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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 with flexible onsite requirements and potential international travel.
- 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 in analytical development.
- Other info: Opportunity to work on complex analytical investigations and lifecycle management.
The predicted salary is between 36000 - 60000 £ per year.
Job Description
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
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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
Network with professionals in the pharmaceutical industry, especially those working in analytical roles. Attend relevant conferences or webinars to connect with potential colleagues and learn about the latest trends in drug product development.
✨Tip Number 2
Familiarise yourself with the specific analytical techniques mentioned in the job description, such as HPLC and GC. Consider reaching out to current employees at StudySmarter or similar companies to gain insights into their experiences and expectations.
✨Tip Number 3
Demonstrate your understanding of regulatory compliance and cGMP principles during any discussions or interviews. Prepare examples from your past experience where you ensured compliance in analytical processes or contributed to successful audits.
✨Tip Number 4
Showcase your collaborative skills by discussing how you've worked with cross-functional teams in previous roles. Highlight any specific projects where you led or contributed to method transfers or lifecycle management to illustrate your technical leadership.
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 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 skills in analytical testing and method development. Mention any experience with cross-functional collaboration and regulatory compliance.
Highlight Relevant Skills: In your application, emphasise your knowledge of cGMP compliance, Lean methodologies, and any hands-on laboratory experience. This will show that you have the technical expertise required for the role.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in the pharmaceutical industry.
How to prepare for a job interview at VRS Recruitment
✨Showcase Your Analytical Expertise
Be prepared to discuss your experience in analytical development, particularly with Oral Solid Dose (OSD) products. Highlight specific projects where you ensured method robustness and regulatory compliance, as this will demonstrate your capability to handle the responsibilities of the role.
✨Emphasise 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 that you can effectively communicate and work within a multidisciplinary environment.
✨Demonstrate Problem-Solving Skills
Prepare to discuss complex analytical investigations you've led or contributed to. Be ready to explain your approach to troubleshooting and how you applied Lean methodologies to improve processes, as this aligns with the company's focus on efficiency.
✨Understand the Company’s Values and Culture
Research the pharmaceutical organisation's mission and values. During the interview, express how your personal values align with theirs, especially regarding quality control and compliance. This will help you stand out as a candidate who is not only qualified but also a good cultural fit.
