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- Tasks: Lead a team ensuring documentation meets quality standards in a dynamic pharmaceutical environment.
- Company: Join a leading manufacturing company in the pharmaceutical industry, known for high-quality products.
- Benefits: Enjoy 33 days holiday, a contributory pension, life insurance, and ongoing training opportunities.
- Why this job: This role offers a chance to develop leadership skills while contributing to impactful healthcare solutions.
- Qualifications: Previous management experience and proficiency in MS Office are essential for this position.
- Other info: Work Monday to Friday with no weekends or night shifts, plus free onsite parking.
The predicted salary is between 36000 - 60000 £ per year.
Salary: Competitive salary plus shift allowance and annual Bonus – details on request
Vacancy Title: Document Control Section Leader Contract Type: Permanent Location: Cheshire Industry: Pharmaceutical SCIENTIFIC Salary: Competitive salary plus shift allowance and annual Bonus – details on request Start Date: 2025-09-01 REF: J91984961 Contact Name: Johnathan Miller Contact Email: Johnathan.miller@russell-taylor.co.uk Vacancy Published: 1 day ago Document Control Section Leader
Runcorn
Permanent
Competitive salary plus shift allowance and annual Bonus – details on request
Monday – Friday. Alternating weekly shifts of 6:30am-2:30pm and 2:15pm-10:15pm
An exciting opportunity has arisen for a Document Control Section Leader to join a leading manufacturing company. This role will see you lead and manage a team of Document Control Officers, ensuring all documentation processes meet strict cGMP standards and supporting the delivery of high-quality products and services.
Key Responsibilities:
• Lead and develop the Document Control team, ensuring performance and compliance with quality standards.
• Oversee the generation, checking, and distribution of documentation (e.g. batch records, labelling, plans, BOMs).
• Monitor KPIs, report on progress, and implement corrective/preventative actions where required.
• Ensure accuracy and timeliness of all documentation to support production schedules.
• Manage training, development, and performance reviews for team members.
• Handle absence management, disciplinary and grievance matters in line with procedures.
• Attend production meetings to communicate documentation requirements and resolve issues quickly.
About You:
• Highly organised with strong time management skills.
• Previous management or supervisory experience, ideally including performance and absence management.
• Strong leadership and people management skills.
• Proficient in MS Office.
What\’s on Offer:
• Monday-Friday role (no weekends or night shifts)
• 33 days holiday (rising with service)
• Contributory pension & life insurance
• Ongoing training and development opportunities
• Free onsite parking
Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us here . Apply Now >
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Document Control Section Leader employer: Russell Taylor Group
Contact Detail:
Russell Taylor Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Document Control Section Leader
✨Tip Number 1
Familiarise yourself with cGMP standards and documentation processes in the pharmaceutical industry. This knowledge will not only help you understand the role better but also demonstrate your commitment to quality and compliance during any discussions.
✨Tip Number 2
Highlight your leadership experience by preparing examples of how you've successfully managed teams in the past. Be ready to discuss specific situations where you improved team performance or resolved conflicts, as this will show your capability to lead the Document Control team.
✨Tip Number 3
Network with professionals in the pharmaceutical sector, especially those involved in document control or quality assurance. Engaging with industry peers can provide insights into the role and may even lead to referrals, increasing your chances of landing the job.
✨Tip Number 4
Prepare to discuss key performance indicators (KPIs) relevant to document control. Understanding how to monitor and report on these metrics will be crucial in your role, so being able to articulate your approach to managing KPIs will set you apart from other candidates.
We think you need these skills to ace Document Control Section Leader
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in document control and management. Emphasise any previous roles where you led a team or ensured compliance with quality standards, as these are key aspects of the Document Control Section Leader position.
Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Discuss your leadership skills and how they align with the responsibilities outlined in the job description. Mention specific examples of how you've successfully managed teams and improved documentation processes.
Highlight Relevant Skills: Ensure you mention your proficiency in MS Office and any other relevant software. Discuss your organisational and time management skills, as well as your ability to monitor KPIs and implement corrective actions, which are crucial for this role.
Follow Application Instructions: Pay close attention to the application instructions provided by the company. Make sure to submit all required documents, including your CV and cover letter, through our website. Double-check for any specific requirements or formats they may request.
How to prepare for a job interview at Russell Taylor Group
✨Showcase Your Leadership Skills
As a Document Control Section Leader, you'll need to demonstrate strong leadership abilities. Prepare examples of how you've successfully managed teams in the past, focusing on your approach to performance management and team development.
✨Understand cGMP Standards
Familiarise yourself with current Good Manufacturing Practices (cGMP) as they are crucial in this role. Be ready to discuss how you have ensured compliance with quality standards in previous positions, and how you would apply this knowledge in the new role.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills, especially regarding documentation processes. Think of specific scenarios where you had to resolve issues related to documentation accuracy or team performance, and be prepared to explain your thought process.
✨Highlight Your Organisational Skills
This role requires excellent time management and organisational skills. Be prepared to discuss how you prioritise tasks and manage multiple projects simultaneously, especially in a fast-paced environment like pharmaceuticals.
