CGMP documentation jobs

QC Specialist

6084-Janssen Research & Development Legal Entity · Posted Nov 9, 2026

Open

Schaffhausen, Schaffhausen, Switzerland
On-site
Full-time · Associate

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QC Specialist

6084-Janssen Research & Development Legal Entity · Posted Nov 9, 2026

Open

Schaffhausen, Schaffhausen, Switzerland
On-site
Full-time · Associate

Apply with Referso

Quality Control Inspector II (3-Month Contract)

Tandem Diabetes Care · Posted Dec 19, 2025

Open

Irvine, California, United States
Contract
$27–$30 per hour
4+ years

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Perform inspections and testing on raw materials and sub-assemblies to identify non-conforming material and product and assist in evaluation of non-conformances.

Compensation

The starting base pay range for this position is $27.00 - $30.00 per hour.

Responsibilities

Performs inspections and testing on raw materials and sub-assemblies to identify non-conforming material and product
Assists in evaluation of non-conformances
Performs routine and non-routine testing of sub-assemblies and finished product
Compiles data for evaluation of department Key Process Indicators (KPIs)
Assists with validating inspection and testing processes

Requirements

HS Diploma or equivalent

Skills

cGMP documentation QSRs sampling methodologies visual inspection systems Microsoft Office

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Manufacturing Engineering Technician II (3 Month Contract)

Tandem Diabetes Care · Posted Dec 15, 2025

Open

San Diego, California, United States
On-site
Contract · Associate
$25–$31 per hour
4+ years

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Performs functions associated with all manufacturing operations, working with engineers in set-up and development of support processes for insulin pump medical devices.

Compensation

The starting base pay range for this position is $25.19 to $31.47 per hour.

Responsibilities

Performs functions associated with all manufacturing operations
Works with engineers in set-up and development of support processes
Assists in the development and execution of protocols and test runs
Design, implement and maintain production support processes
Assess manufacturing processes for compliance with written policies and procedures including QSR’s and cGMP practices

Requirements

Associate degree in a technical discipline
Nice to have: Lean Manufacturing
Nice to have: FDA/GMP/ISO environment

Skills

QSRs cGMP documentation small scale electromechanical device assembly Microsoft Office Internet

Aseptic Technician I

Zoetis · Posted Nov 5, 2026

Open

Charles City, United States
Full-time · Entry

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Responsible for executing aseptic techniques and clean room procedures in a GMP facility, maintaining documentation, operating equipment, and supporting vaccine manufacturing processes.

Responsibilities

Execute aseptic techniques and clean room procedures
Maintain cGMP documentation
Execute batch records and SOPs
Follow financial and safety procedures
Operate departmental equipment

Requirements

High school education or GED required
Post high school education in the sciences or related disciplines preferred
Nice to have: post high school education in sciences
Nice to have: mathematical skills
Nice to have: science skills

Skills

aseptic techniques clean room procedures GMP cGMP documentation batch records SOPs financial procedures

Manager, GMP Quality Assurance

CSBio · Posted Nov 3, 2026

Open

Milpitas, California, United States
Manager
5+ years

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Quality Assurance Manager overseeing cGMP compliance in peptide manufacturing

Responsibilities

Supervise daily QA work, assign priorities, review completion, train staff, and provide practical guidance on cGMP documentation and quality-system requirements.
Review executed batch records, laboratory records, equipment and cleaning records, logbooks, labels, and supporting documentation for completeness and compliance.
Manage or support deviations, investigations, CAPAs, change controls, nonconformances, complaints, and effectiveness checks; ensure actions are documented and completed on time.
Coordinate document control, SOP issuance, periodic review, archival, forms, templates, and controlled-copy practices.
Support employee training assignments, completion tracking, qualification records, and documentation of GMP readiness.

Requirements

Bachelor’s degree in life sciences, chemistry, engineering, pharmacy, or a related field, or equivalent relevant experience.

Skills

deviations CAPAs change controls document control

QC Specialist

QC Specialist

Responsibilities

Requirements

Skills

Quality Control Inspector II (3-Month Contract)

Compensation

Responsibilities

Requirements

Skills

Manufacturing Engineering Technician II (3 Month Contract)

Compensation

Responsibilities

Requirements

Skills

Aseptic Technician I

Responsibilities

Requirements

Skills

Manager, GMP Quality Assurance

Responsibilities

Requirements

Skills

Benefits

Benefits