Senior Quality Officers in Birmingham

Senior Quality Officers in Birmingham

Birmingham Full-Time 60000 - 80000 £ / year (est.) No working from home possible
ZEISS Group

At a Glance

  • Tasks: Lead global Quality for Consumer Eyecare, ensuring top-notch product safety and compliance.
  • Company: ZEISS, a leading tech enterprise in optics and optoelectronics with a global presence.
  • Benefits: Competitive salary, diverse work environment, and opportunities for professional growth.
  • Other info: Dynamic role with international collaboration and career advancement opportunities.
  • Why this job: Join a pioneering company and make a real difference in eye health products worldwide.
  • Qualifications: Experience in quality management and strong leadership skills required.

The predicted salary is between 60000 - 80000 £ per year.

ZEISS is technology and innovation. We develop, manufacture and sell highly innovative products and solutions for our customers in a variety of business fields – always testing the limits of what is feasible.

Lead the global Quality function for Consumer Eyecare across the US, EU, China, and future markets.

  • Build, lead, and continuously improve a scalable global Quality organization covering QMS, Pharmacovigilance / Post-Market Surveillance, Supplier Quality, and Contract Manufacturing Quality.
  • Ensure ZEISS Consumer Eyecare products are developed, sourced, manufactured (including external/contract manufacturing), released, distributed, and monitored in line with applicable quality, safety, and regulatory requirements.
  • Act as the senior Quality partner to the business for launches, market expansion, supplier and contract manufacturing decisions, product changes, and quality risk management across Consumer Eyecare categories such as eye drops, eye vitamins, lid care, and other adjacent eye health products.
  • Define and lead the global Quality strategy, governance, and operating model for Consumer Eyecare, including external and contract manufacturing.
  • Lead local Quality teams in the US, EU, and China, ensuring strong capability, clear accountability, and consistent execution.
  • Own global quality governance for complaints, deviations, non-conformances, investigations, CAPAs, change controls, recalls, and management review.
  • Oversee quality processes for Pharmacovigilance / vigilance / Post-Market Surveillance, including compliant reporting, escalation, trend monitoring, and inspection readiness.
  • Lead Supplier Quality and Contract Manufacturing Quality across CDMOs, contract manufacturers, packers, and critical suppliers.
  • Ensure compliance with applicable regulatory frameworks, including but not limited to: United States: U.S. Food and Drug Administration regulations; China: National Medical Products Administration (NMPA) requirements, China GMP, Medical Device Regulations, filing/registration requirements, and local vigilance reporting obligations.
  • Own supplier and contract manufacturer qualification, audits, onboarding, quality agreements, performance management, and risk-based oversight.
  • Ensure end-to-end quality oversight of externally manufactured products.

Senior Quality Officers in Birmingham employer: ZEISS Group

At ZEISS, we pride ourselves on being a leading technology enterprise that fosters innovation and excellence in the optics and optoelectronics industries. Our collaborative work culture encourages professional growth and development, offering employees the chance to lead impactful global quality initiatives while working alongside talented teams across multiple regions. With a commitment to quality and compliance, we provide a dynamic environment where your contributions directly enhance the health and well-being of consumers worldwide.

ZEISS Group

Contact Details:

ZEISS Group Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Senior Quality Officers in Birmingham

Unlock Networking Opportunities

Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like ZEISS Group. 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 ZEISS Group.

Leverage Internships for Full-time Roles

If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like ZEISS Group. 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 ZEISS Group is looking for. A tailored application can really make you stand out!

We think you need these skills to ace Senior Quality Officers in Birmingham

Quality Management Systems (QMS)
Pharmacovigilance
Post-Market Surveillance
Supplier Quality Management
Contract Manufacturing Quality
Regulatory Compliance
Risk Management

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 ZEISS Group!

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 ZEISS Group 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 ZEISS Group!

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 ZEISS Group, 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 ZEISS Group

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 ZEISS Group 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 ZEISS Group’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.