Analytical Scientist(Technology Transfer)

Kenton Black; England; On-site; GBP 100,000 - 125,000; Full time

Job summary

A global pharmaceutical testing laboratory in Cheshire is seeking an analytical technology transfer scientist to lead analytical method transfers and ensure compliance across operations. Candidates should possess a degree in Chemistry, Pharmacy, or related fields along with proven experience in the pharmaceutical industry. Key responsibilities include acting as the primary contact for oral solid dose products and supporting major product changes. Strong analytical method development skills are essential for this role.

Qualifications

• 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.

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

Strong communication skills

Leadership skills

Knowledge of analytical techniques

Education

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

Job description

Excellent opportunity for an analytical scientist within a global pharmaceutical testing laboratory

This is a permanent opportunity. The salary is negotiable. Kenton Black Scientific is a recruitment partner to a global pharmaceutical testing laboratory based in Cheshire. They are looking to hire an analytical technology transfer scientist to join their team.

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:

• 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