Hello.
We’re Haleon, a new world-leading consumer health company. Shaped by all who join us, we’re improving everyday health for billions of people by growing and innovating our global portfolio of category-leading brands—including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum. We achieve this through a combination of deep human understanding and trusted science, in a company we control, in an environment we co-create, within a culture that’s uniquely ours. Care to join us? It isn’t a question.
Haleon is recruiting for a QC Analyst responsible for analyzing raw materials, intermediates, stability samples, and/or finished products. The role includes peer data review and micro duties/training such as completion of micro environmental testing, micro analysis of raw materials and finished products, among others.
Responsibilities:
1. Promote expected Haleon behaviors and activities.
2. Carry out sampling and testing activities aligned with GLP and business targets.
3. Achieve lead-time targets and proactively address barriers.
4. Maintain full EHS and GLP compliance in all activities.
5. Follow DI expectations and ensure QC documentation complies with cGLP or cGDP practices, including electronic records.
6. Complete CAPAs and other site metrics on time.
7. Complete on-the-job training and maintain training records.
8. Support PPR (Medicinal only) and other site processes.
9. Own laboratory CI processes and support site CI/HAPs projects.
10. Communicate effectively with a customer-support focus.
11. Take accountability for all aspects of work with a can-do attitude.
Impact on Business Objectives:
1. Ensure QC team works safely and in accordance with GxP.
2. Train QC team members for specific tasks per GxP.
3. Make decisions and liaise with internal departments to disposition products per GMP.
4. Coordinate with corporate colleagues to resolve issues.
5. Report issues to relevant managers and directors.
6. Review analytical reports before OQ approval.
7. Prepare and review SOPs.
8. Troubleshoot analytical problems.
9. Schedule functions to maintain efficiency and product lead times.
10. Support site CI/HAPs projects and audits.
Required Skills & Experience:
* Bachelor’s degree or higher in Chemistry or related science.
* 2-3 years of experience in pharmaceutical or healthcare industry.
* Understanding of directives, standards, and quality management systems related to manufacturing of medical devices and medicinal products.
* Ability to contribute to management decisions.
Preferred Skills & Experience:
* Postgraduate science degree preferred.
Join us to discover what life at Haleon is really like: www.haleon.com/careers/
We embrace diversity and strive for an inclusive environment that values unique perspectives, supports communities, and promotes fairness. We believe in flexible working arrangements and encourage open discussions about opportunities.
As part of our application process, you may voluntarily share personal information to help us foster a diverse candidate pool. This information remains confidential and is not accessible to hiring managers.
Haleon is an Equal Opportunity Employer. All qualified applicants will be considered without regard to race, color, religion, sex, sexual orientation, gender identity, age, disability, or protected veteran status.
If you require accommodations during the application process, please inform your recruiter with specific requests. We are committed to supporting all candidates throughout their hiring journey.
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