{"schemaVersion":"jobsearcher.job.v1","id":"017b95598d952eb2a8ac964a","url":"https://jobsearcher.com/jobs/017b95598d952eb2a8ac964a","canonicalUrl":"https://jobsearcher.com/jobs/017b95598d952eb2a8ac964a","title":"PHARMACEUTICAL – SR. CQV ENGINEER","description":"Previous Pharmaceutical/Biotech experience is mandatory for this role\n\nMMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and Validation.\nMMR Consulting has offices in Canada, USA, and Australia.\nThis is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of engineers involved in the design, commissioning & qualification, start-up and project management of various processes, systems, and facilities. The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers.\nThis role is for Sr. CQV Engineer will require to work on the validation of upstream and downstream bioprocess systems/equipment in the biopharmaceutical industry, as well as process equipment in pharma/biotech industries. The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers.\nThe work will require working on-site at client’s facilities, which are located in US. Travel is required to US is required.\n\nResponsibilities\nProvide technical guidance in the commissioning, qualification and start-up of various pharmaceutical / biopharmaceutical cGMP process equipment, utilities & facilities.\nLead the development (for example, write test cases) of key qualification deliverables such as DQ, FAT, SAT, IQ, OQ and PQ during the project lifecycle.\nAble to perform field execution of qualification test cases and protocols.\nSupport development of Project Validation Plans (PVPs) to ensure the action plan to test the system is applicable and relevant.\nLead qualification processes throughout the project lifecycle to ensure timely completion and to ensure all quality and engineering specifications are met.\nPossess knowledge of relevant regulatory requirements and industry best practices on all or any of the following – Process equipment, clean utilities, automation systems, laboratory equipment, building & facilities\nCoordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, and provide updates.\nEngage other departments, as required, in the design reviews and decisions.\nTravel may be occasionally required for meetings with equipment fabrication vendors or Factory Acceptance Testing (FATs).\nWork may require occasional support over shutdowns or extended hours, specifically during installation, construction, commissioning, qualification, and validation phases.\nVisit construction and installation sites, wearing necessary safety PPE.\nYou may be involved with other aspects such as client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and MMR resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc.\nSupervise contractors during critical testing of system and equipment.\nOther duties as assigned by client, and/or MMR, based on workload and project requirements.\nAs this position requires working on client sites, you will need to comply with the client’s safety rules including mandatory vaccination policies for COVID-19, where applicable\nLead/Mentor a team of validation engineers/specialists.\n\nQualifications\n12+ years of experience in commissioning, qualification or validation of various systems within the pharmaceutical/biotech industry.\nPrevious experience in the pharmaceutical / biotech industry, with knowledge of requirements for cGMP operations.\nValidation experience such as cleaning validation, thermal validation, mixing studies, process validation, computer systems validation is an asset but not required.\nExperience with developing and executing validation projects to Risk-Based Commissioning & Qualification approaches, such as ASTM E-2500 or ISPE ICQ, is considered an asset, but not required.\nExperience with commissioning & qualification of process control systems (i.e. PCS, SCADA, Historians) and building automation systems are considered an asset.\nExperience with commissioning and qualifications of biotech process equipment, such as some, but not all, of the following: fermentation, bioreactors, downstream purification processes (chromatography, TFF, UF), CIP systems, Buffer systems, Clean Utilities would be an asset.\nExperience with Qualification or Validation of clean utilities and ISO clean rooms.\nExperience with preparation and execution of URS’s, DQ’s, RTMs, Risk Assessments, CPPs, VPPs, FATs, SATs, IOQs\nLead teams of Validation staff, manage staff priorities, provide mentorship/oversight, help staff resolve issues. Leadership is considered an asset but not required.\nPossess leadership skills, and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexities.\nPossess mentorship skills, to coach and develop junior and intermediate employees.\nEngineering degree, preferably in Mechanical, Electrical or Chemical.\nTravel may be required on occasion.\nAbility to handle multiple projects and work in a fast-paced environment.\nStrong multi-tasking skills\nAbility to lift 50 lbs.\n\nCompensation: 100,000$ - 115,000$ based on experience.\n\nEqual Employment Opportunity and Reasonable Accommodations\n\nMMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.","company":"Mmr Consulting","rawCompany":"mmr consulting","city":"El Paso","state":"TX","isRemote":false,"isActive":false,"createdAt":"2026-07-19T15:22:20.834Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"PHARMACEUTICAL – SR. CQV ENGINEER","description":"Previous Pharmaceutical/Biotech experience is mandatory for this role\n\nMMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and Validation.\nMMR Consulting has offices in Canada, USA, and Australia.\nThis is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of engineers involved in the design, commissioning & qualification, start-up and project management of various processes, systems, and facilities. The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers.\nThis role is for Sr. CQV Engineer will require to work on the validation of upstream and downstream bioprocess systems/equipment in the biopharmaceutical industry, as well as process equipment in pharma/biotech industries. The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers.\nThe work will require working on-site at client’s facilities, which are located in US. Travel is required to US is required.\n\nResponsibilities\nProvide technical guidance in the commissioning, qualification and start-up of various pharmaceutical / biopharmaceutical cGMP process equipment, utilities & facilities.\nLead the development (for example, write test cases) of key qualification deliverables such as DQ, FAT, SAT, IQ, OQ and PQ during the project lifecycle.\nAble to perform field execution of qualification test cases and protocols.\nSupport development of Project Validation Plans (PVPs) to ensure the action plan to test the system is applicable and relevant.\nLead qualification processes throughout the project lifecycle to ensure timely completion and to ensure all quality and engineering specifications are met.\nPossess knowledge of relevant regulatory requirements and industry best practices on all or any of the following – Process equipment, clean utilities, automation systems, laboratory equipment, building & facilities\nCoordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, and provide updates.\nEngage other departments, as required, in the design reviews and decisions.\nTravel may be occasionally required for meetings with equipment fabrication vendors or Factory Acceptance Testing (FATs).\nWork may require occasional support over shutdowns or extended hours, specifically during installation, construction, commissioning, qualification, and validation phases.\nVisit construction and installation sites, wearing necessary safety PPE.\nYou may be involved with other aspects such as client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and MMR resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc.\nSupervise contractors during critical testing of system and equipment.\nOther duties as assigned by client, and/or MMR, based on workload and project requirements.\nAs this position requires working on client sites, you will need to comply with the client’s safety rules including mandatory vaccination policies for COVID-19, where applicable\nLead/Mentor a team of validation engineers/specialists.\n\nQualifications\n12+ years of experience in commissioning, qualification or validation of various systems within the pharmaceutical/biotech industry.\nPrevious experience in the pharmaceutical / biotech industry, with knowledge of requirements for cGMP operations.\nValidation experience such as cleaning validation, thermal validation, mixing studies, process validation, computer systems validation is an asset but not required.\nExperience with developing and executing validation projects to Risk-Based Commissioning & Qualification approaches, such as ASTM E-2500 or ISPE ICQ, is considered an asset, but not required.\nExperience with commissioning & qualification of process control systems (i.e. PCS, SCADA, Historians) and building automation systems are considered an asset.\nExperience with commissioning and qualifications of biotech process equipment, such as some, but not all, of the following: fermentation, bioreactors, downstream purification processes (chromatography, TFF, UF), CIP systems, Buffer systems, Clean Utilities would be an asset.\nExperience with Qualification or Validation of clean utilities and ISO clean rooms.\nExperience with preparation and execution of URS’s, DQ’s, RTMs, Risk Assessments, CPPs, VPPs, FATs, SATs, IOQs\nLead teams of Validation staff, manage staff priorities, provide mentorship/oversight, help staff resolve issues. Leadership is considered an asset but not required.\nPossess leadership skills, and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexities.\nPossess mentorship skills, to coach and develop junior and intermediate employees.\nEngineering degree, preferably in Mechanical, Electrical or Chemical.\nTravel may be required on occasion.\nAbility to handle multiple projects and work in a fast-paced environment.\nStrong multi-tasking skills\nAbility to lift 50 lbs.\n\nCompensation: 100,000$ - 115,000$ based on experience.\n\nEqual Employment Opportunity and Reasonable Accommodations\n\nMMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.","datePosted":"2026-07-19T15:22:20.834Z","dateModified":"2026-07-19T15:22:20.834Z","hiringOrganization":{"@type":"Organization","name":"Mmr Consulting","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"El Paso","addressRegion":"TX","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"017b95598d952eb2a8ac964a"},"url":"https://jobsearcher.com/jobs/017b95598d952eb2a8ac964a"}}