Referso Jobs

Utilities Energy

Sanofi · Posted Nov 5, 2026

Open

Framingham, Massachusetts, United States
On-site
Full-time · Mid
$101K–$145K per year
3+ years

Utilities Energy

Sanofi · Posted Nov 5, 2026

Open

Framingham, Massachusetts, United States
On-site
Full-time · Mid
$101K–$145K per year
3+ years

QC Environmental Monitoring Analyst I

PCI Pharma Services · Posted Nov 6, 2026

Open

Bedford, New Hampshire, United States
3–5 years

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Perform routine environmental monitoring and utility sampling in a cGMP clean room environment.

Responsibilities

Perform routine Environmental Monitoring of classified clean rooms
Perform routine utility sampling of Water for Injection Systems, RO/DI, USP Purified water systems, and Clean Steam systems
Monitor classified clean rooms during manufacturing operations; must be gown qualified
Perform analysis on samples from 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 some supervision
Execute protocols/experiments/SOPs under some supervision

Requirements

High school Diploma
GED
AS degree in Microbiology
BS degree in Microbiology
Nice to have: AS degree in Microbiology

Skills

Environmental Monitoring Utility Sampling Water for Injection System RO/DI USP Purified Water

QC Environmental Monitoring Analyst II

PCI Pharma Services · Posted Nov 6, 2026

Open

Bedford, New Hampshire, United States
5–7 years

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Perform routine environmental monitoring and utility sampling in a cGMP clean room environment.

Responsibilities

Perform routine environmental monitoring of classified clean rooms
Perform routine utility sampling and analysis of Water for Injection Systems, RO/DI, USP Purified water systems, and Clean Steam systems
Monitor classified clean rooms during manufacturing operations; must be gown qualified
Perform routine monitoring and analysis of the Clean Compressed Air System
Execute protocols/experiments/SOPs under minimal supervision

Requirements

High school Diploma, GED, or equivalent credential required
AS degree or BS degree in Microbiology or related scientific field preferred
Nice to have: AS degree in Microbiology
Nice to have: BS degree in Microbiology

Skills

Environmental monitoring Utility sampling Water for Injection Systems RO/DI USP Purified Water

CQV Manager

No deviation · Posted Nov 8, 2026

Open

Yamagata, Yamagata, Japan
Full-time · Manager
8–12 years

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Senior leadership role responsible for directing commissioning, qualification, and validation (CQV) activities across capital projects, facility expansions, equipment installations, and process improvement initiatives in a GMP-regulated manufacturing environment.

Responsibilities

Lead end-to-end CQV activities for capital projects, facility expansions, equipment installations, and process improvement initiatives.
Develop and execute CQV strategies aligned with project timelines, quality requirements, and regulatory expectations.
Establish commissioning and qualification plans covering facilities, utilities, equipment, and computerized systems.
Manage CQV project schedules, milestones, budgets, resources, and risk assessments.
Coordinate internal and external CQV resources, including engineering contractors and validation consultants.

Requirements

Bachelor's degree in Engineering, Pharmaceutical Sciences, Biotechnology, Life Sciences, or a related discipline.
Master's degree is advantageous.

Skills

Commissioning Qualification Validation GMP

Head of Engineering

Teva Pharmaceuticals · Posted Nov 5, 2026

Open

10+ years

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Lead engineering functions at a biopharmaceutical manufacturing site, overseeing plant and campus technical and maintenance aspects, guiding the Site Leadership Team, and ensuring compliance with quality and regulatory standards.

Responsibilities

Provide strategic and operational leadership for all engineering functions
Own plant and campus technical and maintenance aspects
Guide Site Leadership Team on engineering implications
Oversee engineering maintenance and facility management activities
Plan, validate, control and approve engineering decisions, documentation, resources, budget and forecasts

Skills

FDA EU GMP ICH regulations biopharmaceutical unit operations HVAC WFI/PW systems clean steam cleanrooms CIP/SIP process piping (ASME BPE)digital manufacturing technologies (automation, MES, DCS, SCADA)budgeting cost estimation business case development change management

Benefits

company health management system
company doctor
physiotherapy
sports activities
company canteen

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Senior QA Specialist - C&Q

Johnson & Johnson · Posted Nov 4, 2026

Open

Wilson, North Carolina, United States
On-site
Full-time · Senior
6+ years

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Seeking a highly qualified Senior QA Specialist to join a new Biotherapeutics Manufacturing facility in Wilson, NC, ensuring compliance with regulatory requirements and GMP policies throughout the C&Q validation lifecycle.

Responsibilities

Represents Quality Assurance on qualification teams and provides QA oversight of C&Q and validation execution across the capital project lifecycle—user requirements, design review, construction, FAT/SAT, commissioning, qualification and handover.
Supports development and maintenance of site validation program, Validation Master Plan, and project C&Q and validation plans.
Participates in risk assessments (FMEA, HACCP, HAZOP, ICH Q9(R1), CARA) for equipment, utilities and systems.
Reviews and approves commissioning and qualification documentation, including URS, FAT/SAT, IQ/OQ/PQ protocols, and reports.
Ensures Good Documentation Practice and data integrity of vendor, EPCM and CQV contractor documentation.

Requirements

Bachelor's degree in a scientific or engineering discipline
Master's degree in a scientific or engineering discipline
Nice to have: greenfield or start-up facility experience
Nice to have: ASQ certification (CQA, CQE)
Nice to have: Kneat

Skills

Quality Assurance Validation experience

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