Recruitment Agency in Calgary
Suite 1810, Bow Valley Square 2 205 - 5th Avenue SW
T2P 2V7
Calgary
Serving Calgary's vibrant landscape since 1998. Of the recruiting agencies in Calgary, 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.
Location: Mississauga
Branche: Life Sciences
Expertise: HR & Recruiting
Experience: 2 years
Adapt technical user manuals into written procedure for use within laboratory using defined templates. Modernize existing procedures into required templates. Manage the writing and completion of documents and other assigned tasks within established timeline. Manage document review, comment resolution and approval. Provide technical support and troubleshooting for document management and document revision. Perform all job functions in compliance with internal standards. Coordinate with training and laboratory staff to assign training content. Performs work under minimal supervision.
Location: Guelph
Branche: Food Production
Expertise: Production & Manufacturing
Experience: 1 years
We have a current opportunity for a Mechanical and Electrical Assemblers on a contract basis. The position will be based in Oakville. For further information about this position please apply.
Location: Ancaster
Branche: Food Production
Expertise: Production & Manufacturing
Experience: 1 years
We have a current opportunity for a Mechanical and Electrical Assemblers on a contract basis. The position will be based in Oakville. For further information about this position please apply.
Location: Toronto
Branche: Pharmaceuticals
Expertise: Marketing & Sales
Experience: 2 years
Responsibilities Analyze sales, market, and performance data to identify trends and actionable insights. Create clear and impactful data visualizations and reports to support strategic decision-making. Collaborate with cross-functional teams, including sales, marketing, and leadership, to inform business strategies. Contribute to sales and marketing analytics projects, gaining exposure to senior leadership and business-critical initiatives.
Location: Greater Toronto Area
Branche: Pharmaceuticals
Expertise: Production & Manufacturing
Experience: 2 years
Develop and manage project schedules, budgets, resource plans, KPIs, and progress reporting. Support governance meetings by preparing materials, capturing action items, and ensuring follow-through Drive alignment across program teams and ensure adherence to the Manufacturing 4.0 roadmap Act as a liaison between cross-functional teams, including manufacturing, IT, and business process owners. Foster collaboration across various communities of practice, such as MES, Kinaxis, and M&S Plan-to-Manufacture teams. Facilitate stakeholder engagement through effective communication strategies and updates Oversee the deployment of digital tools, such as MES systems, Kinaxis, and iShift. Identify areas for continuous improvement and align solutions with operational excellence goals. Implement change management strategies for smooth adoption of new processes Lead training, workshops, and knowledge-sharing sessions to support cultural and operational shifts Ensure all project activities comply with regulatory requirements and company standards. Maintain documentation to support audits and inspections.
Location: Greater Toronto Area
Branche: Pharmaceuticals
Expertise: Production & Manufacturing
Experience: 2 years
Maintain, troubleshoot, and repair automated systems, including PLCs, HMIs, SCADA, robotics, and other control systems. Diagnose and resolve electrical, mechanical, and software-related issues to minimize downtime and maintain production efficiency. Perform regular calibration of sensors, instruments, and automated equipment to ensure accuracy and compliance with industry standards. Modify/optimize control programs to enhance process performance and production quality. Maintain accurate records of all maintenance activities, calibrations, and software changes. Ensure compliance with Good Manufacturing Practices (GMP), FDA, and other regulatory requirements by adhering to established protocols and guidelines for pharmaceutical industry standards. Identify opportunities to improve automation processes, enhance system reliability, and reduce operational costs. Collaborate with engineering teams to implement upgrades and modifications to systems. Work closely with production, quality assurance, and engineering teams to support manufacturing objectives. Provide training and guidance to operators and junior technicians on the proper use of automated systems. Strong knowledge of PLC programming and industrial automation systems. Experience with control system architecture, including SCADA, HMI interfaces, and networks Proficient in troubleshooting and repairing mechanical, electrical, and software components Familiarity with sensors, actuators, motors, VFDs, and servo systems. Ability to interpret technical drawings, P&IDs, and electrical schematics. Strong analytical and diagnostic skills to identify and resolve system inefficiencies. Proactive mindset with the ability to prioritize and manage tasks in a high-pressure situations
Location: Greater Toronto Area
Branche: Pharmaceuticals
Expertise: Production & Manufacturing
Experience: 2 years
Provide quality oversight for manufacturing process equipment, CIP, SIP, Thermal, Utilities, HVAC qualification and computerized system validation activities pertaining to B100 licensure, start-up and lifecycle management. Review/approve validation deliverables (i.e. URS, specification documents, risk assessment, test strategies, protocols, executed raw data packages, reports, validation plans, SOPs, Equipment registration in SAP) in accordance with internal and regulatory policies. Review, assess and approve change controls, deviations and corrective plans, resulting from validation/qualification studies. As required, represent Quality Operations on project team and/or sub-teams and/or project working groups to provide direction on validation issues with respect to compliance. Responsible for maintaining validation awareness by screening and reporting on significant validation trends and changes through literature reviews, meetings, and peer discussions within the industry.
Location: Quebec City
Branche: Life Sciences
Expertise: Marketing & Sales
Experience: 3 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.
Location: Greater Toronto Area
Branche: Pharmaceuticals
Expertise: Communications & Distribution
Experience: 2 years
Support MICC within assigned therapeutic Ensure quality of the information provided to our customers by supporting and monitoring MICC external supplier who is providing just in time evidence- based information and scientific expertise on the company's products. Provide guidance to MICC external supplier in a timely fashion on day-to-day requests within assigned therapeutic areas. This includes scientific response documents for verbal and written frequently asked questions, as well as response to ad hoc enquiries. Handle escalated Provide support to MICC external supplier for primary intake of adverse events and product complaints, in collaboration with Pharmacovigilance and Quality Assurance teams. Perform quality control of MICC external Provide regular feedback/training to MICC external supplier to optimize Medical Information services. Develop and maintain Canadian product scientific response documents: Contribute to the development, review and update of scientific response documents such as FAQs/Q&As, letters and technical sheets for use in verbal and written responses. Contribute to literature Maintain strong relations with Canadian and Global Medical Information teams to optimize sharing of product information. Ensure Medical Information materials are compliant with Canadian and Global Medical Information good scientific practices. Contribute to product launch readiness within the assigned therapeutic Contribute to optimization of Global Medical Information Assess value of scientific response documents for access through Medical Information self-serve web portal. Collaborate with internal Participate in the development of specific technical/medical responses or analysis to specific situations such as product discontinuation, media attention, crisis situations and responses to Health Canada or other organizations within the assigned therapeutic areas. Analyze and share customer insights with commercial and field teams to meet customer needs. Deliver training on Medical Information services and processes for commercial, field teams and patient support program suppliers.
Location: Montréal
Branche: Life Sciences
Expertise: Marketing & Sales
Experience: 3 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.
Location: Montreal
Branche: Food Production
Expertise: Production & Manufacturing
Experience: 2 years
Monitor and provide guidance to electricians when needed - including contractors. Monitors the respect by contractors of the scope and quality criteria defined in the contract, creates non-conformities when applicable and ensures the application of agreed action plans Create schedules, delegate work and train new employees. Design, implement, maintain, or improve electrical instruments, equipment, facilities, components, products, or systems for commercial, or industrial purposes. Direct or coordinate manufacturing, construction, installation, maintenance, support, documentation, or testing activities to ensure compliance with specifications, codes, or customer requirements Perform detailed calculations to compute and establish manufacturing, construction, or installation standards or specifications Inspect completed installations and observe operations to ensure conformance to design and equipment specifications and compliance with operational, safety, or environmental standards Prepare technical drawings, specifications of electrical systems, or topographical maps to ensure that installation and operations conform to BMS standards and customer requirements Plan layout of electric power generating plants or distribution lines or stations Conduct field surveys or study maps, graphs, diagrams, or other data to identify and correct power system problems Design electrical systems or components that minimize electric energy requirements Ensure the proper maintenance of equipment, compliance with electrical codes and adherence to safety regulations, NEC and NFPA Standards Contribute to improving designs, electrical estimations and manufacturing processes Keep records of electrical operations and timesheets Ensure adequate inventory, plan budgets, prioritize purchases, prepare cost estimates and document their purchases Assist and ensure the correct connections in control panels, I/O check and power supply Studies the technical documentation put together by the Project Team (i.e., Equipment Lists, Electrical Drawings, Electrical Specifications, etc.) and develops commissioning protocols and forms for the Start Up, IQ and OQ of process equipment and installations Perform commissioning on site, instrument installation, electrical installation and maintenance in compliance with electrical standard
Location: Mississauga
Branche: Pharmaceuticals
Expertise: Quality Management
Experience: 2 years
Collaborate with internal teams in locating documentation and reviewing consent related to HBS. Assist the Biobank lead and team in linking samples to consent forms. Duties may include handling of HBS during the reconciliation and curation process. Work with Biobank leads to ensure that learning from HBS related issues are identified and analysed to enable continuous process improvement. Review consent forms for use restriction & storage information. Electronically manage HBS retrievals, including receipt, tracking, review and approval of requests from internal requestors. Confirm requests against the informed consent, raise requests as the need arises. Ensure sample manifests are completed to document the HBS transport or receipt. Assist the Biobank lead in identifying & managing sample sharing between teams. Work with the Biobanks to optimise processes around Biobank requirements for compliance. Work with various Biobanks to ensure sample compliance. Participate & contribute to team meeting & discussions. Support team members in delivering the Departmental goals. Assist in knowledge curation to allow decision making on inventory which maybe in-house, or third parties. Assist with the resolution of issue and queries relating to HBS within the inventory. Maintain records for HBS stored until it meets final disposal and follow destruction process when initiated.