Senior Batch Record Review Specialist at GSK

Zebulon, North Carolina, United States -

Full Time

Start Date

Immediate

Expiry Date

31 Jul, 26

Salary

0.0

Posted On

02 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Batch record review, Quality assurance, cGMP, GDP, Regulatory compliance, CAPA, Deviation management, Change control, Lot release, Root cause analysis, Problem solving, Documentation review, Pharmaceutical manufacturing, Quality guidance, Technical writing

Industry

Pharmaceutical Manufacturing

Description

Site Name: USA - North Carolina - Zebulon Posted Date: May 2 2026 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 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 lead batch record review activities to Release product that is manufactured and/or packaged in compliance with regulatory agencies’ requirements and company standards. Provide quality guidance to Zebulon Production department to ensure their activities are in compliance with regulatory agencies’ requirements and company standards. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Primarily responsible for review, release, and second check of batch record documentation for compliance to cGMPs, SOPs, and internal and regulatory requirements. Coordinates investigations associated with production deviations, as needed. Closes Planned Notifications, as needed. Assists with issues of NRFT for batch documents. Provides quality guidance to production operations, completes work order assessments, and completes atypical comments. Communicates effectively with team members, escalates issues to production and quality team/lead, and provides on-call support, as needed. Supports self-inspections, internal audits and regulatory inspections. Supports Problem Solving/Root Cause Analysis to identify Root Causes and appropriate CAPAs for identified problems. Supports OQ training. Provides end user support for GMP related documentation corrections. Supports continuous improvement processes. Supports certificate (CofA, CofC) creation, review and second check verification in alignment with market requirements and GSK standards along with. Agree personal objectives from the quality strategy and develops oneself. Why You? Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals: High School Diploma plus 4 years relevant experience in the pharmaceutical industry, with a production or quality background. -or- Associates degree plus 2 years relevant experience in the pharmaceutical 3+ years experience in batch record review, quality assurance, or operations within a regulated life sciences environment. Practical knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). Experience reviewing production, laboratory, and control records for compliance. Experience with quality systems such as deviations, CAPA, change control, and lot release. Preferred Qualification If you have the following characteristics, it would be a plus: Bachelor’s degree in a scientific, engineering, or quality discipline. Knowledge of cGMP - FDA and other Regulatory requirements. Understanding of continuous improvement tools. Understanding of IT applications; i.e. MERP, Microsoft office, LIMS. Good communication skills. Good organizational skills. Knowledge of Pharmaceutical Processes. Strong attention to detail, clear written communication, and the ability to follow procedures. Demonstrated serious commitment to accuracy, integrity and quality. Must be able to work independently but also be a strong team player. Entry level experience of MERP. About the Zebulon Site GSK’s Zebulon site is a global supplier of Respiratory and Solid Dose medicines to patients around the globe and the largest GSK Pharmaceutical secondary manufacturing site in North America. The site is located less than 30 minutes from downtown Raleigh, Wendell, Knightdale, Rocky Mount, Wilson, and Wake Forest. Key differentiators about GSK and Zebulon: Our commitment to inclusion is seen as a critical advantage of ours Our focus on cultivating a positive work environment that cares for our employees Demonstrated opportunities for continued career growth driven by individual ambition Leaders that care about their teams and growth of both individuals and the company A priority focus on Safety and Quality Clean and GMP compliant work environment Onsite cafeteria Onsite gym Temperature-controlled climate Licensed, onsite Health & Wellness clinic Work arrangement This position is on-site and may require some nights or weekend work. Shift work on Nights or weekends is eligible to receive a shift premium for work during those scheduled hours. What we value We look for people who act with integrity, put patients first, and work well with others. We welcome applicants from all backgrounds and encourage people who bring different perspectives to apply. If you are ready to grow your career, deepen your quality expertise, and make a real impact, please apply and tell us how your experience fits this role. #LI-GSK Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. 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 - usrecruitment.adjustments@gsk.com 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. 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/

Responsibilities

Lead batch record review activities to ensure product release complies with regulatory and company standards. Provide quality guidance to production operations and coordinate investigations into deviations and root causes.