Operational Quality Specialist

GlaxoSmithKline

Marietta (PA)

On-site

USD 90,000 - 130,000

Full time

5 days ago

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Job summary

GlaxoSmithKline is seeking an on-site QA professional to provide operational quality oversight at a United States manufacturing site. You will collaborate with production, labs, engineering and quality teams to ensure GMP compliance, safety and reliability, while supporting batch record review, deviations and CAPA decisions.

You will coach staff on quality behaviors, maintain inspection readiness, and drive continuous improvement in a fast-paced biologics/pharma environment at the Marietta site.

Qualifications

Bachelor's degree in biology, chemical engineering, life sciences field or a bachelor's degree in another discipline is acceptable if technical depth has been achieved from professional experience.
2+ years of experience in regulated industry with strong quality assurance background; biologics manufacturing preferred.
1+ years of experience with GMPs, NIH Guidelines, FDA and other regulatory compliance requirements.
Experience with validation principles, aseptic processing, quality systems; DMAIC root cause analysis; batch records and GMP documentation.

Responsibilities

Ensure all GMP processes and personnel adhere to GMP, regulations and procedures; minimize non-compliance and maintain inspection readiness.
Maintain shopfloor oversight; be first line of contact for quality issues and escalations.
Provide guidance during GMP activities to detect quality issues in real time for timely interventions.
Spot-check activities across production and lab areas for compliance in production, testing, cleaning and maintenance.
Review cGMP documentation and records; ensure GDP per ALCOA+; review and approve batch records.
Review deviations and CAPA plans; approve related documentation (PQRs, change controls, investigations, validation docs).
Ensure GMPs, validation, quality, safety and environmental regulations are met; follow safety guidelines.
Coach employees on procedures; communicate why non-compliance harms product quality and patient safety.
On-the-floor quality oversight; perform walk-throughs; review batch records, deviations and CAPA for completeness.
Support disposition decisions and lot release; assist with self-inspections and internal audits.

Skills

Data Integrity

Detail-Oriented

Digital Fluency

GxP Regulations

Influencing Without Authority

Lean Management

Pharmaceutical Regulatory Compliance

Problem Solving

Quality Assurance

Risk Awareness

Technical Writing

Education

Bachelor's degree in biology, chemical engineering, life sciences, or related field (or other discipline with technical depth)

Job description

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 quickly, 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:

You will provide operational quality oversight at a United States manufacturing site. You will work closely with production, laboratories, engineering and quality teams to keep processes compliant, safe, and reliable. To ensure adherence to cGxP standards and procedures through the independent oversight of GxP processes. To improve the effectiveness of quality in preventing, identifying and addressing quality issues by encouraging proactive quality culture and continuous improvement. To maintain presence and be accountable for batch record review and approval, key quality decision‑making, and quality escalations. To be a liaison between operations and the site QA Systems, QA Compliance and QA Product Release (QAPR) departments. We value practical problem solvers who make clear decisions and coach others. This role offers hands‑on learning, visible impact on product quality, and growth opportunities that align with our mission of uniting science, technology and talent to get ahead of disease together.

Responsibilities:

Ensure that all GMP processes and operational personnel adhere to current GMP, applicable regulatory requirements, and procedures, minimizing risk of non‑compliance and maintaining inspection readiness at all times.
Maintain shopfloor oversight across area of responsibility and be the first line of contact to support initial management of quality issues, demonstrate quality decision‑making, and provide quality escalations as needed.
Provide guidance during GMP activities to proactively detect potential quality issues through active observation in real‑time, allowing for timely interventions to prevent deviations and defects.
Perform a spot‑check of activities across production and laboratory areas to ensure compliance with quality standards that includes production, testing, cleaning and maintenance activities.
Carry out review of cGMP documentation and records ensuring that the content meets defined criteria, exceptions have been appropriately addressed, and Good Documentation Practice (GDP) is being maintained following ALCOA+ principles for data integrity, audit and traceability. Review and final approve batch records and batch related documentation.
Provide review, initial impact approval, and final approval of deviations and associated CAPA plans. Provide review and approval of documentation which may include procedural revisions, logbooks, PQRs, customer complaint investigations, change controls, validation documents, etc.
Ensure all GMPs, validation, quality, safety and environmental regulations are met. Adhere to all safety guidelines and procedures.
Role model by providing coaching to employees on the importance of following procedures, doing the right thing and explaining the why and the impact non‑compliance can have on product quality and patient safety.
Provide on‑the‑floor quality oversight, perform regular shopfloor walk‑throughs, and detect early quality risks. Review executed and master batch records, deviations, and CAPA plans for completeness and compliance.
Make or recommend disposition decisions and support lot release activities following defined procedures. Support and perform self‑inspections, internal audits, and inspection readiness activities.
Review and approve GMP documentation including change controls, validation summaries, and procedural updates. Investigate quality issues, support root cause analysis, and help implement corrective and preventive actions.

Why You?

This role is on‑site at a United States manufacturing location and requires regular presence in production and laboratory areas. We are building a team that values collaboration, clarity, and continuous learning. We are committed to inclusion and want colleagues who help create a respectful, supportive workplace.

Basic Qualifications:

We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

Bachelor's degree in biology, chemical engineering, life sciences field or a bachelor's degree in another discipline is acceptable if technical depth has been achieved from professional experience.
2 + years of experience in regulated industry. Strong quality assurance background. Experience in biologics manufacturing is strongly preferred. Experience working in pharmaceutical facilities, equipment, and quality systems.
1+ years of experience with GMP's, NIH Guidelines, FDA and other regulatory agency compliance requirements sufficient to apply to quality operations and compliance.
Experience with validation principles, aseptic processing, quality systems and FDA regulations. Experience with training in DMAIC root cause analysis methodology. Experience reviewing batch records and GMP documentation.

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

Experience in biologics or pharmaceutical manufacturing environments with deviations, CAPA, change control, and validation activities. Training or experience in root cause analysis methods such as DMAIC or similar.
Familiarity with inspection readiness and regulatory agency expectations. Demonstrated ability to influence cross‑functional teams and coach others on quality behaviors. Comfortable working in a fast‑paced environment and prioritizing competing demands.
Well‑developed interpersonal skills and decision‑making capabilities with the ability to influence different levels of the Site and Quality organization. Ability to deliver clear communications (written and verbally), coaching, foster a 'Quality Starts With Me' culture and work with a spirit of continuous improvement.
Ability to facilitate and generate the exchange of ideas to resolve problems, prioritize solutions, select optimal quality solutions and implement decisions. Time management skills and ability to prioritize and respond to operational needs and issues within high paced environment. Be a team player prepared to work in and embrace a multi‑skilled team‑based culture.

Skills

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

#LI-GSK

Business Introduction:

We manufacture and supply reliable, high‑quality medicines and vaccines to meet patients' needs and drive our performance.

Our supply chain is not just core to our operations; it's vital to bringing our innovations to patients as quickly, 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.

Position Summary:

Responsibilities:

Ensure that all GMP processes and operational personnel adhere to current GMP, applicable regulatory requirements, and procedures, minimizing risk of non‑compliance and maintaining inspection readiness at all times.
Maintain shopfloor oversight across area of responsibility and be the first line of contact to support initial management of quality issues, demonstrate quality decision‑making, and provide quality escalations as needed.
Provide guidance during GMP activities to proactively detect potential quality issues through active observation in real‑time, allowing for timely interventions to prevent deviations and defects.
Perform a spot‑check of activities across production and laboratory areas to ensure compliance with quality standards that includes production, testing, cleaning and maintenance activities.
Carry out review of cGMP documentation and records ensuring that the content meets defined criteria, exceptions have been appropriately addressed, and Good Documentation Practice (GDP) is being maintained following ALCOA+ principles for data integrity, audit and traceability. Review and final approve batch records and batch related documentation.
Provide review, initial impact approval, and final approval of deviations and associated CAPA plans. Provide review and approval of documentation which may include procedural revisions, logbooks, PQRs, customer complaint investigations, change controls, validation documents, etc.
Ensure all GMPs, validation, quality, safety and environmental regulations are met. Adhere to all safety guidelines and procedures.
Role model by providing coaching to employees on the importance of following procedures, doing the right thing and explaining the why and the impact non‑compliance can have on product quality and patient safety.
Provide on‑the‑floor quality oversight, perform regular shopfloor walk‑throughs, and detect early quality risks. Review executed and master batch records, deviations, and CAPA plans for completeness and compliance.
Make or recommend disposition decisions and support lot release activities following defined procedures. Support and perform self‑inspections, internal audits, and inspection readiness activities.
Review and approve GMP documentation including change controls, validation summaries, and procedural updates. Investigate quality issues, support root cause analysis, and help implement corrective and preventive actions.

Why You?

Basic Qualifications:

We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

Bachelor's degree in biology, chemical engineering, life sciences field or a bachelor's degree in another discipline is acceptable if technical depth has been achieved from professional experience.
2 + years of experience in regulated industry. Strong quality assurance background. Experience in biologics manufacturing is strongly preferred. Experience working in pharmaceutical facilities, equipment, and quality systems.
1+ years of experience with GMP's, NIH Guidelines, FDA and other regulatory agency compliance requirements sufficient to apply to quality operations and compliance.
Experience with validation principles, aseptic processing, quality systems and FDA regulations. Experience with training in DMAIC root cause analysis methodology. Experience reviewing batch records and GMP documentation.

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

Experience in biologics or pharmaceutical manufacturing environments with deviations, CAPA, change control, and validation activities. Training or experience in root cause analysis methods such as DMAIC or similar.
Familiarity with inspection readiness and regulatory agency expectations. Demonstrated ability to influence cross‑functional teams and coach others on quality behaviors. Comfortable working in a fast‑paced environment and prioritizing competing demands.
Well‑developed interpersonal skills and decision‑making capabilities with the ability to influence different levels of the Site and Quality organization. Ability to deliver clear communications (written and verbally), coaching, foster a 'Quality Starts With Me' culture and work with a spirit of continuous improvement.
Ability to facilitate and generate the exchange of ideas to resolve problems, prioritize solutions, select optimal quality solutions and implement decisions. Time management skills and ability to prioritize and respond to operational needs and issues within high paced environment. Be a team player prepared to work in and embrace a multi‑skilled team‑based culture.

Skills

#LI-GSK

#GSKCareers