Analytical Technology Transfer Scientist

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

Job summary

A leading pharmaceutical facility is seeking an Analytical Technology Transfer Scientist in Chester, UK. In this full-time role, you will oversee analytical testing for Oral Solid Dose products, ensure method robustness and compliance, and collaborate across teams. Ideal candidates will have a degree in a relevant field, strong analytical development experience, and excellent communication skills. This role offers a salary of up to £50,000 per annum and hybrid working arrangements.

Qualifications

• Proven experience in drug product analytical development within the pharmaceutical industry.
• Strong knowledge of analytical method development, optimisation, and transfer.
• Familiarity with various analytical techniques.

Responsibilities

• Act as the primary contact for analytical testing of commercial products.
• Ensure compliance across manufacturing sites and CMOs.
• Lead analytical method transfers to global locations.

Skills

Analytical method development

Leadership skills

Communication skills

Root cause analysis

Education

Degree in Chemistry, Pharmacy, or related field

Master’s or PhD preferred

Job description

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Analytical Technology Transfer Scientist, Chester

Client:

Location:

Chester, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

3

Posted:

26.08.2025

Expiry Date:

10.10.2025

Job Description:

Analytical Technology Transfer Scientist

Location: Cheshire

Salary: up to £50,000 per annum

Type: Full-time, Permanent

Hours: 36.5 hours/week (Monday–Friday, 08:00–16:30)

Work arrangement: 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.