Manufacturing Associate - Biotech
Aequor, Vacaville, CA, United States
Job Title: Manufacturing Associate - Biotech
Duration: 12 Months
Shifts and Hours schedule:
Night Shift: 6pm - 7am or 6:30pm - 7:30am
Day Shift: 6am - 7pm or 6:30am - 7:30pm
These roles follow a 3-4-3 shift pattern
Job Responsibility:
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 techniques 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 and 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.
Required skills and education:
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
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Duration: 12 Months
Shifts and Hours schedule:
Night Shift: 6pm - 7am or 6:30pm - 7:30am
Day Shift: 6am - 7pm or 6:30am - 7:30pm
These roles follow a 3-4-3 shift pattern
Job Responsibility:
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 techniques 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 and 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.
Required skills and education:
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
#J-18808-Ljbffr