Current Good Manufacturing Practices (cGMPs) jobs

Supervisor - Quality Assurance (Food Safety and Quality Assurance)

Freshpet Talent Acquisition · Posted Nov 11, 2026

Open

Ennis, Texas, United States
On-site
Full-time · Manager
5+ years

Supervisor - Quality Assurance (Food Safety and Quality Assurance)

Freshpet Talent Acquisition · Posted Nov 11, 2026

Open

Ennis, Texas, United States
On-site
Full-time · Manager
5+ years

Manager, Regulatory Compliance

Catalent Pharma Solutions · Posted Nov 11, 2026

Open

Kansas City, Missouri, United States
On-site
Full-time · Manager
5+ years

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Manages site regulatory compliance processes, including reporting, licensing support, Quality Technical Agreements, and documentation such as the Site Master File and Quality Manual.

Responsibilities

Lead and maintain site regulatory compliance programs to ensure adherence to applicable requirements, commitments, company standards, and current Good Manufacturing Practices.
Manage regulatory submissions, commercial data reporting, licensing activities, and maintenance of regulatory records supporting site operations.
Own and maintain the Site Master File and Quality Manual, ensuring documents remain current, accurate, and compliant.
Develop, review, negotiate, approve, and maintain Quality Technical Agreements with customers, suppliers, contract manufacturers, and business partners.
Support regulatory agency, customer, and pre-approval inspections through documentation preparation, coordination of responses, and follow-up activities.

Requirements

Bachelor’s degree in Chemistry
Bachelor’s degree in Biology
Bachelor’s degree in Pharmaceutical Sciences
Bachelor’s degree in Engineering
Nice to have: Managing Site Master Files and Quality Manuals

Skills

Regulatory submissions Site licensing activities

Team member - Drug Substance

Dr Reddy's Laboratories Limited · Posted Nov 11, 2026

Open

Hyderabad, Telangana, India
18+ years

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Maintain manufacturing equipment and lead continuous improvement initiatives in a pharmaceutical manufacturing setting.

Responsibilities

Maintain manufacturing equipment to ensure correct functionality, calibration compliance, and operation within validated process parameters.
Develop and guide the team toward achieving zero downtime, higher equipment reliability, and maximum availability through proactive maintenance strategies.
Lead continuous improvement initiatives such as LDM, TPM, debottlenecking, and resource optimization, while leveraging cross-site learnings for enhanced productivity and cost efficiency.
Prepare CAPEX proposals, conduct feasibility studies, secure approvals, and ensure timely execution of projects in compliance with regulatory and business requirements.
Manage OPEX budgeting, tracking, and monitoring, along with developing and reviewing KPIs to drive operational efficiency and cost control.

Requirements

Graduation in Mechanical, Electrical, Biotechnology Engineering or related field
Post Graduation in Engineering / MBA
Nice to have: 8+ years in engineering or plant maintenance roles
Nice to have: 5+ years as team lead managing Mechanical / Electrical / HVAC / Instrumentation / Operations / Engineering Projects in pharma manufacturing
Nice to have: Experience in cGMP, EHS, regulatory compliance and audit readiness in pharmaceutical manufacturing

Scientist - Product Development Quality

Zoetis · Posted Nov 3, 2026

Open

Lincoln, United States
On-site
Full-time · Staff
5+ years
Visa sponsorship

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Provide quality assurance and compliance expertise for Veterinary Medicine Research & Development (VMRD), including the design, execution, and transfer of new biological/biopharmaceutical products to ensure department and site objectives are achieved.

Responsibilities

Ensure VMRD production facilities and product transfers comply with USDA, EU, FDA, and Zoetis quality standards.
Work with VMRD Development Science & Technology on scale-up and technical transfers.
Serve as QA consultant for development, clinical, and VICH batches/serials.
Review new product master batch records, manufacturing documents, and analytical documents for compliance.
Review and approve validation protocols and reports.

Requirements

Bachelor's degree in biological or pharmaceutical sciences, engineering, or related discipline (minimum 5 years experience)
Master's degree in biological or pharmaceutical sciences, engineering, or related discipline (minimum 3 years experience)
Nice to have: Master's or PhD degree in a biological science or chemical/bioprocess engineering
Nice to have: Expert-level competency in validation of processes, equipment, cleaning procedures, software, and computerized systems
Nice to have: Solid knowledge of Zoetis biological and biopharmaceutical products

Skills

Quality Assurance auditing

Team Member - OSD Production (Granulation /Compression)

Dr Reddy's Laboratories Limited · Posted Nov 10, 2026

Open

Baddi, Himachal Pradesh, India
On-site
Full-time · Mid
2–4 years

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Production Operator responsible for setting up, calibrating, and operating manufacturing equipment for OSD products, ensuring compliance with GMP, GDP, and safety standards.

Responsibilities

Setting up and calibrating manufacturing machinery
Preparing raw materials
Conducting in-process checks (weight variation, hardness, disintegration)
Recording production activities and maintaining GMP documentation
Cleaning and sanitizing equipment

Requirements

Diploma in Mechanical Engineering
Diploma in Industrial Engineering
Related field
Nice to have: Granulation
Nice to have: Blending

Skills

Batch Production Cleanrooms Equipment Maintenance Incident Reporting Quality Management Pharmaceutical Batch Documentation Pharmaceutical Manufacturing

QA Specialist III

Pfizer · Posted Nov 9, 2026

Open

Andover, Massachusetts, United States
Hybrid
Full-time · Senior
$83K–$138K per year
2+ years

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Provide guidance, lead/co-lead projects for digital solutions, support complex investigations, and ensure product quality assurance and compliance with global regulatory agencies.

Compensation

The annual base salary for this position ranges from $82,700.00 to $137,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary.

Responsibilities

Provide guidance, lead/co-lead projects for digital solutions
Routinely provide updates to the team and management on project milestones
Independently support complex investigations in cross-functional work areas, providing sound quality assurance judgment
Reviews and approves electronic record, protocols and reports
Authors, reviews, and approves SOPs

Requirements

High school diploma (or equivalent) with 8+ years of experience
associate’s degree with 6+ years of experience
BA/BS with 2+ years of experience
Nice to have: quality administered systems
Nice to have: regulatory compliance

Skills

Current Good Manufacturing Practices (GMP)GxP regulations and standards GMP manufacturing role or GMP Quality Assurance role

Project Manager II - R&D(H)

ARL Bio Pharma · Posted Nov 11, 2026

Open

Oklahoma City, Oklahoma, United States
$54–$54 per hour
2+ years

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Compensation

Pay Range: $54.07 per hour

Responsibilities

Develop and validate analytical methods for pharmaceutical products
Manage several research projects and coordinate projects between multiple departments
Communicate with clients regarding project and sample test results
Participate in meetings with scientific and business development personnel
Coach junior department personnel on SOPs and safety

Requirements

Bachelor's degree in Chemistry or related Science Field, or equivalent Diploma
Nice to have: 4 years experience in HPLC, LC-MS/MS method development
Nice to have: Experience in LIMS
Nice to have: Experience in the Pharmaceutical Industry
Nice to have: ARL Experience

Skills

High-Performance Liquid Chromatography (HPLC)Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)Ion Exchange Chromatography (IC)Enzyme-linked immunosorbent assay (ELISA)

CQV Engineer II

PM Group · Posted Nov 9, 2026

Open

Rahway, New Jersey, United States
$85K–$105K per year
2+ years

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CQV Engineer II

Compensation

The pay range for this position is $85,000 – $105,000 annually.

Responsibilities

Performs work in compliance with PM Group’s Service Delivery Platforms and Quality Management System (QMS)
Demonstrates an understanding of project scope of work assigned
Demonstrates an understanding of commercial aspects (hours and capital cost) of their work
Delivers scope of work within budgeted hours
Document development as well as testing execution to meet client qualification needs

Requirements

Bachelor’s degree
Nice to have: engineering degree
Nice to have: knowledge of cGMP manufacturing environments

Skills

CQV commissioning qualification validation documentation practices CGDP CGMP

Production Associate - Pouch (6:45am - 2:45pm)

Baxter International Inc. · Posted Nov 6, 2026

Open

Marion, North Carolina, United States
Full-time
$20–$20 per hour

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Assist in inspecting, over-pouching, and performing quality checks on filled bags for IV therapies and other sterile solutions.

Compensation

This position has a pay rate of $19.90 an hour.

Responsibilities

Over-pouch and seal the over-pouch, enclosing a bag containing solutions or premixed drugs, at a rate consistent with production needs.
Inspect and ensure that the over-pouches, bags and their components meet quality standards.
Perform scheduled quality checks using an assortment of gauges and a scale.
Perform and document scheduled cleaning activities.
Notify the supervisor and take appropriate action if any safety, quality, mechanical or discrepancy issues occur.

Requirements

High School Diploma
GED
equivalent
Nice to have: One year of manufacturing experience
Nice to have: CRC (Career Readiness Certification) at the Silver level

Skills

Inspector Certification Basic English written and oral communication Basic mathematics Safety and quality instruction comprehension

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