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SRG

Development & Regulatory Chemist

SRG Hitchin
32 - 40 hour
new


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    SRG

    Development & Regulatory Chemist

    SRG Hitchin
    32 - 40 hour
    new
    Status Open
    Apply now

    Apply on the employer's website


    What we ask

    Education

    No minimum education required

    What we offer

    Hours
    32 to 40 hours per week
    Employment type
    permanent

    Job description

    Exciting Opportunity: Development & Regulatory Chemist (APIs)

    Are you an analytical development chemist with strong regulatory writing skills and experience supporting API submissions? This organisation is seeking a Development & Regulatory Chemist to join its technical team, playing a key role in API development, analytical method validation, and regulatory documentation for pharmaceutical markets.

    Job Title: Development & Regulatory Chemist
    Vacancy Type: Permanent
    Location: Hertfordshire
    Salary: DOE

    About the Organisation

    You'll be joining a specialist pharmaceutical ingredients business supplying regulated markets across the UK, EU and internationally. The organisation operates within a GMP‑aligned environment and works closely with pharmaceutical customers, contract manufacturers, and regulatory authorities to support API development and lifecycle management.

    The R&D and Technical function is responsible for analytical development, regulatory strategy, and maintaining high‑quality documentation to support existing and new API registrations. The team combines hands‑on scientific work with high‑impact regulatory authorship, making this an ideal role for a chemist who enjoys working across both laboratory and desk‑based technical activities.

    The Role of the Development & Regulatory Chemist

    This is a broad technical role focused on API development and regulatory support. You will contribute across analytical method development, validation, and regulatory documentation, with a key responsibility for ASMF authoring and lifecycle maintenance. Working closely with the Technical Manager and cross‑functional teams, you'll support both existing product portfolios and new API introductions.

    Key responsibilities include:

    Supporting the development and characterisation of pharmaceutical active ingredients (APIs)
    Developing, validating, and transferring analytical methods in line with ICH and GMP expectations
    Authoring, maintaining, and updating Active Substance Master Files (ASMFs)
    Preparing high‑quality technical documentation suitable for direct regulatory submission
    Managing analytical method transfer to internal QC and external contract manufacturers
    Supporting regulatory submissions, variations, and responses to authority questions
    Coordinating analytical work with external laboratories and manufacturing partners
    Overseeing analytical activities at pilot through to commercial scale
    Writing and reviewing technical reports, SOPs, and development documentation
    Providing technical input to commercial and customer discussions when required
    Supporting lifecycle management of registered APIs and ensuring ongoing regulatory compliance

    The Ideal Candidate for the Development & Regulatory Chemist Role

    To succeed in this role, you will bring:

    At least 3 years' of recent experience in pharmaceutical analytical development of APIs
    Proven experience authoring and maintaining ASMF documentation
    Strong understanding of analytical method validation in accordance with ICH guidelines
    Experience supporting regulatory submissions for active substances
    Excellent technical writing skills with the ability to produce regulator‑ready documentation
    A methodical, organised approach with the ability to manage multiple technical priorities
    Strong communication skills and confidence working cross‑functionally

    Why This Role?

    This is an excellent opportunity for a chemist who wants meaningful involvement in both analytical development and regulatory strategy. The role offers clear technical ownership, deep exposure to ASMF preparation and lifecycle management, and the opportunity to play a key role in supporting API registrations across global pharmaceutical markets.

    SRG are the UK's number one recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.
    As scientists ourselves, our specialist sector knowledge and passion are second to none. We're committed to providing outstanding temporary, contract and permanent career opportunities at all levels.

    If this role isn't quite right, feel free to get in touch or visit (url removed) to view our other vacancies.

    Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy
    Apply now

    Apply on the employer's website

    Apply now

    Apply on the employer's website


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