Manufacturing Associate, Biopharma & GMP Operations
Overview
Own hands-on manufacturing tasks in a biopharmaceutical GMP setting at scale. You will operate with strong attention to quality, assist in training, and ensure the integrity of batch records. Join a collaborative team in a fully onsite, 12-hour rotating shift in Plainville, MA. This role emphasizes safety, documentation, and adherence to GDP and cleanroom gowning requirements.
What You'll Do10
- 1Build and execute manufacturing tasks following work instructions to produce compliant products
- 2Maintain batch records and inventory accuracy to support traceability
- 3Inspect finished products against specifications and escalate issues promptly
- 4Assist with batch record reconciliation and preventative maintenance activities
- 5Adhere to Quality Management Systems and close Nonconformance/CAPA items
- 6Identify items requiring escalation and communicate with senior operators or management
- 7Maintain a clean, safe work environment and follow PPE protocols
- 8Participate in training to achieve and maintain full training status and support staff training
- 9Follow cGMP and safety standards and adapt to dynamic priorities
- 10Wear PPE and aseptically gown as needed to prevent contamination
Requirements10
- 1High school diploma or equivalent
- 2Minimum of 1 year of work experience in manufacturing, operations, production, lab setting or related field
- 3Experience in a cGMP environment preferred
- 4Technical expertise in biopharmaceutical manufacturing equipment, principles, and processes
- 5Strong understanding of GMP and safety standards
- 6Ability to work in a dynamic environment and balance multiple priorities
- 7Proficiency in learning new software and tools
- 8Ability to make moderately complex GMP manufacturing decisions with limited supervision
- 9Effective written and verbal communication with peers and management
- 10Ability to read, write, and review documentation for GMP compliance
Salary Insight
$27 - $28k per year
Location
Required Skills
Similar open positions
Explore active roles that match your skills and interests.
Tailstorm Health Inc
VerifiedManufacturing Associate, Pharmaceutical & Sterile Processing
Own daily operations of pharmaceutical manufacturing activities at a cGMP facility with emphasis on sterile injectable products. Scale includes cleanroom environments, standard batch records, and adherence to safety and quality systems. Collaborate with Quality, Engineering, and Maintenance to ensure compliant production and timely delivery. This role offers hands-on equipment operation and a strong documentation practice to support process improvements.
Randstad
VerifiedGMP Manufacturing Associate II, Bioprocessing
You will own bioprocessing operations for clinical and commercial production of transformative medicines, working in a GMP environment in Norwood, MA. You will partner with Quality Assurance, Quality Control, Logistics, and Process Development to ensure quality and compliance. This 6-month contract role offers a supportive, team-oriented culture focused on continuous learning and high standards.
external
VerifiedManufacturing Lead, cGMP (Days)
Lead daily cGMP manufacturing operations on a 2-2-3 days rotation (6 AM-6 PM ET), owning process execution and documentation. Coordinate with the shift Supervisor to schedule tasks, allocate resources, and ensure real-time compliance. Coach associates, investigate deviations, and serve as the operational point of contact for your shift. This role is a proven path to Manufacturing Supervisor, with exposure to Trackwise, Delta V, Syncade, and LIMS. You'll drive output for a 24/7 biomanufacturing site, directly impacting life-saving therapies.
Haemonetics Corp.
VerifiedGMP Manufacturing Associate, Cleanroom Operations
You will support production of high-quality medical devices, operating equipment, packing finished products, and resolving basic equipment faults through HMI screens. You will follow GMP and GDP standards in a cleanroom environment, while collaborating with Quality and Engineering teams to meet production goals. This role offers hands-on experience in a lean manufacturing setting, with opportunities to contribute to continuous improvement initiatives.
BCForward
VerifiedManufacturing Specialist, Pharmaceutical Operations
You will support manufacturing readiness, process improvements, and compliance in a regulated biologics environment at Hillsboro, OR. You own technical changes, deviations, and CAPA execution across a 10-month contract with a leading life sciences client. Collaborate with Manufacturing, Quality, and Engineering teams to drive process capability and reliability. This role offers direct impact on aseptic operations and root cause analysis in a fast-paced production setting.
System One
VerifiedManufacturing Associate, Biopharmaceutical Manufacturing
Own biopharmaceutical manufacturing operations at a Novato site, applying mammalian cell culture and purification techniques to produce bulk drug substance. Collaborate with a cross-functional team in a cGMP environment to support process optimization and technology transfer. This contract role offers $28.00/hr plus shift differential, with a Sunday-Tuesday schedule and alternating Wednesdays, providing a unique work-life balance.