clinical immunologist
Title posted on CareerBeacon - Associate III, Scientific Affairs
Posted on August 09, 2026 by Employer details bioLytical
Job details
Reporting directly to the Product Launch and Sustaining Manager, the the Associate plays a key role in the design and development of new bioLytical rapid point of care tests. Working with a high level of independence and autonomy at the project level, the Associate will plan and carry out necessary activities, problem solve, and drive execution towards project goals and department plans.ABOUT BIOLYTICALBioLytical is a rapidly growing biomedical company. The company?s vision is to develop innovative rapid diagnostic test to help fight several diseases around the world. The company aims to be vertically integrated, producing in house all the materials required for the testing device, from recombinant protein production to the final kit. Thus, bioLytical is looking for people eager to build and help shape the company of the future.bioLytical Laboratories Inc. is a privately-owned Canadian company focused on the research, development and commercialization of rapid in-vitro medical diagnostics using its proprietary INSTI® technology platform.  bioLytical has won several local and industry awards, including BC Exporter of the Year in 2019 and the Globe and Mail?s Fastest Growing Companies list in 2020. We have been named Lifesciences BC?s Growth Stage Med Tech Company of the Year and have been featured on BC?s Fastest Growing Companies six years in a row. bioLytical moved to a significantly larger, state-of-the-art facility in Richmond in 2020 to accommodate the extraordinary growth achieved through our team.HOW YOU WILL CONTRIBUTECo-lead projects and act as Study Director for internal studies Develop project plans, objectives and tasks objectives and participate in project planning and timeline discussionsAssist in preparing Project Management documents Lead the drafting of test plans and execution of scientific studies include but not limited to official verification and validation testing and stability studies Analysis test results and troubleshoot design challengesWrite technical reports on feasibility and performance, and act as reviewer of protocols and reportsParticipate in risk management activities Translate design outputs into procedures, testing methods and quality control release criteria   Support and lead design transfer, to ensure new designs, and design changes are accurately transferred to manufacturingTranslate design outputs into procedures, testing methods and quality control release criteria   Collaborate actively within and outside the department to complete projects and advance creative solutions and act as key contact point between departments and collaboratorsManage the use of resources and ensure their effective usePresent data within the company, routinely communicate complex ideas to those with limited knowledge and understanding as well as to peers using high level skills and a range of mediaAssist with training of team members, laboratory and production or other related personnel WHAT YOU BRINGMaster?s or Bachelor?s degree in a life sciences discipline, preferably in biochemistry, biotechnology, microbiology, medical technology, biology, chemistry, or related science.Minimum 3 years? experience in a research or clinical laboratory Minimum 3 years? industry experience in the development or manufacturing of IVD?sKnowledge of or experience with GLP, GMP work preferredExperience in a BSL2 laboratory an assetExperience of 5S/Lean 6 Sigma an assetExcellent interpersonal skills, oral communication skills, and written communication skills are requiredMust be able to work independently following a brief orientation and training period Must have strong analytical and technical writing skillsExcellent computer skills (MS Office, Access, Excel) Organized and detail-orientedMust be able to work with blood and blood-borne pathogensMust have a go-getter that thrives in high energy environments WHAT WE OFFERA competitive- Location Richmond, BC
- Work location On site
- Salary$99,727 to $535,765YEAR annually
- Terms of employment Permanent employmentFull time
- Starts as soon as possible
- Source CareerBeacon #2495667
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