Manufacturing Batch Reviewer I

Qualifications

• A BSc in a Life Science subject or other equivalent laboratory experience.
• Minimum 1 years’ experience in Sterile Manufacture- and/or Quality-related role.
• Next Steps
• If this sounds like you, then please hit ‘Apply’ now! We will ask you to upload your CV and complete a short application form.
• At RoslinCT, we’re all about inclusivity and creating a fair, welcoming workplace. Our goal is to make sure everyone knows they’re valued and encouraged to be themselves, whether they’re our employees, customers, or partners.
• We take pride in being an equal opportunity employer. We treat all applicants fairly and don’t discriminate based on any protected characteristics. So, no matter who you are, we welcome your application with open arms.
• If you’ve got any specific needs or concerns regarding accessibility during the recruitment process, don’t hesitate to reach out to us at [email protected]. We’re here to assist and make things as smooth as possible for you.
• Background in stem cells, gene or cell therapies, or cell banking within a regulated environment.
• Working knowledge of cGMP principles particularly aseptic processing, documentation and record management with an excellent understanding of UK, EU and FDA regulations.
• Experienced in following SOPs and maintaining high compliance standards.
• Skilled in technical writing and addressing GMP audit findings.
• Highly organised with strong planning, administrative and record-keeping skills.
• Excellent communication and interpersonal skills, building effective relationships across teams.
• Strong attention to detail, with a real desire to continually develop and improve our processes.