Quality Control Analyst (Medical Device)

Job Summary

1. Provide support to Quality Control Department by performingtesting for materials and products.

2. Conduct routine and non-routine analysis of raw materials, in-process items and finished product according to established operating procedures.

3. Compile data for documentation of test procedures that may include stability program testing and formulation studies.

4. Participate in the preparation of investigations, summaries and reports. Reviews data obtained for compliance to specifications and reports abnormalities.

5. Revise and updates standard operating procedures as needed.

6. Responsible for daily log activities including GLP compliance, compliance with safety regulations and maintenance of appropriate levels of needed lab supplies and equipment.

7. Project tracking and coordination.

8. Participation in validation/qualification activities

9. Occasional travel to other STAAR sitesas required.

10. Other duties as assigned.

EDUCATION & TRAINING

• Bachelor’s degree in a science curriculum or equivalent combination of education/experience.

EXPERIENCE

• FDA regulated industry (food, pharmaceutical or medical device) experience is required.

• Minimum of 2years relevant experience required.

SKILLS

• Proficient in MS Office applications, especially Excel and Word.

• Strong work ethic and organizational skills.

• Laboratory skills required.

• Analytical and Microbiological testing highly preferred.

STAAR Surgical is an equal employment opportunity employer.