At a Glance
- Tasks: Ensure quality in manufacturing by reviewing records and supporting investigations.
- Company: Join Jazz Pharmaceuticals, a leader in innovative biopharmaceuticals.
- Benefits: Enjoy competitive salary, health insurance, and career development opportunities.
- Other info: Collaborative culture with exposure to cutting-edge projects.
- Why this job: Make a real impact on patients' lives through quality assurance in pharmaceuticals.
- Qualifications: Experience in regulated environments and strong attention to detail required.
The predicted salary is between 30000 - 40000 £ per year.
Jazz Pharmaceuticals is a global biopharmaceutical company dedicated to transforming the lives of patients and their families through innovative medicines. With leading therapies in neuroscience and oncology, Jazz is committed to advancing science and delivering life-changing treatments to people facing serious diseases.
We are seeking a detail-oriented Production Quality Specialist, Manufacturing to join our Sittingbourne manufacturing facility. In this role, you will be responsible for reviewing Batch Manufacturing Records, supporting quality investigations, maintaining GMP compliance, and driving continuous improvement initiatives across manufacturing operations.
Responsibilities- Review Batch Manufacturing Records (BMRs) to ensure completeness, accuracy, and compliance with GMP requirements and ALCOA+ principles.
- Verify all Critical Process Parameters (CPPs) have been met prior to release to Quality Assurance.
- Document deficiencies and raise deviations where appropriate.
- Author and maintain batch documentation, SOPs, and associated forms.
- Lead and support investigations including deviations, complaints, and quality events.
- Determine root causes and implement corrective and preventive actions (CAPA).
- Report compliance failures, trends, and potential risks.
- Support quality event management and continuous compliance monitoring.
- Participate in strategic projects including Electronic Batch Records (EBR) implementation and process improvement initiatives.
- Conduct GEMBA reviews and collaborate with Production, QA, and Supply Chain teams.
- Identify opportunities for productivity and efficiency improvements.
- Act as a quality ambassador, promoting best practices throughout the department.
- Maintain compliance with Health & Safety regulations and cGMP requirements.
- Report hazards, deficiencies, or safety concerns.
- Ensure all required training and competency assessments remain current.
- Experience reviewing manufacturing or quality documentation within a regulated environment.
- Strong understanding of GMP requirements and documentation practices.
- Experience managing quality events such as deviations, investigations, CAPA, Change Controls, or OOS events.
- Excellent attention to detail and written communication skills.
- Strong organizational and workload prioritization abilities.
- Proficiency with Microsoft Office applications.
- Ability to work independently and collaboratively across departments.
- Experience within the pharmaceutical, biotechnology, or scientific manufacturing industry.
- Familiarity with ERP systems.
- NVQ qualification or equivalent pharmaceutical industry certification.
- Experience supporting electronic batch record systems or digital transformation projects.
- Competitive salary based on experience.
- Medical, dental, and vision insurance.
- Retirement savings plan.
- Career development opportunities within a global pharmaceutical organization.
- Exposure to cutting-edge manufacturing and quality systems projects.
- Collaborative and innovative workplace culture.
Production Quality Specialist - Sittingbourne employer: Jazz Pharmaceuticals
Jazz Pharmaceuticals is an exceptional employer, offering a collaborative and innovative workplace culture at our Sittingbourne manufacturing facility. Employees benefit from competitive salaries, comprehensive medical coverage, and robust career development opportunities within a global biopharmaceutical organisation, all while contributing to life-changing treatments that transform the lives of patients and their families.
StudySmarter Expert Advice🤫
We think this is how you could land Production Quality Specialist - Sittingbourne
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Jazz Pharmaceuticals. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Jazz Pharmaceuticals.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Jazz Pharmaceuticals. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Jazz Pharmaceuticals is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Production Quality Specialist - Sittingbourne
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 Jazz 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 Jazz 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 Jazz 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 Jazz 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 Jazz 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 Jazz 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 Jazz 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.
