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- Tasks: Review quality and batch documentation while ensuring compliance with regulations.
- Company: Join a dynamic life science organisation that's rapidly growing and innovating.
- Benefits: Enjoy a collaborative work environment with opportunities for professional growth.
- Why this job: Be part of a team that values quality and compliance in a meaningful industry.
- Qualifications: HNC/HND minimum; experience in document review in a GMP environment preferred.
- Other info: Great chance to develop your skills in a supportive and engaging workplace.
The predicted salary is between 28800 - 48000 £ per year.
SRG are working with an exciting and growing life science organisation to help them find a QA Document Reviewer. This is a great opportunity for someone with document/batch record review experience and offers the chance to join a growing and dynamic company.
Reporting to the Quality Assurance Manager, the successful candidate will be responsible for maintaining all activities associated with master and working documents, data and records, ensuring compliance with regulatory requirements and company policies/procedures.
The Role:
- Review quality and batch documentation
- Provide document control functions and advice
- Maintain a status tracker and provide accurate status reports on batch record review to support batch compilation activities
- Support document archiving activities when required to ensure the movement of material to and from the archive is properly controlled and documented
- Coordinate the company activities to ensure that SOP are reviewed/revised within the documented revision time span
- Ensure that all documents are updated and mastered according to existing procedures
- Assist in compliance with GMP regulations
Requirements:
- Educated to HNC/HND as minimum - degree preferred
- Experience in document review in a regulated (GMP) environment
- Excellent written and verbal communication skills; able to communicate effectively with all levels within the organisation
- Knowledge of Quality Systems would be beneficial
- Excellent organisational skills
- Ability to work independently and as a member of a team
- Analytical approach to problem solving and decision making
- IT literate with proficiency in Microsoft Office and data entry
If you think this could be the role for you, please apply online!
QA Document Reviewer employer: SRG
Contact Detail:
SRG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA Document Reviewer
✨Tip Number 1
Familiarise yourself with GMP regulations and quality systems. Understanding these concepts will not only help you in the interview but also demonstrate your commitment to the role and the industry.
✨Tip Number 2
Network with professionals in the life sciences sector, especially those working in QA roles. Engaging with them can provide insights into the company culture and expectations, which can be invaluable during your application process.
✨Tip Number 3
Prepare to discuss specific examples of your document review experience in a regulated environment. Highlighting your analytical skills and problem-solving abilities will set you apart from other candidates.
✨Tip Number 4
Showcase your IT proficiency, particularly with Microsoft Office. Being able to efficiently manage data and documentation is crucial for this role, so be ready to discuss how you've used these tools in past positions.
We think you need these skills to ace QA Document Reviewer
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to grasp the responsibilities and requirements of the QA Document Reviewer position. Highlight key skills such as document review experience and knowledge of GMP regulations.
Tailor Your CV: Customise your CV to reflect relevant experience in document control and quality assurance. Emphasise your educational background, particularly if you have an HNC/HND or degree, and showcase any specific achievements in a regulated environment.
Craft a Compelling Cover Letter: Write a cover letter that connects your skills and experiences directly to the job requirements. Mention your excellent communication skills and organisational abilities, and express your enthusiasm for joining a growing life science organisation.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. Ensure that your documents are clear, concise, and professional, reflecting your attention to detail which is crucial for this role.
How to prepare for a job interview at SRG
✨Know Your Documents
Familiarise yourself with the types of documents you'll be reviewing, especially in a GMP environment. Be prepared to discuss your previous experience with document control and how you ensured compliance with regulatory requirements.
✨Showcase Your Communication Skills
As a QA Document Reviewer, effective communication is key. Practice articulating your thoughts clearly and concisely, as you'll need to convey complex information to various stakeholders within the organisation.
✨Demonstrate Organisational Skills
Highlight your ability to manage multiple documents and maintain accurate status reports. Be ready to provide examples of how you've successfully tracked and organised documentation in past roles.
✨Prepare for Problem-Solving Scenarios
Expect questions that assess your analytical skills and decision-making process. Think of specific instances where you identified issues in documentation and how you resolved them, showcasing your proactive approach.
