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Gmp Quality Control Jobs (NOW HIRING)

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Quality Control Analyst I

Camarillo, CA · On-site

$82K - $86K/yr

... GMP procedures accurately • Ability to work independently and manage routine laboratory tasks ... QC laboratory or pharmaceutical industry experience preferred) • Previous experience in a fast ...

Alnylam Pharmaceuticals

Quality Site Head

Norton, MA · Hybrid

$276K - $373K/yr

Lead all GMP Quality functions for the Norton Manufacturing Facility, including Quality Assurance, Quality Control, Site Quality Systems, compliance, validation oversight, and inspection readiness.

Codexis Inc

Sr. Scientist, Quality Control

Plano, TX · On-site

$160K - $175K/yr

... QC laboratory in a GMP manufacturing facility. This is an on-site position initially be based in ... Redwood City, CA, with the potential to transition to our Hayward location in the future or operate ...

Alnylam Pharmaceuticals

Quality Site Head

Norton, MA · On-site

$276K - $373K/yr

Lead all GMP Quality functions for the Norton Manufacturing Facility, including Quality Assurance, Quality Control, Site Quality Systems, compliance, validation oversight, and inspection readiness.

Codexis

Sr. Scientist, Quality Control

Redwood City, CA · On-site

The Sr. Scientist in Quality Control will be leading analytical method transfer and validation for ... Strong scientific judgment and analytical problem-solving skills GMP quality mindset with a focus ...

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Gmp Quality Control information

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How much do gmp quality control jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for gmp quality control in the United States is $21.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.

What is the difference between Gmp Quality Control vs Gmp Quality Assurance?

AspectGmp Quality ControlGmp Quality Assurance
Primary FocusTesting and inspecting products to ensure compliance with standardsDeveloping and maintaining quality systems and processes
ResponsibilitiesSampling, testing, and documenting product qualityAuditing, process validation, and quality system oversight
CertificationsGMP training, laboratory skillsGMP knowledge, quality management system training
Work EnvironmentLaboratories, manufacturing sitesQuality departments, compliance offices

Gmp Quality Control focuses on testing products to verify they meet quality standards, while Gmp Quality Assurance involves establishing and maintaining systems to prevent defects. Both roles are essential in ensuring product safety and compliance in the pharmaceutical and biotech industries.

Is GMP Quality Control a good career path?

GMP Quality Control involves testing and inspecting pharmaceutical products to ensure they meet regulatory standards, making it a stable career with demand in the healthcare and biotech industries. It often requires attention to detail, knowledge of Good Manufacturing Practices, and certifications such as GMP training or laboratory skills. The role offers opportunities for advancement into quality assurance, compliance, or management positions.

Is GMP Quality Control a good career?

GMP Quality Control is a stable career in the pharmaceutical and biotech industries, focusing on ensuring products meet regulatory standards. It involves tasks such as testing, documentation, and compliance, often requiring knowledge of laboratory techniques and certifications like GMP training. The role offers opportunities for advancement and consistent employment due to industry regulation requirements.

What is the role of quality control in GMP?

In GMP, quality control (QC) is responsible for testing and inspecting raw materials, in-process samples, and finished products to ensure they meet specified quality standards. QC helps prevent defective or unsafe products from reaching consumers by verifying compliance with regulatory requirements and maintaining proper documentation. QC professionals often use analytical tools and follow strict protocols to support product safety and efficacy.
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Gmp Quality Control jobs near you
Infographic showing various Gmp Quality Control job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $44,668 per year, or $21.5 per hour.

Quality Control Analyst II

BioPharma Consulting JAD Group

Norton, MA • On-site

$24.25 - $32.75/hr

Contractor

Posted 9 days ago

Job description

The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation. This position enhances QC efficiency and effectiveness.

Key Responsibilities:

  • Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs.
  • Support weekend lab operations and maintain training records.
  • Assist in lab equipment and inventory maintenance, including reagent and sample prep.
  • Review data timely and qualify as a data reviewer Perform operational assignments (raw material processes, environmental monitoring, in-process testing).
  • Contribute to updating controlled documents (SOPs, work instructions, test methods).
  • Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH) Participate in continuous improvement initiatives and cross-functional collaboration.
  • Support regulatory submissions, inspection readiness, and audits.

Requirements

  • B.S. in chemistry, biology, biochemistry, or related field 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent.
  • Experience in method transfer/implementation; understanding of method lifecycle management.
  • Strong technical writing, data analysis, problem-solving, and organizational skills.
  • Proficiency in LabWare LIMS, Excel, Word, and PowerPoint.

Benefits

  • Contract position with possible extension
  • Location: Norton, MA, with occasional responsibilities at other locations.
  • Weekend coverage is required.
  • First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training.