Senior Assembler / Site Technician Mississauga, ON
IntroductionBrunel is seeking a Technician with a solid background in mechanical assembly and maintenance of heavy-duty equipment primarily used in the aggregate and mining industry. Successful applicants must have a demonstrated knowledge of bulk material handling equipment including conveyors (portable, stationary & overland), stackers (telescopic, folding and cable mast), hoppers, belt feeders, crushers and screening plants.
ResponsibilitiesWorking in the assembly bay- Assembling, Testing, & commissioning machines.Perform a detailed functionality test of all mechanical, hydraulic and electrical components.Adjust machinery and repair or replace any defective parts.Cooperate with technical team and share information across the organizationRead blueprints, diagrams and schematic drawings/layouts to assemble & troubleshoot equipment.Document service and installation actions by completing forms, reports, logs, and records.Prepares reports or analysis of product failure trends and service issuesProvide support by examining complaints; identifying solutions; suggesting improved methods and techniques; recommending system & safety improvements.Make improvement recommendations that can reduce cost, increase uptime and enhance safety
RequirementsMinimum 5-8 Years of proven experience in installing and maintaining bulk material equipment in particular rubber belt conveyor systems in outdoor applications.Strong technical writing, communication and interpersonal skills are requiredStrong Electro-Mechanical aptitude with hands-on experienceStrong ability to work in a team environment or autonomously is requiredExperience with tensioning/tracking/training of troughed belt conveyorsExperience in electrical motors, sensors, pneumatics, hydraulics, HMI's is a benefit
Additional Required Competencies:Occasional travel to client sites for service and commissioning may be requested at times – a current validPassport will be required.Must have experience working in extreme environmental conditions (dust, cold, heat, rain) when installing/repairing equipment at customer outdoor site location
Note that this role is a mixture of:90% hands on technician role working in clients manufacturing facility10% field service support on site at customer locationsMajority of clients are in Canada and USA but a number of International projects in places like Australia, Chile, Colombia, Greenland, Indonesia, Slovenia, Mozambique.
What We OfferWhy 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 UsBrunel 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 45 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.
Senior Assembler / Site Technician Mississauga, ON
IntroductionBrunel is seeking a Technician with a solid background in mechanical assembly and maintenance of heavy-duty equipment primarily used in the aggregate and mining industry. Successful applicants must have a demonstrated knowledge of bulk material handling equipment including conveyors (portable, stationary & overland), stackers (telescopic, folding and cable mast), hoppers, belt feeders, crushers and screening plants.
ResponsibilitiesWorking in the assembly bay- Assembling, Testing, & commissioning machines.Perform a detailed functionality test of all mechanical, hydraulic and electrical components.Adjust machinery and repair or replace any defective parts.Cooperate with technical team and share information across the organizationRead blueprints, diagrams and schematic drawings/layouts to assemble & troubleshoot equipment.Document service and installation actions by completing forms, reports, logs, and records.Prepares reports or analysis of product failure trends and service issuesProvide support by examining complaints; identifying solutions; suggesting improved methods and techniques; recommending system & safety improvements.Make improvement recommendations that can reduce cost, increase uptime and enhance safety
RequirementsMinimum 5-8 Years of proven experience in installing and maintaining bulk material equipment in particular rubber belt conveyor systems in outdoor applications.Strong technical writing, communication and interpersonal skills are requiredStrong Electro-Mechanical aptitude with hands-on experienceStrong ability to work in a team environment or autonomously is requiredExperience with tensioning/tracking/training of troughed belt conveyorsExperience in electrical motors, sensors, pneumatics, hydraulics, HMI's is a benefit
Additional Required Competencies:Occasional travel to client sites for service and commissioning may be requested at times – a current validPassport will be required.Must have experience working in extreme environmental conditions (dust, cold, heat, rain) when installing/repairing equipment at customer outdoor site location
Note that this role is a mixture of:90% hands on technician role working in clients manufacturing facility10% field service support on site at customer locationsMajority of clients are in Canada and USA but a number of International projects in places like Australia, Chile, Colombia, Greenland, Indonesia, Slovenia, Mozambique.
What We OfferWhy 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 UsBrunel 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 45 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.
Position: Structural Engineer Location: Regina, SaskatchewanTerm: Permanent - Full TimeTravel: Site travel to project sites when required (Frequent travel to project sites for design walkdowns, inspections, construction support, and coordination)
IntroductionBrunel is currently seeking a Structural Engineer to join one of our leading mining clients in Regina, Saskatchewan. This is an excellent opportunity for an experienced engineer to contribute to the design and analysis of complex underground and surface mining structures, including shafts, headframes, support systems, and heavy industrial infrastructure.
As a Structural Engineer, you will be responsible for delivering technically sound designs and providing field engineering support throughout the project lifecycle — from concept and design development to construction execution. You will apply advanced structural analysis, sound engineering judgment, and practical field experience to ensure safe, efficient, and constructible solutions for challenging mining environments.
ResponsibilitiesPerform structural design and analysis (steel, concrete, shotcrete, reinforcement, etc.) for underground and surface mining structures: headframes, load frames, access galleries, portals, conveyors, foundations, supports, and structural elements of mining infrastructureDevelop structural deliverables: design calculations, structural models, drawings, specifications, and connection detailsPerform site walkdowns, field verifications, and inspections to confirm conditions and adjust design assumptionsCollaborate with geotechnical, civil, mechanical, and mining engineers to integrate structural designs into full project systemsReview vendor/subcontractor structural drawings and connection details for compliance with project requirementsConduct structural assessments, condition inspections, and retrofits / strengthening of existing structures when requiredEvaluate structural risk, redundancy, load cases (dead, live, dynamic, seismic, ground movement) and perform checks under multiple load combinationsEnsure designs comply with applicable codes, standards (e.g. Canadian / provincial codes, mining structural standards) and internal QA/QCSupport construction: respond to requests for information (RFIs), provide design clarifications, and assist in issue resolution in the fieldCoordinate structural scope in bids/proposals (estimate structural costs, prepare structural scope, support tender drawings)
RequirementsBachelor’s degree in civil or Structural Engineering (or equivalent)Registered Professional Engineer (P.Eng.)Minimum 5+ years of structural engineering experience (preferably in heavy industrial, mining, underground, or infrastructure projects)Strong skills in structural modeling and analysis software (e.g. STAAD, SAP2000, ANSYS, RISA, or equivalent)Proficiency in producing structural drawings (e.g. AutoCAD, Revit, Tekla, or equivalent)Excellent understanding of structural principles: load paths, connection design, reinforcement design, dynamic / seismic effects, structural fatigueAbility to interpret geotechnical information and incorporate into structural design (e.g. interaction with rock / ground, ground movement effects)Strong communication skills (verbal, written, with ability to present designs, and interface with multidisciplinary teams)Willingness and ability to travel to project sites (including underground) to validate design conditions and support construction
Preferred / Asset Qualifications:Direct experience in the mining / underground contracting sector (shaft sinking, mine development, tunnelling)Experience in structural assessments, repairs, retrofits, or structural life-extensionFamiliarity with mining structural standards, underground support systems, shotcrete, rock bolts, etc.Experience with structural dynamics, vibration, fatigue, or cyclic loadingExperience in cost estimating of structural scopeExperience with structural risk assessment, reliability, or probabilistic design methods
Working Conditions & TravelPrimary base in Regina office during design phasesFrequent travel to project sites for design walkdowns, inspections, construction support, and coordinationSite exposure may include remote, underground, or constrained environments—must comply with PPE and site safety policiesOccasional extended stays onsite or irregular hours to respond to construction / field issuesSome hybrid / remote flexibility possible when off site
What We OfferWhy 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 UsBrunel 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.
Position: Senior Project EngineerLocation: Vancouver, British Columbia Contract: 1-year initial term, with strong potential for extension.Site: Occasional site visits may be required (Arizona)Work Schedule: Monday - Friday, hours determined by project needs (in office)
IntroductionBrunel is currently hiring a Senior Project Engineer / Project Area Lead on behalf of our major mining client. This contract position will be based in the EPCM consultant’s engineering office in Vancouver, BC, with periodic travel to a remote project site in Arizona. As a Senior Project Engineer, you will play a key leadership role supporting the Owner’s Engineering Manager (EM) and project team in managing the EPCM consultant responsible for developing a new multi-billion-dollar copper concentrator. You will oversee the project through the basic (BE) and detailed engineering (DE) phases and provide technical expertise, guidance, and leadership to the EPCM consultant and other vendors, ensuring project quality, consistency, and progress across your assigned project area(s), as well as engineering support during field execution.
ResponsibilitiesReviews, investigates, and develops appropriate recommendations to EPCM team regarding engineering progress.Serves as an Area Lead on a wide range of small to medium engineering / construction, work packages within the main project scope.Prepares scopes, evaluates proposals and administers awarded contracts with vendors for engineering services, field work and equipment.Coordinates cooperation, and information flow between vendors, particularly at scope battery limits.Coordinates Owner’s disciplines engineers on technical review/supervision of the EPCM and other contractors.Collaborates and provides guidance to the site management team on applicable processes, practices and engineering information. May contribute to site strategic planning and budgeting efforts for designated engineering areas.Includes the Owner’s stake holders in the sharing information about the project, makes sure that their comments are accounted in the design by the EPCM and other vendors.Provides related information about the project to the Owner’s stake holders. May present the project on company’s steering meetings. Performs other duties as required.
Job ScopeNature of work: Works on moderately complex issues, implements solutions through individual effort, but may delegate more routine tasks to others.Level of interaction: Collaborates mostly with peers in the same functional area and has moderate external interaction. Receives instructions from the project EM.Autonomy/decision making: Works under supervision under EM, but has some latitude to set objectives, priorities and timelines impacting the individual assigned area of work as the Area Lead.Budgetary responsibility: Assists with budget preparation and monitoring.Managerial responsibility: may manage Owner’s discipline engineers dedicated to the assigned areas of the project. Manages EPCM and other consultants/vendors.
RequirementsBachelor’s degree in engineering (process, mechanical, electrical, structural, civil) and 10 (ten) to 12 (twelve) years heavy industrial engineering experience, mining strongly preferred, including 2 (two) to 3 (three) years engineering management experience.Experience in EPCM office environment; knowledge of principles and large industrial/mining project engineering execution and management.Demonstrate technical competence in his/her discipline, knowledge of operation of copper concentrator.Experience working in the Owner’s team in the EPCM consultant office will be considered as an asset. Experience with metal mining operations and consulting, with regards to process, machinery, piping, structural, civil, electrical and instrumentation.Skilled in related engineering software (MS Office, AutoCAD, Google Earth, Navis Works, Aconex) scheduling (MS Project).
Language Skills, Certifications and/or TrainingFluency in English.Broad knowledge of the principles and practices of engineering.Ability to research and analyze information of considerable difficulty and draw valid conclusions.Skill in effective communication, both verbal and written, including the ability to actively listen and to adapt behavior and communication style based upon the audience.Ability to develop and maintain awareness of occupational hazards and safety precautions.Skill in following safety practices, and recognizing, controlling and/or eliminating hazards. Ability to build trust and credibility with employees/peers and establish common goals and expectations.Strong analytical skills.
What We OfferWhy 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 UsBrunel 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.
Position: Senior Project EngineerLocation: Vancouver, British Columbia Contract: 1-year initial term, with strong potential for extension.Site: Occasional site visits may be required (Arizona)Work Schedule: Monday - Friday, hours determined by project needs (in office)
IntroductionBrunel is currently hiring a Senior Project Engineer / Project Area Lead on behalf of our major mining client. This contract position will be based in the EPCM consultant’s engineering office in Vancouver, BC, with periodic travel to a remote project site in Arizona. As a Senior Project Engineer, you will play a key leadership role supporting the Owner’s Engineering Manager (EM) and project team in managing the EPCM consultant responsible for developing a new multi-billion-dollar copper concentrator. You will oversee the project through the basic (BE) and detailed engineering (DE) phases and provide technical expertise, guidance, and leadership to the EPCM consultant and other vendors, ensuring project quality, consistency, and progress across your assigned project area(s), as well as engineering support during field execution.
ResponsibilitiesReviews, investigates, and develops appropriate recommendations to EPCM team regarding engineering progress.Serves as an Area Lead on a wide range of small to medium engineering / construction, work packages within the main project scope.Prepares scopes, evaluates proposals and administers awarded contracts with vendors for engineering services, field work and equipment.Coordinates cooperation, and information flow between vendors, particularly at scope battery limits.Coordinates Owner’s disciplines engineers on technical review/supervision of the EPCM and other contractors.Collaborates and provides guidance to the site management team on applicable processes, practices and engineering information. May contribute to site strategic planning and budgeting efforts for designated engineering areas.Includes the Owner’s stake holders in the sharing information about the project, makes sure that their comments are accounted in the design by the EPCM and other vendors.Provides related information about the project to the Owner’s stake holders. May present the project on company’s steering meetings. Performs other duties as required.
Job ScopeNature of work: Works on moderately complex issues, implements solutions through individual effort, but may delegate more routine tasks to others.Level of interaction: Collaborates mostly with peers in the same functional area and has moderate external interaction. Receives instructions from the project EM.Autonomy/decision making: Works under supervision under EM, but has some latitude to set objectives, priorities and timelines impacting the individual assigned area of work as the Area Lead.Budgetary responsibility: Assists with budget preparation and monitoring.Managerial responsibility: may manage Owner’s discipline engineers dedicated to the assigned areas of the project. Manages EPCM and other consultants/vendors.
RequirementsBachelor’s degree in engineering (process, mechanical, electrical, structural, civil) and 10 (ten) to 12 (twelve) years heavy industrial engineering experience, mining strongly preferred, including 2 (two) to 3 (three) years engineering management experience.Experience in EPCM office environment; knowledge of principles and large industrial/mining project engineering execution and management.Demonstrate technical competence in his/her discipline, knowledge of operation of copper concentrator.Experience working in the Owner’s team in the EPCM consultant office will be considered as an asset. Experience with metal mining operations and consulting, with regards to process, machinery, piping, structural, civil, electrical and instrumentation.Skilled in related engineering software (MS Office, AutoCAD, Google Earth, Navis Works, Aconex) scheduling (MS Project).
Language Skills, Certifications and/or TrainingFluency in English.Broad knowledge of the principles and practices of engineering.Ability to research and analyze information of considerable difficulty and draw valid conclusions.Skill in effective communication, both verbal and written, including the ability to actively listen and to adapt behavior and communication style based upon the audience.Ability to develop and maintain awareness of occupational hazards and safety precautions.Skill in following safety practices, and recognizing, controlling and/or eliminating hazards. Ability to build trust and credibility with employees/peers and establish common goals and expectations.Strong analytical skills.
What We OfferWhy 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 UsBrunel 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.
IntroductionBrunel is partnering with a newly built, government-funded GMP biomanufacturing facility dedicated to producing clinical trial materials for innovative biologics and vaccines across Canada. Our client is looking to hire a Senior QC Consultant (Bilingual En/Fr) to focus on specifications, data review, and strategic QC input to ensure compliance with Canadian GMP, FDA cGMP and EU (Eudralex) expectations.
ResponsibilitiesAct as a senior QC subject-matter expert within a multidisciplinary team supporting clinical biologics and vaccine programs.Help develop and refine specifications for biological products, including drug substance, drug product, MCB/WCB and intermediates. Advise on test strategies and panels to be performed for client projects, aligned with relevant regulatory guidance.Review and interpret QC data and environmental monitoring (EM) trending; provide recommendations based on trends and microbiological findings. Support or oversee the generation, review and optimization of QC SOPs, work instructions and related documentation. Contribute to annual QC reports, data summaries and trending analyses, ensuring regulatory and internal policy compliance.Collaborate with the QC lead on weekly progress reviews, deliverables and prioritization of tasks.Support other QC activities as needed (specifications, data analysis, document generation/review).
Requirements7-10 years’ experience in a GMP environment for biologics (QC, QA or related technical roles). Minimum 5 years’ experience in establishing specifications for biological products (clinical and/or commercial). Minimum 5 years’ experience as QA or QC in a biomanufacturing facility for sterile products (e.g., biologics, vaccines). Degree in Sciences (minimum B.Sc. or equivalent). Strong knowledge of Canadian GMP, FDA cGMP and EU (Eudralex) requirements. Demonstrated experience reviewing QC data, identifying trends and translating findings into clear, actionable recommendations.Fluent in both French and English (spoken and written). Legally eligible to work in Canada.Experience supporting new facility start-up, clinical trial material facilities or tech transfer projects.Prior consulting experience or working across multiple products/clients.
What We OfferWhy 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 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.
IntroductionBrunel is partnering with a newly built, government-funded GMP biomanufacturing facility dedicated to producing clinical trial materials for innovative biologics and vaccines across Canada. Our client is looking to hire a Senior QC Consultant (Bilingual En/Fr) to focus on specifications, data review, and strategic QC input to ensure compliance with Canadian GMP, FDA cGMP and EU (Eudralex) expectations.
ResponsibilitiesAct as a senior QC subject-matter expert within a multidisciplinary team supporting clinical biologics and vaccine programs.Help develop and refine specifications for biological products, including drug substance, drug product, MCB/WCB and intermediates. Advise on test strategies and panels to be performed for client projects, aligned with relevant regulatory guidance.Review and interpret QC data and environmental monitoring (EM) trending; provide recommendations based on trends and microbiological findings. Support or oversee the generation, review and optimization of QC SOPs, work instructions and related documentation. Contribute to annual QC reports, data summaries and trending analyses, ensuring regulatory and internal policy compliance.Collaborate with the QC lead on weekly progress reviews, deliverables and prioritization of tasks.Support other QC activities as needed (specifications, data analysis, document generation/review).
Requirements7-10 years’ experience in a GMP environment for biologics (QC, QA or related technical roles). Minimum 5 years’ experience in establishing specifications for biological products (clinical and/or commercial). Minimum 5 years’ experience as QA or QC in a biomanufacturing facility for sterile products (e.g., biologics, vaccines). Degree in Sciences (minimum B.Sc. or equivalent). Strong knowledge of Canadian GMP, FDA cGMP and EU (Eudralex) requirements. Demonstrated experience reviewing QC data, identifying trends and translating findings into clear, actionable recommendations.Fluent in both French and English (spoken and written). Legally eligible to work in Canada.Experience supporting new facility start-up, clinical trial material facilities or tech transfer projects.Prior consulting experience or working across multiple products/clients.
What We OfferWhy 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 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.
IntroductionBrunel is partnering with a newly built, government-funded GMP biomanufacturing facility dedicated to producing clinical trial materials for innovative biologics and vaccines across Canada. Our client is looking to hire a Senior QC Consultant (Bilingual En/Fr) to focus on specifications, data review, and strategic QC input to ensure compliance with Canadian GMP, FDA cGMP and EU (Eudralex) expectations.
ResponsibilitiesAct as a senior QC subject-matter expert within a multidisciplinary team supporting clinical biologics and vaccine programs.Help develop and refine specifications for biological products, including drug substance, drug product, MCB/WCB and intermediates. Advise on test strategies and panels to be performed for client projects, aligned with relevant regulatory guidance.Review and interpret QC data and environmental monitoring (EM) trending; provide recommendations based on trends and microbiological findings. Support or oversee the generation, review and optimization of QC SOPs, work instructions and related documentation. Contribute to annual QC reports, data summaries and trending analyses, ensuring regulatory and internal policy compliance.Collaborate with the QC lead on weekly progress reviews, deliverables and prioritization of tasks.Support other QC activities as needed (specifications, data analysis, document generation/review).
Requirements7-10 years’ experience in a GMP environment for biologics (QC, QA or related technical roles). Minimum 5 years’ experience in establishing specifications for biological products (clinical and/or commercial). Minimum 5 years’ experience as QA or QC in a biomanufacturing facility for sterile products (e.g., biologics, vaccines). Degree in Sciences (minimum B.Sc. or equivalent). Strong knowledge of Canadian GMP, FDA cGMP and EU (Eudralex) requirements. Demonstrated experience reviewing QC data, identifying trends and translating findings into clear, actionable recommendations.Fluent in both French and English (spoken and written). Legally eligible to work in Canada.Experience supporting new facility start-up, clinical trial material facilities or tech transfer projects.Prior consulting experience or working across multiple products/clients.
What We OfferWhy 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 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.
IntroductionBrunel is partnering with a newly built, government-funded GMP biomanufacturing facility dedicated to producing clinical trial materials for innovative biologics and vaccines across Canada. Our client is looking to hire a Senior QC Consultant (Bilingual En/Fr) to focus on specifications, data review, and strategic QC input to ensure compliance with Canadian GMP, FDA cGMP and EU (Eudralex) expectations.
ResponsibilitiesAct as a senior QC subject-matter expert within a multidisciplinary team supporting clinical biologics and vaccine programs.Help develop and refine specifications for biological products, including drug substance, drug product, MCB/WCB and intermediates. Advise on test strategies and panels to be performed for client projects, aligned with relevant regulatory guidance.Review and interpret QC data and environmental monitoring (EM) trending; provide recommendations based on trends and microbiological findings. Support or oversee the generation, review and optimization of QC SOPs, work instructions and related documentation. Contribute to annual QC reports, data summaries and trending analyses, ensuring regulatory and internal policy compliance.Collaborate with the QC lead on weekly progress reviews, deliverables and prioritization of tasks.Support other QC activities as needed (specifications, data analysis, document generation/review).
Requirements7-10 years’ experience in a GMP environment for biologics (QC, QA or related technical roles). Minimum 5 years’ experience in establishing specifications for biological products (clinical and/or commercial). Minimum 5 years’ experience as QA or QC in a biomanufacturing facility for sterile products (e.g., biologics, vaccines). Degree in Sciences (minimum B.Sc. or equivalent). Strong knowledge of Canadian GMP, FDA cGMP and EU (Eudralex) requirements. Demonstrated experience reviewing QC data, identifying trends and translating findings into clear, actionable recommendations.Fluent in both French and English (spoken and written). Legally eligible to work in Canada.Experience supporting new facility start-up, clinical trial material facilities or tech transfer projects.Prior consulting experience or working across multiple products/clients.
What We OfferWhy 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 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.
IntroductionBrunel is partnering with a newly built, government-funded GMP biomanufacturing facility dedicated to producing clinical trial materials for innovative biologics and vaccines across Canada. Our client is looking to hire a Senior QC Consultant (Bilingual En/Fr) to focus on specifications, data review, and strategic QC input to ensure compliance with Canadian GMP, FDA cGMP and EU (Eudralex) expectations.
ResponsibilitiesAct as a senior QC subject-matter expert within a multidisciplinary team supporting clinical biologics and vaccine programs.Help develop and refine specifications for biological products, including drug substance, drug product, MCB/WCB and intermediates. Advise on test strategies and panels to be performed for client projects, aligned with relevant regulatory guidance.Review and interpret QC data and environmental monitoring (EM) trending; provide recommendations based on trends and microbiological findings. Support or oversee the generation, review and optimization of QC SOPs, work instructions and related documentation. Contribute to annual QC reports, data summaries and trending analyses, ensuring regulatory and internal policy compliance.Collaborate with the QC lead on weekly progress reviews, deliverables and prioritization of tasks.Support other QC activities as needed (specifications, data analysis, document generation/review).
Requirements7-10 years’ experience in a GMP environment for biologics (QC, QA or related technical roles). Minimum 5 years’ experience in establishing specifications for biological products (clinical and/or commercial). Minimum 5 years’ experience as QA or QC in a biomanufacturing facility for sterile products (e.g., biologics, vaccines). Degree in Sciences (minimum B.Sc. or equivalent). Strong knowledge of Canadian GMP, FDA cGMP and EU (Eudralex) requirements. Demonstrated experience reviewing QC data, identifying trends and translating findings into clear, actionable recommendations.Fluent in both French and English (spoken and written). Legally eligible to work in Canada.Experience supporting new facility start-up, clinical trial material facilities or tech transfer projects.Prior consulting experience or working across multiple products/clients.
What We OfferWhy 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 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.
