At a Glance
- Tasks: Lead Quality Control teams in Microbiology and Chemistry to ensure product quality and compliance.
- Company: Catalent is a global leader in drug development, delivering over 7,000 life-saving products worldwide.
- Benefits: Enjoy career growth opportunities, work with top pharma companies, and be part of impactful projects.
- Why this job: Join a culture of continuous improvement and make a real difference in patients' lives.
- Qualifications: BSc in Chemistry, Pharmacy, or Biology; experience in pharmaceutical operations is essential.
- Other info: Catalent is an Equal Opportunity Employer committed to inclusivity.
The predicted salary is between 48000 - 72000 £ per year.
Catalent are currently recruiting for an Associate Director – Quality Control to join our busy Swindon site. The QC Associate Director is responsible for providing leadership and quality management support at Catalent’s Swindon site in the area of Quality Control.
This individual will have responsibility for Microbiology and Chemistry Quality Control aspects related to finished product testing and incoming material release. The individual will be expected to deputise for the Senior Quality Director as required.
The role:
- Lead the Microbiology and Chemistry Quality Control teams to consistently and compliantly deliver against performance and financial targets driven by business need.
- Support the development, implementation and communication of a clear strategic vision for Quality to maximize employee focus and develop a competitive advantage.
- Ensure adherence to the standards of quality ruled by current cGMPs and the Company’s Quality Policies and site standard operating procedures.
- Maintain the highest degree of product quality and quality systems, grounded by the ability and vision to anticipate and prevent quality and/or regulatory problems.
- Function as a Quality department liaison and subject matter expert to other department representatives.
- Maintain strong relationships with Commercial customers, regulatory organizations and other industry contacts. Use quality/regulatory intelligence to redesign processes accordingly.
- Support the implementation of EH&S compliance within the QC function, in compliance with local laws and Catalent Policies.
- Ensure QC systems are compliant with corporate and site procedures as well as industry standards such as, but not limited to, testing, training and analytical equipment.
- Author/compile metrics for the QC function; present summary data to site management/customers on a regularly scheduled basis; participate in the site Quality Management Review.
- Facilitate investigations and root cause analyses in the laboratories and broader business.
- Recommend commercial operations priorities from trends in data analyses.
- Develop and/or administer and maintain the QC training program and enforce cGMP compliance.
- Manage, motivate and empower the team, communicating and implementing HR policies within the Department.
- Ensure effective communication and dissemination of site Quality goals and objectives.
- Host and participate in Regulatory Inspections and customer audits as required.
- Drive a culture of continuous improvement within the QC areas, implement best practices and deliver tangible performance improvements; propose, implement and enforce improvements.
The Candidate:
- Minimum BSc preferred in Chemistry, Pharmacy, or Biology with experience in pharmaceutical/GMP operations – essential.
- Strong understanding of the functional areas of manufacturing, sourcing, materials management, quality assurance and control, microbiology and laboratory operations in a solid dosage manufacturing environment is preferred.
- A strong background in continuous improvement; experience of ‘Lean Lab’ and certification as a Lean Six Sigma Green Belt (or above) is preferred.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability.
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Associate Director, Quality Control employer: Catalent
Contact Detail:
Catalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director, Quality Control
✨Tip Number 1
Familiarize yourself with the latest cGMP regulations and quality control standards in the pharmaceutical industry. This knowledge will not only help you understand the expectations of the role but also demonstrate your commitment to maintaining high-quality standards.
✨Tip Number 2
Highlight your experience in leading teams and driving continuous improvement initiatives. Be prepared to discuss specific examples of how you've implemented Lean practices or Six Sigma methodologies in previous roles, as this aligns closely with the responsibilities of the Associate Director position.
✨Tip Number 3
Network with professionals in the pharmaceutical and quality control sectors. Engaging with industry contacts can provide valuable insights into the company culture at Catalent and may even lead to referrals that can strengthen your application.
✨Tip Number 4
Prepare to discuss your approach to managing regulatory inspections and audits. Being able to articulate your strategies for ensuring compliance and maintaining strong relationships with regulatory bodies will be crucial in demonstrating your fit for this leadership role.
We think you need these skills to ace Associate Director, Quality Control
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Associate Director - Quality Control position at Catalent. Understand the key responsibilities and required qualifications, especially in areas like Microbiology and Chemistry Quality Control.
Tailor Your CV: Customize your CV to highlight relevant experience in pharmaceutical/GMP operations, quality assurance, and continuous improvement methodologies such as Lean Six Sigma. Emphasize any leadership roles or projects that align with the responsibilities outlined in the job description.
Craft a Compelling Cover Letter: Write a cover letter that not only showcases your qualifications but also demonstrates your understanding of Catalent's mission and values. Mention specific examples of how you have led teams or improved quality processes in previous roles.
Highlight Compliance Knowledge: Since adherence to cGMPs and quality policies is crucial for this role, make sure to include any relevant certifications or training related to quality control and compliance. Discuss your experience with regulatory inspections and audits if applicable.
How to prepare for a job interview at Catalent
✨Showcase Your Leadership Skills
As an Associate Director, you'll be leading teams in Quality Control. Be prepared to discuss your leadership style and provide examples of how you've successfully managed teams in the past, especially in high-pressure environments.
✨Demonstrate Your Knowledge of cGMP Standards
Since adherence to current Good Manufacturing Practices (cGMP) is crucial for this role, make sure you can articulate your understanding of these standards and how you've implemented them in previous positions.
✨Prepare for Technical Questions
Expect to face technical questions related to microbiology and chemistry quality control. Brush up on relevant testing methods and quality assurance processes to demonstrate your expertise.
✨Emphasize Continuous Improvement Experience
Catalent values a culture of continuous improvement. Be ready to share specific examples of how you've driven process improvements in your previous roles, particularly any experience with Lean methodologies or Six Sigma.