QC Laboratory Analyst, Finished Products Specialist

4 weeks ago


Brighton, Brighton and Hove, United Kingdom Custom Pharma Services Full time

About the Role

We are seeking an experienced Finished Products Analyst to join our Quality Control Laboratory Team at Custom Pharma Services.

Key Responsibilities

  • Carry out day-to-day scheduling work of the QC routine and/or investigative analytical work to ensure adherence to the plan and meet customer requirements.
  • Ensure equipment is properly maintained and take personal responsibility for some equipment.
  • Ensure the QC laboratories are well-organized, reagents/standards are available and controlled.
  • Participate in the timely analysis and release of incoming starting materials.
  • Apply expertise and a systematic approach to problem-solving to achieve prompt and effective results.
  • Ensure equipment is qualified and calibrated.
  • Ensure methods are validated and developed/enhanced to meet current Regulatory requirements.
  • Participate in the transfer of new and modified analytical methods into the lab and perform the acquisition, qualification, maintenance, and calibration of existing and new laboratory equipment.
  • Participate in achieving site KPIs by completing QC and customer objectives and focusing on tasks linked to overall site performance.
  • Provide input to various projects on site as required to maintain company obligations with respect to laboratory activities, release activities, validation, and compliance.
  • Improve adherence to customer quality requirements by applying principles of GMP/GLP.
  • Propose new ideas to improve performance within own area of responsibility.

Requirements

  • A degree in a related science subject, such as Chemistry or Pharmaceutical Chemical Science.
  • A chemistry background and previous experience as a Quality Control Analyst.
  • Previous experience within a QC or development environment in the pharmaceutical industry is preferred.
  • A practical working knowledge of GMP and GLP.
  • A familiarity with laboratory equipment/techniques/procedures and documentation systems.
  • Understanding of EU and other specific analytical regulations for the pharmaceutical industry would be a bonus but is not essential.
  • Attention to detail.
  • Knowledge of information flow and decision-making processes.
  • Follow written procedures with accuracy and efficiency.
  • The ability to prioritize workload and work with minimum supervision.
  • Excellent verbal and written communication skills.
  • Competent in Microsoft Word and Excel.
  • A high level of literacy and numeracy.
  • A flexible attitude to meet changing priorities.
  • A continuous improvement mindset.

What We Offer

  • Rising holiday allowance to 26 days holiday plus UK bank holidays.
  • Group personal pension scheme.
  • Annual profit-related company and individual bonus payment based on successful performance.
  • Life assurance at twice annual salary.
  • Health Plan with Simply Health including access to a GP or Counselling Services 24/7, money back on prescriptions, optical, dental, and physiotherapy.
  • Ride to work scheme.
  • Subsidized Gym Membership.
  • Discount Shopping Portal.
  • Enhanced Maternity/Paternity Pay.
  • Employee Referral Scheme bonus of £1,000.
  • Values-based awards.
  • Free hot drinks vending.

Successful candidates will be required to complete a basic disclosure check.

Strictly no agencies please.



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