We are excited to announce an internal opportunity for a proactive and experienced candidate to join our Quality Control Team as a Stability Lead. This is a full-time, on-site position based on a 37.5-hour work week; Monday to Friday, playing a key role in the day-to-day operations of the department.
We’re looking for someone with strong leadership capabilities and a proven track record in managing teams. The ideal candidate will be detail-oriented, committed to compliance, and passionate about fostering a positive and productive working environment. If you're ready for a new challenge within a collaborative and supportive QC setting, we encourage you to apply!
Key Responsibilities:
1. Champion Health and Safety by adhering to policies, reporting incidents, identifying risks, and promoting a strong safety culture.
2. Support the Head of QC in cultivating a culture of quality, compliance, and continuous improvement (GMP, GLP, Data Integrity, Housekeeping).
3. Provide leadership and technical guidance to analysts, including training and mentorship.
4. Ensure timely review and approval of QC testing across raw materials, in-process, finished products, stability, and validation samples.
5. Oversee the closure of CAPAs, incidents, change controls, audits, SOPs, and method updates.
6. Manage laboratory systems and processes to maintain efficiency and regulatory compliance.
7. Participate in client and project meetings, ensuring seamless process management and timely invoicing.
8. Maintain accurate planning and scheduling, including 12-week visibility and timely completion of PQRs.
9. Ensure effective stability sample management and documentation.
10. Drive adherence to SOPs, GMP standards, and company policies.
11. Deliver on-site KPIs across Customer Service, Stability, HSE, Quality, and Financial metrics.
12. Provide timely client feedback and implement process improvements to enhance efficiency.
13. Promote team development through coaching, training, and encouraging adaptability.
You will have:
14. Strong knowledge of GMP and Global Pharmaceutical Regulations.
15. Demonstrated leadership experience in a laboratory or technical environment.
16. Expertise in chemistry, laboratory techniques, and chromatography systems/software.
17. Proficiency in analytical method development, transfer, and technical documentation (e.g., SOPs, reports).
18. Excellent communication, conflict resolution, and resource management skills.
19. Strong Microsoft Office skills, particularly in Excel.
20. A collaborative, solution-oriented mindset with a focus on continuous improvement.
21. Ability to mentor, multitask, and adapt to evolving priorities.
22. High energy, accountability, and alignment with company values.
** Please note the closing date for this role will be Monday 16th June 2025, if you are interested in applying, please send your CV to the HR Team for review**