Analytical Technology Transfer Scientist

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

Job summary

A leading pharmaceutical company is hiring an Analytical Technology Transfer Scientist in Ipswich. This full-time role involves leading analytical method transfers, collaborating with cross-functional teams, and ensuring compliance across manufacturing sites. Candidates should have a degree in Chemistry or a related field and experience in drug product analytical development. Salary up to £50,000 per annum, offering a hybrid work model.

Qualifications

• Degree, Master’s, or PhD in Chemistry, Pharmacy, or Pharmaceutical Sciences required.
• Proven experience in drug product analytical development.

Responsibilities

• Act as the primary contact for analytical testing of commercial OSD products.
• Lead analytical method transfers to multiple global locations.
• Collaborate with cross-functional teams including QA, QC, and Manufacturing.

Skills

Analytical method development

Leadership skills

Communication skills

Problem-solving

Education

Degree in Chemistry, Pharmacy, or related field

Tools

Analytical techniques

Job description

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Analytical Technology Transfer Scientist, Ipswich

Job Category: Other

EU work permit required: Yes

Job Views: 3

Posted: 26.08.2025

Expiry Date: 10.10.2025

Job Description:

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.