Manufacturing Associate-2nd Shift-Bulk
Alkermes
August 26, 2026
On-site
Cincinnati Metropolitan Area
Operations
2nd shift (2:00pm–12:30am) Monday, Tuesday, Wednesday, and Friday.
Responsibilities:
- Perform bulk manufacturing operations: equipment cleaning, equipment set-up, equipment/automation operation, batch processing.
- Read and follow detailed SOPs/procedures and document operations according to cGMP.
- Perform sample collection, equipment/process monitoring, and minor maintenance.
- Maintain training proficiency via the Learning Management System.
- Write and review SOPs and cGMP documentation.
- Perform facility/equipment cleaning and set-up; assist with development activities and validation as required.
- Abide by safety requirements; work independently and in a team environment; follow internal policies.
- Other tasks as assigned; shift coverage and weekend work may be required.
Knowledge/Skills:
- General math skills (simple algebra).
- Adherence to Current Good Manufacturing Practices; knowledge of HAZCOM, RCRA, and other safety requirements.
- Mechanical aptitude for minor non-routine adjustments and diagnosing equipment.
- Basic computer word processing/spreadsheet skills.
- Good written communication and excellent documentation skills.
- Ability to gown in an aseptic manner for clean room operations.
Qualifications:
Manufacturing Associate 1
- HS diploma or equivalent.
- Preferred: 0–1 year sterile pharmaceutical operation; Associate degree+ in science/technical.
Manufacturing Associate 2
- HS diploma or equivalent; 1–3 years pharma manufacturing.
- Preferred: 1+ year sterile operation; Associate degree+ in science/technical.
Manufacturing Associate 3
- HS diploma or equivalent; 4–5 years pharma manufacturing.
- Preferred: 2–3 years sterile operation; Associate degree+ in science/technical.
Physical requirements:
- Lifting/moving up to 50 lbs (team lift up to 100 lbs), walking/standing, reaching, climbing, bending; stand in steel-toed shoes for 7+ hours; operate production equipment; read/follow SOPs.
Responsibilities:
- Perform bulk manufacturing operations: equipment cleaning, equipment set-up, equipment/automation operation, batch processing.
- Read and follow detailed SOPs/procedures and document operations according to cGMP.
- Perform sample collection, equipment/process monitoring, and minor maintenance.
- Maintain training proficiency via the Learning Management System.
- Write and review SOPs and cGMP documentation.
- Perform facility/equipment cleaning and set-up; assist with development activities and validation as required.
- Abide by safety requirements; work independently and in a team environment; follow internal policies.
- Other tasks as assigned; shift coverage and weekend work may be required.
Knowledge/Skills:
- General math skills (simple algebra).
- Adherence to Current Good Manufacturing Practices; knowledge of HAZCOM, RCRA, and other safety requirements.
- Mechanical aptitude for minor non-routine adjustments and diagnosing equipment.
- Basic computer word processing/spreadsheet skills.
- Good written communication and excellent documentation skills.
- Ability to gown in an aseptic manner for clean room operations.
Qualifications:
Manufacturing Associate 1
- HS diploma or equivalent.
- Preferred: 0–1 year sterile pharmaceutical operation; Associate degree+ in science/technical.
Manufacturing Associate 2
- HS diploma or equivalent; 1–3 years pharma manufacturing.
- Preferred: 1+ year sterile operation; Associate degree+ in science/technical.
Manufacturing Associate 3
- HS diploma or equivalent; 4–5 years pharma manufacturing.
- Preferred: 2–3 years sterile operation; Associate degree+ in science/technical.
Physical requirements:
- Lifting/moving up to 50 lbs (team lift up to 100 lbs), walking/standing, reaching, climbing, bending; stand in steel-toed shoes for 7+ hours; operate production equipment; read/follow SOPs.