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Salary
≈ $57k – $117k per year (Estimated)
Location
In office (Bedford)
Seniority
Middle · 3+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 21, 2026. First seen by Alion on Oct 14, 2026. PCI Pharma Services scores B on the Alion truth index.

Overview
Company
Impact
Profile match
PCI Pharma Services is a contract development and manufacturing organisation (CDMO) headquartered in Philadelphia serving pharmaceutical and biotech companies. Founded in 1971, it runs sterile and non-sterile operations, including injectable fill-finish, drug-device combination products, clinical trial services and commercial packaging, at sites in the US, Ireland, the UK, Spain, Canada and Australia, including Bedford, Rockford and San Diego. It hires manufacturing associates, maintenance mechanics, QC microbiologists, quality and QMS investigators, warehouse staff, project managers and business development executives.

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

Position Title: QC Microbiologist

Location: Bedford, New Hampshire

Department: Quality Control (QC)

Reporting To: QC Supervisor

Shift: 1st (Monday - Friday)

Hours: 8:30am-5:00pm

Job Summary:

Conducts sampling and testing of production environments, and/or facility clean utilities, as per approved procedures. Performs Lab work and other tasks as assigned by management.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

  • Perform routine Environmental Monitoring of the classified clean rooms
  • Monitor classified clean rooms during manufacturing operations, must gown qualify
  • Sample and test the Water for Injection System, USP Purified Water systems and Clean Steam systems; perform and document plate reads for all environmental and utility testing with minimal supervision
  • Write and execute protocols/experiments/SOPs under limited supervision
  • Reviews work of peers and SOP document changes under limited supervision
  • May assist senior staff in preparation of investigations, reports and execution of complex protocols
  • Visual inspection of media fill vials and plates
  • Perform general lab maintenance/housekeeping
  • Training of staff in routine processes
  • Other duties as assigned

QUALIFICATIONS:

Required:

  • 3-5 years’ experience in a cGMP environment. Two years of experience may be replaced by Associates/Non- Scientific Bachelor’s degree. Four years of experience may be replaced with BS/BA degree in Microbiology or related scientific field.

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future

Equal Employment Opportunity (EEO) Statement:

PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

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