Analytical Method Development Analyst

Marketplace Technical
30 Sep 2017
03 Nov 2017
Contract Type
Full Time

Pharmaceutical Manufacturer based in Hertfordshire requires a Analytical Method Development Analyst to provide analytical method development support to existing and new products and technology transfer to QC team.

·Develop analytical methods appropriate for raw materials, In-process controls and Intermediate/Final API’s

·Attention to detail with ability to prioritize and manage the workload, and, as required, be able to manage shifting priorities based on critical deadlines so that production needs are always met.

·Demonstrate excellent communication skills (verbal and written).

·Ability to develop and give presentations on technical topics.

·Ability to train/mentor associates.

·Ability to effectively deal with a variety of conflicting issues and diplomatically solve those issues.

·Ability to read, analyse, and interpret complex technical documents and manuals

·Ability to define problems, collect data, establish facts, and draw valid conclusions.

·Ability to use trends and data to review and improve performance

·Ensure methods are developed in accordance with current regulatory expectations and are suitable for ASMF submissions

·Work closely with R&D/Process Development Chemists and QC analysts to ensure methods are developed and implemented in time to meet project/customer deadlines


Degree in Analytical chemistry


Relevant experience within pharmaceutical industry (Minimum 2- 3 years’ experience):

·Strong knowledge of using HPLC, MS, GC, IR, UV, TLC, Particle size analysis and dry powder method development & Wet chemical techniques.

·Respective method developments and Validation as per ICH requirements

·Technology transfer of newly developed methods to QC team both internally and externally

·Setting specification for raw materials, in-process checks and finish product

·Knowledge of general analytical methods used for herbal raw materials and API’s will be useful

·Writing and reviewing SOP’s

·Knowledge of current GMP requirements

·Understanding of Lean/Six sigma

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