At a Glance
- Tasks: Ensure quality compliance in analytical projects and operations while driving GMP improvements.
- Company: Join Almac Sciences, a leader in life sciences with a commitment to quality.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Be part of a team that values quality and compliance in every project.
- Why this job: Make a real impact on quality assurance in a dynamic and innovative environment.
- Qualifications: Life Sciences degree and experience in quality or laboratory settings.
The predicted salary is between 30000 - 40000 £ per year.
The Quality Compliance Officer within the Analytical Services team will provide quality assurance support across analytical projects and routine analytical operations, including the review and approval of quality‑related documentation. The role involves actively promoting Quality Compliance activities and driving GMP improvement initiatives across Almac Sciences. The post holder will support the effective implementation of the Quality Management System, contribute to quality investigations, and ensure robust CAPA actions are implemented. They will review and approve GMP analytical data and documentation, represent QA on relevant analytical project activities, and take ownership of quality assurance aspects, escalating issues where appropriate to maintain regulatory and GMP compliance at all times.
Key Requirements
- Life Sciences degree level qualification
- Experience working in a quality or laboratory environment operating to GMP principles or a recognised quality system (e.g., ISO)
- Experience preparing and/or reviewing analytical documents such as analytical method validation reports and Certificates of Analysis
- Experience performing investigations into quality issues such as Unplanned Deviations and OOS’s
- Experience reviewing analytical data (e.g., stability data)
- Experience performing internal audits to identify GMP compliance gaps
Quality Compliance Officer- Analytical Services employer: HIRANI
HIRANI is an exceptional employer located in the vibrant city of Belfast, offering a collaborative work culture that fosters innovation and growth. Employees benefit from comprehensive professional development opportunities and the chance to lead transformative projects that drive economic impact. With a commitment to supporting local manufacturing and supply chains, HIRANI provides a unique platform for meaningful contributions to the community and industry.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Compliance Officer- Analytical Services
✨Tip Number 1
Network like a pro! Reach out to professionals in the quality compliance field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Quality Compliance Officer role.
✨Tip Number 2
Prepare for interviews by brushing up on GMP principles and quality assurance practices. We recommend practising common interview questions related to quality investigations and CAPA actions, so you’re ready to impress!
✨Tip Number 3
Showcase your analytical skills! Bring examples of your previous work with analytical documents and quality systems to the table. We want to see how you’ve contributed to quality compliance in past roles.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. We’re always on the lookout for passionate candidates who are ready to drive GMP improvement initiatives.
We think you need these skills to ace Quality Compliance Officer- Analytical Services
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Quality Compliance Officer role. Highlight your experience in quality assurance and any relevant GMP principles you've worked with. We want to see how your background fits perfectly with what we're looking for!
Showcase Your Experience:When writing your application, don’t just list your qualifications. Share specific examples of your experience in preparing and reviewing analytical documents or performing investigations into quality issues. This helps us understand how you can contribute to our team.
Be Clear and Concise:Keep your application clear and to the point. Use straightforward language and avoid jargon unless it’s relevant to the role. We appreciate a well-structured application that makes it easy for us to see your skills and experiences.
Apply Through Our Website:We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to submit all the necessary documents in one go. Plus, it shows us you’re serious about joining our team!
How to prepare for a job interview at HIRANI
✨Know Your GMP Principles
Make sure you brush up on Good Manufacturing Practice (GMP) principles before the interview. Be ready to discuss how you've applied these in your previous roles, especially in quality assurance or laboratory settings.
✨Familiarise Yourself with Quality Documentation
Get comfortable with the types of analytical documents you'll be reviewing, like method validation reports and Certificates of Analysis. Being able to talk about your experience with these documents will show that you're prepared and knowledgeable.
✨Prepare for Quality Investigations Questions
Expect questions about how you've handled quality issues in the past, such as Unplanned Deviations or Out of Specification results. Have specific examples ready to demonstrate your problem-solving skills and your approach to CAPA actions.
✨Show Your Audit Experience
If you've performed internal audits, be ready to discuss what you learned from them and how you identified compliance gaps. This will highlight your proactive approach to maintaining quality standards and your ability to drive improvements.
