Manufacturing Operator I
Portsmouth, New Hampshire, United States
Job Description
Job Description:
Supports cGMP manufacturing suites by ensuring proper stocking, cleaning, material preparation, and equipment maintenance while following GMP and aseptic practices.
Responsibilities:
Requirements:
Mandatory Requirements:
Supports cGMP manufacturing suites by ensuring proper stocking, cleaning, material preparation, and equipment maintenance while following GMP and aseptic practices.
Responsibilities:
- Perform daily 6S, stocking, and cleaning of suites and parts.
- Prepare, assemble, and autoclave materials for production.
- Handle material movement across production areas.
- Perform routine equipment maintenance and cleaning.
- Complete weekly/monthly cleaning (e.g., inoculum rooms).
- Maintain GMP/GDP-compliant documentation.
- Follow aseptic techniques and contamination control practices.
- Support training, meetings, and assigned tasks
Requirements:
- 0-2 years in pharma/biotech/manufacturing (freshers with relevant exposure can apply).
- Bachelor's in Life Sciences / Biotechnology / related field.
Mandatory Requirements:
- Basic cGMP knowledge.
- septic technique awareness.
- SOP & documentation (GDP) understanding.
- ttention to detail and teamwork.
Apply
Career Focus: Manufacturing
This role is part of a curated selection of life science opportunities featured on Xtalks. Employers may request edits or removal here.
Similar Jobs
Manufacturing Operator III – Fluid...
POSITION SUMMARY The Manufacturing Operator III performs functions relat...
Manufacturing Operator III – Granulation
Job Summary – The Manufacturing Operator III – Granulation p...
Supervisor, Manufacturing
About Company Mizuho OSI is the leader in the markets for specialty surg...
Manufacturing Specialist – Scheduling
We’re here for one reason and one reason only – to cure canc...