New · posted Oct 27
GSK · Pharmaceuticals
Operational Quality Specialist - QC
- Marietta, PA
- On-site
- Full-time
- Associate & Specialist
The role
Principle Decisions and Complexity
- Decisions made for Quality directly impact the quality and suitability of the products produced at the Marietta site including the release of clinical trial materials and commercial products. Decisions must be made in accordance with regulations of the USP, CFR, EP and FDA.
- Manage a high number of projects in parallel. Priorities can change very quickly due to new business opportunity or new sales projection. High adaptability required for ability to keep teams motivated when priorities change. Facilitate opposing views among departments to resolution.
Oversee all Quality Control (QC) SOPs, QC Methods, unplanned events, Change Controls, CAPAs, continuous method validation, and QMS events for drug substance quality control activities. Drive excellence in Quality Control.
Join us as an Operational Quality Specialist in Quality Control. You will be at the heart of ensuring high-quality standards are met across manufacturing and testing operations. Working closely with production, laboratories, engineering, and quality teams, you’ll protect product quality and patient safety through clear decisions and hands-on support. We seek proactive problem-solvers who communicate openly and foster a strong quality culture. This role offers you growth, learning, and a chance to contribute to GSK’s mission of uniting science, technology, and talent to get ahead of disease together.
Responsibilities:
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
What you need
Basic Qualifications
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- Bachelor’s degree in chemistry, biochemistry, pharmaceutical sciences, or related scientific discipline. 2+ years of quality control experience and experience overseeing quality control testing..
- Prior experience with licensed biopharmaceutical or biological products preferred. Hands on experience using Analytical laboratory equipment/systems, such as HPLC, GC-MS, TOC, FTIR, ELISA is preferred. Hands on experience with Aseptic Environmental Monitoring programs, microbiological testing methods, such as, Sterility test USP<71>, Endotoxin testing USP<85>, Bioburden testing.
- Experience in quality systems, Quality Control Laboratories, including validation, documentation, compliance in a high volume, rapid turnaround release office or compliance department. Understanding of industry and science practices related to the business. Versed in GMP’s, NIH Guidelines, FDA and other regulatory agency requirements for validation and operations, analytical and stability functions and compliance. Demonstrated ability to drive initiatives across multiple business units under tight deadlines.
- Strong communication and problem-solving skills with demonstrated ability to work well with and influence others without direct reporting relationships. Ability to work in a high complex matrix environment with a sense of urgency, flexibility and accountability. Must be a committed team player prepared to work in and embrace a multi-skilled team-based culture. Proven record of providing excellent internal and external customer service.
- Stay current on developments in the field and GSK- Standards. Demonstrate a serious commitment to accuracy and quality while meeting goals or deadlines. This role is responsible for approving GMP quality control test methods for drug product and must understand the requirements for documentation related to QC testing.
Data Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Influencing Without Authority, Lean Management, Pharmaceutical Regulatory Compliance, Problem Solving, Quality Assurance (QA), Risk Awareness, Technical Writing
Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
Preferred Qualificationsnice to have
- Experience in a pharmaceutical or biologics manufacturing environment focusing on drug substance or product testing. Knowledge of laboratory information management systems (LIMS) or electronic lab notebooks. Training or experience in root cause analysis and structured investigation techniques. Experience supporting regulatory inspections and audit readiness activities.
- Ability to influence and coach laboratory staff and cross-functional teams on quality behaviors. Comfortable working in a fast-paced environment with multiple priorities.
Where you'll work
Marietta, PAOn-siteOpen in Maps (opens in a new tab)
More jobs in Marietta, PAWorking conditions
Work Arrangement
This role is on-site at a United States manufacturing location. Regular presence in production and laboratory areas is required. Hybrid or remote work is not available.
Ready to apply?
If this role feels like the right fit for your skills and ambitions, please apply. Tell us how your experience aligns with these responsibilities and qualifications. Share examples of how you helped improve quality processes or supported teams through change. We look forward to hearing from you and exploring how you can help make a real difference for patients.
From the posting
About GSK
Business Introduction
We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.
Position Summary:
- Provide oversight to all QC related quality system activities and take initiative to resolve and/or escalate concerns including Deviations, CAPAs, Change Controls, Validation, Analytical Method Transfers, Risk Assessment, and PQRs. Provide advice and counsel on cGMP and related quality assurance issues to QC managers and personnel.
- Demonstrated familiarity and compliance with GMPs, EHS procedures and regulations, facility regulatory guidelines and standard operating procedures. Provide on the floor QA support and perform QA Operation's activities (documentation review, logbook review, facility cleaning records for quarterly walkthroughs).
- Responsible for release of the rooms after the Return to Service testing for the lab areas and for status changes of lab areas in response to maintenance work or unplanned events. Responsible for QA oversight of the Stability and Retention program for the GSK Marietta site.
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - [email protected]
Equal opportunity, accessibility and legal noticesGSK's statements, word for word
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Job intelligence
The context around this role
Live data · October 28, 2026
Salary intelligence
How the pay compares
Associate & Specialist roles in the US130 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $49,125 | $61,250 | $78,500 |
Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 28, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 341 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not GSK's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 13 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods6
- Collaboration and leadership6
- GMP and compliance5
- Documentation and SOPs5
- Validation and qualification2
- Quality systems and risk2
- Data and digital systems2
- Investigations and CAPA1
- Regulatory submissions1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticals
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and Answers
- ICHICH quality guidelines(official source, opens in a new tab)Q1 stability, Q2(R2) analytical validation, Q7, Q9 risk management, Q10 quality systems
- USPUSP compendial chapters(official source, opens in a new tab)Bioburden (USP <61>), endotoxin (USP <85>), TOC (USP <643>) and water testing
Company hiring pulse
GSK on Regulatory Jobs
- 17
- Open roles
- 16
- Distinct roles
- 6
- Locations
By discipline
- Quality14 82%
- Regulatory2 12%
- Compliance & Safety1 6%
By level
- Associate & Specialist9 53%
- Manager3 18%
- Senior & Principal3 18%
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Operational Quality Specialist - QC at GSK
Open until filled.