PR · On-site
This 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 ...
PR · On-site
This 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 ...
The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers. This role is forSr. CQV Engineerwill require to work on the validation of upstream and ...
The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers. This role is forSr. CQV Engineerwill require to work on the validation of upstream and ...
PR · On-site
The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers. This role is forSr. CQV Engineerwill require to work on the validation of upstream and ...
Quick apply
PR · On-site
The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers. This role is forSr. CQV Engineerwill require to work on the validation of upstream and ...
PR · On-site
MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and ... This role is for Sr. CQV Manager/PM will require to lead commissioning, qualification, and ...
PR · On-site
MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and ... This role is for Sr. CQV Manager/PM will require to lead commissioning, qualification, and ...
PR · On-site
Its services include Engineering, Project Management, and Validation. MMRConsulting ... CQV Manager/PMwill require to lead commissioning, qualification, and validation activities for ...
PR · On-site
Its services include Engineering, Project Management, and Validation. MMRConsulting ... CQV Manager/PMwill require to lead commissioning, qualification, and validation activities for ...
PR · On-site
Its services include Engineering, Project Management, and Validation. MMRConsulting ... CQV Manager/PMwill require to lead commissioning, qualification, and validation activities for ...
Quick apply
PR · On-site
Its services include Engineering, Project Management, and Validation. MMRConsulting ... CQV Manager/PMwill require to lead commissioning, qualification, and validation activities for ...
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Quick apply
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Quick apply
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
CQV Specialist - Upstream Process Equipment & Downstream Biotech Process Equipment
Juncos, PR · On-site
As a world leader in life science engineering and technical solutions, MTG has the knowledge and ... Maintain accurate and up-to-date CQV records and documentation in accordance with industry ...
CQV Specialist - Upstream Process Equipment & Downstream Biotech Process Equipment
Juncos, PR · On-site
As a world leader in life science engineering and technical solutions, MTG has the knowledge and ... Maintain accurate and up-to-date CQV records and documentation in accordance with industry ...
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Quick apply
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Quick apply
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Quick apply
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Quick apply
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Quick apply
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Quick apply
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Quick apply
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelors degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelors degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Quick apply
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Quick apply
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Quick apply
PR · On-site
Provide training and technical guidance to CQV engineers and contractors executing test protocols. Qualifications: * Bachelor's degree in Chemical, Mechanical, or Biochemical Engineering (or ...
Cqv Engineer information
What does a CQV engineer do?
A CQV (Commissioning, Qualification, and Validation) engineer is responsible for ensuring that manufacturing equipment, systems, and processes in industries like pharmaceuticals and biotech meet regulatory standards and quality requirements. They develop protocols, perform testing, and document procedures to verify that systems operate correctly and consistently. CQV engineers often work with validation tools, follow strict compliance guidelines, and collaborate with cross-functional teams during project execution.
How much do CQV engineers make in the US?
CQV (Commissioning, Qualification, and Validation) engineers in the US typically earn between $80,000 and $130,000 annually, depending on experience, location, and industry. Senior or specialized engineers with certifications and extensive expertise can earn higher salaries, often exceeding $150,000. The role often requires knowledge of regulatory standards and validation tools.
What engineers make $300,000 a year?
Senior engineers in specialized fields such as petroleum, aerospace, or software engineering can earn $300,000 or more annually, especially with extensive experience, advanced skills, and leadership roles. High-paying engineering positions often require advanced degrees, certifications, and working in high-demand industries or executive-level positions.
What is a CQV Engineer job?
A CQV (Commissioning, Qualification, and Validation) Engineer is responsible for ensuring that equipment, systems, and processes within regulated industries, such as pharmaceuticals or biotechnology, meet regulatory and operational requirements. They develop and execute test protocols, troubleshoot issues, and document compliance with industry standards (e.g., FDA, GMP). Their role ensures that manufacturing facilities produce safe and effective products. CQV Engineers often collaborate with cross-functional teams, including quality, engineering, and operations.
What are some common challenges faced by CQV Engineers in the pharmaceutical industry?
CQV Engineers in the pharmaceutical industry often encounter challenges such as managing strict timelines while ensuring full compliance with regulatory standards and adapting to evolving project requirements. They must coordinate with multiple departments including QA, production, and engineering to align project goals and documentation. Additionally, troubleshooting unexpected technical issues and staying updated with the latest industry guidelines can be demanding. However, overcoming these challenges is rewarding, as it directly contributes to the safe and effective delivery of life-saving products.
What are the key skills and qualifications needed to thrive in the Cqv Engineer position, and why are they important?
To thrive as a CQV (Commissioning, Qualification, and Validation) Engineer, you need a solid background in engineering principles, GMP regulations, and life sciences or pharmaceutical processes, often supported by a relevant degree. Familiarity with quality management systems, risk assessment tools, and software for documentation and validation such as TrackWise or Veeva is commonly required, and certifications like Six Sigma or CQV-specific credentials are valuable. Strong analytical thinking, attention to detail, effective communication, and collaboration skills set top performers apart. These competencies are essential to ensure compliance, project success, and seamless interaction with cross-functional teams in highly regulated environments.
What engineer makes $500,000 a year?
Highly experienced engineers in specialized fields such as petroleum engineering, aerospace engineering, or certain senior roles in software engineering can earn $500,000 or more annually, often including bonuses and stock options. These positions typically require advanced skills, extensive experience, and often involve leadership or executive responsibilities.
What are popular job titles related to Cqv Engineer jobs in Puerto Rico? For Cqv Engineer jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Cqv Engineer jobs in Puerto Rico look for? The top searched job categories for Cqv Engineer jobs in Puerto Rico are:
Other
Posted 20 days ago
Job description
Previous Pharmaceutical/Biotech experience is mandatory for this role
MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and Validation.
MMR Consulting has offices in Canada, USA, and Australia.
This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of engineers involved in the design, commissioning & qualification, start-up and project management of various processes, systems, and facilities. The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers.
This role is for Sr. CQV Engineer will require to work on the validation of upstream and downstream bioprocess systems/equipment in the biopharmaceutical industry, as well as process equipment in pharma/biotech industries. The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers.
The work will require working on-site at client's facilities, which are located in US. Travel is required to US is required.
Responsibilities
Qualifications
Compensation: 100,000$ - 115,000$ based on experience.
Equal Employment Opportunity and Reasonable Accommodations
MMR 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.
MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and Validation.
MMR Consulting has offices in Canada, USA, and Australia.
This 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.
This 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.
The work will require working on-site at client's facilities, which are located in US. Travel is required to US is required.
Responsibilities
- Provide technical guidance in the commissioning, qualification and start-up of various pharmaceutical / biopharmaceutical cGMP process equipment, utilities & facilities.
- Lead the development (for example, write test cases) of key qualification deliverables such as DQ, FAT, SAT, IQ, OQ and PQ during the project lifecycle.
- Able to perform field execution of qualification test cases and protocols.
- Support development of Project Validation Plans (PVPs) to ensure the action plan to test the system is applicable and relevant.
- Lead qualification processes throughout the project lifecycle to ensure timely completion and to ensure all quality and engineering specifications are met.
- Possess 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
- Coordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, and provide updates.
- Engage other departments, as required, in the design reviews and decisions.
- Travel may be occasionally required for meetings with equipment fabrication vendors or Factory Acceptance Testing (FATs).
- Work may require occasional support over shutdowns or extended hours, specifically during installation, construction, commissioning, qualification, and validation phases.
- Visit construction and installation sites, wearing necessary safety PPE.
- You 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.
- Supervise contractors during critical testing of system and equipment.
- Other duties as assigned by client, and/or MMR, based on workload and project requirements.
- As 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
- Lead/Mentor a team of validation engineers/specialists.
Qualifications
- 12+ years of experience in commissioning, qualification or validation of various systems within the pharmaceutical/biotech industry.
- Previous experience in the pharmaceutical / biotech industry, with knowledge of requirements for cGMP operations.
- Validation experience such as cleaning validation, thermal validation, mixing studies, process validation, computer systems validation is an asset but not required.
- Experience 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.
- Experience with commissioning & qualification of process control systems (i.e. PCS, SCADA, Historians) and building automation systems are considered an asset.
- Experience 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.
- Experience with Qualification or Validation of clean utilities and ISO clean rooms.
- Experience with preparation and execution of URS's, DQ's, RTMs, Risk Assessments, CPPs, VPPs, FATs, SATs, IOQs
- Lead teams of Validation staff, manage staff priorities, provide mentorship/oversight, help staff resolve issues. Leadership is considered an asset but not required.
- Possess leadership skills, and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexities.
- Possess mentorship skills, to coach and develop junior and intermediate employees.
- Engineering degree, preferably in Mechanical, Electrical or Chemical.
- Travel may be required on occasion.
- Ability to handle multiple projects and work in a fast-paced environment.
- Strong multi-tasking skills
- Ability to lift 50 lbs.
Compensation: 100,000$ - 115,000$ based on experience.
Equal Employment Opportunity and Reasonable Accommodations
MMR 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.
About MMR Consulting
Sourced by ZipRecruiter
Company size
51 - 200 Employees
Headquarters location
Orland Park, IL, US
Year founded
2017