Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Electrical Project Manager

Description:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Electrical Project Manager

Description:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Electrical Project Manager

Description:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Electrical Project Manager

Description:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Electrical Project Manager

Description:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Electrical Project Manager

Description:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Electrical Project Manager

Description:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Validation Process Project Manager

Responsibilities:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Validation Process Project Manager

Responsibilities:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Validation Process Project Manager

Responsibilities:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Validation Process Project Manager

Responsibilities:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Validation Process Project Manager

Responsibilities:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Validation Process Project Manager

Responsibilities:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Validation Process Project Manager

Responsibilities:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Validation Process Project Manager

Responsibilities:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Validation Process Project Manager

Responsibilities:

Owner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle). Focus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.Manage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.Change Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity. Deliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.Lead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.Interface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.Reviewing project plans and specifications.Monitoring contractor performance and ensuring adherence to contractual obligations.Conducting regular site walkdowns to review quality and progress.Ensuring compliance with safety regulations and quality standards.Develop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.Work closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.Provide engineering expertise and technical guidance throughout the project lifecycle.Maintain documentation of project activities, plans, designs, reports, and updates.Monitor project costs, manage budgets, and report on financial status.Identify potential risks and develop mitigation strategies to ensure project success.Ensure all project activities meet or exceed industry standards, regulations, and company quality guidelines.Regularly update stakeholders on project progress, challenges, and changes in scope.Address technical issues and project challenges, providing solutions to keep the project on track.

Qualifications:

Bachelor's Degree in Engineering or Science.Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.Experience in direct process / manufacturing areas.Must be fully bilingual (English / Spanish) with excellent oral skills.Must be proficient using MS Windows and Microsoft Office applications.Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.Technical Writing skills and investigations processes.Available to work extended hours, possibility of weekends and holidays. Read Less

Job DescriptionJob DescriptionABOUT US

Falcón Sánchez & Associates, a leading local CPA and Consulting firm, is looking for a talented Tax Manager that will add value to our firm and to our clients. Join us as we provide work-life balance during your experience of growth!

SUMMARY OF RESPONSIBILITIES

We are seeking an experienced Tax Manager to serve as a key liaison between our clients, tax team, and firm leadership. This role is responsible for managing multiple tax engagements across diverse industries in both the United States and Puerto Rico, ensuring high-quality compliance, advisory services, and client satisfaction.

The Tax Manager will lead engagement planning, supervise and develop staff, review complex tax returns, and drive engagement performance, including budgeting, billing, and collections. This role plays a critical part in maintaining technical excellence, strengthening client relationships, and supporting the firm’s growth initiatives.

DUTIES AND RESPONSIBILITIES

Manage the full lifecycle of tax engagements, including planning, execution, review, and delivery.Take ownership of assigned engagements, ensuring responsive communication and high-quality service experience.Lead engagement planning meetings and coordinate resources to meet deadlines.Ensure proper documentation, workpaper quality, and compliance with firm standards and filing requirements. Review complex federal and Puerto Rico tax returns (corporate, partnership, fiduciary, and individual).Provide technical guidance on U.S. and Puerto Rico tax matters, including research, tax memos, and advisory projects.Stay current on tax law changes and proactively identify planning opportunities and risk areas.Maintain responsibility for the overall quality and accuracy of tax compliance and consulting deliverables.Build and maintain strong client relationships and identify opportunities for additional services.Participate in business development and networking activities aligned with firm growth strategies.Collaborate with Partners, Directors, and Operations to address client needs and engagement risks.Support firm initiatives and promote a culture of trust, inclusion, and continuous improvement.Supervise, coach, and mentor Tax Seniors and Associates to ensure timely and accurate results.Provide constructive feedback, performance evaluations, and career development recommendations.Delegate work effectively based on staff skills and engagement needs.Support recruitment efforts, including resume reviews and candidate interviews.Deliver internal training and contribute to the professional development of the tax team.

QUALIFICATIONS

Active CPA license requiredMinimum 3+ years of experience as a Senior Tax Accountant in a public accounting firmStrong technical knowledge of U.S. and Puerto Rico taxationExperience reviewing complex tax returns and managing multiple engagementsProven ability to supervise staff and manage client relationshipsBilingual proficiency (Spanish and English)Advanced skills in tax software and Microsoft OfficeMaster’s degree in Accounting, Taxation, Finance, Economics, or related field (preferred)Experience with tax research tools and workflow management systems Read Less

Job DescriptionJob DescriptionABOUT US

Falcón Sánchez & Associates, a leading local CPA and Consulting firm, is looking for a talented Tax Manager that will add value to our firm and to our clients. Join us as we provide work-life balance during your experience of growth!

SUMMARY OF RESPONSIBILITIES

We are seeking an experienced Tax Manager to serve as a key liaison between our clients, tax team, and firm leadership. This role is responsible for managing multiple tax engagements across diverse industries in both the United States and Puerto Rico, ensuring high-quality compliance, advisory services, and client satisfaction.

The Tax Manager will lead engagement planning, supervise and develop staff, review complex tax returns, and drive engagement performance, including budgeting, billing, and collections. This role plays a critical part in maintaining technical excellence, strengthening client relationships, and supporting the firm’s growth initiatives.

DUTIES AND RESPONSIBILITIES

Manage the full lifecycle of tax engagements, including planning, execution, review, and delivery.Take ownership of assigned engagements, ensuring responsive communication and high-quality service experience.Lead engagement planning meetings and coordinate resources to meet deadlines.Ensure proper documentation, workpaper quality, and compliance with firm standards and filing requirements. Review complex federal and Puerto Rico tax returns (corporate, partnership, fiduciary, and individual).Provide technical guidance on U.S. and Puerto Rico tax matters, including research, tax memos, and advisory projects.Stay current on tax law changes and proactively identify planning opportunities and risk areas.Maintain responsibility for the overall quality and accuracy of tax compliance and consulting deliverables.Build and maintain strong client relationships and identify opportunities for additional services.Participate in business development and networking activities aligned with firm growth strategies.Collaborate with Partners, Directors, and Operations to address client needs and engagement risks.Support firm initiatives and promote a culture of trust, inclusion, and continuous improvement.Supervise, coach, and mentor Tax Seniors and Associates to ensure timely and accurate results.Provide constructive feedback, performance evaluations, and career development recommendations.Delegate work effectively based on staff skills and engagement needs.Support recruitment efforts, including resume reviews and candidate interviews.Deliver internal training and contribute to the professional development of the tax team.

QUALIFICATIONS

Active CPA license requiredMinimum 3+ years of experience as a Senior Tax Accountant in a public accounting firmStrong technical knowledge of U.S. and Puerto Rico taxationExperience reviewing complex tax returns and managing multiple engagementsProven ability to supervise staff and manage client relationshipsBilingual proficiency (Spanish and English)Advanced skills in tax software and Microsoft OfficeMaster’s degree in Accounting, Taxation, Finance, Economics, or related field (preferred)Experience with tax research tools and workflow management systems Read Less

Job DescriptionJob DescriptionAsiste en las operaciones de día a día de la tienda.Supervisa, adiestra y evalúa los empleados a su cargo.Responsable por las ganancias, gastos, dinero en efectivo, inventario y compras de la estación o tienda.Analiza resultados, tendencias operacionales y establece planes de acción proveyendo dirección en las áreas de las oportunidades.Mantiene la documentación requerida por la empresa.Responsable por las auditorías y cumplimiento con las regulaciones estatales y federales.Verifica disponibilidad de los productos y localización de la mercancía en la tienda.Establece relaciones con los clientes y la comunidad en que sirve.Responsable de todo lo relacionado al departamento de “Food Service”, ventas, gastos, control de calidad, manejo de alimentos, procedimientos de “Serv Safe”, entre otros.Responsable de auditar y autorizar los registros de asistencia de su equipo de trabajo, así como notificar y completar la documentación requerida para la aprobación de licencias.Responsable de cumplir con todos los procesos relacionados al manejo de combustible, incluyendo pero sin limitarse a: Cumplir con las normas de la Junta de Calidad ambiental / Manejo u control de inventario de gasolina / Asegurarse del buen funcionamiento de equipos / Áreas de seguridad / Survey de precios / Identificar y estar alerta a cualquier cambio o situación que pueda impactar las ventas en su área; entre otros

Qualifications and Skills

Bachillerato en Administración de Empresas o su equivalente en Experiencia, por lo menos 3 años.

Dominio de Programas de Computadoras como Microsoft Office

Habilidad para aprender y trabajar con sistemas de informacion

Dominio en Controles de Inventario

Excelentes Destrezas Interpersonales

Experiencia en Supervision y Liderazgo

Habilidad para trabajar multiples tareas

Beneficios

Salario + Programa de IncentivoEstipendio para gasolinaPlan MédicoSeguro de VidaLicencia de Vacaciones/EnfermedadPrograma de Consumo de AlimentosPrograma de AdiestramientoOportunidades de Crecimiento Read Less

Job DescriptionJob DescriptionAsiste en las operaciones de día a día de la tienda.Supervisa, adiestra y evalúa los empleados a su cargo.Responsable por las ganancias, gastos, dinero en efectivo, inventario y compras de la estación o tienda.Analiza resultados, tendencias operacionales y establece planes de acción proveyendo dirección en las áreas de las oportunidades.Mantiene la documentación requerida por la empresa.Responsable por las auditorías y cumplimiento con las regulaciones estatales y federales.Verifica disponibilidad de los productos y localización de la mercancía en la tienda.Establece relaciones con los clientes y la comunidad en que sirve.Responsable de todo lo relacionado al departamento de “Food Service”, ventas, gastos, control de calidad, manejo de alimentos, procedimientos de “Serv Safe”, entre otros.Responsable de auditar y autorizar los registros de asistencia de su equipo de trabajo, así como notificar y completar la documentación requerida para la aprobación de licencias.Responsable de cumplir con todos los procesos relacionados al manejo de combustible, incluyendo pero sin limitarse a: Cumplir con las normas de la Junta de Calidad ambiental / Manejo u control de inventario de gasolina / Asegurarse del buen funcionamiento de equipos / Áreas de seguridad / Survey de precios / Identificar y estar alerta a cualquier cambio o situación que pueda impactar las ventas en su área; entre otros

Qualifications and Skills

Bachillerato en Administración de Empresas o su equivalente en Experiencia, por lo menos 3 años.

Dominio de Programas de Computadoras como Microsoft Office

Habilidad para aprender y trabajar con sistemas de informacion

Dominio en Controles de Inventario

Excelentes Destrezas Interpersonales

Experiencia en Supervision y Liderazgo

Habilidad para trabajar multiples tareas

Beneficios

Salario + Programa de IncentivoEstipendio para gasolinaPlan MédicoSeguro de VidaLicencia de Vacaciones/EnfermedadPrograma de Consumo de AlimentosPrograma de AdiestramientoOportunidades de Crecimiento Read Less