QC Senior Laboratory Technical Support
We Are Rosemont
For over 50 years, Rosemont Pharmaceuticals has been a trusted name in the development and manufacture of oral liquid medicines. With a portfolio of over 130 products – including 70 licensed medicines – we’re proud to support healthcare professionals and patients, especially those with swallowing difficulties.
Our purpose is clear: to improve patient outcomes through innovation in liquid formulations. We’re highly respected across the pharmaceutical industry and have played a key role in establishing best practices for dysphagia care.
Our mission is to create a globally connected, people‑focused organisation where every individual is empowered to thrive and achieve their best. If you’re passionate about making a meaningful impact to patients across the world and want to be part of a company with a strong heritage and ambitious vision, we’d love to hear from you.
About the Role
As QC Senior Laboratory Technical Support, you will play a pivotal role in ensuring the availability, compliance, and effective management of Quality Control laboratory equipment. Acting as a subject‑matter expert, you’ll support QC operations by coordinating equipment qualification/validation, maintenance, calibration, CAPEX projects, and data integrity activities within a GMP environment.
This role operates with minimal supervision and is key in supporting audits, quality events, and continuous improvement across the QC function.
This role requires the successful candidate to be based at our Leeds site Monday – Friday each week.
Key Responsibilities
- Coordinate and support all QC instrumentation maintenance and routine calibration activities
- Manage QC equipment lifecycle activities, including purchasing, qualification, and capitalisation through site CAPEX programmes
- Own and manage equipment‑related deviations, non‑conformances, incident reports, and “as‑found” calibration failures
- Maintain strong vendor relationships, including service contract review and renewal
- Coordinate software access and IT‑related QC support activities
- Review, update, and maintain equipment SOPs and work instructions
- Provide in‑house coaching and technical troubleshooting support to QC equipment team members
- Support regulatory inspections and customer audits, representing QC as required
- Contribute to site Quality Management System activities, including CAPA, change control, and data integrity risk assessments
- Collaborate cross‑functionally with Production, R&D, PMO, and other internal stakeholders
Skills, Knowledge & Experience
- Degree‑level qualification in a scientific discipline
- Experience in a GMP laboratory environment, with strong analytical and equipment knowledge
- Proven experience managing QC instrumentation, calibration, and compliance activities
- Strong understanding of Quality Management Systems and regulatory expectations
- Confident communicator with the ability to work cross‑functionally and support audits
- Proactive, organised, and able to manage complex technical issues with minimal supervision
- Flexible approach, with willingness to support activities outside standard working hours when required
Benefits
At Rosemont, we believe great benefits go beyond salary. That’s why our offering is shaped by what our people truly value:
Annual Bonus – Recognising your contribution to Rosemont
Healthcare Cash Plan or Private Medical Cover – Personal cover to support your health and wellbeing
3% Employee / 5% Company Pension Contribution – Helping you plan for the future
26 Days Annual Leave + Bank Holidays
Flexible Working – Including hybrid and flexible working hours available
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