Analytical Chemist

2 months ago


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

Join our team at Mundipharma as an Analytical Chemist Apprentice and take the first step in your career in pharmaceutical testing laboratories.

About the Role:

We are seeking a highly motivated and detail-oriented individual to join our Quality Department laboratories as an Analytical Chemist Apprentice. As an Analytical Chemist, you will provide high-quality scientific and analytical expertise for a variety of pharmaceutical dosage forms.

Key Responsibilities:
  • Act as an analytical expert on a wide range of projects, developing supervisory skills by undertaking more responsibility for the day-to-day operation of the laboratory.
  • Conduct the execution of analytical method transfers between laboratories, ensuring all aspects of analytical development and validation are delivered to the required standard of science, quality, and regulatory compliance.
  • 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.
  • 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, by applying expert scientific knowledge, demonstrating a practical approach, and providing appropriate and innovative solutions.
  • Be proficient and proactive in the use of regulatory and other relevant guidelines, including pharmacopoeias, to ensure appropriate compliance within projects.
  • Provide appropriate and 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:

We offer a flexible benefits package, opportunities for learning & development, a collaborative, inclusive work environment, and a chance to work with a talented team of professionals.

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