What are the responsibilities and job description for the Manufacturing Process Associate position at Katalyst Healthcares & Life Sciences?
Summary
The Manufacturing Process Associate supports daily production activities in a GMP-regulated manufacturing environment. This position is responsible for operating equipment, maintaining documentation, performing inspections, and ensuring products meet quality standards.
Key Responsibilities
The Manufacturing Process Associate supports daily production activities in a GMP-regulated manufacturing environment. This position is responsible for operating equipment, maintaining documentation, performing inspections, and ensuring products meet quality standards.
Key Responsibilities
- Operate manufacturing equipment according to SOPs and work instructions.
- Monitor production processes and complete batch documentation.
- Perform equipment setup, cleaning, and changeovers.
- Conduct visual inspections and report quality concerns.
- Maintain inventory of production materials.
- Follow GMP, safety, and quality procedures.
- Support continuous improvement initiatives.
- Perform other assigned duties.
- High School Diploma or Associate Degree preferred.
- Knowledge of GMP and manufacturing practices.
- Ability to follow written procedures.
- Basic computer skills.
- Good communication and teamwork.
- Strong attention to detail.
- 1–3 years of manufacturing or production experience preferred.
- Medical device, pharmaceutical, or food manufacturing experience is a plus.