Analytical Testing Chemist I

Found in: Jooble CA O C2 - 2 weeks ago

Cambridge ON, Canada Mundipharma International Full time

Principal Chemical Analyst page is loaded Principal Chemical Analyst
Apply locations GB Cambridge time type Full time posted on Posted 10 Days Ago job requisition id JR1218
Principal Chemical Analyst 
Cambridge (Lab Based) 
Job type: 24-Months Fixed Term Contract
We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees.
Working within the Analytical Services section of the Quality Department laboratories a Senior Analyst will provide high quality scientific and analytical expertise for a variety of pharmaceutical dosage forms. Seek out improvement opportunities and make suggestions to management for changes in practice and technical innovation. Act as an Analytical expert on a wide range of projects. Will be expected to develop supervisory skills by undertaking more responsibility for the day to day operation of the laboratory.
Lead the execution of analytical method transfers between laboratories. 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 in accordance with agreed timelines.
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, this can be 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.
Minimum 5 years of 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.
flexible benefits package
Diversity and inclusion
Building an inclusive environment where people can thrive, grow and achieve their full potential is a priority. If you’re not sure this role is right for you but you’re keen to hear about future opportunities at Mundipharma, join our talent community and be the first to hear about new roles.
Fixed Term Contract (Fixed Term) About Us
Mundipharma is a global healthcare company with a presence across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East.
Mundipharma is dedicated to bringing innovative treatments to patients in the areas of Pain Management, Infectious Disease and Consumer Healthcare as well as other severe and debilitating disease areas. For more information about Mundipharma's guiding principles and commitment to diversity and inclusion visit:
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