Analytical Technology Transfer Scientist

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

Job summary

A leading pharmaceutical firm in Slough is seeking an enthusiastic Analytical Technology Transfer Scientist. This full-time role offers a salary up to £50,000 per annum with a hybrid working model. You will act as the primary contact for analytical testing of commercial Oral Solid Dose products and collaborate with various teams to ensure method robustness and compliance.

Qualifications

• Proven experience in drug product analytical development within the pharmaceutical industry.
• Strong knowledge of analytical method robustness, performance, and compliance.
• Familiarity with analytical techniques and root cause analysis tools.

Responsibilities

• Act as the primary contact for analytical testing of commercial Oral Solid Dose (OSD) products.
• Ensure analytical method robustness and compliance across manufacturing sites.
• Collaborate with cross-functional teams including QA, QC, Regulatory Affairs, and Manufacturing.

Skills

Analytical method development

Analytical testing

Communication skills

Strong knowledge of OSD

Education

Degree in Chemistry, Pharmacy, Pharmaceutical Sciences or related field

Job description

Social network you want to login/join with:

Analytical Technology Transfer Scientist, Slough

Client: [Client Name]

Location: Slough, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views: 3

Posted: 26.08.2025

Expiry Date: 10.10.2025

Job Description:

We are hiring an enthusiastic and innovative Analytical Scientist to join a leading pharmaceutical facility in Cheshire. This full-time, permanent role offers a salary up to £50,000 per annum, with a 36.5-hour workweek (Monday–Friday, 08:00–16:30) and hybrid working (3 days on site).

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 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.