Analytical Chemist

7 days ago


Tetbury, Gloucestershire, United Kingdom Mundipharma Full time
Job Title: Analytical Chemist

Location: Cambridge (Lab Based)

Job Type: 24-Months Fixed Term Contract

As an Analytical Chemist at Mundipharma, you will be responsible for providing high-quality scientific and analytical expertise for various pharmaceutical dosage forms. Your key responsibilities will include:

Key Responsibilities:
  • Act as an analytical expert on a wide range of projects, ensuring the highest level of quality and compliance.
  • Develop supervisory skills by undertaking more responsibility for the day-to-day operation of the laboratory, ensuring efficient and effective processes.
  • Conduct the execution of analytical method transfers between laboratories, ensuring seamless integration and minimal disruption.
  • Support and help to develop analytical validation strategies, ensuring all aspects of analytical development and validation are delivered to the required standard of science, quality, and regulatory compliance.
  • Assist with and ensure Quality Management System processes such as Change Controls, Deviations, CAPAs, and Quality Risk management procedures are undertaken and progressed as required.
  • Plan, coordinate, and conduct laboratory work to support analytical projects, including analysis of raw materials, intermediates, and finished products.
  • Record, evaluate, and present data generated during laboratory work both internally and by third parties, applying expert scientific knowledge and providing innovative solutions.
  • Be proficient and proactive in the use of regulatory and other relevant guidelines, including pharmacopoeias, to ensure appropriate compliance within projects.
  • Provide consolidated CMC or pharmaceutical analysis opinion to ensure successful project outcomes.

Requirements:

  • Proven years of experience in pharmaceutical testing laboratories.
  • Proven track record in analytical chemistry and/or analytical development for drug product formulations, as well as experience in CMC/regulatory guidelines and filings.
  • Significant industrial experience working in or maintaining a GMP/GLP compliant analytical environment.
  • Experience with EU regulatory guidelines, quality management systems, and quality risk assessments.

What We Offer:

  • Flexible benefits package.
  • Opportunities for learning and development.
  • Collaborative and inclusive work environment.

Diversity and Inclusion:

Mundipharma is committed to building an inclusive environment where people can thrive, grow, and achieve their full potential.


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