Scientist, Quality Projects

2 weeks ago


Windsor, Canada BioVectra Inc. Full time

BIOVECTRA Inc. is a leading bio-science business in Prince Edward Island and Nova Scotia, focused on contract manufacturing and product development of active pharmaceutical ingredients, pharmaceutical intermediates, and bioreagents.

At BIOVECTRA, we are passionate about improving patient care by making better therapeutics as a contract drug manufacturing organization (CDMO) that supports the top pharmaceutical and biotech companies in the world. Be part of a team with a global reach that also has a great community vibe. We care about each other and live our values of teamwork, respect, professionalism, and quality. Diversity is one of our strengths as we strive to offer a welcoming and inclusive environment.

**BIOVECTRA Inc.** has an opening for a** Scientist, Quality Projects.**This is a permanent, full-time position located in **Windsor, Nova Scotia.**
- Developing, verifying, and validating analytical methods
- Carrying out literature searches to evaluate currently known methods and preparing research and development/validation plan.
- Assisting in project evaluations and with _pro forma _costing of custom projects.
- Training and knowledge transfer to technical staff as a member of the project team working effectively with both the R & D and Quality Control groups.
- Technical writing including Quality control procedures, cGMP protocols and reports.
- Leading laboratory investigations into product quality and/or analytical method performance
- Adhering to BIOVECTRA’s Health and Safety Policy as outlined in CP0010 Occupational
- Health and Safety Policy, Statements of Principle, and Responsibilities.
- Following the company’s quality standard (quality management system procedures and cGMP regulations).
- Additional duties assigned, based on business needs and the department supervisor’s request
- Bachelor of Science degree in Chemistry, Biochemistry or Molecular Biology
- MSc or PhD degree is an asset
- Two years of relevant laboratory experience - HPLC, GC, ELISA assay and PCR experience preferred
- Technical writing experience.
- Experience leading laboratory investigations in a GMP environment.
- Experience leading (inter)departmental meetings and/or communications with clients.
- Knowledge of cGMP guidelines an asset.

**Closing Date: December 27, 2024


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