Lead QC Environmental Monitoring Analyst

PCI Pharma Services

Bedford (NH)

On-site

USD 90,000 - 120,000

Full time

3 days ago
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Job summary

PCI Pharma Services in Bedford, NH is seeking a QC Environmental Monitoring Analyst III Lead to oversee routine environmental monitoring in classified clean rooms and support water systems and clean steam analyses.

You will write and review SOPs, train staff, and coordinate cross-functional activities while ensuring GDP/ALCOA+ compliance; requires 7–9 years in a cGMP environment and strong attention to detail.

Qualifications

  • High school Diploma, GED, or equivalent; AS or BS in Microbiology preferred.
  • 7–9 years of experience in a cGMP environment.
  • Highly detail-oriented with exceptional organizational skills.
  • Professional verbal communication and computer skills; ability to learn new software.
  • Experience with ISO-8 to ISO-5 gowning and cleanroom protocols.

Responsibilities

  • Perform routine Environmental Monitoring of classified clean rooms.
  • Monitor clean room operations; sample Water for Injection (WFI)/RO/DI, USP purified water, and clean steam systems.
  • Write/execute protocols, experiments, and notebook studies; review SOPs.
  • Train staff in routine and advanced processes; participate in cross-functional meetings.
  • Ensure GDP and ALCOA+ data integrity; assist with investigations and data reviews.

Skills

Attention to detail
Organizational skills
Professional verbal communication
Computer skills
Gowning proficiency
Ability to work varied hours

Education

BS in Microbiology or related
AS/ASc in Microbiology or related
High school Diploma or GED

Tools

Lab equipment knowledge

Job description

PCI Pharma Services in Bedford, NH is seeking a QC Environmental Monitoring Analyst III Lead to oversee routine environmental monitoring in classified clean rooms and support water systems and clean steam analyses.

You will write and review SOPs, train staff, and coordinate cross-functional activities while ensuring GDP/ALCOA+ compliance; requires 7–9 years in a cGMP environment and strong attention to detail.

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