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Quality Assurance Lead
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Quality Assurance Lead
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Wrexham, Wrexham, United Kingdom Meet Full timeAbout the RoleWe are seeking a highly skilled Quality Assurance Lead to join our dynamic QA Operations department. As a key member of our team, you will play a pivotal role in ensuring the highest standards of quality across our manufacturing processes.Key ResponsibilitiesProvide expert quality guidance and solutions based on a deep understanding of GMP,...
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Quality Control Specialist
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Quality Control Specialist
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Quality Control Specialist
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Quality Control Specialist
1 month ago
Wrexham, Wrexham, United Kingdom Kenton Black Ltd Full timeQC Analyst Job DescriptionAbout the Role:We are seeking an experienced QC Analyst to join our team at Kenton Black Ltd. As a QC Analyst, you will play a crucial role in ensuring the quality of our pharmaceutical products.Key Responsibilities:Perform analytical testing on pharmaceutical raw materials and finished products using HPLC/UPLC/UV/GC...
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Experienced Quality Assurance Specialist
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Quality Control Lead
2 months ago
About Meet:
Meet is a leading pharmaceutical company specializing in the development and manufacturing of innovative therapies. Our mission is to deliver high-quality products that improve patients' lives while fostering a culture of excellence, collaboration, and continuous improvement.
About the Role:
We are seeking a highly skilled Quality Assurance Manager to join our dynamic QA Operations team. As a key member of our organization, you will play a pivotal role in ensuring the highest standards of quality across our manufacturing processes.
This role will involve overseeing and supporting a wide range of activities, from drug substance production to biologics development, and engineering validations. Your expertise will be integral in maintaining compliance, driving improvements, and acting as a Subject Matter Expert (SME) across the product lifecycle.
Key Responsibilities:
- Provide expert quality guidance and solutions based on a deep understanding of GMP, QRM, and relevant manufacturing processes.
- Lead initiatives to enhance practices and procedures, ensuring alignment with GMP requirements for sterile medicinal products.
- Take charge of critical quality documentation, including review and approval of all drug substance release materials.
- Liaise with leadership and cross-functional teams, providing expert opinions and contributing to key quality discussions.
- Serve as a trusted SME within QA, offering coaching and learning opportunities to drive continuous improvement.
- Act as a deputy for the QA Operations Process Leader when needed, ensuring seamless quality operations.
Requirements:
- Extensive knowledge of cGMP and QRM in pharmaceutical manufacturing.
- Exceptional organizational skills, with the ability to prioritize, manage time, and assess risk effectively.
- A logical, process-oriented thinker with strong communication skills, capable of working collaboratively in a team.
- Proficiency in evaluation and root cause analysis, with a track record of leading quality improvements.
- Ability to be a point of contact for quality events and escalations, providing expert guidance and solutions.
What We Offer:
- A competitive salary and an enhanced benefits package, including an annual bonus, a generous pension scheme, and wellness allowances.
- A supportive environment with a fantastic culture and a strong commitment to Diversity & Inclusion.
- Opportunities for professional development and growth within a rapidly expanding company.
- A workplace recognized as a 'Best Workplace' and 'Best Workplace for Wellbeing,' with a genuine commitment to sustainability, powered by 100% renewable energy.