QC Analyst

Location Maidenhead
Discipline: Pharmaceutical
Job type: Permanent
Salary: £Negotiable
Contact name: Liam Smith

Contact email: admin@superadmin.sciencesr
Job ref: BBBH4031_1664265846
Published: over 1 year ago
Startdate: ASAP

Responsibilities

  • Carry out Quality Control analysis on Incoming Materials, Components and Products (including stability and other samples) as well as data in support of the onsite manufacturing and QC functions
  • Help to ensure that QC functions operate in a fully current GMP compliant manner and in compliance with the filed regulatory dossiers for the products supported.
  • You will have involvement in the writing, reviewing and implementing of SOP's, methods, protocols and reports as required.
  • You must be able to follow and understand specifications for sample analysis.
  • The successful candidate will need to be able to provide technical support/advice for QC testing whilst ensuring that the test methods are followed correctly.
  • Participate in documentation, laboratory systems and processes to include updating existing ones as required.

    Required Skills

    Degree in Chemistry, Pharmaceutical Science, analytical or related

    Proven experience of 2-4 years as QC Analyst.

    Strong hands-on experience of undertaking testing, analysis and development using instrumentational analysis such as

    HPLC

    GC

    Dissolution

    UV

    FTIR in a cGMP environment.

    Good knowledge of GMP, ICH guidelines, BP/EP/USP methods with an understanding of QA processes and methodologies.

    Experience of LIMS or equivalent system is desirable.

    Sound understanding of MHRA guidelines

    Good understanding of FDA guidelines and other governing bodies is desirable but not essential

Please contact Liam Smith at Science Solutions