Current jobs related to Associate Iii, Scientific Affairs - Richmond - bioLytical
-
Associate Iii, Scientific Affairs
3 weeks ago
Richmond, Canada bioLytical Full timeReporting 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...
-
Associate Iii, Scientific Affairs
2 weeks ago
Richmond, Canada bioLytical Full timeReporting 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...
-
Associate, Scientific Affairs
3 weeks ago
Richmond, Canada bioLytical Full timeReporting to the Manager, Research & Development, the Associate III 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...
-
Research Associate Lv. Iii
3 weeks ago
Richmond, Canada Lepzi Biotechnology Ltd. Full timeLepzi Biotechnology Ltd. (LBio) is an innovative ground for the development of high-performance solutions for _in-vitro_ diagnostics. Our platform technology is designed to provide fast and reliable measurement of specific analytes in human whole blood and plasma for a wide range of medical conditions, including heart failure, kidney failure, preeclampsia,...
-
Associate, Scientific Affairs
3 weeks ago
Richmond, Canada bioLytical Full timeReporting to the Manager, Research & Development, the Associate II 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...
-
Associate, Scientific Affairs
7 days ago
Richmond, Canada bioLytical Full timeReporting directly to the R&D Manager, the the Associate plays a key role in the design and development of new bioLytical rapid point of care tests. **HOW YOU WILL CONTRIBUTE** - Develop project or task objectives and proposals; - Plan for design verification and validation testing - Plan, design and execute stability studies - Troubleshoot test results and...
-
Content Licensing Associate
4 weeks ago
Richmond Hill, Canada Photo Affairs, inc. Full time_Content Licensing Associate _ Photo Affairs, inc. is seeking a Content Licensing Associate to assist senior staff with intellectual property rights clearances, predominantly image/video/text based materials on behalf of various high-profile content producers, internationally. work remotely - comfortable with independent, self-guided work and time...
-
Warehouse - Warehouse Associate Iii
3 weeks ago
Richmond, Canada Russell A. Farrow Limited Full timeFarrow is a diversified, family-owned business that facilitates international trade by executing comprehensive customs brokerage and integrated logistics solutions. We provide our clients peace of mind with our customs brokerage, shipping, and freight-forwarding capabilities for Canada and the United States. Farrow Prides itself on providing exceptional...
-
Associate Director Regulatory Affairs
2 weeks ago
Richmond Hill, Canada Apotex Inc. Full timeAbout Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the...
-
Associate Director Regulatory Affairs
2 weeks ago
Richmond Hill, Canada Apotex Inc. Full timeAbout Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the...
-
Account Manager Iii
2 weeks ago
Richmond, Canada Thermo Fisher Scientific Full timeThermo Fisher Scientific Inc. (NYSE: TMO) takes pride in being the leader in serving science. We help our customers accelerate life sciences research, respond to challenges, improve patient diagnostics, deliver medicines to market and increase laboratory efficiency. Our work has a real-world effect and you’ll be supported in achieving your career...
-
Manager, Regulatory Affairs
3 weeks ago
Richmond, Canada bioLytical Full time**bioLytical**is hiring an experienced Regulatory Affairs (RA) Manager. You will be responsible for defining and implementing regulatory strategies to obtain global approvals for new/modified devices to meet bioLytical’s corporate objectives. This role requires the ability to analyze complex technical and medical information and formulate strong...
-
Manager, Regulatory Affairs
2 weeks ago
Richmond, Canada bioLytical Full time**bioLytical** is hiring an experienced Regulatory Affairs (RA) Manager. You will be responsible for defining and implementing regulatory strategies to obtain global approvals for new/modified devices to meet bioLytical’s corporate objectives. This role requires the ability to analyze complex technical and medical information and formulate strong...
-
Medical Affairs Strategist
13 hours ago
Richmond Hill, Ontario, Canada Brunel International Full timeClinical and Medical Affairs Career OpportunityThe Clinical and Medical Affairs Manager will be responsible for ensuring compliance with relevant regulations, overseeing clinical trials, and evaluating investigational sites in North America. Additionally, they will maintain the Trial Master File, collaborate with vendors for medical writing and data...
-
Summer Leader Iii
3 weeks ago
Richmond, Canada Thompson Community Association Full timeApplications are now being accepted for **Summer Leader III **positions with Richmond community associations in Parks and Recreation. This person reports to the Summer Coordinator or Director of Childcare Services at each facility and is responsible for planning the daily activities and weekly themes for daycamp programs. The Leader III instructs program...
-
Lead Associate, Regulatory Affairs
3 weeks ago
Richmond, Canada bioLytical Full time**bioLytical**is hiring a demonstrated Regulatory Affairs (RA) Associate. You will actively support operations for the market entry of new IVD products and the maintenance of licenses for commercially marketed products. You will share your expertise and help train team members. As a RAC certified professional with US FDA experience, you play a vital role in...
-
Lead Associate, Regulatory Affairs
3 weeks ago
Richmond, Canada bioLytical Full time**bioLytical** is hiring an demonstrated Regulatory Affairs (RA) Associate. You will actively support operations for the market entry of new IVD products and the maintenance of licenses for commercially marketed products. You will share your expertise and help train team members. As a RAC certified professional with US FDA experience, you play a vital role...
-
Medical Affairs Specialist
14 hours ago
Richmond Hill, Ontario, Canada Brunel International Full time**About the Role:**We are seeking a highly skilled Clinical and Medical Affairs Manager to join our team at Brunel International. In this role, you will be responsible for ensuring compliance with regulations (SOPs, GCPs, FDA, Health Canada) and managing clinical trials.The ideal candidate will have a strong background in clinical research management,...
-
Medical Affairs Manager Lead
6 days ago
Richmond Hill, Ontario, Canada Brunel International Full timeJob DescriptionThe Clinical and Medical Affairs Manager will be responsible for ensuring full compliance with regulations, managing clinical trials, and evaluating investigational sites in North America. The role also involves maintaining the Trial Master File, collaborating with vendors for medical writing and data management, securing IRB approvals, and...
-
Clinical and Medical Affairs Manager
4 weeks ago
Richmond Hill, Canada Brunel International Full timeWhat are you going to doThe Clinical and Medical Affairs Manager will be responsible for ensuring compliance with regulations (SOPs, GCPs, FDA, Health Canada), managing clinical trials, and evaluating investigational sites in North America. Additionally, maintain the Trial Master File, collaborate with vendors for medical writing and data management, secure...

Associate Iii, Scientific Affairs
4 weeks ago
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 BIOLYTICAL**
BioLytical 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 CONTRIBUTE**
- Co-lead projects and act as Study Director for internal studies
- Develop project plans, objectives and tasks objectives and participate in project planning and timeline discussions
- Assist 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 challenges
- Write technical reports on feasibility and performance, and act as reviewer of protocols and reports
- Participate 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 manufacturing
- Translate 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 collaborators
- Manage the use of resources and ensure their effective use
- Present 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 media
- Assist with training of team members, laboratory and production or other related personnel
**WHAT YOU BRING**
- Master’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’s
- Knowledge of or experience with GLP, GMP work preferred
- Experience in a BSL2 laboratory an asset
- Experience of 5S/Lean 6 Sigma an asset
- Excellent interpersonal skills, oral communication skills, and written communication skills are required
- Must be able to work independently following a brief orientation and training period
- Must have strong analytical and technical writing skills
- Excellent computer skills (MS Office, Access, Excel)
- Organized and detail-oriented
- Must be able to work with blood and blood-borne pathogens
- Must have a go-getter that thrives in high energy environments
**WHAT WE OFFER**
- A competitive compensation package
- Extended health benefits including dental - 100% employer contribution
- Flexible working hours
- Paid sick days
- Bonus day off with pay on your birthday every year
- Full-size in-house fitness gym and shower facilities
- Complimentary reserved parking
- Opportunity to work with industry experts who are motivated and passionate about what they do but know how to have some fun
- A chance to show off your dance moves and singing voice at the company parties and jump in to score a victory or lead the way in our outdoor games at the summer barbeques
- The opportunity to join an ‘off the charts’ foodie culture in our large kitchen and try out your favourite recipes or enjoy the culinary delights as they hit the share table
The annual base salary for this job ranges from:
$65,000-$70,000
bioLytical's pay range is based on multiple factors including experience, education, job-related skills, and equity within the team or organization.
**CORE VAL