About Company
GSK (GlaxoSmithKline) is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We are committed to impacting the health of billions worldwide through the discovery, development, and delivery of innovative medicines and vaccines. Our dedication extends across therapeutic areas including infectious diseases, HIV, oncology, immunology, and respiratory conditions. At GSK, we foster an environment where scientific curiosity thrives, where talent is nurtured, and where diversity of thought leads to groundbreaking solutions. We believe in being a responsible corporate citizen, upholding the highest ethical standards, and striving for a sustainable future. Join a team where your work truly matters, contributing to a healthier world and shaping the future of medicine. We are driven by our values: Patient Focus, Transparency, Respect, and Integrity, and supported by our behaviors: Courage, Accountability, Development, and Teamwork.
Job Description
We are seeking a highly motivated and detail-oriented Quality Assurance Associate to join our dedicated team in East Hill, Pensacola. This is an incredible opportunity to contribute to GSK’s mission of improving human health by ensuring the highest standards of quality and compliance in our pharmaceutical operations. As a Quality Assurance Associate, you will play a critical role in upholding GSK’s rigorous quality management systems, safeguarding product integrity, and ensuring adherence to Good Manufacturing Practices (GMP) and regulatory requirements. You will be instrumental in the review of production records, batch documentation, and supporting investigations to resolve quality issues. This position is ideal for an individual passionate about quality excellence, keen on learning, and eager to make a tangible impact within a world-leading biopharmaceutical company. Your work will directly influence the safety and efficacy of products reaching patients globally. We are looking for someone who thrives in a fast-paced environment, possesses strong analytical skills, and is committed to continuous improvement. If you are ready to apply your expertise in a role that combines scientific rigor with real-world impact, then we encourage you to apply and become a vital part of our quality journey. We are building a future-ready quality organization focused on innovation, efficiency, and unwavering commitment to patient safety. Your contributions will not only ensure compliance but also drive process enhancements that elevate our operational excellence.
Key Responsibilities
- Review and approve batch production records, laboratory control records, and other GMP documentation for completeness and accuracy.
- Perform line clearances and in-process checks to ensure adherence to manufacturing procedures and quality standards.
- Participate in deviation investigations, root cause analysis, and the implementation of corrective and preventive actions (CAPAs).
- Support the preparation for and execution of internal and external audits, including regulatory inspections.
- Contribute to the development and revision of Standard Operating Procedures (SOPs) and other quality-related documents.
- Monitor and ensure compliance with all applicable local, federal, and international regulations (e.g., FDA, EMA).
- Assist in the training of manufacturing personnel on quality procedures and GMP requirements.
- Support the release of raw materials, in-process materials, and finished products.
- Identify opportunities for continuous improvement within the quality system and participate in improvement projects.
Required Skills
- 2+ years of experience in Quality Assurance within a regulated industry (Pharmaceutical, Biotechnology, Medical Devices).
- Strong understanding of Good Manufacturing Practices (GMP) and relevant regulatory requirements.
- Excellent attention to detail and strong analytical skills.
- Proficiency in reviewing technical documentation and identifying discrepancies.
- Effective written and verbal communication skills.
- Ability to work independently and collaboratively in a team environment.
- Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
Preferred Qualifications
- Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Pharmacy, Engineering).
- Experience with electronic Quality Management Systems (eQMS).
- Knowledge of aseptic processing and sterile manufacturing.
- Certifications in Quality Assurance (e.g., ASQ Certified Quality Associate).
Perks & Benefits
- Competitive salary and performance-based bonuses.
- Comprehensive health, dental, and vision insurance plans.
- 401(k) retirement plan with company match.
- Generous paid time off (PTO) and holidays.
- Opportunities for professional development and continuous learning.
- Employee assistance programs.
- Inclusive and diverse company culture.
- Life and disability insurance.
How to Apply
Interested candidates are encouraged to click on the application link below to submit their resume and cover letter directly through the GSK careers portal. Please ensure your application highlights your relevant experience and qualifications for this role. Only applications submitted through the official portal will be considered.