At a Glance
- Tasks: Lead a team in microbiological testing and ensure compliance with GMP standards.
- Company: Ipsen, a global biopharmaceutical company focused on transformative medicines.
- Benefits: Hybrid working, career development, and a supportive workplace culture.
- Other info: Join a diverse team committed to innovation and quality in healthcare.
- Why this job: Make a real impact on patient lives while leading a passionate team.
- Qualifications: Degree in Life Science and experience in a cGMP-regulated environment.
The predicted salary is between 37800 - 46200 £ per year.
About Ipsen
Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation. Our passionate teams in more than 40 countries are focused on what matters and endeavour every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society!
Job Description
QC Microbiology Shift Team Leader
Location: Wrexham
Hybrid Working Available
Leadership Opportunity | GMP Manufacturing | Pharmaceutical Quality Lead Quality. Drive Compliance. Develop Talent.
Are you an experienced microbiology professional looking for your next leadership challenge in a highly regulated pharmaceutical environment? At Ipsen, we're looking for a QC Microbiology Shift Team Leader to lead a talented team responsible for critical microbiological testing and environmental monitoring activities that help ensure the delivery of safe, high-quality medicines to patients worldwide. This is an exciting opportunity to combine your technical microbiology expertise with people leadership, continuous improvement, and cross-functional collaboration in a site that places quality, innovation, and patient outcomes at the heart of everything we do.
What You'll Be Doing
- Providing day-to-day leadership for the QC Microbiology team, ensuring the timely delivery of microbiological testing and environmental monitoring activities while maintaining the highest standards of GMP compliance and data integrity.
- Leading, coaching and developing a high-performing team of microbiologists.
- Managing laboratory schedules, resources and priorities to ensure on-time delivery.
- Reviewing microbiological data including bioburden, sterility, endotoxin and environmental monitoring results.
- Supporting batch certification and release activities through microbiological assessment and reporting.
- Driving investigations relating to OOS, OOT and OOE events.
- Partnering with Sterility Assurance, QA, Production and Technical Operations teams to assess microbiological risks and support decision-making.
- Leading continuous improvement initiatives across QC Microbiology operations.
- Monitoring and reporting team performance through meaningful KPIs.
- Ensuring audit and inspection readiness at all times.
- Supporting regulatory inspections and customer audits.
- Promoting a strong quality and safety culture across the laboratory.
What We're Looking For
We're interested in hearing from candidates who bring both strong technical expertise and proven people leadership experience.
- Essential Requirements
- Degree in a Life Science discipline.
- Experience working within a cGMP-regulated pharmaceutical or biopharmaceutical microbiology laboratory.
- Strong knowledge of microbiological testing including: Bioburden, Sterility testing, Endotoxin testing, Environmental monitoring.
- Experience leading investigations relating to OOS, OOT and OOE results.
- Experience managing laboratory resources, schedules and priorities.
- Previous experience leading, coaching or developing teams.
- Good understanding of GMP requirements and regulatory expectations.
- Highly Desirable
- Degree in Microbiology.
- Strong knowledge of EU GMP Annex 1 and ICH Q9.
- Experience with contamination control strategies and aseptic processing environments.
- Knowledge of isolator technology.
- Experience managing CAPAs, change controls and audit readiness programmes.
We are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace 'The Real Us'. The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve.
If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application.
At Ipsen, each employee makes a real impact. Our teams are passionate about what they do because they care about making a difference in patients' lives. We invest in our employees to support life-changing projects that create positive impact for patients and society.
QC Microbiology Shift Team Leader employer: Ipsen
Ipsen in Wrexham is an excellent employer, offering a collaborative work culture that prioritises innovation and excellence. Employees benefit from a supportive environment with opportunities for professional growth, all while working in a state-of-the-art packing facility that operates on a convenient Monday to Friday schedule. Join us to be part of a team that values your expertise and contributions in mechanical engineering and vision systems.
StudySmarter Expert Advice🤫
We think this is how you could land QC Microbiology Shift Team Leader
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We think you need these skills to ace QC Microbiology Shift Team Leader
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 Ipsen!
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 Ipsen 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 Ipsen!
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 Ipsen, 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 Ipsen
✨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 Ipsen that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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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.
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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.