Associate Buyer/Planner
San Carlos, CA
W2 Contract to Possible Hire
$28/hr
Please scroll to the bottom of this posting to review an important Candidate Safety & Fraud Awareness Disclaimer from TCWGlobal.
We are seeking a highly organized and detail-oriented Associate Buyer/Planner to support our growing reagent manufacturing operations. This role is responsible for purchasing, material planning, receiving, inventory control, and ERP data management to ensure uninterrupted supply of materials required for reagent production.
The successful candidate will play a critical role in supporting manufacturing by managing raw materials, reagents, consumables, and packaging components while maintaining inventory accuracy and supplier performance. This position is ideal for someone who enjoys working across procurement, planning, warehouse operations, and ERP systems in a fast-paced biotechnology environment.
Responsibilities
Maintain supplier pricing, lead times, and purchasing parameters within NetSuite.Plan and manage inventory to support reagent manufacturing schedules and customer demand.Utilize NetSuite MRP to generate and execute purchasing and replenishment plans.Create and manage purchase orders for raw materials, reagents, consumables, and packaging components.Monitor supplier deliveries, open orders, and lead times to ensure on-time material availability.Receive, inspect, and process incoming materials, chemicals, reagents, and laboratory supplies and verify shipments against purchase orders, packing slips, and Certificates of Analysis (CoA).Coordinate incoming inspection and release activities with Quality and Manufacturing teams.Manage temperature-sensitive shipments including ambient, refrigerated, frozen, and dry-ice materials.Maintain accurate item master records and inventory data within NetSuite.Manage material attributes including units of measure, lead times, storage conditions, and supplier information.Ensure data integrity across purchasing, planning, inventory, and manufacturing modules.Generate inventory, purchasing, and supplier performance reports to support business decisions.Assist with internal and external audits and support compliance with quality system requirements.
Required Qualifications
Associate's or bachelor’s degree in supply chain, Operations, Business, Life Sciences, or related field.3+ years of experience in purchasing, inventory control, material planning, receiving, or supply chain operations.Deep understanding of inventory control methodologies (cycle counting, ABC analysis)Experience working in biotechnology, life sciences, diagnostics, pharmaceutical, or medical device manufacturing environments.Hands-on experience with ERP systems, preferably NetSuite.Strong understanding of inventory control, MRP, and purchasing processes.Experience handling lot-controlled and expiration-controlled materials.Strong analytical, organizational, and problem-solving skills.Identify system and process gaps; implement scalable solutionsAbility to work independently and collaborate across multiple departments.
TCWGlobal is an equal opportunity employer. We do not discriminate based on age, ethnicity, gender, nationality, religious belief, or sexual orientation.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Important Candidate Safety Notice
This position has been verified and officially approved by TCWGlobal.
Please be aware that fraudulent recruiters and fake job postings may attempt to impersonate legitimate companies online. For your protection:
Only trust communication from verified TCWGlobal representativesEnsure a TCWGlobal recruiter is present on all official phone or video interviewsTCWGlobal will never request payment, gift cards, cryptocurrency, or sensitive banking information during the hiring processDo not share sensitive personal information with unverified individuals or suspicious third partiesIf you are unsure whether a posting or recruiter is legitimate, we encourage you to verify active opportunities directly through https://www.tcwglobal.com/client-jobs or by contacting hello@tcwglobal.comTCWGlobal is committed to protecting candidates and maintaining a safe, transparent, and professional hiring experience.
Read LessSupply Chain Buyer (Direct Materials, SAP) – $37.30–$45/hr | Onsite M–F | 3-Month Assignment
Are you a detail-driven procurement professional who thrives in fast-paced manufacturing environments? This is an opportunity to step into a critical supply chain role where your work directly impacts production continuity, supplier performance, and operational efficiency.
In this role, you’ll take ownership of purchasing direct materials that keep manufacturing moving—partnering cross-functionally with planning, scheduling, and suppliers to ensure the right materials arrive at the right time, every time.
What You’ll Do
Manage end-to-end purchasing activities for direct materials supporting manufacturing operationsPlace and track purchase orders through SAP to meet production and inventory requirementsProactively manage supplier relationships to ensure on-time delivery, quality, and performanceMonitor inventory levels and adjust purchasing strategies to align with production demandsIdentify and resolve supply chain disruptions, shortages, and delivery risksPartner with scheduling and production teams to expedite materials when neededResolve invoice discrepancies and coordinate with internal teams to prevent delaysSupport supplier audits and business reviews to drive continuous improvementProcess return-to-vendor (RTV) transactions for non-conforming materialsMaintain accurate purchasing records, documentation, and system dataIdentify opportunities to improve purchasing efficiency and streamline workflows
What You Bring
Bachelor’s degree in Supply Chain, Business, Logistics, or related field (or equivalent experience)1–3 years of experience in purchasing, procurement, or production planning within a manufacturing environmentHands-on experience issuing purchase orders and expediting materialsStrong understanding of MRP-driven purchasing processesExperience working in SAP or similar ERP systemsSolid Excel and Microsoft Office skillsAbility to manage multiple priorities and solve problems proactivelyStrong communication skills with the ability to collaborate across teams and with suppliers
Nice to Have
Exposure to CPM and/or CPIM certification courseworkExperience supporting supplier performance reviews or auditsBackground in regulated or quality-driven manufacturing environments
Why This Role Stands Out
Direct impact on production success and supply continuityHigh visibility across supply chain, operations, and supplier networkOpportunity to strengthen SAP and MRP-driven procurement experienceFast-paced environment where your problem-solving skills will be highly valuedIf you’re someone who enjoys owning the purchasing process, building strong supplier partnerships, and keeping operations running smoothly, this is a great opportunity to make an immediate impact.
TCWGlobal is an equal opportunity employer. We do not discriminate based on age, ethnicity, gender, nationality, religious belief, or sexual orientation.
Supervisor, Factory Service Engineer
Full Time, Direct Hire
Monday-Friday 7am-4:30pm or 6pm-6am (5 Days On/5 Days Off)
Bridgewater, NJ
$60-70/hr
Please scroll to the bottom of this posting to review an important Candidate Safety & Fraud Awareness Disclaimer from TCWGlobal.
We are seeking an experienced, hands-on Supervisor, Factory Service Engineer to lead the Night Shift Factory Service Engineering team at our Bridgewater, NJ Smart Factory.
This role is responsible for supporting the reliability, performance, and GMP compliance of our cell therapy manufacturing equipment and associated process equipment. The Supervisor will provide day-to-day leadership to Factory Service Engineers responsible for preventive maintenance, corrective maintenance, calibration, repair, troubleshooting, qualification, retrofits, upgrades, and End of Line testing.
This is a hands-on leadership role requiring strong technical troubleshooting skills, GMP equipment support experience, and the ability to mentor and manage a technical team in a fast-paced, mission-driven manufacturing environment.
Key Responsibilities
Supervise daily Night Shift Factory Service Engineering activities, including workload planning, shift coverage, scheduling, mentorship, and performance feedback.Serve as the primary technical escalation point for complex equipment failures, troubleshooting issues, and maintenance challenges during Night Shift.Oversee preventive maintenance, corrective maintenance, repairs, calibrations, retrofits, upgrades, qualifications, and End of Line testing on Cell Shuttle and process equipment.Ensure all maintenance and service activities comply with GMP standards, regulatory requirements, SOPs, and internal procedures.Review and approve maintenance documentation, equipment logs, and CMMS entries for accuracy and completeness.Partner with Quality, Manufacturing, Engineering, Procurement, and Inventory teams to support compliance, uptime, parts availability, vendor coordination, and issue resolution.Lead or support equipment-related Change Controls, CAPA investigations, and deviation reports.Author, review, and maintain SOPs and Work Instructions for maintenance and service activities.Ensure tools and test equipment are properly maintained, calibrated, and safe for use.Drive continuous improvement initiatives to reduce downtime, improve reliability, and increase service team efficiency.Facilitate shift handovers and escalate critical equipment issues to the Manager, Factory Service Engineering.Support onboarding, technical training, and ongoing development of Factory Service Engineers.Participate in and help manage the after-hours on-call rotation through PagerDuty.Stay current on GMP best practices, equipment advancements, and industry trends to support team development and operational excellence.
Requirements
Bachelor’s degree or equivalent experience in Engineering or a related technical field.5+ years of experience in a GMP manufacturing environment, preferably in cell therapy, biopharmaceuticals, or advanced biomanufacturing.2+ years in a lead, senior, or supervisory role overseeing technical or engineering personnel.Strong understanding of GMP regulations and quality standards related to cell therapy or bioprocessing equipment.Experience serving as a technical or service lead on multi-subsystem equipment installations and qualifications.Strong troubleshooting and repair experience with complex automated manufacturing equipment.Ability to read and interpret technical documents, schematics, and engineering drawings.Experience using a CMMS and maintaining accurate maintenance documentation.Strong organizational, prioritization, communication, and documentation skills.Proven ability to lead, coach, and develop team members in a fast-paced operational environment.Ability to collaborate effectively with Quality, Manufacturing, Engineering, Procurement, Inventory, and other cross-functional teams.Detail-oriented, compliance-focused, and committed to high-quality standards.Must be able to work full-time Night Shift, including weekends and holidays as required to support business needs.Must be onsite at the Bridgewater plant; onsite attendance is an essential function of the role.Must be able to lift and carry up to 50 lbs.Strong verbal, written, organizational, presentation, and interpersonal skills.Demonstrates self-awareness, integrity, authenticity, and a growth mindset.
Nice to Have
Experience with PLC automated control systems.Experience with 6-axis robots.Experience working safely with 208V high-voltage systems.Experience with Blue Mountain CMMS.Prior supervisory experience in a cell therapy or advanced biomanufacturing facility.
TCWGlobal is an equal opportunity employer. We do not discriminate based on age, ethnicity, gender, nationality, religious belief, or sexual orientation.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Important Candidate Safety Notice
This position has been verified and officially approved by TCWGlobal.
Please be aware that fraudulent recruiters and fake job postings may attempt to impersonate legitimate companies online. For your protection:
Only trust communication from verified TCWGlobal representativesEnsure a TCWGlobal recruiter is present on all official phone or video interviewsTCWGlobal will never request payment, gift cards, cryptocurrency, or sensitive banking information during the hiring processDo not share sensitive personal information with unverified individuals or suspicious third partiesIf you are unsure whether a posting or recruiter is legitimate, we encourage you to verify active opportunities directly through https://www.tcwglobal.com/client-jobs or by contacting hello@tcwglobal.comTCWGlobal is committed to protecting candidates and maintaining a safe, transparent, and professional hiring experience.
Read LessOffice Security Coordinator
Location: San Francisco, CA (SF HQ – Onsite | Local SF candidates within commuting distance)
Pay Rate: $26–$28/hr (commensurate with experience)
Schedule: Monday – Friday, 8:00 AM – 5:00 PM
Duration: 6 months (possible extension)
This role requires experience working in a corporate setting in a customer-facing / front office capacity.
Please scroll to the bottom of this posting to review an important Candidate Safety & Fraud Awareness Disclaimer from TCWGlobal.
About The Role
We are looking for a reliable, professional, and security-minded Office Security Coordinator to support our San Francisco headquarters. This role serves as the primary point of contact for all visitor management and front-of-house security operations, and requires someone calm under pressure, polished, and deeply committed to creating a safe and welcoming environment for employees and guests. This is a fully onsite role and requires consistent attendance, professionalism, and strong communication skills.
What You’ll Do
• Greet and assist all visitors, candidates, and external guests; manage lobby flow and ensure a warm, professional first impression
• Verify guest identity and manage visitor check-in in accordance with SB 553 and Cal/OSHA IIPP requirements
• Coordinate with employees ahead of scheduled visits to ensure seamless arrivals
• Administer access control via Brivo, including badge provisioning, deactivation, and audit support
• Maintain visitor logs and support periodic SB 553 compliance documentation and reporting
• Serve as the day-of point of contact for building security coordination and escalations
• Partner with the Workplace team on office events requiring guest access planning
• Work with the building on evacuation plans and disaster management protocols
What We’re Looking For
• 1–3 years of experience in a front desk, security, facilities, or hospitality role
• Familiarity with access control systems (Brivo or similar) – or coachable and eager to learn
• Strong interpersonal skills – you default to “yes, and how can I help?”
• Calm under pressure; able to de-escalate situations professionally
• Working knowledge of, or willingness to learn, California SB 553 requirements
• Reliable, punctual, and detail-oriented
• Basic Google Suite proficiency (Gmail, Calendar, Drive)
Nice to Have
• Experience in a fast-paced tech office or co-working environment
• CPR/First Aid certified
• Familiarity with visitor management software
TCWGlobal is an equal opportunity employer. We do not discriminate based on age, ethnicity, gender, nationality, religious belief, or sexual orientation.
Important Candidate Safety Notice
This position has been verified and officially approved by TCWGlobal.
Please be aware that fraudulent recruiters and fake job postings may attempt to impersonate legitimate companies online. For your protection:
Only trust communication from verified TCWGlobal representativesEnsure a TCWGlobal recruiter is present on all official phone or video interviewsTCWGlobal will never request payment, gift cards, cryptocurrency, or sensitive banking information during the hiring processDo not share sensitive personal information with unverified individuals or suspicious third partiesIf you are unsure whether a posting or recruiter is legitimate, we encourage you to verify active opportunities directly through https://www.tcwglobal.com/client-jobs, or by contacting hello@tcwglobal.comTCWGlobal is committed to protecting candidates and maintaining a safe, transparent, and professional hiring experience.
Title: Digital Content Programmer - Fitness Experiences (Contract)
Location: Cupertino, CA (Hybrid)
Pay Rate: $41 - $46/hr
Duration: 12-month assignment
Please scroll to the bottom of this posting to review an important Candidate Safety & Fraud Awareness Disclaimer from TCWGlobal.
Summary:
We are seeking an Editorial Programmer to support the programming and delivery of digital fitness and wellness content across mobile, tablet, and connected TV platforms. In this role, you will execute weekly content plans, manage editorial programming within a content management system (CMS), and ensure digital content is accurately published and optimized for customers.
This position requires a highly organized individual with experience in digital content programming, online media, or eCommerce. The ideal candidate is detail-oriented, enjoys working with technology, and thrives in a collaborative, fast-paced environment while partnering with content, engineering, marketing, design, and production teams.
What You'll Do:
· Program and publish weekly digital fitness and wellness content using internal content management systems
· Execute editorial content plans across mobile, tablet, and connected TV platforms
· Manage the timely publication of workouts, guided meditations, featured collections, instructor content, and other editorial initiatives
· Ensure content assets, metadata, imagery, and supporting deliverables are complete, accurate, and published on schedule
· Collaborate with content, production, business, marketing, engineering, and design teams to support new content launches and ongoing programming initiatives
· Partner with engineering teams to improve internal content management systems, publishing tools, and editorial workflows
· Support testing and validation of new platform features by programming content within development and testing environments
· Monitor content quality and recommend enhancements that improve the customer experience
· Track project timelines, priorities, and deliverables while managing multiple concurrent initiatives
· Identify opportunities to improve operational efficiency, publishing workflows, and content management processes
What You Bring:
· Bachelor's degree or equivalent professional experience
· 3+ years of experience in digital content programming, online media, eCommerce, digital publishing, or editorial operations
· Experience working with content management systems (CMS) and digital publishing platforms
· Strong organizational skills with the ability to prioritize multiple projects in deadline-driven environments
· Excellent communication and cross-functional collaboration skills
· Experience working with web-based production tools and digital publishing technologies
· Strong attention to detail with a focus on content accuracy and quality assurance
· Ability to work independently while managing competing priorities
· Passion for digital fitness, wellness, health, or consumer content experiences
Bonus Points If You Have:
· Experience supporting subscription-based digital products or consumer content platforms
· Experience working with metadata management and digital asset workflows
· Familiarity with CMS optimization, editorial workflows, or content operations
· Experience collaborating with engineering teams on publishing tools or platform enhancements
· Interest in fitness, wellness, meditation, or health-focused digital products
TCWGlobal is an equal opportunity employer. We do not discriminate based on age, ethnicity, gender, nationality, religious belief, or sexual orientation.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Important Candidate Safety Notice
This position has been verified and officially approved by TCWGlobal.
Please be aware that fraudulent recruiters and fake job postings may attempt to impersonate legitimate companies online. For your protection:
• Only trust communication from verified TCWGlobal representatives
• Ensure a TCWGlobal recruiter is present on all official phone or video interviews
• TCWGlobal will never request payment, gift cards, cryptocurrency, or sensitive banking information during the hiring process
• Do not share sensitive personal information with unverified individuals or suspicious third parties
• If you are unsure whether a posting or recruiter is legitimate, we encourage you to verify active opportunities directly through https://www.tcwglobal.com/client-jobs or by contacting hello@tcwglobal.com
TCWGlobal is committed to protecting candidates and maintaining a safe, transparent, and professional hiring experience.
Warehouse Associate
Monday-Friday 8am-5pm
Long Beach, CA
$20/hr
Please scroll to the bottom of this posting to review an important Candidate Safety & Fraud Awareness Disclaimer from TCWGlobal.
We are seeking a Warehouse Associate I to join our team. This person is responsible for all general warehouse activities, including but not limited to Receiving, Unpacking, Material Handling Activities and Shipping.
What you’ll do:
Primary Responsibilities:
Pack customer orders while verifying part number, qty and condition of each line item on packing slips, BOL’s Stock materials in their respective inventory locations Picking inventory and prepare customer orders for shipment Maintain the workplace and warehouse in a neat, clean and orderly condition Performs other duties as assigned
What you need to know:
Experience/Skills/Education:
Required:
Must be able to speak, read and write English Ability to lift up to 55lbs unassisted Basic Math Skills Required
Desired:
Previous warehouse experienceTCWGlobal is an equal opportunity employer. We do not discriminate based on age, ethnicity, gender, nationality, religious belief, or sexual orientation.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Important Candidate Safety Notice
This position has been verified and officially approved by TCWGlobal.
Please be aware that fraudulent recruiters and fake job postings may attempt to impersonate legitimate companies online. For your protection:
• Only trust communication from verified TCWGlobal representatives
• Ensure a TCWGlobal recruiter is present on all official phone or video interviews
• TCWGlobal will never request payment, gift cards, cryptocurrency, or sensitive banking information during the hiring process
• Do not share sensitive personal information with unverified individuals or suspicious third parties
• If you are unsure whether a posting or recruiter is legitimate, we encourage you to verify active opportunities directly through https://www.tcwglobal.com/client-jobs or by contacting hello@tcwglobal.com
TCWGlobal is committed to protecting candidates and maintaining a safe, transparent, and professional hiring experience.
GMP Production Support Engineer
Full Time, Direct Hire
Monday-Friday 7am-4:30pm OR 6pm-6am (5 days on/5 days off)
Bridgewater, NJ
$40-50/hr + Benefits
Please scroll to the bottom of this posting to review an important Candidate Safety & Fraud Awareness Disclaimer from TCWGlobal.
Position Summary
We are seeking Factory Service Engineers to support fully automated gene and cell therapy manufacturing platforms. These systems are actively running patient products in a GMP cell therapy manufacturing environment.
This role is focused on keeping the process running, identifying issues quickly, performing basic equipment troubleshooting, and clearly communicating what is happening on the production floor. The ideal candidate has GMP manufacturing, process support, MSAT, biotech/pharma production, or equipment support experience, plus enough hands-on mechanical ability to troubleshoot basic equipment issues.
What You’ll Do
Support gene therapy systems that are already built and processing patient cartridgesMonitor equipment and process performance during production runsIdentify process or equipment issues and communicate observations clearly to technical teamsPerform basic hands-on troubleshooting, including loose cables, sensor adjustments, simple mechanical issues, and equipment alarmsSupport preventive maintenance, repairs, calibration, and troubleshooting activitiesWork with manufacturing, quality, engineering, and service teams to resolve production issuesDocument maintenance, troubleshooting, and support activities in a GMP-compliant mannerSupport change controls, CAPA investigations, SOPs, and work instructions as neededParticipate in training to learn gene and cell therapy manufacturing platforms and process flowSupport after-hours/on-call needs as required for GMP operations
What We’re Looking For
Bachelor’s degree in engineering, life sciences, or related field, or equivalent technical experience3+ years of experience in GMP manufacturing, biotech, pharma, cell therapy, or regulated production supportStrong process understanding; able to recognize when a process is not running as expectedBasic hands-on mechanical aptitude and troubleshooting abilityAbility to clearly explain what you are seeing so engineers or technical teams can resolve the issueExperience supporting automated manufacturing equipment, process equipment, or production systemsStrong documentation skills and understanding of GMP expectationsComfortable working in a fast-paced manufacturing environment where patient product is involvedAble to lift up to 50 lbs and work onsite in Bridgewater, NJ
Strong Backgrounds for This Role
Process TechnicianManufacturing TechnicianManufacturing Associate with strong equipment/process experienceMSAT AssociateBioprocess TechnicianGMP Production Support TechnicianEquipment Support EngineerMaintenance Technician from pharma, biotech, or medical deviceCell therapy or gene therapy manufacturing technician
Nice to Have
Cell therapy, gene therapy, or biologics manufacturing experienceExperience with automated GMP manufacturing equipmentExperience with CMMS systems such as Blue Mountain, Maximo, SAP PM, or eMaintExperience with deviations, CAPAs, change controls, SOPs, and GMP documentationBasic electrical or mechanical troubleshooting experienceTCWGlobal is an equal opportunity employer. We do not discriminate based on age, ethnicity, gender, nationality, religious belief, or sexual orientation.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Important Candidate Safety Notice
This position has been verified and officially approved by TCWGlobal.
Please be aware that fraudulent recruiters and fake job postings may attempt to impersonate legitimate companies online. For your protection:
• Only trust communication from verified TCWGlobal representatives
• Ensure a TCWGlobal recruiter is present on all official phone or video interviews
• TCWGlobal will never request payment, gift cards, cryptocurrency, or sensitive banking information during the hiring process
• Do not share sensitive personal information with unverified individuals or suspicious third parties
• If you are unsure whether a posting or recruiter is legitimate, we encourage you to verify active opportunities directly through https://www.tcwglobal.com/client-jobs or by contacting hello@tcwglobal.com
TCWGlobal is committed to protecting candidates and maintaining a safe, transparent, and professional hiring experience.
Factory Service Engineer, Installation
W2 Contract to Hire
Monday-Friday 7am-4:30pm
Bridgewater, NJ
$40-50/hr + Benefits
Please scroll to the bottom of this posting to review an important Candidate Safety & Fraud Awareness Disclaimer from TCWGlobal.
Position Summary
We are seeking hands-on Factory Service Engineers to support the build, installation, commissioning, and testing of fully automated gene and cell therapy manufacturing platforms.
This role is ideal for someone with strong mechanical, electrical, robotics, equipment assembly, or machine-build experience who enjoys building complex systems from the ground up. You will work closely with senior engineers to assemble and test highly customized equipment used in GMP cell therapy manufacturing.
What You’ll Do
Build, assemble, install, and commission gene and cell therapy manufacturing platforms and related equipmentFollow CAD drawings, schematics, work instructions, and detailed build documentationSupport equipment start-up, end-of-line testing, functional checks, and troubleshootingTest BPS and SLTS instruments before they are installed into the gene and cell therapy manufacturing platforms.Identify and correct issues such as loose connections, assembly errors, alignment problems, or shipping-related damageUse hand tools and test equipment such as Allen wrenches, sockets, box/open-end wrenches, hammer drills, torque wrenches, multimeters, Loctite, and anti-seizeSupport equipment upgrades, retrofits, preventative maintenance, and repairs as neededMaintain accurate documentation in a GMP environmentWork under senior technical leads while learning custom equipment and build process
What We’re Looking For
Bachelor’s degree in engineering or related field, or equivalent hands-on technical experience3+ years of experience with complex equipment, automation, robotics, mechanical/electrical systems, or manufacturing equipmentStrong hands-on mechanical aptitude and comfort using toolsAbility to read and follow schematics, CAD drawings, technical drawings, and assembly instructionsHigh attention to detail; comfortable working to tight tolerancesExperience troubleshooting mechanical, electrical, robotic, or automated equipment issuesStrong documentation and communication skillsComfortable working in a regulated GMP manufacturing environmentAble to lift up to 50 lbs and work onsite in Bridgewater, NJ
Nice to Have
Experience with PLC-controlled systemsExperience with 6-axis robotsExperience working around 208V systemsGMP, biotech, pharma, cell therapy, or medical device manufacturing experienceExperience with Blue Mountain or another CMMS
Strong Backgrounds for This Role
Electrical EngineerMechanical EngineerRobotics EngineerElectricianField Service EngineerAutomation TechnicianEquipment Installation EngineerMachine BuilderControls TechnicianCNC / robotics / complex equipment technicianData center buildout or infrastructure technician with strong hands-on skillsTCWGlobal is an equal opportunity employer. We do not discriminate based on age, ethnicity, gender, nationality, religious belief, or sexual orientation.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Important Candidate Safety Notice
This position has been verified and officially approved by TCWGlobal.
Please be aware that fraudulent recruiters and fake job postings may attempt to impersonate legitimate companies online. For your protection:
• Only trust communication from verified TCWGlobal representatives
• Ensure a TCWGlobal recruiter is present on all official phone or video interviews
• TCWGlobal will never request payment, gift cards, cryptocurrency, or sensitive banking information during the hiring process
• Do not share sensitive personal information with unverified individuals or suspicious third parties
• If you are unsure whether a posting or recruiter is legitimate, we encourage you to verify active opportunities directly through https://www.tcwglobal.com/client-jobs or by contacting hello@tcwglobal.com
TCWGlobal is committed to protecting candidates and maintaining a safe, transparent, and professional hiring experience.
Title: Clinical Laboratory & Diagnostics Specialist (2nd Shift)
Payrate: $30-32/hour
Duration: 1-year contract (Excellent potential for permanent)
Hours: Full-time | Monday-Friday | 3pm-11:30pm
Start Date: ASAP
Location: Irvine, CA 92618 (Onsite - Local candidates only)
Summary:
Ready to be part of a global mission to help people live longer, healthier lives? Join a world-class team of innovators, leaders, and problem solvers who develop state-of-the-art instruments and reagents for life science research laboratories and healthcare facilities worldwide. As a Clinical Laboratory & Diagnostics Specialist on our 2nd shift team, you'll play a crucial role in supporting finished product testing and release of company controls. Working in our Quality Control department, you'll combine technical expertise with collaborative teamwork to ensure the highest standards in clinical diagnostic testing. If you're passionate about precision, thrive in a fast-paced lab environment, and want to make a real impact on global healthcare, this is your opportunity to shine.
What You'll Do:
Operate, maintain, calibrate, and troubleshoot clinical diagnostic laboratory instruments with precision and expertiseFollow good laboratory practices (GLP) and good documentation practices (GDP) to ensure compliance and qualityWork collaboratively with team members to achieve daily testing goals and objectivesEvaluate assay runs for accuracy and acceptability according to Quality Control proceduresEnter results into appropriate software and database systems with attention to detailOrder supplies required for testing on assigned instrumentation to maintain seamless operationsSupport finished product testing and release of company controls during 2nd shift operationsPerform daily maintenance and troubleshooting on clinical diagnostic instrumentationWhat You Bring:
Associate's degree or higher in science field or equivalent clinical lab experience2+ years of experience in clinical laboratory and diagnostics settingExperience performing daily maintenance of instrumentation or relevant school experienceFamiliarity with clinical laboratory instruments from manufacturers like Beckman, Roche, Siemens, or AbbottAbility to operate, maintain, calibrate, and troubleshoot clinical diagnostic lab instrumentsExcellent multitasking and organizational skills in fast-paced environmentsBasic knowledge of Microsoft Excel, Outlook, and WordStrong attention to detail and commitment to quality standardsBonus Points If You Have:
Experience running chemistry/immunoassay/immunology analyzers and/or ELISAsKnowledge of LIMS (Laboratory Information Management System)Advanced certifications in clinical laboratory technologyExperience with regulatory compliance in clinical settingsBackground in quality control or quality assurance processesMake a meaningful impact on global healthcare while advancing your career in a cutting-edge laboratory environment. With competitive hourly pay, weekly pay, and comprehensive benefits, plus excellent potential for permanent placement, you'll have the foundation to excel in this vital role. Apply now to become our next Clinical Laboratory & Diagnostics Specialist and help us continue our mission of improving lives worldwide.
TCWGlobal is an equal opportunity employer. We do not discriminate based on age, ethnicity, gender, nationality, religious belief, or sexual orientation.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
**Important Candidate Safety Notice**
This position has been verified and officially approved by TCWGlobal.
Please be aware that fraudulent recruiters and fake job postings may attempt to impersonate legitimate companies online. For your protection:
• Only trust communication from verified TCWGlobal representatives
• Ensure a TCWGlobal recruiter is present on all official phone or video interviews
• TCWGlobal will never request payment, gift cards, cryptocurrency, or sensitive banking information during the hiring process
• Do not share sensitive personal information with unverified individuals or suspicious third parties
• If you are unsure whether a posting or recruiter is legitimate, we encourage you to verify active opportunities directly through https://www.tcwglobal.com/client-jobs, or by contacting hello@tcwglobal.com
TCWGlobal is committed to protecting candidates and maintaining a safe, transparent, and professional hiring experience.
