Quantum Pharmaceutical Ltd
Validation Officer

How your CV stacks up
Upload your CV to see how well it fits this job role
?%
Job Ref: JM160231526 VO
Location: 26 Harbour Court, 9 Heron Road, Belfast
Postcode: BT3 9HB
Type of contract: Permanent
Posted Date: Thursday, June 18, 2026
Closing Date: Thursday, July 16, 2026
Validation Officer
At Target Healthcare, we are driven by a powerful mission: to transform healthcare and profoundly impact the lives of patients everywhere. Quantum Pharmaceutical, an integral part of the Target Group, stands at the forefront of this mission as the UK’s leading manufacturer of aseptic medicines, ensuring that critical medications reach those who need them most.
We are looking for a Validation Officer who shares our commitment to quality, compliance, and patient safety. This role is more than a technical position; it is an opportunity to make a meaningful impact by ensuring the highest standards across our operations. We need someone with a keen eye for detail who can work collaboratively to support validation and quality assurance activities, helping to maintain compliance with GMP, GDP, and internal quality systems while contributing to the delivery of safe, effective products to patients.
Key Responsibilities
As a Validation Officer your responsibilities will include
Reasons to use Rodeo
I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?
Honest answer — it depends on where you want to end up. A lot of top grad schemes (Big 4, civil service, banking) don’t need a masters. Let’s look at the ones you’d be competitive for now, and we can decide if a masters actually adds anything.
Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
Graduate Consultant — 2026 Scheme
Why you're a good match
StrongYour economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.
See breakdownIt searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Why you're a good match
You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.
Experience fit
Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
- Support validation and quality assurance activities to ensure compliance with GMP, GDP, and internal quality systems.
- Assist in the delivery and maintenance of the Site Validation Master Plan across manufacturing, facilities, equipment, processes, and computerised systems.
- Prepare, review, and approve validation documentation, including protocols, reports, risk assessments, and lifecycle records.
- Provide validation and quality guidance to stakeholders and support cross-functional projects across the business.
- Support investigations, deviations, CAPAs, change controls, and quality risk management activities.
- Contribute to internal, supplier, customer, and regulatory audits, including audit preparation and follow-up actions.
- Promote a culture of quality, compliance, and continuous improvement throughout the organisation.
- Monitor validation and quality performance metrics and support training activities where required.
- Deputise for the Validation Manager when appropriate.
To be successful in this role, you should be able to demonstrate:
- Experience working in the pharmaceutical, healthcare, or life sciences industry (essential)
- Experience in a validation or quality assurance role (essential)
- Experience in computer system validation (desirable)
- Strong knowledge of GMP and GDP
- Hands-on experience with validation documentation across the full lifecycle (equipment, systems, facilities, processes)
- Ability to work independently and make sound decisions
- Confident communicating with stakeholders at all levels
- Highly computer literate with strong Microsoft Office skills
- GCSE (or equivalent) in English and Mathematics at grades A–C
- Willingness to travel occasionally to other group sites to support validation activities


Get help with your application
Your very own career expert that helps elevate your application to the next level.
Benefits Of Working With Us
We believe in fostering growth, learning and development within our organisation you'll have the opportunity to work as part of a high performing team, progress and develop your skills and career within a diverse and inclusive environment.
- Generous pension plan
- Vibrant social committee
- Cycle to work scheme
- Electric vehicle scheme
- Eyecare vouchers
Please note: This role is not eligible for sponsorship.
All applicants are subject to enhanced DBS check along with two references.
Apply
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Skills