At a Glance
- Tasks: Ensure compliance with quality standards and validation activities in a dynamic team.
- Company: Join Almac Group, a global leader in advancing human health.
- Benefits: Enjoy competitive salary, 34 days leave, healthcare, and professional development.
- Other info: Flexible schedules, wellness programs, and opportunities for advancement await you.
- Why this job: Make a real impact in the pharmaceutical industry while growing your career.
- Qualifications: Level 5 qualification or relevant experience in scientific, engineering, or IT fields.
The predicted salary is between 30000 - 40000 £ per year.
Full time, Contract
Closing date: June 16, 2026 4:00 PM
Who We Are
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
Description
Business Unit: Pharma Services
Open To: Internal & External Applicants
Please note if you have applied for this position within the past 6 months, we will be unable to accept your re-application at this time.
The Role
Working as part of the Technical Quality team based in our Global Headquarters in Craigavon, the Technical Quality Specialist will be responsible for working within the Technical Quality team to ensure compliance with the principles of GMP and Almac’s quality standards. The post holder is responsible for a range of validation activities within Almac Pharma Services to ensure that all critical facilities, systems, processes and procedures achieve compliance with EU and FDA requirements in a timely manner.
For a full list of job specific responsibilities please see attached Job Description.
Further information on the role from a current Technical Quality Specialist can be viewed on the video below:
Qualifications
- Level 5 qualification (or equivalent) OR relevant experience within scientific, engineering or IT related discipline
- Experience or working knowledge of an established quality system (e.g. GMP, ISO)
(The following criteria may be applied if a large pool of applicants exist)
- Bachelor’s degree (or above) in a scientific (e.g. Chemistry, Biology or Pharmacy/Pharmaceutical Sciences) or technical (Engineering or IT) discipline OR Significant experience within a Quality, Validation, Manufacturing, Packaging, Engineering or IT role
- Experience of working within a quality system or within a validation role
- Experience of computerised systems for labs and / or pharmaceutical processing equipment
- Experience of equipment or facility qualification
- Experience of Process or Packaging Validation
Reward
For the successful candidate, we offer an attractive benefits package which will include a competitive salary, annual bonus, employer pension contributions, 34 days paid annual leave, healthcare benefits and much more. Please see benefits tab for further details.
Apply Now
Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible.
Closing Date Tuesday 16th June 2025 at 5pm
RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CV’s received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.
Benefits Include:
- Paid Time-Off for Vacation and Sick Days
- Flexible Schedules
- Professional Development + Growth
- Free onsite tea/coffee
- EAP (Employee Assistance Programme)
- Staff Discounts
- Professional Coaching
- Team Bonding Events
- Opportunities for Advancement
- Attractive Compensation Package
- Work/Life Balance
- Relocation Assistance
- Wellness Programs
- Lunch & Learns
- Employee Recognition
- Employee Referral Bonus
- Rewards for Years Of Service
- Death in Service Pension Scheme
Almac Group is an Equal Opportunity Employer
Technical Quality Specialist (12 Month Contract) in Craigavon employer: OASIS Group
Almac Group is an exceptional employer, offering a dynamic work environment at our Global Headquarters in Craigavon, where you can contribute to advancing human health. We pride ourselves on our supportive culture that fosters professional development and growth, alongside a comprehensive benefits package that includes competitive salaries, generous annual leave, and wellness programmes. Join us to be part of a team that values work-life balance and recognises your contributions through various employee recognition initiatives.
StudySmarter Expert Advice🤫
We think this is how you could land Technical Quality Specialist (12 Month Contract) in Craigavon
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like OASIS Group. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like OASIS Group.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like OASIS Group. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what OASIS Group is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Technical Quality Specialist (12 Month Contract) in Craigavon
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at OASIS Group!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show OASIS Group that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at OASIS Group!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At OASIS Group, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at OASIS Group
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at OASIS Group that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with OASIS Group’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
