Analytical Technology Transfer Scientist

JR United Kingdom; Peterborough; Hybrid; GBP 42,000 - 50,000; Full time

Job summary

A leading pharmaceutical company in Cheshire is looking for an enthusiastic Analytical Technology Transfer Scientist. In this full-time, permanent role, you will act as the primary contact for analytical testing of commercial products. Responsibilities include ensuring analytical method compliance and leading method transfers globally. A degree in a relevant field and experience in the pharmaceutical industry are required. The position offers a salary of up to £50,000 per annum and a hybrid working model.

Qualifications

• Proven experience in drug product analytical development within the pharmaceutical industry.
• Strong knowledge of analytical method development, optimisation, and transfer.
• Understanding of the product life cycles.

Responsibilities

• Act as the primary contact for analytical testing of commercial Oral Solid Dose products.
• Ensure analytical method robustness, performance, and compliance across manufacturing sites.
• Lead analytical method transfers to multiple global locations.

Skills

Analytical method development

Communication skills

Leadership skills

Root cause analysis

Education

Degree, Master's, or PhD in Chemistry, Pharmacy, Pharmaceutical Sciences

Job description

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Analytical Technology Transfer Scientist, Peterborough

Client:

Location:

Peterborough, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

Job Views:

3

Posted:

26.08.2025

Expiry Date:

10.10.2025

Job Description:

Analytical Technology Transfer Scientist
Cheshire
Salary up to £50,000 per annum
Full-time, Permanent
36.5 hours/week (Monday–Friday, 08:00–16:30)
Hybrid working – 3 days on site
My client is hiring an enthusiastic and innovative Analytical Scientist to join their team at a leading pharmaceutical facility in Cheshire. This is a fantastic opportunity to contribute to high-impact commercial products in a collaborative and dynamic environment.

Key Responsibilities:

• Act as the primary contact for analytical testing of commercial Oral Solid Dose (OSD) products.
• Ensure analytical method robustness, performance, and compliance across manufacturing sites and CMOs.
• Lead analytical method transfers to multiple global locations (international travel may be required).
• Collaborate with cross-functional teams including QA, QC, Regulatory Affairs, and Manufacturing.
• Support market access projects and major product changes.
• Potential involvement in hands-on analytical activities.

Qualifications & Experience:

• Degree, Master’s, or PhD in Chemistry, Pharmacy, Pharmaceutical Sciences, or a related field.
• Proven experience in drug product analytical development within the pharmaceutical industry.
• Strong knowledge of analytical method development, optimisation, and transfer.
• Understanding of OSD, Inhalation, and Parenteral product life cycles.
• Familiarity with a broad range of analytical techniques and root cause analysis tools.
• Solid grasp of SHE principles and cGMP.
• Excellent communication and leadership skills.
• Desirable: Experience in CMC functions and Lean methodologies.