Director Operational Readiness Position Summary CRB is looking for an energetic self-motivated individual for the role of Director Operational Readiness. The Director will lead cross-functional teams in the integration and delivery of Operational Readiness services (Turnover CQV and Startup Operations) on capital projects for our Life Science Food Beverage Semi-Conductor and Data Center clients. Their main focus will be to become a business partner with Clients in achieving a Make Product Faster mindset which enables licensable facilities to be production online sooner utilizing risk-based and lifecycle methodologies. This role will also include helping clients navigate through regulatory requirements devising and executing strategies that meets timelines and assessing / mitigating risk all while driving leaner processes to achieve the end goal. The Director will provide oversight guidance and team formation for all regional projects from business development to proposal stage to facility turnover. This position requires a high level of organization communication and leadership; and the qualified candidate will have excellent interpersonal skills with internal and external clients. They will represent CRB in a professional manner assist in winning work and understand how their strategy directly impacts our collective success. Responsibilities Maintain PL responsibilities for business team and accountable to achieve Regional Team Revenue and Profit goals Coordinate/collaborate with Regional leadership in business development and account management on Market Focus Trends and developing New Client Solutions Lead and Support the Operational Readiness approach internally and externally with clients Design Operations Quality and Regulatory teams Manage regulatory reviews be part of operational design reviews develop overall risk-based approach for testing/documentation Active management of internal and/or external Operational Readiness resources on projects Lead the development of specific Turnover Operation and CQV plans to ensure integration with design automation and construction plans Work with Construction and Digital Innovation to deliver streamlined data management across various platforms Manage our partners and/or build a group to execute the integrated delivery strategy Develop and maintain relationships with ley stakeholders for successful projection execution Collaborate/Support the Digital Innovation team in the delivery of project data to Clients using best practices and AI integration Future assist in regulatory filings and agency reviews; operational training/staffing for clients Knowledge of US FDA (21 CFR) ISO 9001 and EU EMEA regulations Knowledge of primary industry guidance on CQV and CSV including but not limited to: ISPE Baseline Guide 5 Commissioning and Qualification edition 2 ISPE GAMP V A Risk Based Approach to Compliant GMP Computerized Systems ASTM E2500 Standard Guide for Specification Design and Verification of Pharmaceutical and Biopharmaceutical Manufacturing Systems and Equipment ISPE Guideline Science and Risk-based Approach for the Delivery of Facilities Systems and Equipment 2011 ISPE Good Practice Guide Applied Risk Management for Commissioning and Qualification 2011 Qualifications : Bachelors Degree in Architecture Engineering Life Sciences Construction Management or similar degree preferred or equivalent years of relevant industry experience. Professional licensure strongly preferred. Minimum of 15 years of Commissioning Qualification Validation Compliance and Operations experience in the Life Science industry; Sound technical knowledge of both US and global regulatory requirements . Demonstrated effective leadership financial management and collaboration skills. Interpersonal and leadership skills necessary to communicate clearly and effectively manage qualification/validation activities with all levels of personnel from various disciplines across the organization. Direct experience in producing and managing commissioning qualification and operational deliverables. Familiarity with all phases of design and construction required; direct experience in Life Sciences capital projects preferred. Excellent organizational interpersonal presentation and communication skills. Commitment to technical excellence as well as creating world-class experiences for our clients and employees. Flexible and willing to travel as needed. Expectation of 50% travel initially with eventual expectation of up to 25% travel in support of client projects and regional leadership. Additional Information : All your information will be kept confidential according to EEO guidelines. CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer and it is our policy to provide equal opportunity to all people without regard to race color religion national origin ancestry marital status veteran status age disability pregnancy genetic information citizenship status sex sexual orientation gender identity or any other legally protected category. Employment is contingent on background screening. CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please no phone calls or emails. CRB offers a complete and competitive benefit package designed to meet individual and family needs. If you are unable to complete this application due to a disability contact this employer to ask for an accommodation or an alternative application process. Remote Work : No Employment Type : Full-time Key Skills Computer Science,Operational Risk Management,Risk Management,Six Sigma,Continuous Improvement,Lean,Process Improvement,Pricing,Customer Support,Alteryx,Kaizen,Project Management Lifecycle Experience: years Vacancy: 1
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