Manufacturing Associate - Biotech
Aequor JD ·www.aequor.com
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Rate details:
Day shift (Shift 1): ***/hr
Night shift (Shift 3): ***/hr
- Please keep these standard pay rates aligned with the rest of the department.
- Only submit candidates that are flexible and open to either day or night shift. The hiring team will do their best to adhere to a preference. However, shift details will be confirmed once offer has been extended.
Shifts and Hours schedule:
Upstream Day Shift: 6am - 7pm
Upstream Night Shift: 6pm - 7am
Downstream Day Shift: 6:30am - 7:30pm
Downstream Night Shift: 6:30pm - 7:30am
- These roles follow a 3-4-3 shift pattern
Role Purpose:
The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.
40% Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate
20% Attain qualification for all assigned tasks and maintain individual training plan
10% Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc.
10% Perform material movements, transfer raw materials, chemicals into, out of, across the production areas.
10% Maintain facility and equipment through routine cleaning and sanitization, support 6S programs
10% Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects, perform other duties as assigned.
High School Diploma or Equivalent minimum; AS/BS preferred
Preferred area of study: Science related discipline
0-3 years experience; some prior experience in a manufacturing setting preferred.
Proven logic and decision making abilities, critical thinking skills
Day shift (Shift 1): ***/hr
Night shift (Shift 3): ***/hr
- Please keep these standard pay rates aligned with the rest of the department.
- Only submit candidates that are flexible and open to either day or night shift. The hiring team will do their best to adhere to a preference. However, shift details will be confirmed once offer has been extended.
Shifts and Hours schedule:
Upstream Day Shift: 6am - 7pm
Upstream Night Shift: 6pm - 7am
Downstream Day Shift: 6:30am - 7:30pm
Downstream Night Shift: 6:30pm - 7:30am
- These roles follow a 3-4-3 shift pattern
Role Purpose:
The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.
40% Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate
20% Attain qualification for all assigned tasks and maintain individual training plan
10% Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc.
10% Perform material movements, transfer raw materials, chemicals into, out of, across the production areas.
10% Maintain facility and equipment through routine cleaning and sanitization, support 6S programs
10% Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects, perform other duties as assigned.
High School Diploma or Equivalent minimum; AS/BS preferred
Preferred area of study: Science related discipline
0-3 years experience; some prior experience in a manufacturing setting preferred.
Proven logic and decision making abilities, critical thinking skills
Frequently asked questions
Who is hiring for the Manufacturing Associate - Biotech role?
Aequor JD is hiring for the Manufacturing Associate - Biotech position, a Shazamme client. Apply directly on the employer's career site.
Where is the Manufacturing Associate - Biotech job located?
The Manufacturing Associate - Biotech role with Aequor JD is based in Vacaville, CA, US. The role is hybrid-friendly.
Is the Manufacturing Associate - Biotech role remote?
Yes — the Manufacturing Associate - Biotech position at Aequor JD is hybrid. Candidates based in US are preferred.
What does the Manufacturing Associate - Biotech role pay?
Aequor JD lists the Manufacturing Associate - Biotech role at USD 12–26 per hour.
Is the Manufacturing Associate - Biotech role full-time or contract?
This is a full time position at Aequor JD.
What experience level is the Manufacturing Associate - Biotech role?
The Manufacturing Associate - Biotech position is aimed at junior-level candidates.
How do I apply for the Manufacturing Associate - Biotech role at Aequor JD?
Apply directly on Aequor JD's career page via the Apply button on this listing. ZammeJobs links straight through to the employer's ATS — no third-party form, no resume database.