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- Tasks: Review batch documentation for accuracy and compliance in a fast-paced environment.
- Company: Join Catalent, a global leader in drug development and manufacturing, dedicated to improving lives.
- Benefits: Enjoy competitive salary, bonuses, generous holidays, and discounts at national retailers.
- Why this job: Be part of a dynamic team making a real impact on patient health with innovative products.
- Qualifications: Strong communication skills and previous GMP experience are essential; IT proficiency is a plus.
- Other info: Work a unique 4 days on, 4 days off shift pattern for better work-life balance.
The predicted salary is between 30000 - 42000 ÂŁ per year.
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.
Are you detail-oriented, quality-driven, and passionate about operational excellence? Catalent is looking for aDocument Review Technicianto join our Zydis Operations team. This is your opportunity to play a vital role in the production of our innovative Zydis tablets — a fast-dissolving oral dosage form that transforms patient experience.
As a Document Review Technician, you’ll be the key link between manufacturing and quality assurance, ensuring that all batch documentation is accurate, complete, and audit-ready.
The Role:
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Reviewing batch documentation post-manufacture for accuracy and compliance.
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Coordinating with QA Officers, QPs, and support teams to maintain document flow.
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Acting as the primary point of contact for production documentation queries.
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Supporting training and development of team members in documentation standards.
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Driving continuous improvement in documentation processes and SOPs.
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Ensure compliance with cGMP and “Always Audit Ready” standards.
The Candidate:
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Strong written and verbal communication skills.
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Good IT proficiency; experience with PASX and Zydose is a plus.
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Previous GMP and Pharma manufacturing experience is essential
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Proactive, self-motivated, and able to manage own workload
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Strong interpersonal and teamwork skills.
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Ability to identify and drive improvements.
Why You Should Join Catalent:
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Competitive Salary – Reflecting your experience and skills.
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Bonus & Benefits – Includes a site performance bonus, a pension scheme matching up to 8% and life assurance. Enjoy a generous holiday entitlement that increases with tenure, with the option to purchase additional leave. Plus, gain access to Reward Gateway, offering discounts at many national retailers.
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Career Development – Access high-quality training, mentoring, and cross-functional opportunities within Catalent’s global network. Benefit from a subscription to LinkedIn Learning, providing access to 10,000+ online courses.
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Health & Wellbeing – Includes an employee assistance programme, on-site canteen facilities, and an active safety and “Patient First” culture. Take advantage of a Cycle to Work Scheme and an Electric Vehicle car scheme.
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Excellent Location – Just a two-minute drive from J16 of the M4, with free on-site parking.
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.
personal initiative. dynamic pace. meaningful work.
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 DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
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Document Review Technician (4 days on 4 days off shift) employer: Catalent
Contact Detail:
Catalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Document Review Technician (4 days on 4 days off shift)
✨Tip Number 1
Familiarise yourself with Good Manufacturing Practices (GMP) and the specific documentation standards used in the pharmaceutical industry. This knowledge will not only help you during interviews but also demonstrate your commitment to quality and compliance.
✨Tip Number 2
Network with professionals in the pharmaceutical sector, especially those who have experience in document review or quality assurance roles. Engaging with them on platforms like LinkedIn can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples of how you've contributed to process improvements in previous roles. Highlighting your proactive approach and ability to drive change will resonate well with the hiring team at Catalent.
✨Tip Number 4
Research Catalent's products and their impact on patient care. Being knowledgeable about their innovative Zydis tablets and other offerings will show your genuine interest in the company and its mission during the interview.
We think you need these skills to ace Document Review Technician (4 days on 4 days off shift)
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Document Review Technician. Familiarise yourself with terms like cGMP and audit-ready standards, as these are crucial for the role.
Tailor Your CV: Highlight your relevant experience in GMP and Pharma manufacturing. Be specific about your previous roles and how they relate to the skills required for this position, such as attention to detail and communication skills.
Craft a Strong Cover Letter: Use your cover letter to express your passion for operational excellence and how your proactive nature aligns with Catalent's mission. Mention any specific experiences that demonstrate your ability to drive improvements in documentation processes.
Proofread Your Application: Ensure that your CV and cover letter are free from errors. A well-presented application reflects your attention to detail, which is essential for the Document Review Technician role.
How to prepare for a job interview at Catalent
✨Understand the Role
Make sure you thoroughly understand the responsibilities of a Document Review Technician. Familiarise yourself with batch documentation processes, compliance standards, and the importance of being audit-ready. This will help you answer questions confidently and demonstrate your knowledge.
✨Showcase Your Attention to Detail
As this role requires a keen eye for detail, prepare examples from your past experiences where your attention to detail made a significant impact. Be ready to discuss how you ensure accuracy in documentation and how you handle discrepancies.
✨Highlight Your Communication Skills
Strong written and verbal communication skills are essential for this position. Prepare to discuss how you've effectively communicated with team members and other departments in previous roles, especially in relation to quality assurance and documentation queries.
✨Demonstrate Continuous Improvement Mindset
Catalent values continuous improvement in documentation processes. Think of instances where you've identified areas for improvement in your previous roles and be prepared to share these examples. This shows your proactive nature and commitment to operational excellence.