drjobs Analytical Chemist - Eurofins CDMO Alphora Inc

Analytical Chemist - Eurofins CDMO Alphora Inc

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

Oakville - Canada

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

You possess a high degree of initiative and are a team player with excellent communication abilities. You have a strong understanding of API (active pharmaceutical ingredient) analytical method validation and development. You are comfortable in a modern state of the art laboratory and are proficient with HPLC/UPLC GC IC KF and various wet chemistry techniques. Proficiency with LCMS and/or GCMS are definite assets. Your attention to detail a comprehensive understanding of cGMP strong organizational skills with the ability to drive projects to completion make you the ideal candidate to become a member of our team.

Description of Department:

The Analytical Services Department is responsible for providing analytical method development and analytical support for Synthetic Process Development. In addition to support in process development  analytical method validation forced degradation studies stability testing are routinely performed.   

Description of Major Job Responsibilities: Reporting to the Analytical Chemist Team Leader

  • Work effectively within interdepartmental project teams including analytical quality assurance process development and manufacturing.
  • Develop and author analytical test methods (raw material in process control synthetic intermediate and API) for use in GMP manufacturing.
  • Perform analytical method validations and prepare data for review and reports.
  • Provide analytical support to both process development and stability.
  • Conduct scientific investigations in support of process development and manufacturing
  • Work in accordance with established GMP and safety requirements.

Instrumentation:

  • HPLC/UPLC (Empower) GC GC/Headspace IR KF Ion Chromatography

Qualifications :

  • B.Sc. in a related field with a minimum of 5 years relevant experience in pharmaceutical analysis development and validation.
  • Excellent skills in technical writing and GMP documentation.
  • Excellent problemsolving planning and organizational skilled coupled with a strong attention to detail.


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.

NO AGENCIES CALLS OR EMAILS PLEASE


Remote Work :

No


Employment Type :

Fulltime

Employment Type

Full-time

Company Industry

About Company

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.