Trace Analysis Scientist — LC-MS Method Development

Eurofins Uk Pss

Macclesfield

On-site

GBP 42,000 - 62,000

Full time

3 days ago
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Job summary

Eurofins UK PSS in Macclesfield, England, United Kingdom is seeking an Analytical Product Development Scientist to support the analysis of pharmaceutical Oral Drug Products and New Mod alities with accurate results within an acceptable timeframe. This is a full-time, permanent position with a 36.5 hour work week, Monday–Friday.

You will perform routine and non-routine analyses, review GMP data, and contribute to method development and validation using LC-MS and LC-MS/MS.

Qualifications

  • A degree in Chemistry or related discipline is required.
  • Experience in pharmaceutical analysis in a development lab or equivalent.
  • Competent with traditional analytical and chromatographic techniques.
  • Significant trace analysis experience, especially LC-MS and LC-MS/MS.

Responsibilities

  • Perform routine and non-routine analysis using traditional and modern analytical techniques as required by the Lead Scientist or customer representative.
  • Review analytical data for GMP compliance and prepare and approve results after training and competency.
  • Support development and validation of analytical procedures for Oral Drug Products and New Modalities like peptides with trace analysis using LC-MS and LC-MS/MS.
  • Initiate and follow up on OOS results and action limits per customer procedures.
  • Participate in the preparation of reports.

Skills

Trace analysis experience
Analytical thinking
Problem solving

Education

Degree in Chemistry or related discipline

Tools

LC-MS
LC-MS/MS
Chromatography

Job description

Eurofins UK PSS in Macclesfield, England, United Kingdom is seeking an Analytical Product Development Scientist to support the analysis of pharmaceutical Oral Drug Products and New Mod alities with accurate results within an acceptable timeframe. This is a full-time, permanent position with a 36.5 hour work week, Monday–Friday.

You will perform routine and non-routine analyses, review GMP data, and contribute to method development and validation using LC-MS and LC-MS/MS.

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