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 ...
Apply Early
Boston, MA · On-site
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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Boston, MA · On-site
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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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 ...
Cary, NC · Hybrid
We are seeking a CQV Subject Matter Expert with a dual mandate: (1) Business Development / PreSales to shape opportunities, lead solutioning, and win new CQV programs; and (2) Delivery Oversight to ...
Cary, NC · Hybrid
We are seeking a CQV Subject Matter Expert with a dual mandate: (1) Business Development / PreSales to shape opportunities, lead solutioning, and win new CQV programs; and (2) Delivery Oversight to ...
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 ...
Apply Early
We are seeking CQV Engineers with at least 3 years of direct CQV experience to support execution of GMP equipment qualification deliverables. These roles will focus on protocol execution ...
We are seeking CQV Engineers with at least 3 years of direct CQV experience to support execution of GMP equipment qualification deliverables. These roles will focus on protocol execution ...
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 ...
The Director of Commissioning, Qualification, and Validation (CQV) is responsible for leading the site-wide CQV program to ensure facilities, utilities, equipment, computerized systems, manufacturing ...
The Director of Commissioning, Qualification, and Validation (CQV) is responsible for leading the site-wide CQV program to ensure facilities, utilities, equipment, computerized systems, manufacturing ...
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 ...
New
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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 ...
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.
Charlotte, NC · On-site
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 ...
New
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Charlotte, NC · On-site
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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Huntsville, AL · On-site
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 ...
Huntsville, AL · On-site
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 ...
Richmond, VA · On-site
Turner & Townsend is seeking an experienced 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 ...
Richmond, VA · On-site
Turner & Townsend is seeking an experienced 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 ...
Turner & Townsend is seeking an experienced 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 ...
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Turner & Townsend is seeking an experienced 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 ...
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Lebanon, IN · On-site
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 ...
Lebanon, IN · On-site
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 ...
Turner & Townsend is seeking an experienced 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 ...
Turner & Townsend is seeking an experienced 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 ...
Senior CQV Engineer/Manager Location: Remote / Hybrid / Onsite (Depending on Project Requirements) Duration: Long-Term Contract Position Overview We are seeking an experienced CQV (Commissioning ...
Senior CQV Engineer/Manager Location: Remote / Hybrid / Onsite (Depending on Project Requirements) Duration: Long-Term Contract Position Overview We are seeking an experienced CQV (Commissioning ...
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 ...
$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 8 days ago
Be an early applicant
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
