Analytical Technology Transfer Scientist

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

Job summary

A leading pharmaceutical facility in Basildon is seeking an Analytical Technology Transfer Scientist. The role involves overseeing analytical testing, leading method transfers, and collaborating across teams. Candidates should have a degree in Chemistry or Pharmacy along with proven analytical development experience. The position offers up to £50,000 per annum with hybrid working options.

Qualifications

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

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.
• Lead analytical method transfers to multiple global locations.

Skills

Analytical method development

Communication skills

Leadership skills

Root cause analysis

Education

Degree, Master’s, or PhD in Chemistry, Pharmacy, or related field

Tools

Analytical techniques

Job description

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Analytical Technology Transfer Scientist, Basildon

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Client:

Location:

Basildon, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

3

Posted:

26.08.2025

Expiry Date:

10.10.2025

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Job Description:

We are seeking an enthusiastic and innovative Analytical Technology Transfer Scientist to join a leading pharmaceutical facility in Basildon. This full-time, permanent role offers a salary up to £50,000 per annum, with a 36.5-hour work week (Monday–Friday, 08:00–16:30) and hybrid working arrangements (3 days onsite).

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.