At a Glance
- Tasks: Perform and lead analytical testing to ensure quality and safety of pharmaceutical products.
- Company: Target Healthcare Group, a pioneer in the pharmaceutical industry.
- Benefits: Top-tier salary, comprehensive benefits, and a balanced work-life environment.
- Other info: Join a dynamic team with excellent career growth and mentoring opportunities.
- Why this job: Make a real impact in healthcare while working with cutting-edge technology.
- Qualifications: Bachelor’s or Master’s in relevant field and 5-8 years of QC lab experience.
The predicted salary is between 40000 - 50000 £ per year.
At Target Healthcare Group, we are pioneers in the pharmaceutical industry, committed to revolutionising healthcare. As the UK’s leading manufacturer and supplier of unlicensed medicines and hard-to-source products, we serve retail pharmacies, hospitals, pharmaceutical wholesalers, and homecare markets with unmatched expertise and passion. With a diverse team of over 500 professionals, including top pharmacists, skilled technicians, and dedicated support staff, we ensure excellence and innovation in everything we do.
Why Top Talent Chooses Us
- Impact - Ensure the safety and efficacy of life-saving medicines.
- Innovation - Work with cutting-edge technology and groundbreaking processes in a rapidly growing environment.
- Career Growth - Enjoy unparalleled opportunities for continuous learning and professional advancement.
- Collaborative Excellence - Be part of a passionate, international team dedicated to making a real difference in healthcare.
- Competitive Rewards - Receive a top-tier salary, comprehensive benefits, and enjoy a balanced work-life environment.
We are looking for a QC Technical Specialist to join our growing and forward-thinking team. You will be responsible for performing, reviewing, and leading analytical testing to ensure the quality, safety, and efficacy of pharmaceutical products in accordance with current Good Manufacturing Practices (cGMP), internal procedures, and regulatory requirements. This role provides technical expertise, supports method validation and transfer, and assists in troubleshooting analytical issues while mentoring junior analysts within the QC laboratory.
Your responsibilities will include, although not limited to:
- Perform qualitative and quantitative chemical and microbiological analyses of raw materials, in-process samples, finished products, and stability samples using validated methods (e.g., HPLC, GC, UV, FTIR, Dissolution).
- Review and verify analytical data, ensuring accuracy, completeness, and compliance with cGMP and SOPs.
- Lead out-of-specification (OOS), out-of-trend (OOT), and deviation investigations, including root cause analysis and CAPA development.
- Support release testing and timely completion of batch records to ensure uninterrupted product supply.
- Participate in method validation, method transfer, and equipment qualification activities.
- Develop and optimise analytical methods as required to support new product development or process changes.
- Troubleshoot complex analytical and instrumentation issues independently and provide guidance to peers.
- Ensure all activities comply with cGMP and ICH, and other applicable regulatory guidelines.
- Prepare, review, and maintain laboratory documentation including test records, logbooks, and SOPs.
- Support internal and external audits and respond to audit findings.
- Mentor and train junior analysts in analytical techniques, data integrity, and laboratory best practices.
- Participate in continuous improvement initiatives to enhance laboratory efficiency, quality, and safety.
- Collaborate cross-functionally with QA and Production teams to resolve quality issues.
To be successful in this role, you should be able to demonstrate:
- Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.
- Minimum 5–8 years of QC laboratory experience in the pharmaceutical or biopharmaceutical industry.
- Strong working knowledge of analytical techniques such as HPLC, GC, UV-Vis, FTIR, TOC and dissolution.
- Proven experience in method validation, instrument troubleshooting, and data integrity compliance.
- Excellent understanding of cGMP, GLP, and regulatory requirements.
- Strong attention to detail and analytical thinking.
- Proficiency in laboratory software including Chromeleon.
- Strong communication, leadership, and mentoring skills.
- Ability to work independently and manage multiple priorities under tight timelines.
Benefits of Working with Us
- Active Social and charity committee
- Cycle to Work Scheme
- Electric Vehicle Scheme
- Eye Care Vouchers
If you are passionate about quality and aspire to make a significant impact in healthcare, we want you on our team. Join Target Healthcare Group as QC Technical Specialist and become a key player in our mission to transform healthcare.
Please note: this role is not eligible for sponsorship. Successful applicants will be subject to a DBS check and satisfactory employment references.
QC Technical Specialist in North East employer: Quantum Pharmaceutical Limited
At Target Healthcare Group, we pride ourselves on being a leading employer in the pharmaceutical industry, offering a dynamic and collaborative work environment where innovation thrives. Our commitment to employee growth is evident through continuous learning opportunities and mentorship programmes, ensuring that our team members can advance their careers while making a meaningful impact on healthcare. With competitive rewards and a strong focus on work-life balance, we create a supportive culture that values each individual's contribution to our mission of revolutionising healthcare.
Contact Details:
Quantum Pharmaceutical Limited Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land QC Technical Specialist in North East
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