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For Companies At a Glance
- Tasks: Ensure quality and compliance of pharmaceutical products while collaborating across departments.
- Company: Almac Group, a global leader in advancing human health.
- Benefits: Hybrid working, paid time off, and a supportive work environment.
- Other info: Flexible working hours with excellent career development opportunities.
- Why this job: Make a real impact on patient health by ensuring product integrity.
- Qualifications: Degree in Life Science or significant industry experience with GMP knowledge.
The predicted salary is between 30000 - 40000 £ per year.
Almac Group is a global leader in advancing human health. We provide a range of expert services across the drug development lifecycle to pharmaceutical and biotech companies, supporting them in finding treatments for patients.
Skills and attributes:
- Quality System Knowledge of GMP Pharmaceutical Manufacturing
The Role:
The role focuses on ensuring and enhancing the quality and GMP (Good Manufacturing Practice) compliance of pharmaceutical products within Almac Pharma Services. The post holder will be responsible for monitoring and reviewing various operational areas—including manufacturing, quality control, product development, and distribution—to assess and maintain compliance with regulatory standards. They will provide expert quality assurance support across departments, collaborating with internal and external stakeholders to uphold product integrity and meet project timelines.
In addition to oversight responsibilities, the post holder will actively contribute to the development and continuous improvement of quality systems such as deviation management, CAPA, change control, and risk assessments. They will participate in internal and external audits, review critical documentation, and support supplier management processes. The role also involves reviewing production and laboratory data, compiling product quality reviews, and serving as a key contact for compliance-related queries, all with the overarching goal of safeguarding the quality and regulatory compliance of pharmaceutical products.
Key Requirements:
- Have eligibility to work in the UK OR possess a valid work permit that will allow you to take up full time employment in the UK
- Degree (or equivalent) in a Life Science or closely related field OR significant experience working within the Pharmaceutical Industry along with demonstrable knowledge may be considered as sufficient to meet educational requirements for this role.
- Significant experience working within an established Quality System (e.g. GMP, ISO)
- Comprehensive, working knowledge of the regulatory requirements for pharmaceutical products are essential, including familiarity with the principles of Good Manufacturing Practice, Pharmaceutical Quality Systems, Quality Risk Management and Pharmaceutical Product Lifecycles.
Further Information:
The working pattern for this role is a flex pattern between the hours of 07:00 – 19:00 with core hours of 10:00 – 16:00. You will be eligible for hybrid working following the successful completion of probation. This role requires coverage beyond normal working hours on a regular basis and it is a condition of your employment that you are able to fulfil this requirement of the role. Paid Time-Off for Vacation and Sick Days. Almac Group is an Equal Opportunity Employer.
Quality Assurance Specialist employer: OASIS Group
Contact Detail:
OASIS Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Specialist
✨Tip Number 1
Network like a pro! Reach out to people in the pharmaceutical industry, especially those who work at Almac Group. A friendly chat can open doors and give you insider info about the company culture and what they really value in a Quality Assurance Specialist.
✨Tip Number 2
Prepare for interviews by brushing up on GMP and quality systems. We recommend having specific examples ready that showcase your experience with compliance and quality assurance. This will help you stand out as someone who truly understands the role.
✨Tip Number 3
Don’t just apply and wait! Follow up on your application through our website. A quick email or message shows your enthusiasm and keeps you on their radar. Plus, it’s a great way to ask any questions you might have about the role.
✨Tip Number 4
Showcase your continuous improvement mindset. Almac values innovation, so be ready to discuss how you've contributed to quality system enhancements in the past. This will demonstrate that you're not just about maintaining standards but also about pushing them forward.
We think you need these skills to ace Quality Assurance Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Assurance Specialist role. Highlight your experience with GMP and any relevant quality systems you've worked with. We want to see how your background aligns with what we do at Almac!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance in the pharmaceutical industry. Let us know how your skills can contribute to our mission of advancing human health.
Showcase Relevant Experience: When filling out your application, be sure to showcase any significant experience you have in quality systems or regulatory compliance. We love seeing candidates who understand the ins and outs of the pharmaceutical lifecycle!
Apply Through Our Website: Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team at Almac!
How to prepare for a job interview at OASIS Group
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of Good Manufacturing Practice (GMP) and how it applies to the pharmaceutical industry. Be ready to discuss specific examples of how you've ensured compliance in previous roles, as this will show your understanding and experience.
✨Showcase Your Quality System Experience
Prepare to talk about your experience with quality systems like ISO or any other relevant frameworks. Highlight any specific projects where you contributed to quality improvements or compliance, as this will demonstrate your hands-on expertise.
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations related to quality assurance. Think about how you would handle deviations, CAPA processes, or risk assessments. Practising these scenarios can help you articulate your thought process clearly during the interview.
✨Engage with Your Interviewers
Don’t just answer questions—engage with your interviewers! Ask insightful questions about their quality systems and challenges they face. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.