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Gmp Quality Control Jobs (NOW HIRING)

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

$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 ...

IntelliPro Group Inc.

NC · On-site

$40/hr

GMP Quality Assurance Duration: 06/29/2026--- 04/04/2027 with possible extension Office: Research ... Provide timely support of Learning Management System, Change Control, Deviation Management Systems ...

Epicurean Butter

Quality Control Supervisor

Thornton, CO · On-site

$24 - $30/hr

Quality Control Technician Supervisor Department: QA Direct Supervisor/Manager: Director of Quality ... Assists with Food Safety/GMP quality related audit preparation * Responsible for QA final product ...

New

Cayman

QC Chemist I, GMP

Ann Arbor, MI · On-site

Currently, we are looking to add a GMP QC Chemist I to the team: Responsibilities and Duties: * Perform routine sampling and GMP analytical testing to support the timely release of raw materials, in ...

New

DivIHN

QA Contractor, GMP Quality Assurance

NC · On-site

QA Contractor, GMP Quality Assurance Location: Onsite at Research Triangle Park, NC Duration: 9 ... Provide timely support of Learning Management System, Change Control, Deviation Management Systems ...

AllSTEM Connections

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 ...

Lancesoft

NC · On-site

$40/hr

The QA Contractor, GMP Quality Assurance, reporting to the Manager, GMP Quality Assurance, or ... Provide timely support of Learning Management System, Change Control, Deviation Management Systems ...

Vrtx

Manager GMP Quality Operations

Boston, MA

$118K - $177K/yr

The GMP Quality Operations Manager is recognized internally as an expert in the principles and ... data, EM data, QC release testing, and other quality systems documentation, while advancing ...

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Gmp Quality Control information

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How much do gmp quality control jobs pay per hour?

As of Jul 13, 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.

Which pays more, QA or QC?

In the context of GMP Quality Control, QA (Quality Assurance) roles typically pay more than QC (Quality Control) positions because QA involves broader responsibilities such as process audits and compliance oversight. QC roles focus on testing and inspection of products, often with more routine tasks. Salary differences can vary based on experience, certifications, and industry, but generally QA positions offer higher compensation.

Is QC a high paying job?

Quality Control (QC) roles in industries like pharmaceuticals and manufacturing can offer competitive salaries, especially with experience and relevant certifications. However, pay varies based on location, company size, and level of expertise, and QC positions are generally considered mid-range in terms of salary compared to other technical roles.

Is quality control part of GMP?

Yes, quality control is an essential component of Good Manufacturing Practice (GMP) standards. GMP requires quality control processes, including testing and validation, to ensure products meet safety and quality specifications. Quality control professionals in GMP environments perform inspections, sampling, and testing to maintain compliance and product integrity.

What is the highest paying job in pharmaceuticals?

In pharmaceuticals, senior roles such as Vice President of Quality or Director of Quality Control typically have the highest salaries, often exceeding six figures. These positions require extensive experience, leadership skills, and knowledge of Good Manufacturing Practices (GMP) and regulatory compliance.
More about Gmp Quality Control jobs
What cities are hiring for Gmp Quality Control jobs? Cities with the most Gmp Quality Control job openings:
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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, 76% Full Time, 19% Part Time, 1% Temporary, and 3% Contract. 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.

Director, GMP Quality Assurance

Jade Biosciences

On-site, Remote

Full-time

Posted 17 days ago

Job description

About Jade Biosciences
Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases. Jade's lead candidate, JADE101, targets the cytokine APRIL, and is currently being evaluated in a Phase 1 clinical trial for the treatment of immunoglobulin A nephropathy. Jade's pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as JADE301, an undisclosed antibody candidate, both currently in preclinical development. Jade was launched based on assets licensed from Paragon Therapeutics, an antibody discovery engine founded by Fairmount. For more information, visit JadeBiosciences.com and follow the Company on LinkedIn.
Role Overview
The Director, GMP Quality Assurance (QA) provides QA support across Jade's product pipeline across various stages of development. This role serves as a key partner to CMC and cross-functional teams, offering QA expertise, guidance and risk-based input to support development and product quality strategies.
The role provides QA oversight of contract manufacturers (CMOs) and service providers supporting cell bank, drug substance (DS), drug product (DP), finished drug product (FDP) packaging and labeling, and product distribution, ensuring alignment with GMP requirements and Jade quality standards.
Additionally, the position coordinates day-to-day GMP quality activities for outsourced manufacturing, including the intake, routing, tracking, and timely archival of quality records such as batch disposition, deviations, CAPAs, change controls, expiry/retest extensions, and product complaints. The Director collaborates with internal and external stakeholders to support timely, compliant documentation and batch release decisions. Additionally, the role may also support other QA Leads to promote cross-program alignment, consistency in QA practices, and balanced workload distribution.
This is a fully remote role, preferably based on the U.S. West Coast, with occasional domestic and international travel. The position reports to the Senior Director, GMP Quality Assurance.
Key Responsibilities
  • Serve as the QA lead for assigned GMP-related activities including quality oversight of CDMOs, tech transfer, scale-up, manufacturing (cell bank, DS, DP, FDP), and disposition of clinical materials
  • Quality reviewer and approver for quality records such as change controls, CAPAs, deviations, temperature excursions, product complaints, expiry/retest, stability protocols/reports, master batch records, method qualifications, etc.
  • Collaborate with CMC, Supply Chain, Analytical Development and Program Management to ensure on-time delivery of products and compliance with all relevant cGMP regulations and guidelines as they pertain to manufacturing and supply operations
  • Supports archival of documents/records, quality metrics and develop/maintain QA related tracking logs
  • Work directly with operating entities (internal and CMOs) to ensure that product(s) meet all required quality standards and specifications
  • Supports management of Quality Agreements, including project coordination, cross-functional review, and approval workflows
  • Represent the Quality function in product development (CMC) teams to provide proactive quality guidance and decisions
  • Influence other functional departments to ensure that CMOs achieve and maintain the appropriate levels of GMP compliance and provide the highest level of quality services to Jade
  • Lead quality risk management activities to proactively identify, assess, and mitigate GMP-related risks across manufacturing and supply operations
  • Facilitate resolution of quality issues with internal and external parties in a timely manner
  • Coordinate communications with CMOs and internal technical product teams on quality issues
  • Review CMC sections of regulatory filings, as needed
  • Collaborate cross-functionally with CMC, Regulatory, Clinical Supply Chain, and Program Leadership teams to ensure quality is embedded across development and manufacturing activities
  • Participate in and support regulatory authority inspections and internal audits
  • Supports development/maintenance of Quality SOPs
  • Contribute to the development and maintenance of a positive team-focused company culture
  • Other duties, as assigned

Qualifications
  • Bachelor's degree and 15 years of experience or a master's degree with 12+ years of experience in scientific discipline or comparable experience
  • 10+ years of experience in GMP Quality Assurance at an operational level supporting manufacturing and 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 regulations, device and combo product related guidelines, and other ICH guidelines
  • Ability to research and interpret international GMP related regulations and guidance
  • Experience managing CDMOs
  • Experience related to managing technology transfer, scale up, and validation
  • Experience supporting regulatory authority/notified body inspections
  • Experience supporting regulatory submissions (e.g. IND, BLA) and responses to health authority queries (e.g., FDA, EMA)
  • Strategic thinker with a hands-on approach; comfortable balancing long-term planning with day-to-day execution
  • Proven experience developing strong partnerships with cross functional key stakeholders to ensure that strategic business goals are met through the sharing of knowledge and teamwork
  • Must have excellent verbal, written, interpersonal and organizational skills
  • Strong communication and influencing skills, as well as problem solving ability to evaluate quality matters and make decisions utilizing risk-based approach
  • Must be self-motivated with the ability to thrive in a fast-paced, ambiguous environment while managing competing priorities
  • Excellent computer skills with working knowledge of MS Office such as Word and Excel, Visio and Adobe Acrobat professional, and familiarity with SharePoint
  • Commitment to fostering a diverse and inclusive workplace

Position Location
This is a remote role; up to 15% travel to team and company events is required.
The anticipated salary range for candidates for this role is $210,000 - $235,000. The final salary offered will depend on several factors, which may include, but not limited to, relevant years of experience, educational background, and geography.
As part of the I-9 verification of authorization to work in the United States, Jade Bioscience participates in E-Verify. To learn more about E-Verify please review this poster.
Jade Biosciences is proud to be an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.

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