What are the responsibilities and job description for the Production Associate O1 position at Cytiva?
Transforming Human Health
Working at Cytiva means being at the forefront of providing innovative solutions to improve human health. Our customers undertake life-saving activities ranging from fundamental biological research to developing new medicines and cell and gene therapies.
As a Production Associate O1, you will be responsible for production and ensuring that day-to-day work tasks are completed in an ethical and safe manner.
Key Responsibilities:
- Read and follow work policies and procedures, EHS, Quality control inspections, and GMPs.
- Complete all planned Quality & Compliance training within defined deadlines.
- Identify and report quality or compliance concerns and take immediate corrective action as required.
Requirements:
- High School Diploma/GED or local equivalent.
- Ability to work well with team lead, engineers, supervisors, and managers to improve quality and process efficiency.
- Ability to frequently move, climb stairs and ladders daily, lift, carry, push or pull weight up to 50 lbs.
Preferred Qualifications:
- Manufacturing or production experience.
- MS Office programs.
Benefits:
We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance, and 401(k) to eligible employees.
Equal Opportunity Employer:
Cytiva is committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
