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: Flexible working hours, hybrid options, paid time off, and career development opportunities.
- Other info: Dynamic role with opportunities for growth and learning in a supportive environment.
- Why this job: Make a real impact on patient health by ensuring top-quality pharmaceutical products.
- Qualifications: Degree in Life Science or significant industry experience with Quality Systems.
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 in Craigavon employer: OASIS Group
Contact Detail:
OASIS Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Specialist in Craigavon
✨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 creating a list of common interview questions related to quality assurance and practising your answers. This will help you feel confident and ready to showcase your expertise!
✨Tip Number 3
Don’t forget to follow up after your interview! A quick thank-you email can leave a lasting impression. Mention something specific from your conversation to show you were engaged and are genuinely interested in the role.
✨Tip Number 4
Apply through our website for the best chance of landing that Quality Assurance Specialist role. It shows you’re serious about joining Almac Group and gives us a direct line to your application. Plus, we love seeing candidates who take that extra step!
We think you need these skills to ace Quality Assurance Specialist in Craigavon
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 our needs!
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. Share specific examples of how you've contributed to compliance and quality improvements in past roles.
Showcase Your Skills: Don’t forget to showcase your skills that match the job description. Whether it's your knowledge of regulatory requirements or your experience with audits, we want to know how you can contribute to our team at Almac Group.
Apply Through Our Website: We encourage you to apply through our website for the best chance of success. It’s straightforward and ensures your application gets to the right people. Plus, you’ll find all the details you need about the role there!
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 commitment to quality assurance.
✨Showcase Your Quality System Experience
Prepare to talk about your experience with established 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 scenario-based questions that assess your problem-solving skills in quality assurance. Think of situations where you had to manage deviations, CAPA, or risk assessments, and be prepared to explain your thought process and actions taken.
✨Engage with Stakeholders
Since collaboration is key in this role, think of examples where you've worked with internal and external stakeholders. Be ready to discuss how you communicated quality standards and resolved compliance-related queries, showcasing your teamwork and communication skills.