Analytical Technology Transfer Scientist

JR United Kingdom; Bournemouth; Hybrid; GBP 45,000 - 50,000; Full time

Job summary

A leading pharmaceutical company in Bournemouth is seeking an Analytical Technology Transfer Scientist to oversee analytical testing of Oral Solid Dose products. This full-time permanent role offers a salary of up to £50,000 per annum and a hybrid working arrangement. Candidates should have a relevant degree and proven experience in the pharmaceutical industry. Strong communication skills and knowledge of analytical method development are essential.

Qualifications

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

Responsibilities

• Serve 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

Drug product analytical development

Excellent communication

Leadership skills

Education

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

Job description

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Analytical Technology Transfer Scientist, Bournemouth

Client:

Location:

Bournemouth, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

3

Posted:

26.08.2025

Expiry Date:

10.10.2025

Job Description:

Position: 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)
Working arrangement: Hybrid (3 days on site)

My client is seeking an enthusiastic and innovative Analytical Scientist to join their team at a leading pharmaceutical facility in Cheshire. This role offers the opportunity to contribute to high-impact commercial products in a collaborative environment.

Key Responsibilities:

• Serve 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.
• Potentially participate in hands-on analytical activities.

Qualifications & Experience:

• Degree, Master’s, or PhD in Chemistry, Pharmacy, Pharmaceutical Sciences, or 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 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.