At a Glance
- Tasks: Lead quality control investigations and ensure compliance in microbiology lab operations.
- Company: Rosemont Pharmaceuticals, a trusted name in oral liquid medicine development.
- Benefits: Annual bonus, healthcare cash plan, flexible working, and 26 days annual leave.
- Other info: Join a culture that champions inclusion, growth, and meaningful career paths.
- Why this job: Make a real impact on patient care while working in a dynamic pharmaceutical environment.
- Qualifications: Degree in Microbiology and experience in GMP laboratory settings required.
The predicted salary is between 35000 - 44962 £ per year.
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
We are looking for an experienced Senior Analyst to join our Quality Control team focussing on Microbiology.
This role plays a key part in ensuring the quality, compliance and continuous improvement of our laboratory operations.
Reporting to the QC leadership team, you will provide advanced analytical expertise, lead investigations, support method validation activities, and contribute to the successful delivery of business-critical projects.
This is an exciting opportunity for an analytical professional who enjoys solving complex problems, driving improvement initiatives and working collaboratively across multiple departments to support the delivery of high-quality medicines to patients.
This role requires the successful candidate to be based at our Leeds facility Monday – Friday each week.
Key Responsibilities
- Lead and support Out of Specification (OOS) investigations and root cause analysis activities.
- Perform QC compliance gap assessments against relevant pharmacopoeial and regulatory requirements.
- Support method optimisation, verification, validation and transfer activities.
- Review validation, stability and risk assessment reports.
- Prepare and review technical transfer protocols and reports.
- Participate in CAPA implementation, change controls and continuous improvement programmes.
- Support audit readiness activities and contribute during regulatory and customer audits.
- Represent Quality Control with key internal stakeholders including Production, R&D and Project Management teams.
- Contribute to New Product Development (NPD) projects and QC deliverables.
- Provide coaching, training and technical support to colleagues while deputising for Team Leaders when required.
- Maintain compliance with GMP, Quality Management Systems and company procedures.
What We're Looking For
Essential
- Degree in Microbiology or equivalent relevant experience.
- Strong Microbiology Skills and experience in performing Microbiology laboratory work such as Preservative efficacy testing, total viable counts, environmental monitoring and water testing
- Significant experience working within a GMP laboratory environment.
- Strong understanding of analytical testing, method validation and laboratory compliance requirements.
- Experience leading investigations, CAPAs and continuous improvement initiatives.
- Excellent report writing, problem-solving and risk assessment skills.
- Ability to work independently whilst managing complex technical issues.
- Strong communication and stakeholder management capabilities.
- Strong Team work and organisation skills.
- Experience in scheduling and planning team activities.
Desirable
- 4+ years' experience in a Quality Control analytical laboratory environment.
- Experience supporting regulatory inspections and customer audits.
- Leadership, coaching or mentoring experience.
- Experience supporting pharmaceutical product development or technical transfer activities.
- Success in this Role
The successful candidate will be a proactive and detail-oriented quality professional with strong business awareness, customer focus, communication skills and a passion for teamwork.
You will thrive in a fast-paced pharmaceutical environment and be motivated by delivering high-quality outcomes that ultimately benefit patients.
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 – 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.
Ready to Make a Difference?
If you're looking for an opportunity to apply your Quality Control expertise in a role that directly supports patient care and product quality, we'd love to hear from you.
Apply today and become part of a team dedicated to improving patient outcomes and shaping the future of oral liquid medicines!
StudySmarter Expert Advice🤫
We think this is how you could land Senior Analyst – Quality Control (Microbiology) in Bradford
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We think you need these skills to ace Senior Analyst – Quality Control (Microbiology) in Bradford
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Rosemont Pharmaceuticals!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Rosemont Pharmaceuticals that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Rosemont Pharmaceuticals!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Rosemont Pharmaceuticals, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Rosemont Pharmaceuticals
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Rosemont Pharmaceuticals that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Rosemont Pharmaceuticals’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
