Manufacturing Associate
Listed on 2026-01-10
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Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing Production, Manufacturing Engineer
Manufacturing Associate I – Second Shift
Manufacturing Associate I is responsible for completing production orders in accordance with the daily production schedule. Candidates will work on manufacturing biological reagents and finished products such as reagent formulations, antibody conjugation, component lyophilization, filling, and assembly of final products.
Position DescriptionWe are seeking a disciplined, energetic, fast‑learning candidate to join our Manufacturing team on the second shift. Experience under ISO 13485 and/or cGMP in a biotechnology or pharmaceutical industry is highly preferred.
Work Schedule10 am – 6:30 pm Thursday, Friday, Saturday, Sunday, and Monday.
Second Shift Expectations- Minimal supervision is provided over the weekend; candidates must demonstrate experience working independently and making sound decisions in a manufacturing environment.
- Strong organizational skills and self‑motivation are essential to maintain productivity and quality standards during off‑hours.
- Effective communication skills to provide regular updates and document activities for review by weekday supervisors.
- Commitment to safety, quality, and continuous improvement, even when working independently.
- Perform standardized lyophilization of critical components for downstream manufacturing.
- Formulate biochemical and chemical reagents in accordance with manufacturing records, SOPs, and QSR regulations.
- Support manufacturing activities such as filling, packaging, label printing, etc.
- Follow Good Documentation Practices to maintain detailed and accurate records for the manufacturing of reagents/products.
- Track inventory of consumables and raw materials; perform routine cycle count to ensure inventory accuracy.
- Perform general laboratory maintenance such as basic equipment calibration, routine cleaning, and housekeeping.
- Assist in troubleshooting manufacturing issues.
- Participate in product validation for new product/process introductions from R&D into Manufacturing.
- Participate in internal and external safety and quality inspections.
- Maintain a safe working environment and comply with all safety laboratory practices.
- B.S. or B.A. degree in Biology, Chemistry, or equivalent.
- Minimum one year of relevant experience in reagent manufacturing; lyophilization experience highly desired.
- Demonstrated good biochemistry laboratory skills.
- Strong organizational skills, attention to detail, and problem‑solving skills.
- Experience following SOPs and maintaining clear, accurate records.
- Experience working independently with minimal supervision, especially during weekend or off‑hour shifts.
- Strong team player, motivated, and willing to learn new techniques in a fast‑paced environment.
- Experience in ISO 13485 and GMP environment a plus.
- Strong verbal and written communication skills.
- Ability to lift up to 25 lbs.
- Position requires standing for long periods of time daily.
The base salary range for this full‑time position is $72,000 – $85,000 plus bonus, equity, and benefits. Salary ranges are determined by work location, job‑related skills, experience, and applicable education or training.
Seniority LevelMid‑Senior level
Employment TypeFull‑time
Job FunctionResearch, Analyst, and Information Technology
IndustriesBiotechnology Research and Pharmaceutical Manufacturing
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