Job Title:  Senior Technical Specialist

Role Details

Analytical Support Senior Analyst - Pharmaceutical Quality Control

Location: Barnstaple, Devon
Contract: Full-Time, Permanent
Working Hours: Monday to Friday, 08:00 to 16:30
Salary: Competitive + Bonus + Benefits

The Role

We are seeking an experienced and highly motivated Analytical Support Senior Analyst to join our Quality Control team at our Barnstaple manufacturing site.

This is an exciting opportunity for an analytical scientist with strong technical expertise and a passion for problem-solving, method development, and continuous improvement. Working within the Analytical Support Team, you will play a pivotal role in supporting method development, technology transfers, validation activities, laboratory investigations, and the introduction of new analytical technologies.

Key Responsibilities

• Perform complex analytical laboratory testing using a range of techniques.
• Lead and support laboratory investigations, including drug substance and drug product investigations.
• Develop, optimise and validate analytical methods in line with ICH guidelines.
• Write and review method validation protocols and reports.
• Support technology transfer projects, product development and line extensions.
• Provide analytical support for cleaning validation, process validation, trial batches and stability studies.
• Assess and introduce new analytical technologies that improve quality, efficiency and cost-effectiveness.
• Respond to analytical queries arising from global marketing authorisation applications.
• Act as a Power User for the Chromatography Data System (Empower CDS).
• Support Supplier Item Qualification (SIQ) activities and deliver work within agreed timelines.
• Train, coach and mentor laboratory personnel in analytical techniques and procedures.
• Ensure all testing activities are conducted in accordance with GMP and approved procedures.

The Person

You are someone who combines scientific expertise with a practical, results-focused approach. You enjoy taking ownership, building effective relationships and using your technical knowledge to make a real impact on product quality, operational efficiency and business performance.

Essential Skills & Experience

• Extensive experience in analytical testing with experience in several of the following techniques: HPLC, GC, Dissolution, UV Spectroscopy, FTIR, TLC, Titrations, and Particle Size Analysis
• Strong knowledge of ICH method development and validation requirements.

• Expert knowledge and experience using Empower CDS or similar chromatography data systems.
• Experience troubleshooting and resolving laboratory technical issues.
• Experience writing technical reports and validation documentation.
• Strong understanding of GMP requirements within a pharmaceutical environment.
• Ability to coach, mentor and develop colleagues.
• Excellent communication and presentation skills.
• Proactive, organised and results-focused approach.
• Ability to manage multiple priorities and work effectively under pressure.

Desirable Experience

• Experience with quality management systems, deviations and investigations.
• Supplier Item Qualification (SIQ) experience.
• Understanding of pharmaceutical regulatory requirements.
• Cleaning validation method development and validation experience.

Qualifications

Essential:

• ‘A’ level in chemistry or relevant qualification preferably in Analytical Science, Pharmaceutical Science or a related field.
• Or extensive relevant experience in an Analytical Chemistry laboratory, preferably Pharmaceutical or small molecule analysis

Desirable:

• Degree in a science related discipline

The Rewards

In return, we offer a competitive salary and rewards package. Not to mention the opportunity to genuinely make a difference in a new and dynamic role within a progressive and expanding business, at an exciting time of growing international reach.

How to Apply

If you have the experience, passion and ability to make this role a success then we would love to hear from you. Please complete your Candidate Profile on our careers site to apply for this role. The closing date is 5th November 2026. For more information, you can contact us on: careers@accord-healthcare.com

A Bit About Us

Accord Healthcare Europe is one of the fastest growing pharmaceutical companies in Europe. Accord has one of the largest market footprints of any European generic and biosimilars companies selling generic medicines in over 80 countries around the world. This global footprint enables us to deliver vital, affordable medicines to national health systems supporting healthcare professionals to transform patient lives worldwide. The approach of Accord is agile and inventive, always seeking to improve products and patients' access to them. Accord are driven to think differently and deliver more for the benefit of patients worldwide.

To continue our growth, we’re looking for the best and brightest technical minds and forward-thinking business professionals. Keeping our people at the heart of all we do, we offer rewarding opportunities for those looking for continued personal and professional growth, investing in training and development tailored to each individual’s focus. So, if you’re looking for an inclusive company to take your career to the next level, you’re certainly in the right place; come and join us to make it better.

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All applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability.

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