QC Analyst

4 weeks ago

Skipton, North Yorkshire, United Kingdom Dechra Full time

Job Introduction

QC Analyst
12 Month Fixed Term Contract
Early shift

We are seeking a highly skilled and experienced QC Analyst to join our team at Dechra. As a QC Analyst, you will be responsible for carrying out testing and evaluation of raw materials, packaging materials, semi-finished products, and end products to ensure they meet Good Manufacturing Practice (GMP) requirements.

Role Responsibilities

Key Responsibilities

  • Perform analytical and physical tests on raw materials, packaging materials, semi-finished products, and end products to ensure they meet GMP requirements.
  • 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.
  • Work with a wide range of analysis equipment, including 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.
  • Conduct 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 the laboratory rooms and the individual workplace.
  • Provide training and 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 them according to regulations.
  • Perform all other tasks that can reasonably be requested and approved by management.
  • Collaborate with team colleagues to ensure that the workplace environment remains at a high level regarding quality and cleanliness and complies with company and legislative standards at all times.
  • Ensure both your own health and safety and that of others, ensure that all company safety and quality systems and relevant legislation are complied with, ask questions, and report any incidents or suggestions to the manager.
  • Ensure that all waste is safely removed and is in line with business processes.
  • Stay abreast of developments in the field through training, reading of literature, documentation, and the like.

The Ideal Candidate

We are looking for a highly skilled and experienced QC Analyst who has a strong background in analytical chemistry and quality control. The ideal candidate will have a minimum of 3 years of relevant experience in a pharmaceutical GMP quality control laboratory and raw materials testing.

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 knowledge of 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 the applicable procedures and their application.
  • BSc Hons in Chemistry or equivalent in a scientific field.
  • Occasional global travel is required with this role.

Package Description

  • 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.

Dechra Pharmaceuticals PLC

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