Lab Operations Specialist, GMP & Lab Ops in Cambridge
Overview
Own sample management and laboratory operations within a GMP environment at scale in Cambridge. You will manage sample accessioning, inventory, data entry, and cleanroom activities across multiple departments. You will collaborate with lab, manufacturing, and quality teams to maintain documentation accuracy and regulatory compliance. This role blends hands-on material handling with data integrity and process adherence to support manufacturing and quality goals.
What You'll Do10
- 1Build and manage sample accessioning, tracking, and documentation to ensure chain-of-custody accuracy.
- 2Enter and maintain sample information in ERP and quality systems to support compliance and traceability.
- 3Assist with laboratory operations including material handling, inventory control, and media preparation.
- 4Transport materials and samples across lab and manufacturing areas to maintain workflow efficiency.
- 5Support cleanroom operations including gowning and contamination-control practices.
- 6Maintain accurate records using Excel and electronic systems to support audits and reporting.
- 7Monitor inventory levels and perform ERP-based inventory control tasks with RF scanning.
- 8Collaborate with laboratory, manufacturing, and quality teams to optimize throughput and compliance.
- 9Perform biopsy accessioning and related documentation activities with precision.
- 10Support data entry and documentation efforts across programs to sustain GMP adherence.
Requirements7
- 1High School Diploma or Associate Degree
- 2Minimum of 4 years of experience in a GMP or cGMP environment
- 3Experience with sample management, receiving, accessioning, or laboratory operations
- 4Strong data entry and documentation skills with high accuracy
- 5Proficiency in Microsoft Excel and electronic data management systems
- 6Experience using ERP systems and quality management systems
- 7Ability to manage multiple priorities in a fast-paced environment while maintaining attention to detail
Salary Insight
$50 - $58k per year
Location
Required Skills
Similar open positions
Explore active roles that match your skills and interests.
Kelly Services
VerifiedDocument Control Assistant, GMP Manufacturing & GLIMS
You will coordinate production sampling, batch documentation, and GLIMS data entry to support GMP manufacturing in Durham, NC. You will ensure accurate batch record review, sample handoffs, and timely batch release. Work onsite 5 days a week alongside cross-functional teams to meet production and quality targets. This role stands out for its hands-on exposure to PAS-X and LIMS systems in a regulated pharmaceutical environment.
Actalent
VerifiedLab Operations Specialist Actalent
Lab Operations Specialist at Actalent in San Francisco, California. This contract-to-hire role involves managing laboratory inventory, collaborating with cross-functional teams, and ensuring compliance with GMP standards while supporting research outcomes.
Labcorp
VerifiedMaterials Management Specialist Labcorp
Labcorp seeks a Materials Management Specialist to lead inventory processes in Baltimore MD. This role drives physical allocations and record keeping for reagent and consumable stock while overseeing shipping and expiry monitoring. The specialist will act as SME for audits and support new product development initiatives.
Lancesoft INC
VerifiedQuality Control Analyst, Biochemistry & GMP Lab
You will own document authoring and revision for GMP raw materials testing in a biochemistry lab at LanceSoft. You will execute experiments and procedures with limited supervision, ensuring compliance with regulatory standards. This role sits on the QC Raw Materials team, supporting daily operations for manufacturing release. You will drive instrument and method projects from initiation to documentation, collaborating with biochem staff and lab managers. The work directly impacts product quality and regulatory readiness, offering hands-on experience with Matlab and chemometric software.
RoslinCT US
VerifiedCell Processing Associate I Boston
Join RoslinCT as a Cell Processing Associate I to lead manufacturing processes for cell therapies. This role drives production in an ISO V and VII cleanroom environment. You will collaborate across teams to ensure compliance and deliver high-quality clinical materials.
Lantheus Contractors
VerifiedQC Lab Services Analyst, Radiopharmaceuticals & GMP Compliance
QC Lab Services Analyst will own daily lab operations at our Springfield NJ site, ensuring accurate sample tracking, materials management, and regulatory compliance for radiopharmaceutical processes. You will join a cross functional team supporting continuous improvement, workflow optimization, and partner with Quality, Operations, and Facilities. This role emphasizes on site presence five days a week and attention to GMP GLP OSHA standards. What makes this role different is the opportunity to contribute to a fast paced lab services function within a leading radiopharmaceutical company.