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Tailored Recruitment Services

Serving the city's dynamic landscape since 1998, Brunel has emerged as one of the top recruitment agencies in Toronto. Brunel is the trusted partner of top clients in the oil and gas, mining, life sciences, and renewable energy sectors.

 

We have quickly become woven into the fabric of Alberta's community. As champions of Calgary's diverse talent pool, and with consideration of its valuable natural resources, we take pride in our role as recruitment leaders. We excel in Canadian executive search. Our dedicated teams of headhunters and large talent networks across the country equip your organization with top tailored recruitment.

 

Whether you're seeking top-tier talent for a local venture or embarking on an international endeavor, let us be your partner in success. Reach out to us today and discover how we can help you exceed your goals in the heart of Alberta and beyond.

Explore our vacancies

Pharmacovigilance Associate

Location: Ontario or Quebec

Branche: Pharmaceuticals

Expertise: Production & Manufacturing

Experience: 2 years

Responsibilities Data Entry of Individual Case Safety Reports (ICSRs) to the pharmacovigilance (PV) safety databases as per corporate and local requirements and timelines. Ensure that ICSRs for marketed products and medical devices subject to expedited reporting according to Canadian regulations are submitted to Health Canada within prescribed timelines. Monitor and support the preparation of written follow up requests to ensure timelines prescribed by local/global and corporate requirements are met. Perform reconciliations of the company's third party vendors programs, licensed partners as well as inter-departmental teams, as per corporate requirements and monitor key performance indicators. Provide support for the compliance monitoring of Individual Case Safety Reports (ICSRs) and generating metrics on case handling. Manage the external vendor training records including the launching of annual refresher training. Process Canada Vigilance queries and Access to Information requests/results. Support the analysis of reports in PV databases. Respond to queries and requests from internal and external stakeholders. Support the company's Project Leaders in compiling information for the LPSMF on a regular basis. Collaborate in developing and maintaining the local Pharmacovigilance standard operating procedures (SOPs), working instructions and job aids. Participate in the maintenance of the PV paper and electronic filing and archiving system according to corporate and Canadian requirements. Participate in the ongoing optimization of PV procedures as well as inter-departmental procedures affecting PV. Provide overall support to PV team activities.

Mechanical Equipment Installer

Location: Montréal

Branche: Life Sciences

Expertise: Production & Manufacturing

Experience: 2 years

Responsibilities Install large medical equipment while collaborating with Installation Project Manager to schedule product installation in coordination with equipment delivery, Customer availability, and construction schedules. Prior to installation, verify rough-in dimensions and utilities are adequate to meet equipment specifications. Ensure doorways, elevators, and hallways are sufficient to allow equipment transport to installation site. Install large medical equipment, including, but not limited to uncrating, assembling, setting, or lifting product into place, and leveling. Must be capable of independent work. Complete service documentation electronically. Provide daily email updates to keep all parties informed and ensure timely service, hand off to local technicians and Customer satisfaction. Ensure Customer satisfaction through post-installation activities to include disposal of all associated packing and shipping crate material, ensuring equipment is wiped down and fingerprints are removed, and addressing any questions/issues before leaving the site. Utilize Customer protocols when entering and exiting facilities and abide by all of the company's and Customer Health & Safety protocols and procedures.

Surgical Sales Representative

Location: Ottawa

Branche: Medical devices

Expertise: Marketing & Sales

Experience: 2 years

Strategically manage a large territory, which will require regular travel, including 2-3 days in a hotel each month. Set territory goals and develop action plans to achieve growth objectives. Protect existing business and seek opportunities to expand the territory using innovative sales and marketing techniques. Negotiate pricing effectively while balancing a variety of conflicting interests. Confidently introduce new products and provide detailed information about existing products. Develop and maintain strong professional relationships with customers. Respond promptly and satisfactorily to customer inquiries. Contribute positively to the sales team through conference calls and regular communication. Complete sales reports in a timely manner and respond quickly to requests from head office. Maintain sample inventory in good condition and track its movement accurately. Educate oneself on materials related to the position, products, and industry. Manage expenses appropriately while striving to minimize extraneous costs. Represent ethically and professionally at all times.

Senior Scientist

Location: Richmond Hill

Branche: Medical devices

Expertise: Research & Development

Experience: 5 years

Drives the execution of technical development plans spanning preclinical animal studies through process validation to support IDE and PMA submission by leveraging expertise of Prollenium's Technical Subject Matter Experts (SME) and external Contract Manufacturing Organization (CMOs) Initiator of new projects for the R&D team for the purposes of commercialization to consistently sustain Prollenium's product pipeline Supervise project related scientific/technical activities and contribute to strategic decision by reviewing and evaluating data, interpreting results and drawing relevant conclusions Ensures technical readiness by designing, reviewing, and approving the animal study protocols for commencing preclinical studies in support of IDE submission Providing technical expertise by authoring drug and medical device IDE and PMA modular components covering product background, device description, preclinical testing, product biocompatibility, manufacturing process and product testing and characterization Partnering with Quality/Regulatory and Analytical Technical experts to prepare Technical Files and Design Dossiers in line with the different market requirements (Canada, US, Europe, Rest of the World) Assisting the Global Chief Scientific Officer in the evaluation key technologies of biotech companies and analyzing their technological capabilities for the purposes of Merger & Acquisition (M&A) activities Assisting the Global Chief Scientific Officer in evaluating budgetary proposals from Contract Manufacturing Organizations (CMOs) to determine the optimum budget for product characterization and biocompatibility studies Being a key member of the R&D, Regulatory and Clinical bi-weekly team meeting in the preparation of IDE and PMA submissions Communicating current scientific findings to the Global Chief Scientific Officer through peer-review journals, ISO standards and clinical trials in order to assist in Prollenium's product development pipeline Other duties as assigned

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