Analytical Technology Transfer Scientist

JR United Kingdom; Belfast; Hybrid; GBP 50,000; Full time

Job summary

A leading pharmaceutical company is seeking an enthusiastic Analytical Technology Transfer Scientist for a hybrid role in Belfast. You will be responsible for analytical testing and leading method transfers globally. Ideal candidates will have a degree in Chemistry or a related field, strong experience in analytical development, and excellent communication skills. The role offers a salary up to £50,000 per annum.

Qualifications

• Proven experience in drug product analytical development within the pharmaceutical industry.
• Solid grasp of cGMP and SHE principles.
• Understanding of OSD, Inhalation, and Parenteral product life cycles.

Responsibilities

• Act as the primary contact for analytical testing of commercial products.
• Lead analytical method transfers to multiple global locations.
• Collaborate with teams in QA, QC, Regulatory Affairs, and Manufacturing.

Skills

Analytical method development

Communication skills

Leadership skills

Knowledge of SHE principles

Familiarity with analytical techniques

Education

Degree in Chemistry, Pharmacy, or related field

Job description

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Analytical Technology Transfer Scientist, Belfast

Client:

Location:

Belfast, 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
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.