Contract Manufacturing Quality Specialist - #146351

A collective energy and ambition. A place where you can make a real difference.

We’re a company that genuinely cares about our people, our products, our consumers and the environment.

Our unique, informal culture champions courage, determination and collaboration. Knowing we have an open and supportive team means each of us has the freedom to take responsibility and ownership. We have a shared passion to work hard, innovate and push boundaries.

United by the belief that when we strive for growth, anything is possible. While we might not be the largest company in our industry, we believe we can have the biggest impact because: Together We Have the Power to Win.

Are You Ready to Ensure Quality Excellence in Pharmaceutical Manufacturing? Do you have a passion for quality assurance and a keen eye for detail? Are you adept at navigating complex regulatory environments and fostering strong cross-functional relationships? If so, we have the perfect opportunity for you!

Join Our Team as a Contract Manufacturing Specialist!

About The Role

As a Contract Manufacturing Specialist, you will play a crucial role in ensuring the release of finished pharmaceutical, medical device, and cosmetic products within their approved specifications. You'll work closely with Contract Manufacturers, Supply Chain, and distribution partners to support and resolve non-conformances that impact Contract Manufactured finished products.

Key Responsibilities

• Champion Quality Culture: Foster a quality-driven environment within Supply Chain, GMS, and R&D teams.
• Cross-Functional Collaboration: Work effectively with key stakeholders both internally and at Contract Manufacturers.
• Support 3PL Warehouses: Address quality-related issues with Contract Manufactured finished products.
• Certificates of Analysis: Provide CofAs for stakeholders as needed.
• Product Release: Ensure finished products meet approved specifications before release.
• Non-Conformance Management: Document, investigate, and resolve non-conformances through the Agile system.
• Complaint Investigation: Assist in probing adverse complaints related to Contract Manufactured products.
• Metric Reporting: Support the reporting of monthly metrics and KPIs, driving continuous improvements.
  
  

What We’re Looking For

• Attention to Detail: Your meticulous nature ensures nothing slips through the cracks.
• Tech-Savvy: Proficient in Microsoft Word and Excel.
• Proactive: You plan ahead and take initiative.
• Decision Maker: Strong analytical skills to make accurate, timely decisions.
• Relationship Builder: Foster strong multi-functional relationships.
• Adaptable: Respond positively to change.
  
  

Education & Experience

• Experience: Proven experience in Quality Assurance within regulated industries is desirable.
• Education: Background in science or engineering.
• Knowledge: Familiarity with GMP/GDP, ISO22716, and/or ISO13485 is a plus.
  
  

Health & Safety Commitment

• Safety First: Support safety as a top priority.
• Awareness: Understand and follow all Health & Safety instructions.
• Reporting: Report accidents or near misses to the Health & Safety Manager.
  
  

Why Join Us?

• Impactful Work: Play a vital role in ensuring the quality and safety of essential products.
• Collaborative Environment: Work with a dynamic team dedicated to excellence.
• Growth Opportunities: Continuous learning and professional development.
• Competitive package: including 24 days annual leave (with the opportunity to purchase up to an additional 3 days), a pension matched up to 9%, discretionary annual bonus, life assurance cover and membership of a health cash plan.
  
  

Ready to take the next step in your career? Apply now and become a key player in ensuring the highest standards of quality in pharmaceutical manufacturing!

For more information on our company, our brands and our culture visit us at http://www.churchdwight.co.uk/

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