Analyst Stability Lab

Haleon is a global leader in consumer healthcare, committed to enhancing everyday health for millions of people worldwide. The company’s portfolio includes well-known brands such as Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum. Haleon combines deep human insight with trusted scientific innovation to drive growth and improve health outcomes. The organization promotes a collaborative and inclusive culture that values agility and shared success. Supporting a hybrid working model, Haleon encourages employees to maintain a healthy work-life balance and to bring their authentic selves to the workplace.

Key Responsibilities
- Conduct timely and accurate analysis of stability samples, including accelerated, ongoing, and long-term studies, ensuring full compliance with key performance indicators (KPIs).
- Perform analysis on New Product Introduction (NPI) batches, validate and verify analytical methods, and test reference standards for qualification purposes.
- Prepare stability protocols and reports, manage sample receipt, update schedules, and ensure correct labeling and retrieval of samples within designated timelines.
- Maintain comprehensive documentation such as worksheets, logbooks, protocols, and reports in accordance with data integrity principles (ALCOA+).
- Regularly monitor stability chambers and promptly report any malfunctions or irregularities.
- Identify and report any Out of Trend (OOT), Out of Specification (OOS), atypical results, events, or deviations without delay.
- Ensure proper disposal of laboratory waste following established safety standards.
- Provide timely stability data to the Quality Systems (QS) department to support Periodic Product Review (PPR) reporting.
- Accurately archive stability data and maintain trackers to facilitate easy retrieval and regulatory compliance.
- Support the Finished Goods Testing department in achieving Confirm to Release (CTR) targets.
- Assist in audit preparation activities in coordination with the reporting manager.
- Adhere strictly to Good Manufacturing Practices (GMP), company quality policies, legal requirements, and Haleon guidelines.
- Comply with Environmental, Health, and Safety (EHS) policies and legal standards.
- Perform additional duties as assigned to meet evolving business needs.

Required Qualifications
- Master’s degree in Chemistry or Pharm D.
- 1-2 years of experience as an analyst within a Quality Control (QC) laboratory environment.
- Strong analytical skills and a solid understanding of pharmaceutical industry standards and best practices.

Preferred Qualifications and Benefits
Haleon fosters a dynamic and inclusive workplace where diversity is celebrated and employees are empowered to innovate and grow. The company embraces an agile working culture that offers flexibility in work arrangements, tailored to role requirements and agreed upon between employees and managers. Haleon is committed to equal opportunity employment and provides reasonable accommodations throughout the recruitment process to support all candidates. Joining Haleon means contributing to a mission focused on making everyday health more accessible, inclusive, and sustainable on a global scale.

If you are passionate about advancing healthcare and want to be part of a company that values your unique perspective while supporting your professional development, Haleon invites you to explore this opportunity and build a rewarding career with them.