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Analytical Technology Transfer Scientist

JR United Kingdom

Bath

Hybrid

GBP 42,000 - 50,000

Full time

23 days ago

Job summary

A leading pharmaceutical firm in Bath is seeking an Analytical Technology Transfer Scientist to manage analytical testing of commercial products. This full-time role involves ensuring method compliance and leading transfers globally in a collaborative, hybrid work setting. Suitable candidates should have a degree in Chemistry or related fields and strong experience in the pharmaceutical industry.

Benefits

Hybrid working model

Qualifications

  • Proven experience in drug product analytical development within the pharmaceutical industry.
  • Solid grasp of SHE principles.
  • Desirable: Experience in CMC functions and Lean methodologies.

Responsibilities

  • Act as the primary contact for analytical testing of commercial OSD products.
  • Ensure analytical method robustness, performance, and compliance across sites.
  • Lead analytical method transfers to multiple global locations.

Skills

Analytical method development
Communication skills
Leadership skills
Knowledge of cGMP
Root cause analysis

Education

Degree in Chemistry, Pharmacy, or related field
Job description

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Analytical Technology Transfer Scientist, Bath

Client:

Location:

Bath, 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 (Note: Location discrepancy in original description, verify if necessary)

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

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