The Sr. Research Chemist will be responsible for overseeing and executing analytical services in support of Drug Product development and GMP operations. Primary responsibilities will include analytical services such as method transfer method development and phase appropriate method validation. The Sr. Research Chemist will also support QC drug product release stability and any required investigations. The Sr. Research Chemist may also be responsible for direct reports as required.
DUTIES AND RESPONSIBILITIES:
- Draft GMP documentation such as test methods material/product specifications protocols and SOPs as required.
- Develop and execute analytical methods in support of oral drug product development. Methods include but are not limited to Assay Impurity Dissolution Water Content and Residual Solvent.
- Conduct OOT/OOS/Deviation investigations as required.
- Troubleshoot maintain and perform equipment qualifications for HPLCs GCs KF and other analytical equipment as required.
- Conduct prototype and GMP stability studies in accordance with ICH or other regulatory guidelines.
- Ensure all work is performed in compliance with applicable SOPs cGMPs and GLPs.
- Promote and maintain a safe and healthy working laboratory environment in compliance with established health and safety procedures.
- Other duties as assigned.
COMMUNICATION AND CONTACTS:
Within the Company
- Interact with all staff throughout the company as necessary to implement the business objectives.
Outside of the Company
- Interact with various outsource vendors clients contractors and industry bodies to support the business objectives.
Qualifications :
- B.Sc. or M.Sc. in Chemistry with >10 years experience or Ph.D in Chemistry with >5 years experience in the pharmaceuticalrelated field industry
- Must have a strong knowledge of drug product development and handson experience in analytical development
- Must be highly motivated and have a proven record of success in multiple projects
- Must be well organized and able to meet project timeline commitments
- Must work well in a multidisciplinary team environment and have excellent written and verbal communication skills
- B.Sc. or M.Sc. in Chemistry with >10 years experience or Ph.D in Chemistry with >5 years experience in the pharmaceuticalrelated field industry
- Must have a strong knowledge of drug product development and handson experience in analytical development
- Must be highly motivated and have a proven record of success in multiple projects
- Must be well organized and able to meet project timeline commitments
- Must work well in a multidisciplinary team environment and have excellent written and verbal communication skills
Additional Information :
At Eurofins we offer excellent fulltime benefits including health & dental coverage life and disability insurance RRSP with 3% company match paid holidays paid time off.
Accommodation: Persons with disabilities who need accommodation in the application process or those needing job postings in an alternative format may email a request via the website at
As a Eurofins employee you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins please explore our website at
We thank all applicants within commuting distance of GTA Ontario for showing an interest in this position. Only those selected for an interview will be contacted.
This posting is supported by AI technology to assist in screening candidates and resumes.
NO AGENCIES CALLS OR EMAILS PLEASE
Remote Work :
No
Employment Type :
Fulltime