Job Description: Assist in manufacturing therapeutic proteins under cGMP conditions by operating equipment performing basic lab tests documenting work and maintaining a clean safe production environment.
Responsibilities: - Operate and monitor production equipment (CIP/SIP processes).
- Follow SOPs and process recipes accurately.
- Perform basic lab tests (pH conductivity sampling).
- Record work per Good Documentation Practices (GDP).
- Handle and transfer materials safely.
- Clean and sanitize equipment and facility.
- Attend meetings training and shift handovers.
Requirements: - High School Diploma or equivalent.
- Basic understanding of manufacturing or lab processes.
- Ability to follow written instructions.
- Attention to detail and record-keeping accuracy.
- Good teamwork and communication skills.
- Willingness to work in a cGMP-regulated environment.