What is the role of an R&D scientist?
Research and development (R&D) scientists play a central role in driving innovation and advancing scientific knowledge within their respective fields, including in (bio-)technology, pharmaceuticals, medicine, materials science and more.
They are responsible for spearheading research initiatives, conducting experiments, and analyzing data to push the boundaries of scientific understanding. Their work is instrumental in developing new technologies, products, and solutions while upholding rigorous scientific standards and ethical principles.
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Sales Operations Coordinator
Location: Toronto
Branche: Pharmaceuticals
Expertise: Marketing & Sales
Experience: 2 years
Responsibilities Collaborate with the sales, marketing and forecasting teams to manage the operations related to the sales incentive programs (calculation, analysis, adjustments, reports, payouts) Collaborate with the sales leads to keep the Sales Reps Performance Ranking up to date Validate reports like Sales Validation Report, Eligibility Validation Report which enhances the robustness and accuracy of the process Extract and validate the reps lists for the processing of the incentive payouts based on their performance Collaborate with The Sales Insight Manager, Data Scientist, Sales and Marketing leads to determine how to best optimize the HCPs target lists Coordinate the end-to-end process and all efforts related to the updating of customer targeting lists (list extract, refresh, validation, upload) across all BUs each semester Identify areas of improvement in the processes, individual performance, and team dynamics through process analysis. Support the logistics related to Sales Force redesign and optimization (alignment of reps to district
Materials Engineering Specialist
Location: Fort McMurray
Branche: Conventional Energy
Expertise: Production & Manufacturing
Experience: 5 years
Support Production Units in managing threats by endorsing Materials Engineer assessment on applicable damage mechanisms, likelihood of failure, metallurgical controls needed for successful repairs, repair/replacement decisions, risk mitigation support through advanced analysis and knowledge/experience sharing as required Provide Metallurgical expertise for critical repairs (for Reactors, HP-High Pressure Separators, SMRs-Steam Methane Reformers, PSA-Pressure Swing Adsorbers), Hot tap welding on live piping and equipment etc. Support Management of Equipment Strategies/RBI by acting as a Cold Eye reviewer for Equipment Strategies with highlighted risks / Risk Rank I & II. Provide metallurgical expertise to Equipment Strategy/RBI team for high-risk items Support the PU through review of identified risk and mitigation measures Act as an expert for metallurgical aspects of failures, investigations, material selection and welding Provide oversight for the work outsourced to 3rd party contractors and ensure technical deliverables meet company requirements Involvement in identified risk scenarios to drive technical decisions related to Materials Engineering Oversee assessment of Materials Engineering / corrosion related IOWs - selection, exceedance, and mitigation Provide specialized Materials engineering support to TA organization and outages Participate in Joint Industry Project (JIP), external technical committees and conferences as needed Mentor Materials Engineers on the team on material selection, welding, repair methodology, failure analysis and metallurgical assessment Develop and deliver technical mentoring sessions and knowledge sharing Lead Targeted Knowledge Transfer (TKT) sessions as required to develop advanced engineering analysis skills Act as the Technical Authority for Metallurgical Engineering aspects and authorize TDNs (as per OEMS - Technical Authority) Custodian of special metallurgical procedures followed at the site (for e.g. Weldability Procedure, Solution Annealing Procedure) Provide Metallurgical Engineering support for Project Initiatives #BRUCAD
Bilingual Medical Information Specialist
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.
Cost Control Manager
Location: Vancouver or Calgary
Branche: Mining
Expertise: Controlling
Experience: 5 years
A courageous safety leader who adheres to and sponsors safety and environmental rules and procedures. Maintains and demonstrate commitment to safety and environmental protection as a core value. An effective problem solver with a results-oriented approach and ability. Responsible for mentoring, coaching, evaluating and providing feedback to a team of project accountants, project cost controllers. Responsible for conducting formal performance reviews and career advancement discussions, either as a direct line supervisor or matrix supervisor. Responsible for regular planning of the resource requirements across a range of project stages and execution models. Responsible to support, as required, any ad-hoc Project Controls, Projects or related initiatives. Responsible to review and approve internal Project Controls Management Plans and internal project setups in the various cost systems. Responsible for periodic review and modifications to the appropriate Overviews/Standards/ Templates of the Projects, Project Procedures Manual. Responsible for performing audits of projects and/or service providers for conformance to Projects Overviews and Standards. Responsible to support the independent review of a project at various points in its lifecycle via Setup Reviews, Health Checks, Stage Gates, or ad-hoc audits. Responsible to participate in Independent Peer Reviews of Projects led projects, other non-Projects led projects, or joint venture partnership projects, as required. Responsible to provide input to strategic direction of project controls department. Project Accounting specific: Responsible to develop project focused accounting policies, procedures and templates for best practices related to accounting in a project setting. Responsible to define roles and responsibilities of the Project Accounting function vs other accounting functions within the Organization. Responsible to interface with other Business Units on relevant matters to ensure alignment of expectations and requirements. Responsible to analyze Projects needs as they related to Project Accounting and ensure they are incorporated into overall strategic plans. Responsible to plan, organize, direct, control and evaluate Project Accounting operations, audits of project contracts and other financial services as required. Responsible to alert and report to senior management all critical trends with respect to the financial performance of various projects in the Projects portfolio.
Engineering Manager II
Location: Calgary
Branche: Shipbuilding
Expertise: Production & Manufacturing
Experience: 4 years
Ensure scope definition for the appropriate Stage Gate meets company requirements before commencing work. Approve Engineering Execution Plans (EEP) and contribute to Project Execution Plans (PEP), ensuring effective scope development and change management. Review and manage engineering budgets to align with project scope and execution plans. Oversee the development of Engineering Work Packages (EWPs) for all deliverables and time-based functions. Review and align engineering schedules with overall project timelines. Coordinate with Procurement, Construction, Commissioning, Operations, and other corporate functional groups to integrate input and conduct necessary reviews. Manage and appraise the structure of the engineering project team, ensuring it meets both short and long-term objectives. Ensure Engineering Systems and 3D intelligent design environments are properly set up and utilized effectively. Direct and review engineering activities to ensure work quality aligns with company objectives. Promote safety awareness and apply corporate design for safety principles. Conduct engineering risk assessments and HAZOPs, ensuring all identified issues are addressed. Arrange and facilitate design reviews and key engineering review milestones. Coordinate quality audit verifications to ensure compliance with engineering standards and internal procedures. Identify and implement value optimization opportunities across all project disciplines. Provide technical guidance to discipline engineers and project engineers regarding scope, design criteria, and safety considerations. Ensure compliance with company technical standards throughout project development and execution phases. Contribute to the development of an integrated engineering management methodology across studies and execution projects. Maintain the flow of analyzed information and reporting to the Corporate Management Team related to Contracts Management plans and project status. Develop and maintain a Project Engineering Management framework for world-class delivery of capital projects.
Documentation Specialist
Branche: Life Sciences
Expertise: Controlling
Experience: 1 years
Responsibilities Organize, maintain, and manage electronic regulatory documents including applications, submissions, dossiers, and correspondence, on shared directories and other electronic platform, Support regulatory project leaders to prepare administrative M1 documents for various typeds of Health Canada regulatory submissions (NDS, SNDS, Response to Clarifaxes etc.) efficiently and accurately in accordance with current Health Canada Guidelines and Corporate Guidance. Overview and maintain regulatory shared mailbox by facilitating effective communication and coordinating correspondence to internal stakeholders. Maintain accurate records of regulatory documents and submissions by upload regulatory dossiers and supportive information into corporate internal database and platform. Act as a backup to the regulatory Regulatory Coordinator to provide operational support as needed. Collaborate with regulatory affairs professionals, subject matter experts, and cross-functional local and global teams to gather necessary documentation and information for regulatory submissions and pharmacovigilance related safety reports. Participate in any ad-hoc or special regulatory projects as needed.
Pharmacovigilance Specialist
Location: Quebec or Ontario
Branche: Pharmaceuticals
Expertise: Planning & Testing
Experience: 3 years
Responsibilities Analyze and process adverse events and safety reports with utmost quality and timeliness in accordance with Global and Local Pharmacovigilance procedures. Collect, pursue follow-up information to complete quality adverse event reports and transmit all local adverse events to Global Pharmacovigilance. Evaluate domestic and foreign ICSRs (marketed and non-marketed drugs) for submission to Health Canada according to Canadian regulations and within prescribed timelines. Submit the Canadian reportable adverse reactions to Health Canada according to their regulations and guidance's. Respond to queries and requests from Global Pharmacovigilance. Run monthly submissions compliance report and communicate with team members. Organize and ensure maintenance of the electronic filing and archiving system according to corporate and Canadian requirements. Document and update case information into the global safety database. Interact with other functional areas/departments to process adverse events efficiently & reliably. Collaborate in developing and maintaining the local Pharmacovigilance SOPs and procedures. Update the list of all Canadian drug licensing status and renewals, in conjunction with Regulatory Affairs. Participate in training of PV Associate on their assigned activities. Support associate with inbound and outbound case management activities as needed and as per corporate and local requirements and timelines. Provide overall support to the PV on all team activities. Maintain current knowledge of all relevant local Pharmacovigilance regulations in regard to drug, natural health and cosmetics products. Coordinate responses to questions and requests from Regulatory Authorities.
Automation Engineer
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
What are the required skills for an R&D scientist?
To excel as an R&D scientist, individuals must possess exceptional analytical and critical thinking skills, which are indispensable for experimental design, data interpretation, and drawing insightful conclusions. Effective communication skills are essential for collaborating with cross-functional teams and disseminating research findings to peers and the wider audience.
Additionally, R&D scientists should demonstrate proficiency in laboratory techniques pertinent to their specific domain, such as molecular biology, chemistry, or engineering. Staying current with advancements in their field and upholding the highest ethical standards in research and experimentation are also imperative.
Where do R&D scientists work?
R&D scientists find rewarding career opportunities in diverse settings, including research institutions, industrial companies, pharmaceutical firms, and government research agencies. They frequently collaborate with experts from various disciplines, bridging the gap between scientific research and practical applications.
Common R&D scientist responsibilities
- Maintain and operate laboratory equipment, ensuring optimal functionality, and manage lab material inventories;
- Plan and execute laboratory experiments and research projects to explore scientific phenomena and potential innovations;
- Conceptualize and validate experimental protocols, including the development of novel methodologies;
- Collaborate with multidisciplinary teams to integrate research findings into practical applications and solutions;
- Analyze complex data sets, extract meaningful insights, and provide recommendations based on research outcomes;
- Author research papers, technical reports, and scholarly articles for dissemination in scientific journals;
- Stay abreast of cutting-edge developments in their field and incorporate emerging technologies into research endeavors;
- Maintain meticulous records of experiments, protocols, and findings, adhering to industry-standard practices;
- Adhere to the highest ethical standards in research, ensuring the responsible conduct of experiments;
- Present research findings at conferences and contribute to knowledge exchange within the scientific community;
- Drive the development of innovative technologies and products that advance scientific understanding and benefit society.
Qualifications for R&D scientists
To pursue a career as an R&D scientist, candidates typically hold a Bachelor's degree in a relevant field, such as physics, chemistry, biology, engineering, or a related discipline. Many R&D scientists also pursue advanced degrees such as Master's or Ph.D. for research-intensive roles.
Other important qualifications include:
- Expertise in laboratory techniques and research methodologies;
- Exceptional analytical and critical thinking abilities;
- Effective written and verbal communication skills;
- A strong foundation in ethical principles governing research and experimentation;
- A willingness to adapt and embrace new tech and methodologies;
- Collaborative aptitude, enabling effective teamwork in interdisciplinary research environments;
- A steadfast commitment to advancing scientific knowledge and driving innovation for the betterment of society.
