Holly Springs, NC · On-site
$88K - $116K/yr
Title - CQV Lead, Upstream Location: Holly Springs, North Carolina Visa - OPEN NEED LEAD CANDIDATE ONLY WITH LINKEDIN PROFILE seeking a highly experienced CQV (Commissioning, Qualification, and ...
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Holly Springs, NC · On-site
$88K - $116K/yr
Title - CQV Lead, Upstream Location: Holly Springs, North Carolina Visa - OPEN NEED LEAD CANDIDATE ONLY WITH LINKEDIN PROFILE seeking a highly experienced CQV (Commissioning, Qualification, and ...
CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100% Onsite) Type: Long-Term Contract Start Date: ASAP Overview We are seeking experienced CQV ...
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CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100% Onsite) Type: Long-Term Contract Start Date: ASAP Overview We are seeking experienced CQV ...
CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100% Onsite) Type: Long-Term Contract Start Date: ASAP Overview We are seeking experienced CQV ...
Quick apply
CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100% Onsite) Type: Long-Term Contract Start Date: ASAP Overview We are seeking experienced CQV ...
Somerset, NJ · On-site
Overview The CQV Engineer III position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team at a client site near Somerset, NJ . Together are sharing ...
Somerset, NJ · On-site
Overview The CQV Engineer III position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team at a client site near Somerset, NJ . Together are sharing ...
Hiring: Sr. CQV Specialist (2 Openings) Raritan, NJ (100% Onsite) Long-Term Contract (2+ Years) Looking for professionals with: 8+ years of CQV/Validation experience GMP Pharma, Biotech, or Cell ...
Hiring: Sr. CQV Specialist (2 Openings) Raritan, NJ (100% Onsite) Long-Term Contract (2+ Years) Looking for professionals with: 8+ years of CQV/Validation experience GMP Pharma, Biotech, or Cell ...
Onsite in Sacramento, California CQV Consultant . The selected candidate will be responsible for commissioning, qualification, and validation activities related to GMP utilities, manufacturing ...
Onsite in Sacramento, California CQV Consultant . The selected candidate will be responsible for commissioning, qualification, and validation activities related to GMP utilities, manufacturing ...
Bend, OR · On-site
POSITION: Sr Manager, CQV Engineering JOB LOCATION: 63045 Corporate Place, Bend, OR 97701 DUTIES: Move projects in the readiness stage from commissioning to IOQ approval and handed off to operations.
Bend, OR · On-site
POSITION: Sr Manager, CQV Engineering JOB LOCATION: 63045 Corporate Place, Bend, OR 97701 DUTIES: Move projects in the readiness stage from commissioning to IOQ approval and handed off to operations.
CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100% Onsite) Type: Long-Term Contract Start Date: ASAP Overview We are seeking experienced CQV ...
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CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100% Onsite) Type: Long-Term Contract Start Date: ASAP Overview We are seeking experienced CQV ...
Kenosha, WI · On-site
Arcadis is seeking a CQV PM to manage the entire program for our client in Wisconsin. Role accountabilities: • Refine Program Level Strategy for assigned workstream • Develop detailed activity ...
Kenosha, WI · On-site
Arcadis is seeking a CQV PM to manage the entire program for our client in Wisconsin. Role accountabilities: • Refine Program Level Strategy for assigned workstream • Develop detailed activity ...
Greenville, SC · On-site +1
CQV Specialist Summary: We are seeking a CQV Specialist to support commissioning, qualification, and validation activities for sterile liquid pharmaceutical manufacturing and packaging equipment and ...
Greenville, SC · On-site +1
CQV Specialist Summary: We are seeking a CQV Specialist to support commissioning, qualification, and validation activities for sterile liquid pharmaceutical manufacturing and packaging equipment and ...
Senior CQV Scheduler to join our team to support scheduling as a project controls function on a large-scale project. The ideal individual will have a proven track record of successfully delivering ...
Senior CQV Scheduler to join our team to support scheduling as a project controls function on a large-scale project. The ideal individual will have a proven track record of successfully delivering ...
Greenville, SC · On-site +1
CQV Specialist Summary: We are seeking a CQV Specialist to support commissioning, qualification, and validation activities for sterile liquid pharmaceutical manufacturing and packaging equipment and ...
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Greenville, SC · On-site +1
CQV Specialist Summary: We are seeking a CQV Specialist to support commissioning, qualification, and validation activities for sterile liquid pharmaceutical manufacturing and packaging equipment and ...
Senior CQV Scheduler Turner & Townsend is a global professional services company with over 22,000 people in more than 60 countries. Working with our clients across real estate, infrastructure, energy ...
Senior CQV Scheduler Turner & Townsend is a global professional services company with over 22,000 people in more than 60 countries. Working with our clients across real estate, infrastructure, energy ...
CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100% Onsite) Type: Long-Term Contract Start Date: ASAP Overview We are seeking experienced CQV ...
Quick apply
CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100% Onsite) Type: Long-Term Contract Start Date: ASAP Overview We are seeking experienced CQV ...
We are seeking an experienced Senior CQV Project Manager to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives.
We are seeking an experienced Senior CQV Project Manager to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives.
Summary We are seeking a highly motivated Senior CQV Engineer to support commissioning, qualification, and validation activities for pharmaceutical and biotechnology manufacturing facilities. The ...
Summary We are seeking a highly motivated Senior CQV Engineer to support commissioning, qualification, and validation activities for pharmaceutical and biotechnology manufacturing facilities. The ...
Greenville, SC · On-site
CQV Specialist Summary: We are seeking a CQV Specialist to support commissioning, qualification, and validation activities for sterile liquid pharmaceutical manufacturing and packaging equipment and ...
Greenville, SC · On-site
CQV Specialist Summary: We are seeking a CQV Specialist to support commissioning, qualification, and validation activities for sterile liquid pharmaceutical manufacturing and packaging equipment and ...
Summary We are seeking a highly motivated Senior CQV Engineer to support commissioning, qualification, and validation activities for pharmaceutical and biotechnology manufacturing facilities. The ...
Quick apply
Summary We are seeking a highly motivated Senior CQV Engineer to support commissioning, qualification, and validation activities for pharmaceutical and biotechnology manufacturing facilities. The ...
Senior CQV Scheduler to join our team to support scheduling as a project controls function on a large-scale project. The ideal individual will have a proven track record of successfully delivering ...
Senior CQV Scheduler to join our team to support scheduling as a project controls function on a large-scale project. The ideal individual will have a proven track record of successfully delivering ...
Our CQV Project Managers deliver comprehensive support to clients across all phases of the CQV lifecycle, including manufacturing facility expansion and capital project initiatives. This includes ...
Our CQV Project Managers deliver comprehensive support to clients across all phases of the CQV lifecycle, including manufacturing facility expansion and capital project initiatives. This includes ...
$91K - $96.1K
4% of jobs
$96.1K - $101.2K
5% of jobs
$101.2K - $106.3K
13% of jobs
$107.4K is the 25th percentile. Wages below this are outliers.
$106.3K - $111.4K
12% of jobs
$111.4K - $116.5K
12% of jobs
The median wage is $118.3K / yr.
$116.5K - $121.5K
12% of jobs
$121.5K - $126.6K
11% of jobs
$129.9K is the 75th percentile. Wages above this are outliers.
$126.6K - $131.7K
11% of jobs
$131.7K - $136.8K
15% of jobs
$136.8K - $141.9K
5% of jobs
$141.9K - $147K
1% of jobs
$91K
$120K
$147K
A CQV (Commissioning, Qualification, and Validation) job involves ensuring that equipment, systems, and processes in industries like pharmaceuticals and biotechnology meet regulatory and operational requirements. CQV professionals develop protocols, execute tests, and document compliance to ensure that facilities maintain safety and efficacy standards. They work closely with engineers, quality teams, and regulatory bodies to achieve validated systems.
CQV specialists in the pharmaceutical industry frequently encounter challenges such as managing tight project deadlines, adapting to evolving regulatory requirements, and coordinating across multi-disciplinary teams. Balancing compliance with operational efficiency demands a thorough understanding of documentation and attention to detail. Working with new or complex equipment can also present learning curves that require problem-solving and collaboration with engineering, production, and quality assurance teams. However, overcoming these challenges offers valuable experience and opportunities to build a robust skill set highly regarded in regulated industries.
To thrive as a CQV (Commissioning, Qualification, and Validation) specialist, you need a strong background in engineering or life sciences, along with expertise in equipment qualification, validation protocols, and regulatory compliance. Familiarity with industry standards such as cGMP, FDA, and tools like validation software and document management systems is highly valuable. Strong analytical thinking, attention to detail, communication, and teamwork skills are crucial for ensuring project success and regulatory adherence. These skills ensure that pharmaceutical and biotech manufacturing processes meet rigorous quality standards and regulatory requirements.
$88K - $116K/yr
Contractor
Posted 14 days ago
Title - CQV Lead, Upstream
Location: Holly Springs, North Carolina
Visa - OPEN
NEED LEAD CANDIDATE ONLY WITH LINKEDIN PROFILE
seeking a highly experienced CQV (Commissioning, Qualification, and Validation) Lead to oversee all CQV activities related to Upstream Manufacturing
This leadership role will be responsible for ensuring end-to-end CQV delivery for upstream systems including single-use bioreactors, large-scale stainless steel bioreactors, and centrifuges, from inoculation through harvest.
Best Regards
Piyush Kumar
Technical Recruiter
Stellent IT
Email: piyush@stellentit.com
Call- +1 609 546-9245
Gtalk: piyush@stellentit.com
Sourced by ZipRecruiter
Stellent IT, based in St Augustine, Florida, USA, is a renowned company in the IT sector whose primary focus is providing top-tier IT consulting and staffing services. Stellent IT's expertise lies not just in fulfilling IT staffing needs but in offering comprehensive technological solutions that enhance and drive business performance. Despite the limited information about their founding history, the company has earned a name for itself in the IT industry due to its commitment to quality and consistent delivery. With a mission centered around helping businesses efficiently navigate the IT landscape by providing strategic technology-inspired solutions, Stellent IT prides itself as a leader in its field.
Recruiting and staffing services
11 - 50 Employees
St Augustine, FL, US
