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QC Analyst

2 months 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 evaluating the results obtained in order to guarantee the quality of packaging materials, semi-finished products, raw materials, and end products.

Role Responsibility

Key Responsibilities

  • Perform analytical and physical tests and evaluate the results obtained in order to guarantee the quality of packaging materials, semi-finished products, raw materials, and end products.
  • Meet established specifications and customer requirements.
  • Collection, receipt, and archiving of samples of raw materials.
  • Ensure an efficient division of the work, taking into account the 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.
  • Working knowledge of raw materials testing, testing according to Pharmacopoeia.
  • Perform analysis for process, product, cleaning, and equipment validation studies.
  • Conducting analysis for stability studies.
  • Carry out analysis for method transfers to or from other laboratories.
  • Checking analysis data, documents, methods, and procedures.
  • Correct interpretation, processing, and reporting of analysis data in electronic data systems and validation protocols.
  • Conducting examinations as a result of Out-of-Specification results, deviations, and other quality-related investigations.
  • Keeping 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.
  • Providing training/training to new employees or colleagues.
  • Arranging the execution of external research, sending samples, processing reports, and checking the progress of the work to be carried out.
  • Drafting of specifications incl. Analytical regulations for raw materials.
  • Drafting of procedures relating to the departmental work and handling it according to the regulations.
  • All other tasks that can reasonably be requested and approved by the 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

  • Very precise and concentrated work
  • Can work in a team
  • Good communicative skills
  • Good problem-solving ability
  • Strong attention to detail
  • 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 the applicable procedures and their application
  • BSc Hons in Chemistry or equivalent in 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