Stability Lead - Internal Candidates Only

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:

• Champion Health and Safety by adhering to policies, reporting incidents, identifying risks, and promoting a strong safety culture.


• Support the Head of QC in cultivating a culture of quality, compliance, and continuous improvement (GMP, GLP, Data Integrity, Housekeeping).


• Provide leadership and technical guidance to analysts, including training and mentorship.


• Ensure timely review and approval of QC testing across raw materials, in-process, finished products, stability, and validation samples.


• Oversee the closure of CAPAs, incidents, change controls, audits, SOPs, and method updates.


• Manage laboratory systems and processes to maintain efficiency and regulatory compliance.


• Participate in client and project meetings, ensuring seamless process management and timely invoicing.


• Maintain accurate planning and scheduling, including 12-week visibility and timely completion of PQRs.


• Ensure effective stability sample management and documentation.


• Drive adherence to SOPs, GMP standards, and company policies.


• Deliver on-site KPIs across Customer Service, Stability, HSE, Quality, and Financial metrics.


• Provide timely client feedback and implement process improvements to enhance efficiency.


• Promote team development through coaching, training, and encouraging adaptability.

You will have:

• Strong knowledge of GMP and Global Pharmaceutical Regulations.


• Demonstrated leadership experience in a laboratory or technical environment.


• Expertise in chemistry, laboratory techniques, and chromatography systems/software.


• Proficiency in analytical method development, transfer, and technical documentation (e.g., SOPs, reports).


• Excellent communication, conflict resolution, and resource management skills.


• Strong Microsoft Office skills, particularly in Excel.


• A collaborative, solution-oriented mindset with a focus on continuous improvement.


• Ability to mentor, multitask, and adapt to evolving priorities.


• 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**