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Gmp Quality Control Jobs (NOW HIRING)

Olema Oncology

Associate Director, GMP Quality

Boston, MA · On-site

$160K - $180K/yr

There will be associated responsibilities for reviewing Analytical Development / Quality Control results. In this position you will perform GMP activities such as, but not limited to, review of ...

Kellton Tech

QC Analyst III

Portsmouth, NH · On-site

$33/hr

GMP QC lab experience required. * Strong communication and problem-solving skills. * Experience with TrackWise, LIMS, and Microsoft Office Suite a plus.

Jade Biosciences

... quality control in a pharmaceutical or biotech environment * Experience with all phases of development (Ph 1-4 including commercial) * In-depth knowledge and full understanding of GMP FDA, EMA ...

Novartis

QC Chemist

Indianapolis, IN · On-site

$97K - $146K/yr

On-time and GMP-compliant release of dosage forms * Support Quality Control and AS&T as a valued business partner, with a culture of safety, quality, * delivery to patients, cost, compliance, and ...

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How much do gmp quality control jobs pay per hour?

As of Aug 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.

Is GMP quality control inspection a good career?

GMP quality control inspection is a stable career in the pharmaceutical and biotech industries, focusing on ensuring products meet regulatory standards. It often requires attention to detail, knowledge of Good Manufacturing Practices, and certifications such as GMP training. The role offers opportunities for advancement and consistent employment in regulated environments.

What is the role of quality control in GMP?

In GMP, quality control (QC) is responsible for testing and verifying raw materials, in-process samples, and finished products to ensure they meet specified quality standards. QC helps prevent contaminated or substandard products from reaching consumers and maintains compliance with regulatory requirements through proper documentation and testing procedures.

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?

GMP Quality Control is a vital role in the pharmaceutical and biotech industries, focusing on ensuring products meet regulatory standards through testing and documentation. It often requires attention to detail, knowledge of Good Manufacturing Practices, and certifications such as GMP training. The career offers stability, opportunities for advancement, and the chance to work in regulated environments that prioritize quality and safety.
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Gmp Quality Control jobs near you
Infographic showing various Gmp Quality Control job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 74% Full Time, 20% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $44,668 per year, or $21.5 per hour.

GMP QC Systems Consultant

Stark Pharma Solutions Inc

Frankford, DE • On-site

Contractor

Posted 14 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on GMP QC Systems Consultant position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Position: GMP QC Systems Consultant

Location: Frankford, DE (100% Onsite)
Duration: 12+ Month Contract

Job Overview

We are seeking an experienced GMP QC Systems Consultant to support the implementation, integration, and validation of Quality Control laboratory systems in a regulated pharmaceutical environment. The ideal candidate will have strong expertise in GMP laboratory systems, Computer System Validation (CSV/CSA), and cross-functional project execution.

Key Responsibilities

  • Lead implementation and integration of GMP QC laboratory systems.
  • Coordinate system configuration, data migration, deployment, and go-live activities.
  • Manage project timelines, risks, budgets, and stakeholder communications.
  • Support Computer System Validation (CSV/CSA), including IQ/OQ/PQ execution and documentation.
  • Perform risk assessments, testing, and validation activities in compliance with GAMP5 and GxP requirements.
  • Collaborate with QA, IT, laboratory teams, vendors, and business stakeholders to ensure successful project delivery.
  • Ensure compliance with GxP, Data Integrity, and internal quality standards.
  • Prepare project status reports and support release readiness activities.

Required Qualifications

  • 8+ years of experience in Pharmaceutical, Biotechnology, or other GMP-regulated environments.
  • Strong experience implementing and validating QC/Laboratory systems.
  • Hands-on knowledge of CSV, CSA, GAMP5, GxP, IQ/OQ/PQ, and risk-based validation.
  • Experience with system integration, data migration, and cross-functional project coordination.
  • Familiarity with laboratory platforms such as LIMS, SDMS, Empower, LabX, QuantStudio, SoftMax Pro, or similar systems.
  • Excellent communication, documentation, and stakeholder management skills.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com