Analytical R&D Specialist: Method Validation & Trials

955 ACM UK

York and North Yorkshire

On-site

GBP 48,000 - 62,000

Full time

14 days+

Get more replies from employers

Send a job-specific resume in minutes.

Job summary

ACM Global Laboratories in the United Kingdom is seeking a Research and Development Specialist to design, develop and validate analytical procedures, and to manage studies from method development through validation and investigational work.

You will lead validation planning, ensure adherence to GCP/GLP/GCLP and CAP, liaise with clients and cross‑functional teams, and support regulatory submissions with robust documentation.

Qualifications

  • BSc (or equivalent) or higher in a relevant scientific subject.
  • Minimum of 4 years’ experience within a laboratory environment.
  • Proven experience with external client interactions and managing deliverables from a laboratory, scientific, or technical standpoint.
  • Demonstrable experience managing validation activities within a laboratory setting (clinical laboratory experience highly preferred).
  • Strong analytical, problem‑solving and communication skills.
  • Highly organized with the ability to manage multiple projects simultaneously.
  • Ability to interpret complex technical information and translate findings into clear recommendations.

Responsibilities

  • Develop validation plans, validation summary reports, stability summary reports, correlation plans and correlation summary reports to meet regulatory requirements.
  • Provide supporting information to Scientific Affairs in the evaluation of appropriate testing and/or methodology.
  • Liaise with technical staff on feasibility of testing for new study requirements.
  • Provide pricing as needed to the Proposals team.
  • Select appropriate test methods; research and identify suppliers of laboratory consumables and equipment options for new tests to support clinical trial opportunities.
  • Facilitate assay development, conduct instrument validations and implement new testing to satisfy the needs of clinical trials protocols, clients and regulatory requirements.
  • Be responsible for assay/panel pre‑validation and validation and correlation testing worldwide.

Skills

Analytical skills
Communication skills
Problem solving
Organization

Education

BSc or equivalent in a relevant scientific subject

Job description

ACM Global Laboratories in the United Kingdom is seeking a Research and Development Specialist to design, develop and validate analytical procedures, and to manage studies from method development through validation and investigational work.

You will lead validation planning, ensure adherence to GCP/GLP/GCLP and CAP, liaise with clients and cross‑functional teams, and support regulatory submissions with robust documentation.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Analytical Method Validation Specialist (Clinical Trials)
Analytical Method Validation Specialist (Clinical Trials)

ACM Global Laboratories, Inc. • York and North Yorkshire

On-site
GBP 42,000 - 64,000
Analytical R&D Specialist: Method Validation & Trials
Analytical R&D Specialist: Method Validation & Trials

ACM UK • York and North Yorkshire

On-site
GBP 63,000 - 85,000
Clinical Laboratory Scientist I — GCP & Quality Analysis
Clinical Laboratory Scientist I — GCP & Quality Analysis

ACM Global Laboratories • York and North Yorkshire

On-site
GBP 27,000 - 37,000
Analytical Scientist - HPLC/GC Method Development
Analytical Scientist - HPLC/GC Method Development

MedPharm Ltd • Guildford

On-site
GBP 35,000 - 55,000
Research & Development Specialist
Research & Development Specialist

955 ACM UK • York and North Yorkshire

On-site
GBP 48,000 - 62,000
Laboratory Technician: GMP‑Driven QC & R&D Testing
Laboratory Technician: GMP‑Driven QC & R&D Testing

Accord Healthcare • Barnstaple

On-site
GBP 32,000 - 42,000
Bonus scheme
Pension scheme
Training and development
Analytical Development Chemist - GMP/Pharma
Analytical Development Chemist - GMP/Pharma

OASIS Group • Craigavon

On-site
GBP 30,000 - 45,000
Paid Time-Off for Vacation and Sick ^
Clinical Laboratory Scientist I - GCP & QC Specialist
Clinical Laboratory Scientist I - GCP & QC Specialist

ACM UK • York and North Yorkshire

On-site
GBP 28,000 - 38,000
Senior Analytical Development Scientist, Biotech Methods
Senior Analytical Development Scientist, Biotech Methods

Hyper Recruitment Solutions • England

On-site
GBP 65,000 - 90,000
Competitive benefits
Development opportunities
Research & Development Specialist
Research & Development Specialist

ACM Global Laboratories, Inc. • York and North Yorkshire

On-site
GBP 42,000 - 64,000