Medical Packaging QC Scientist – GMP Lab Testing

Eurofins; Indianapolis (IN); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Medical, Dental, Vision

Life Insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins Scientific is seeking a qualified candidate in Indianapolis, IN for a full-time laboratory testing role. The position involves evaluating and testing primary container-closure components, secondary packaging, and shipping systems using mechanical testing equipment and LIMS.

You will document results, help develop test methods, collaborate with cross-functional teams, and ensure adherence to GMP and safety standards. US work authorization is required. Benefits included.

Qualifications

• Associates with related experience.
• BS with 4–6 years of experience; MS with 2–4 years.
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Responsibilities

• Perform evaluations and laboratory testing on primary container-closure components and system, critical secondary packaging, and shipping systems utilizing mechanical testing equipment, dimension measurement instruments, and container closure integrity testing systems
• Execute methods, collect data, and document results in lab notebooks and LIMS
• Participate in the development of laboratory test methods or equipment to ensure reliability and accuracy of results
• Interact with colleagues in other groups on a routine basis
• Ensure all activities follow established safety standards, regulatory requirements and Good Manufacturing Procedures (GMP)

Skills

Laboratory testing

Quality control

Education

Associate degree in related field

BS in related field

MS in related field

Tools

LIMS

Job description

Eurofins Scientific is seeking a qualified candidate in Indianapolis, IN for a full-time laboratory testing role. The position involves evaluating and testing primary container-closure components, secondary packaging, and shipping systems using mechanical testing equipment and LIMS.

You will document results, help develop test methods, collaborate with cross-functional teams, and ensure adherence to GMP and safety standards. US work authorization is required. Benefits included.