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Technical lc/ms/ms bioanalyst

Oldham
Russell Taylor Management
Posted: 5h ago
Offer description

Job Specification: Technical LC-MS/MS Bioanalyst

Location: Lancashire
Salary: Competitive
Working Hours: Mon - Fri Standard business hours (Flexibility available)

THE ROLE

Russell Taylor are seeking an experienced a Technical LC-MS/MS Bioanalyst to join a global pharmaceutical company providing senior technical leadership across bioanalytical studies for UK and international clients. This role will work closely with Project Management and Business Development teams, taking ownership of the technical oversight, quality and delivery of complex bioanalytical projects.
You will use your expertise in LC-MS/MS bioanalysis to deliver compliant, high-quality and commercially sound solutions, while acting as a trusted technical partner to clients and supporting the development of laboratory teams.

KEY RESPONSIBILITIES

• Provide technical leadership for bioanalytical studies involving small and large molecules using LC-MS/MS
• Develop and validate bioanalytical methods in accordance with ICH M10 and MHRA-aligned GxP expectations
• Ensure work is delivered in compliance with GLP, GCP and/or GMP, as applicable
• Act as a key technical contact for clients, providing clear, accurate and timely updates
• Define and scope complex projects from early-stage or evolving client requirements
• Produce high-quality technical and client-facing reports
• Support Business Development through technical input, study design, timelines and cost estimates
• Build and maintain strong client relationships, contributing to new business wins
• Mentor and support laboratory staff, promoting best practice, quality and continuous improvement

SKILLS & EXPERIENCE

• At least 10 years' industry experience in LC-MS/MS bioanalysis within a pharmaceutical, CRO or contract laboratory environment
• Demonstrated ability to develop bioanalytical methods from first principles across multiple projects
• Strong experience working with small molecules, large molecules and new drug modalities across a range of biological matrices
• In-depth knowledge of UK and international regulatory requirements, including MHRA expectations and Good Working Practices
• Strong commercial awareness, with the ability to provide accurate project timelines and costings
• Experience working alongside Project Management and Business Development teams
• Excellent knowledge of laboratory safety, including COSHH, SHE and quality management systems
• Strong communication skills with the confidence to engage with senior stakeholders and clients

WHAT WE OFFER

• Opportunities for career development and progression within a global organisation
• A collaborative, high-performing and supportive working environment

Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us

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