QC Microbiologist I - Environmental Monitoring Specialist

PCI TRGR Penn Pharmaceutical Services Ltd

Bedford (NH)

On-site

USD 60,000 - 75,000

Full time

12 days ago

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Job summary

PCI Pharma Services in Bedford, New Hampshire, is seeking a QC Microbiologist to support environmental monitoring and utility testing in a cGMP setting. You will perform sampling, testing, and routine lab tasks in a fast-paced quality control lab.

The role requires 3–5 years of cGMP experience, a degree in Microbiology or related field, and the ability to write protocols and SOPs under limited supervision; shift is 1st, 8:30am–5:00pm, Monday–Friday.

Qualifications

  • 3–5 years' experience in a cGMP environment; 2 years 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 field.
  • Position requires ability to write and execute procedures under limited supervision.

Responsibilities

  • Perform routine Environmental Monitoring of the classified clean rooms.
  • Monitor classified clean rooms during manufacturing operations; gown qualify as required.
  • Sample and test Water for Injection, USP Purified Water, and Clean Steam systems; perform plate reads with minimal supervision.
  • Write and execute protocols/experiments/SOPs; review peers' work and SOP changes.
  • Assist senior staff with investigations, reports, and complex protocols.
  • Visually inspect media fill vials and plates; train staff in routine processes.

Skills

Environmental Monitoring
Gowning qualification
Laboratory testing
Protocol writing
SOP documentation

Education

BS/BA in Microbiology or related field
Associates or non-scientific Bachelor's degree acceptable with 2 years experience

Job description

PCI Pharma Services in Bedford, New Hampshire, is seeking a QC Microbiologist to support environmental monitoring and utility testing in a cGMP setting. You will perform sampling, testing, and routine lab tasks in a fast-paced quality control lab.

The role requires 3–5 years of cGMP experience, a degree in Microbiology or related field, and the ability to write protocols and SOPs under limited supervision; shift is 1st, 8:30am–5:00pm, Monday–Friday.

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