Introduction: We are seeking a detail-oriented and proactive Commercial Quality Specialist to join our client’s team, a global leader in the pharmaceutical industry committed to upholding the highest standards of product quality and regulatory compliance. Based out of the Saint-Laurent, Montreal Head Office , this position offers a hybrid work model (three days in-office, with Tuesday and Wednesday mandatory ) and is a contract opportunity through April 30, 2026 . Working four days per week (29 hours weekly) , this role is ideal for a professional with a strong understanding of Good Manufacturing Practices (GMP) who thrives in both independent and collaborative environments. As the Commercial Quality Specialist, you will independently support Commercial Quality operations across the affiliate, ensuring compliance with quality system requirements related to pharmaceutical products, biologics, medical devices, combination products, and cosmetics. You will play a key role in maintaining and enhancing quality systems, supporting audits and inspections, managing quality events, and ensuring adherence to corporate and regulatory standards. Responsibilities: Integrate and apply local quality regulations for drugs, biologics, devices, combination products, and cosmetics. Design and implement effective quality systems, procedures, and processes within cross-functional teams to ensure compliance and operational efficiency. Perform assessments to determine compliance with procedures and regulations; identify potential gaps and support the development and execution of improvement plans. Plan, prepare, review, and approve quality documentation such as change controls, product quality reviews, and other local requirements. Support self-inspections, internal audits, external audits, and Ministry of Health inspections as directed by management. Coordinate and investigate quality events such as deviations and non-conformances, and manage corresponding action plans and decisions. Execute supplier qualification programs and monitor performance for key suppliers. Monitor key quality metrics and KPIs to ensure ongoing compliance and effectiveness. Support activities governed by Good Storage and Distribution Practices, including controlled temperature and cold chain monitoring. Support the Management Review process at the affiliate level. Represent Commercial Quality in cross-functional projects and initiatives as assigned by management. Requirements: Bachelor’s Degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering, or other relevant scientific or technical field (required). 2+ years of experience in Quality Assurance within a GMP or GDP environment (preferred). Comprehensive understanding of local GxP requirements, including applicable regulations and standards for pharmaceuticals, biologics, devices, and cosmetics. Strong computer skills, with proficiency in SAP, TrackWise, ComplianceWire, and OneVault. Ability to work effectively both independently and collaboratively within cross-functional teams. Demonstrated ability to learn quickly, manage multiple priorities, and make sound decisions in partnership with management. Excellent organizational, analytical, and communication skills with high attention to detail. Experience supporting or participating in audits, inspections, or other quality compliance activities is an asset. What We Offer Why apply through Brunel? Finding the next step in your career can be a full-time job. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with onboarding. We’ll get you going while you get on with the job. About Us Brunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Over 45 years, we’ve created a global network of interesting clients and talented individuals working together through a vast array of services.
Production Supervisor Montreal, QC Introduction Brunel is partnering with one of our leading radiopharmaceutical clients to support the hire of a Production Supervisor. This is an exciting opportunity to join a growing organization dedicated to improving patient lives through the production of high-quality radiopharmaceutical products. As the Production Supervisor, you will oversee daily manufacturing operations, ensuring production runs safely, efficiently, and in compliance with Good Manufacturing Practices (GMP). You will play a key role in maintaining quality standards, supporting your team’s development, and fostering a culture of excellence across operations. Responsibilities Team Leadership Supervise and motivate production employees to meet departmental goals. Maintain strong communication with Quality, Engineering, and Technical Services teams. Lead ongoing cGMP training and employee development. Manage scheduling, absenteeism, and overtime while maintaining engagement on the production floor. Production Oversight Coordinate and execute radiopharmaceutical production batches per customer orders. Monitor and report on production performance metrics. Manage inventory of raw materials and oversee HVAC monitoring. Review and maintain SOPs, production documentation, validation reports, and change controls. Conduct investigations and implement corrective actions with proper documentation. Support process improvements, equipment maintenance, and SAP-related production activities. Quality, Health & Safety Promote and sustain a strong culture of quality throughout production. Ensure strict adherence to health, safety, and radiation protection procedures. Requirements B.Sc. or M.Sc. in Science or Chemical Engineering. 4+ years of pharmaceutical manufacturing experience, with at least 2 years in a supervisory role (unionized environment preferred). Strong understanding of GMP and production operations. Proficiency in Microsoft Word and Excel. Bilingual – French and English. Must be comfortable working 6:00 AM to 2:00 PM shifts. What We Offer Why apply through Brunel? Finding the next step in your career can be a fulltime job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with on-boarding. We’ll get you going while you get on with the job. About Us Brunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Over 45 years, we’ve created a global network of interesting clients and talented individuals working together through a vast array of services.
Introduction We are seeking a strategic and analytically minded Business Analyst to join our client’s team. Our client is dedicated to improving lives through the discovery of life-changing medicines, advancing disease management, and supporting patients, families, and caregivers. Their work—spanning research programs to volunteer initiatives—reflects a deep commitment to uniting caring with discovery to make life better for people around the world. This is a 6-month contract opportunity offered on a hybrid work schedule located in downtown Toronto, ON . As the Business Analyst, you will play a critical role in leading and supporting the development of analytics capabilities across the organization. You will enable business teams to leverage data effectively by identifying analytics needs, enhancing data literacy, and driving adoption of tools, platforms, and methodologies that support advanced analytics and strategic decision-making. This role offers an exciting opportunity to combine technical understanding, business acumen, and leadership to influence analytics strategy and organizational performance. Responsibilities Partner with business units to assess current analytics maturity and identify capability gaps. Define and prioritize analytics use cases aligned with strategic business goals. Support the development and rollout of analytics frameworks, governance models, and best practices. Collaborate with stakeholders to gather and document business requirements for analytics solutions, dashboards, and data products. Translate business needs into functional specifications for data integrators, engineers, developers, and BI teams. Facilitate workshops to align on KPI definitions, metrics, and reporting standards. Drive adoption of analytics and visualization platforms (e.g., Power BI, Tableau) across business units. Provide training, onboarding, and support to users to improve data literacy and self-service capabilities. Evaluate and recommend new tools and technologies to enhance analytics and reporting performance. Work with data governance teams to ensure consistent definitions, data lineage, and metadata management. Monitor and resolve data quality issues in coordination with technical teams. Promote responsible data usage and ensure compliance with applicable privacy and data protection regulations. Define success metrics for analytics initiatives and track performance against business objectives. Conduct post-implementation reviews to evaluate outcomes and identify improvement opportunities. Stay current with industry trends, emerging technologies, and best practices in analytics, data governance, and business intelligence. Requirements Bachelor’s or Master’s degree in Business, Information Systems, Data Analytics, or a related field. 3–6 years of experience in business analysis, analytics strategy, or data product management. Experience working with datasets from Healthcare, Pharmaceutical, or Health Insurance industries. Strong understanding of key performance indicators (KPIs) and metrics relevant to the pharma and biotech sectors. Proficiency in analytics platforms and data visualization tools (e.g., Power BI, Tableau). Familiarity with data architecture concepts and cross-functional collaboration with data engineers, BI developers, and business teams. Experience with Canadian datasets (e.g., IQVIA, EMRs, Claims). Excellent communication, facilitation, and stakeholder management skills. Proficiency in SQL and familiarity with data modeling and reporting concepts. Strong organizational, analytical, and problem-solving abilities with attention to detail. Ability to manage multiple priorities in a dynamic environment and drive alignment across teams. Commitment to continuous learning, innovation, and professional growth. What We Offer Why apply through Brunel? Finding the next step in your career can be a full-time job. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with onboarding. We’ll get you going while you get on with the job. About Us Brunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Over 45 years, we’ve created a global network of interesting clients and talented individuals working together through a vast array of services.
Position: Project Manager Location: Saskatoon, Saskatchewan Industry: Mining - Potash Introduction Our client, a leading global mining organization, is seeking an experienced Project Manager – Technology to join their team in Saskatchewan. This role will be part of a large-scale greenfield mining and infrastructure development and is responsible for managing the planning, coordination, and execution of key technology and infrastructure work packages. The Project Manager will ensure delivery within established scope, budget, schedule, and safety parameters, while driving digital integration and continuous improvement across disciplines. Responsibilities Manage full lifecycle delivery of assigned technology and infrastructure scopes, including planning, engineering, procurement, fabrication, and construction coordination. Lead project execution activities, ensuring alignment with schedule, budget, and quality objectives. Develop and maintain detailed project plans, risk registers, and cost forecasts in accordance with project governance. Coordinate with multi-disciplinary teams, including engineering, construction, commissioning, and operations, to ensure seamless integration. Manage vendor performance, contract deliverables, and interface points across multiple contractors and internal stakeholders. Implement digital delivery and modular fabrication strategies using BIM and data-centric project controls. Identify and mitigate schedule or cost risks, and develop corrective actions to maintain project performance. Ensure all activities adhere to safety, environmental, and regulatory standards. Prepare regular progress reports, dashboards, and presentations for leadership review. Foster collaboration, communication, and alignment across internal and external project partners. Requirements Bachelor’s degree in Engineering (Mechanical, Civil, Electrical, Mining, or related discipline). 8+ years of project management experience in large-scale mining, industrial, or infrastructure projects. Proven experience managing technology, automation, or modular infrastructure scopes. Strong knowledge of project management principles, methodologies, and contract management. PMP certification Experience with scheduling tools (e.g., Primavera P6), cost control systems, and project reporting. Demonstrated ability to manage complex stakeholder interfaces and multiple work fronts simultaneously. Strong leadership and coordination abilities with a proactive, results-driven approach. Excellent communication, negotiation, and interpersonal skills. Sound understanding of digital project delivery (BIM, model coordination, data integration). High attention to detail and commitment to safety, quality, and environmental standards. Adaptable and resilient in dynamic project environments. Team-oriented and able to build trust across diverse stakeholders. What We Offer Why work with Brunel? We are proud to offer exciting career opportunities from over 100 offices globally in 42 countries. Advancing your career takes time and effort – let us match you to your ideal position. About Us Brunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Brunel provides the global recruitment and workforce services you need to lead your industry. With 50 years of market experience in Renewable Energy, Automotive, Oil & Gas, Life Sciences, Mining, and Infrastructure, we help you finish major projects safely, compliantly, on-time, within budget and at the highest quality, so you can keep growing – anywhere in the world.
Introduction Our client is a leading Canadian public research organization that develops innovative biologics and vaccines to improve the health of people in Canada and around the world, offering a highly collaborative, mission-driven environment with excellent stability and benefits. As a Downstream Processing (DSP) Technician, you will support the manufacture of clinical biologics in a cGMP environment. You’ll be involved in downstream pre-viral steps (elution, clarification, nanofiltration) and post-viral steps (concentration and bulk filling) for clinical-scale batches, ensuring products are manufactured, handled, and documented according to regulatory and internal quality standards. Responsibilities Execute downstream manufacturing steps according to approved batch records and cGMP requirements. Prepare and review SOPs, working formulas, and related production documentation. Perform in-process assays using equipment such as filter integrity testers, pH meters, and analytical balances. Weigh, transfer, and mix chemicals and solutions as required for DSP activities. Perform product filtrations, nanofiltration steps, and bulk filling operations for clinical batches. Prepare glassware and single-use assemblies and install them on the appropriate purification equipment. Verify instrument calibration prior to production and document checks in accordance with procedures. Transfer filled bulk containers to designated cold storage (e.g., refrigerators) and complete associated records. Review and correct logbooks and other production records to ensure data integrity and completeness. Support cleaning activities in collaboration with production support team members. Develop autoclave loads with the department manager and ensure compliant sterilization cycles. Monitor stock levels of common laboratory and production supplies and flag replenishment needs. Respond appropriately to emergency notifications, following site procedures and training. Participate in quality system activities such as CAPAs, Change Controls, and Deviation Reports, as applicable. Perform other related duties as required to support production and continuous improvement. Requirements Diploma or Bachelor’s degree in Biotechnology, Biochemistry, Chemistry, Pharmaceutical Sciences, or related field. Experience in GMP biologics, pharmaceutical, or sterile manufacturing (downstream processing experience is a strong asset). Hands-on experience with filtration, clarification, and/or bulk filling operations, preferably in a clinical or commercial setting. Comfortable working with SOPs, batch records, and logbooks, with strong attention to detail and documentation accuracy. Familiarity with basic laboratory and production equipment (pH meters, balances, filtration systems, single-use assemblies, etc.). Ability to follow detailed procedures, work within a highly regulated environment, and meet production timelines. Strong teamwork, communication, and problem-solving skills. Willingness to work on-site in a cleanroom/GMP environment; flexibility for occasional off-hours or weekend work to support production is an asset. What We Offer Why apply through Brunel? Finding the next step in your career can be a full-time job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with onboarding. We’ll get you going while you get on with the job. About Us Brunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Over 45 years, we’ve created a global network of interesting clients and talented individuals working together through a vast array of services.
Introduction Our client is a leading national research and innovation organization advancing human health through cutting-edge biotherapeutics and vaccines, offering the stability of the public sector with the innovation of a high-tech biotech environment. As an Upstream Processing (USP) Technician , you will support the manufacture of clinical biologics under current Good Manufacturing Practices (cGMP). You’ll work hands-on with mammalian cell culture, bioreactors, and upstream operations to produce material for clinical studies in a highly regulated, team-oriented environment. Responsibilities Execute upstream manufacturing steps according to batch records and cGMP requirements Perform mammalian cell culture operations, including propagation, expansion, and clinical-scale production in bioreactors Carry out in-process testing using spectrophotometers, pH meters, metabolite analyzers, and related lab equipment Perform master cell bank manufacturing and filling under biosafety cabinet conditions Weigh, transfer, and mix chemicals and media components according to procedures Set up, install, and operate single-use assemblies and related upstream processing equipment Conduct product filtration, centrifugation, and related upstream clarification steps Prepare and organize glassware and disposable assemblies for production runs Verify instrument calibration status prior to each production batch and document results Complete and review logbooks and other GMP documentation, performing corrections as required Support cleaning and autoclave activities in collaboration with production support teams Monitor stocks of common lab supplies and notify management of inventory needs Respond to emergency notifications following established procedures Participate in CAPA, Change Control, and Deviation reporting activities as needed Requirements Diploma or degree in Biotechnology, Biology, Biochemistry, or related life science (or equivalent experience in GMP manufacturing) Experience with mammalian cell culture and aseptic techniques (academic, co-op, or industry) Familiarity with cGMP, batch records, and controlled documentation practices Comfort working with bioreactors, filtration systems, and common analytical instruments (e.g., pH meters, spectrophotometers) Strong attention to detail and commitment to data integrity and product quality Ability to follow SOPs precisely and maintain accurate documentation Team-oriented mindset with good communication skills and willingness to support cross-functional activities Flexibility to work in a regulated, production-driven environment (shift work or occasional off-hours may be required) What We Offer Why apply through Brunel? Finding the next step in your career can be a full-time job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with onboarding. We’ll get you going while you get on with the job. About Us Brunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Over 45 years, we’ve created a global network of interesting clients and talented individuals working together through a vast array of services.
Senior Director, Quality Assurance and Regulatory AffairsToronto, ON
IntroductionBrunel is partnering with a leading Canadian retail pharmacy network to support the search for a Senior Director, Quality Assurance. This role will provide leadership and oversight of Quality and Regulatory functions across multiple business units within a national healthcare organization. The successful candidate will be responsible for maintaining compliance with Health Canada regulations and ensuring effective implementation of Quality Management Systems across licensed facilities and distribution channels.
Reporting directly to the Vice President, Pharmaceutical Sourcing and Commercial Operations, the Senior Director, Quality Assurance will oversee the design, implementation, and continuous improvement of quality and regulatory programs. This position requires advanced leadership, sound regulatory knowledge, and the ability to drive compliance in a complex, multi-site environment.
ResponsibilitiesQuality Management SystemsEstablish, implement, and maintain Quality Management Systems (QMS) and Risk Management Programs in accordance with Health Canada regulations.Develop and update Standard Operating Procedures (SOPs).Oversee Health Canada inspections and manage all required regulatory licenses (e.g., DEL, MDEL, NBCP Wholesale License).Ensure compliance across all Health Product licensed facilities and the Import Drug Products QMS.Oversee the Computerized System Validation process and the QMS for the organization’s e-commerce platform.Regulatory OversightManage SAP Master Data for pharmacy schedules, drugs, medical devices, and natural health product attributes.Lead third-party audits and perform vendor qualification assessments, including Quality Agreements.Conduct internal GMP self-inspections and report on findings to ensure ongoing compliance.Oversee the Product Quality Complaint Program.Provide quality and regulatory oversight for multiple business units, including Shoppers Drug Mart, MediSystem Pharmacy, Central Pharmacy Services, Sanis Inc., and Specialty Health Network.Leadership and CollaborationLead, mentor, and develop quality teams across multiple locations.Collaborate cross-functionally with operations, supply chain, and senior leadership to support business objectives.Ensure alignment with corporate compliance and regulatory expectations.Occasional travel to national sites as required.
RequirementsBachelor of Science (B.Sc.) or equivalent in a related field (e.g., Chemistry, Biology, or Chemical Engineering).Minimum 15 years of experience in the GMP pharmaceutical industry with at least 5 years in senior Quality Assurance leadership.Experience working with Health Canada and regulatory inspections.Experience in Medical Devices; Supply Chain and Logistics background considered an asset.Strong knowledge of GMP, GDP, and quality system management.Advanced communication and interpersonal skills with the ability to influence across departments.Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).Key CompetenciesStrategic problem-solving and analytical decision-making.Strong organizational and prioritization skills.Ability to manage complexity and multiple stakeholders.Excellent written and verbal communication skills in English; French considered an asset.
What We OfferWhy apply through Brunel? Finding the next step in your career can be a fulltime job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with on-boarding. We’ll get you going while you get on with the job.
About UsBrunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Over 45 years, we’ve created a global network of interesting clients and talented individuals working together through a vast array of services.
Senior Director, Quality Assurance and Regulatory AffairsToronto, ON
IntroductionBrunel is partnering with a leading Canadian retail pharmacy network to support the search for a Senior Director, Quality Assurance. This role will provide leadership and oversight of Quality and Regulatory functions across multiple business units within a national healthcare organization. The successful candidate will be responsible for maintaining compliance with Health Canada regulations and ensuring effective implementation of Quality Management Systems across licensed facilities and distribution channels.
Reporting directly to the Vice President, Pharmaceutical Sourcing and Commercial Operations, the Senior Director, Quality Assurance will oversee the design, implementation, and continuous improvement of quality and regulatory programs. This position requires advanced leadership, sound regulatory knowledge, and the ability to drive compliance in a complex, multi-site environment.
ResponsibilitiesQuality Management SystemsEstablish, implement, and maintain Quality Management Systems (QMS) and Risk Management Programs in accordance with Health Canada regulations.Develop and update Standard Operating Procedures (SOPs).Oversee Health Canada inspections and manage all required regulatory licenses (e.g., DEL, MDEL, NBCP Wholesale License).Ensure compliance across all Health Product licensed facilities and the Import Drug Products QMS.Oversee the Computerized System Validation process and the QMS for the organization’s e-commerce platform.Regulatory OversightManage SAP Master Data for pharmacy schedules, drugs, medical devices, and natural health product attributes.Lead third-party audits and perform vendor qualification assessments, including Quality Agreements.Conduct internal GMP self-inspections and report on findings to ensure ongoing compliance.Oversee the Product Quality Complaint Program.Provide quality and regulatory oversight for multiple business units, including Shoppers Drug Mart, MediSystem Pharmacy, Central Pharmacy Services, Sanis Inc., and Specialty Health Network.Leadership and CollaborationLead, mentor, and develop quality teams across multiple locations.Collaborate cross-functionally with operations, supply chain, and senior leadership to support business objectives.Ensure alignment with corporate compliance and regulatory expectations.Occasional travel to national sites as required.
RequirementsBachelor of Science (B.Sc.) or equivalent in a related field (e.g., Chemistry, Biology, or Chemical Engineering).Minimum 15 years of experience in the GMP pharmaceutical industry with at least 5 years in senior Quality Assurance leadership.Experience working with Health Canada and regulatory inspections.Experience in Medical Devices; Supply Chain and Logistics background considered an asset.Strong knowledge of GMP, GDP, and quality system management.Advanced communication and interpersonal skills with the ability to influence across departments.Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).Key CompetenciesStrategic problem-solving and analytical decision-making.Strong organizational and prioritization skills.Ability to manage complexity and multiple stakeholders.Excellent written and verbal communication skills in English; French considered an asset.
What We OfferWhy apply through Brunel? Finding the next step in your career can be a fulltime job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with on-boarding. We’ll get you going while you get on with the job.
About UsBrunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Over 45 years, we’ve created a global network of interesting clients and talented individuals working together through a vast array of services.
Production SupervisorMontreal, QC
IntroductionBrunel is partnering with one of our leading radiopharmaceutical clients to support the hire of a Production Supervisor. This is an exciting opportunity to join a growing organization dedicated to improving patient lives through the production of high-quality radiopharmaceutical products.
As the Production Supervisor, you will oversee daily manufacturing operations, ensuring production runs safely, efficiently, and in compliance with Good Manufacturing Practices (GMP). You will play a key role in maintaining quality standards, supporting your team’s development, and fostering a culture of excellence across operations.
ResponsibilitiesTeam LeadershipSupervise and motivate production employees to meet departmental goals.Maintain strong communication with Quality, Engineering, and Technical Services teams.Lead ongoing cGMP training and employee development.Manage scheduling, absenteeism, and overtime while maintaining engagement on the production floor.Production OversightCoordinate and execute radiopharmaceutical production batches per customer orders.Monitor and report on production performance metrics.Manage inventory of raw materials and oversee HVAC monitoring.Review and maintain SOPs, production documentation, validation reports, and change controls.Conduct investigations and implement corrective actions with proper documentation.Support process improvements, equipment maintenance, and SAP-related production activities.Quality, Health & SafetyPromote and sustain a strong culture of quality throughout production.Ensure strict adherence to health, safety, and radiation protection procedures.
RequirementsB.Sc. or M.Sc. in Science or Chemical Engineering.4+ years of pharmaceutical manufacturing experience, with at least 2 years in a supervisory role (unionized environment preferred).Strong understanding of GMP and production operations.Proficiency in Microsoft Word and Excel.Bilingual – French and English.Must be comfortable working 6:00 AM to 2:00 PM shifts.
What We OfferWhy apply through Brunel? Finding the next step in your career can be a fulltime job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with on-boarding. We’ll get you going while you get on with the job.
About UsBrunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Over 45 years, we’ve created a global network of interesting clients and talented individuals working together through a vast array of services.
Production SupervisorMontreal, QC
IntroductionBrunel is partnering with one of our leading radiopharmaceutical clients to support the hire of a Production Supervisor. This is an exciting opportunity to join a growing organization dedicated to improving patient lives through the production of high-quality radiopharmaceutical products.
As the Production Supervisor, you will oversee daily manufacturing operations, ensuring production runs safely, efficiently, and in compliance with Good Manufacturing Practices (GMP). You will play a key role in maintaining quality standards, supporting your team’s development, and fostering a culture of excellence across operations.
ResponsibilitiesTeam LeadershipSupervise and motivate production employees to meet departmental goals.Maintain strong communication with Quality, Engineering, and Technical Services teams.Lead ongoing cGMP training and employee development.Manage scheduling, absenteeism, and overtime while maintaining engagement on the production floor.Production OversightCoordinate and execute radiopharmaceutical production batches per customer orders.Monitor and report on production performance metrics.Manage inventory of raw materials and oversee HVAC monitoring.Review and maintain SOPs, production documentation, validation reports, and change controls.Conduct investigations and implement corrective actions with proper documentation.Support process improvements, equipment maintenance, and SAP-related production activities.Quality, Health & SafetyPromote and sustain a strong culture of quality throughout production.Ensure strict adherence to health, safety, and radiation protection procedures.
RequirementsB.Sc. or M.Sc. in Science or Chemical Engineering.4+ years of pharmaceutical manufacturing experience, with at least 2 years in a supervisory role (unionized environment preferred).Strong understanding of GMP and production operations.Proficiency in Microsoft Word and Excel.Bilingual – French and English.Must be comfortable working 6:00 AM to 2:00 PM shifts.
What We OfferWhy apply through Brunel? Finding the next step in your career can be a fulltime job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with on-boarding. We’ll get you going while you get on with the job.
About UsBrunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Over 45 years, we’ve created a global network of interesting clients and talented individuals working together through a vast array of services.
