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QC Analyst

2 months ago

Skipton, North Yorkshire, United Kingdom Dechra Pharmaceuticals Limited Full time
About Dechra Pharmaceuticals Limited

We are a global specialist in the world of veterinary pharmaceuticals, dedicated to developing, manufacturing, marketing, and selling high-quality products exclusively for veterinarians worldwide.

Job Summary

We are seeking a highly skilled QC Analyst to join our team in a 12-month fixed-term contract. As a key member of our quality control team, you will be responsible for ensuring the quality of our products and processes.

Main Responsibilities
  • Perform analytical and physical tests to guarantee the quality of packaging materials, semi-finished products, raw materials, and end products.
  • Meet established specifications and customer requirements.
  • Collect, receive, and archive samples of raw materials.
  • Ensure an efficient division of work, taking into account production planning and agreed lead times.
  • Perform regular maintenance and minor repairs, keeping clean and calibrating equipment, materials, and spaces.
  • Perform tests on raw materials using a wide range of analysis equipment.
  • Work knowledge of raw materials testing, testing according to Pharmacopoeia.
  • Perform analysis for process, product, cleaning, and equipment validation studies.
  • Conduct analysis for stability studies.
  • Carry out analysis for method transfers to or from other laboratories.
  • Check analysis data, documents, methods, and procedures.
  • Correct interpretation, processing, and reporting of analysis data in electronic data systems and validation protocols.
  • Conduct examinations as a result of Out-of-Specification results, deviations, and other quality-related investigations.
  • Keep in touch with relevant departments to ensure that analytical tests are performed on time.
  • Ensure the cleanliness in laboratory rooms and the individual workplace.
  • Provide training/training to new employees or colleagues.
  • Arrange the execution of external research, send samples, process reports, and check the progress of the work to be carried out.
  • Draft specifications, including analytical regulations for raw materials.
  • Draft procedures relating to departmental work and handle it according to regulations.
  • All other tasks that can reasonably be requested and approved by management.
Requirements
  • Minimum of 3 years of relevant experience in a pharmaceutical GMP quality control laboratory and raw materials testing.
  • Knowledge of chemical and physical analysis techniques; HPLC, UV-VIS, DLC, MID-IR, (auto) titration, water determination Karl Fischer, TOC, physicochemical tests as density, melting point determination, color measurement, viscosity measurement, pH measurement.
  • Knowledge of laboratory equipment to be used.
  • Working in Word and Excel and with HPLC data system (CDS).
  • Knowledge of environmental, health, and safety, GMP, and company regulations.
  • Global knowledge of production method.
  • Knowledge of applicable procedures and their application.
  • BSc Hons in Chemistry or equivalent in a scientific field.
  • Occasional global travel is required with this role.
What We Offer
  • Average 36-hour working week (with a day off every other Friday).
  • Earlies.
  • Plenty of training and development opportunities.
  • 22.5 days annual leave + Bank holidays.
  • Option to buy a week's holiday each year.
  • 8% Employer Pension Contribution.
  • Free access to the Headspace App.
  • Employee Assistance Programme.
  • Discounted gym membership.
  • Free on-site parking and electric charging.