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- Tasks: Lead analytical testing for drug products and support global manufacturing sites.
- Company: Join a globally renowned pharmaceutical organisation with a state-of-the-art facility in Macclesfield.
- Benefits: Enjoy a hybrid working model and potential international travel opportunities.
- Why this job: Make a real impact in the pharmaceutical sector while collaborating with diverse teams.
- Qualifications: Degree, MSc or PhD in a scientific field with strong industry experience required.
- Other info: Ideal for those passionate about analytical chemistry and drug product lifecycle management.
The predicted salary is between 28800 - 43200 £ per year.
Are you an experienced Analytical Scientist looking to make an impact in the pharmaceutical sector? This is a fantastic opportunity for a driven and innovative scientist to take a leading role in supporting drug products manufacturing at our clients’ globally renowned pharmaceutical organisation at their state-of-the-art facility based in Macclesfield. You will ensure analytical performance, method robustness, and regulatory compliance across a portfolio of mainly Oral Solid Dose (OSD) medicines. Key responsibilities: Serve as the key point of contact for analytical testing of drug products Support global manufacturing sites and CMOs with analytical expertise Collaborate across departments including Manufacturing, QA, QC, Regulatory Affairs, and External Sourcing Oversee method transfers, change control assessments, and market access projects Provide technical leadership on complex analytical investigations and lifecycle management Potential involvement in hands-on laboratory support and occasional international travel About You Degree, MSc or PhD in a Scientific field Strong industry experience in drug product analytical development and strong understanding of the life cycle of OSD, inhalation, or parenteral drug products—from late-stage development and launch through commercial production and post-launch management Working knowledge of SHE principles and cGMP compliance Proven ability to communicate and collaborate across cross-functional teams Exposure to Lean methodologies and multi-disciplinary CMC roles is a plus The job holder will also be able to follow a hybrid working model (minimum 3 days onsite). Key words: Senior Analyst, Analyst, Scientist, Lab-based, Analytical Chemistry, Method Development, Method Validation, Method transfer, Method optimisation, HPLC, GC, chromatography, Oral Solid Dose (OSD), inhalation drug products, parenteral drug products, drug product lifecycle, stability testing, dissolution testing, cGMP compliance, lifecycle management, commercial manufacturing, global pharmaceutical, contract manufacturing organizations (CMOs), quality control (QC), CMC, Chemistry, Manufacturing, and Controls, process improvement, laboratory support, Macclesfield, Manchester, Stockport, Wilmslow, Knutsford, Altrincham, Congleton, Buxton, Stoke-on-Trent, Crewe, Sandbach, Northwich, Warrington, Nantwich, Chester, Liverpool, Glossop, Derbyshire, Cheshire, Greater Manchester, Staffordshire, VRS9087MP Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website .41bf1e1f-b16b-4260-a40a-17c77a06fd15
Analytical Technology Transfer Scientist employer: VRS Recruitment
Contact Detail:
VRS Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Analytical Technology Transfer Scientist
✨Tip Number 1
Familiarise yourself with the specific analytical techniques mentioned in the job description, such as HPLC and GC. Being able to discuss your hands-on experience with these methods during interviews will demonstrate your technical expertise and readiness for the role.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who work in analytical roles. Attend relevant conferences or webinars to connect with potential colleagues and learn more about current trends and challenges in drug product development.
✨Tip Number 3
Prepare to discuss your experience with cross-functional collaboration. Think of specific examples where you worked with teams from Manufacturing, QA, or Regulatory Affairs, as this will highlight your ability to communicate effectively across departments.
✨Tip Number 4
Research the company’s recent projects or innovations in the pharmaceutical sector. Being knowledgeable about their work will not only impress your interviewers but also allow you to tailor your responses to align with their goals and values.
We think you need these skills to ace Analytical Technology Transfer Scientist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in analytical development, particularly with Oral Solid Dose (OSD) medicines. Use keywords from the job description to demonstrate your fit for the role.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for the pharmaceutical sector and your specific achievements in analytical science. Mention any experience with method transfers and regulatory compliance to align with the key responsibilities.
Highlight Cross-Functional Collaboration: In your application, emphasise your ability to work across departments such as Manufacturing, QA, and Regulatory Affairs. Provide examples of successful collaborations that led to improved outcomes in previous roles.
Showcase Technical Expertise: Detail your technical skills in analytical methods like HPLC and GC, and your understanding of cGMP compliance. This will demonstrate your capability to provide the technical leadership required for the position.
How to prepare for a job interview at VRS Recruitment
✨Showcase Your Analytical Expertise
Be prepared to discuss your experience with analytical methods, particularly in relation to Oral Solid Dose (OSD) products. Highlight specific projects where you ensured method robustness and regulatory compliance.
✨Demonstrate Cross-Functional Collaboration
Since the role involves working with various departments, share examples of how you've successfully collaborated with teams like Manufacturing, QA, and Regulatory Affairs. This will show your ability to communicate effectively across functions.
✨Highlight Your Technical Leadership
Prepare to talk about instances where you've provided technical leadership on complex analytical investigations. Discuss how you approached problem-solving and the impact of your contributions on project outcomes.
✨Familiarise Yourself with cGMP and SHE Principles
Make sure you understand current Good Manufacturing Practices (cGMP) and Safety, Health, and Environment (SHE) principles. Be ready to discuss how you've applied these in your previous roles to ensure compliance and safety in laboratory settings.
