Job Description
Associate Analyst QC – Pharmaceutical Microbiologist – 18m FTC
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 an Associate Analyst in our Quality Control – Microbiology team, you’ll play a vital role in ensuring the safety, quality and compliance of our raw materials and finished products. Working in accordance with cGMP standards, you’ll perform microbiological testing, support investigations, ensure accurate documentation and contribute to our continuous improvement culture.
This is an excellent opportunity for someone with analytical laboratory experience who is looking to develop deeper technical expertise in a fast‑paced pharmaceutical QC environment.
This role is an 18 Month Fixed Term Contract.
Key Responsibilities
* Conduct visual inspections and microbiological TVC/PET testing to USP, EP and BP monographs.
* Ensure laboratory cleanliness, safety compliance and high standards of housekeeping.
* Review internal and contract laboratory data to ensure regulatory compliance and accuracy.
* Participate in OOS, OOT, aberrant result and failure investigations; recommend corrective actions.
* Troubleshoot equipment issues and conduct routine calibrations according to SOPs and work instructions.
* Write, revise and maintain QC SOPs, work instructions and technical reports.
* Support key QC systems such as stability studies, RM risk assessments, reference standards and environmental monitoring.
* Collate QC data for regulatory submissions and support method transfer documentation.
* Uphold QC best practices, company values, safety standards and good documentation practices.
About You
We’re looking for someone who brings:
Experience & Knowledge
* 2–4 years’ experience in a GMP analytical laboratory.
* Previous experience with TVC/PET (AET) testing is essential.
* Bachelor’s degree in a relevant scientific discipline or A-level / scientific background with extensive analytical laboratory experience.
* Proficiency in microbiology techniques.
* Experience with GMP documentation and QC laboratory processes.
Skills & Competencies
* Strong problem-solving skills and attention to detail.
* Effective communication and the ability to work collaboratively within a team.
* Ability to investigate quality events and support root-cause analysis.
* Good business awareness and customer service mindset.
* Flexibility to support business needs, including occasional out-of-hours work.
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
Free On-Site Parking – Convenient access to our Leeds facility
Rosemont Rewards Platform – Discounts, free perks, and wellbeing tools for all employees
We are committed to fostering an environment of enablement where our people can grow, develop their talents, and pursue meaningful career paths. By placing patients and customers at the heart of everything we do, we drive high performance through accountability, consistency, and a strong governance structure. We champion inclusion, community, and a rewarding employee experience - creating a culture that supports development, celebrates achievement, and empowers individuals to thrive.
Diversity & Inclusion is integral to our culture and reflecting the patients we serve. At Rosemont, we believe equal opportunity for all is fundamental to our company's values and all our applicants can expect fairness and transparency in our recruitment process.
If this sounds like the perfect next step in your QC career, we’d love to hear from you - apply today and help us shape the future of patient-focused medicines!