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.

The candidate will be responsible for:

• 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

The successful candidate for this position should have:

• 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.

BIOVECTRA offers a competitive salary and benefit package. Interested candidates are asked to apply by choosing the "Apply Now" button

Closing Date: December 27, 2024

Individual accommodations due to a disability are available upon request for candidates taking part in all aspects of the selection process. All qualified applicants will receive consideration for employment without regard to age, race, religion, ethnicity, gender, disability, citizenship status, marital status, actual or perceived sexual orientation. BIOVECTRA is committed to creating an inclusive environment and building a team that represents a variety of backgrounds, perspectives, and skills. We value diversity and recognize that experience comes in many forms and skills are transferable. Please view this description as a general overview, but not a mandatory comprehensive list. If you feel passionate about our efforts and believe that you have the skills to contribute and lead in this role, apply! We thank all interested parties; however, only those applicants considered for an interview will be contacted.