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Quality Assurance Lead - Environmental Monitoring & Facility Validation

Eurofins USA BioPharma Services · Lancaster, PA · Quality Systems

Employment type

Full-time

Work setting

On-site

Location

Lancaster, PA

Schedule

Day shift

Posted

Travel

Required

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Job overview

The Quality Assurance Lead is an onsite role based in Lancaster, PA. Compensation is not specified for this position, which supports the quality systems at Eurofins USA BioPharma Services. This role exists to maintain quality systems for environmental monitoring and facility validation. The lead contributes to the company's mission by drafting procedures, supporting accreditation, and ensuring compliance with GMP/GLP standards across the laboratory network.

What you'll do

  • Draft SOPs, assist with accreditation, work with subject matter experts, maintain training records, and support data integrity requirements.

What we're looking for

Skills & competencies
full-time
day shift
lancaster pa
eurofins
quality assurance
environmental monitoring
validation
gmp
pharma
onsite
Work arrangement
  • Weekend coverage required

Benefits & perks

  • Medical, dental, vision, life/disability insurance, 401(k) with match, and paid vacation.

Why this role

Requires 3+ years of GMP-regulated experience and 10-25% travel.

About the employer

Eurofins USA BioPharma Services is hiring for this role. Industry: Testing Laboratories and Services. Sector: 54.

Additional details

Industry sector
54
Industry
Testing Laboratories and Services
Occupation code
17-2112.00
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