Manufacturing Associate II - 12hr Day Shift
About The Position
Discover Impactful Work: You will supply solutions (buffers and media) for upstream and downstream campaigns via GMP Manufacturing. You will drive the operational heartbeat of our manufacturing plant by ensuring our cleanrooms are flawlessly staged and supplied. Your impact will be felt daily through the precise staging and kitting of single-use assemblies, raw materials, and sterile components required for complex upstream and downstream manufacturing. By maintaining rigorous inventory controls, optimizing materials flow into classified spaces, and managing cGMP waste streams safely, you prevent costly process bottlenecks and enable our core manufacturing teams to execute their runs seamlessly and safely. A Day in the Life: Attend the morning Tier 1 shift huddle to review the day's production campaign schedule and cross-reference material inventory. Step into a MFG suite to measure raw chemical components or execute a 500 L bioreactor growth-media preparation. Perform in-process testing (pH, conductivity, Osmolarity along with Endotoxin/bioburden sampling) on the finished solution before sterile-filtering it directly into a storage tote for the upstream team.
Requirements
- High school diploma or equivalent required.
- Minimum of 1 year of work experience in a manufacturing, operations, production, lab setting or related field.
- Proficiency in weighing raw chemicals, calculating mass/volume metrics, and operating specialized equipment (e.g., mixers, floor scales, SUMs, pH/Conductivity Meters and sterile filtration assemblies) to formulate media and buffers.
- Working knowledge of cleanroom behavior, contamination controls, and the operation of MFG mixing equipment.
- Exceptional attention to detail in real-time documentation, with the ability to accurately complete batch records, equipment logs, and material tracking forms to maintain flawless regulatory compliance.
- Constantly lifting, scooping, and pouring chemical powder bags weighing up to 50 lbs, and pushing/pulling wheeled tanks/totes.
- Spending 75% to 90% of a 12-hour shift on your feet, which includes frequent bending, squatting, and reaching to connect cleanroom equipment lines.
- Stamina to work for hours while wearing restrictive Personal Protective Equipment (PPE), including full-body bunny suits, frocks, face masks, and multiple layers of gloves.
Nice To Haves
- Experience in a cGMP environment.
Responsibilities
- Supply solutions (buffers and media) for upstream and downstream campaigns via GMP Manufacturing.
- Ensure cleanrooms are flawlessly staged and supplied.
- Stage and kit single-use assemblies, raw materials, and sterile components.
- Maintain rigorous inventory controls.
- Optimize materials flow into classified spaces.
- Manage cGMP waste streams safely.
- Attend morning Tier 1 shift huddles to review production schedules and material inventory.
- Measure raw chemical components or execute bioreactor growth-media preparation.
- Perform in-process testing (pH, conductivity, Osmolarity along with Endotoxin/bioburden sampling).
- Sterile-filter solutions into storage totes.
Benefits
- Competitive Pay
- Performance Related Bonus where eligible
- Annual merit performance-based increase
- Medical benefits
- Paid Time Off/Annual Leave
- Employee Referral Bonus
- Choice of national medical and dental plans, and a national vision plan, including health incentive programs
- Employee assistance and family support programs, including commuter benefits and tuition reimbursement
- At least 120 hours paid time off (PTO)
- 10 paid holidays annually
- Paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave)
- Accident and life insurance
- Short- and long-term disability
- 401(k) U.S. retirement savings plan
- Employees’ Stock Purchase Plan (ESPP)
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
