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Ceritypartners

Investment Associate

New York, NY

$100K - $115K/yr

CerityPartners Ventures (CPV) is hiring Investment Associates for our Built World team. Founded as Touchdown Ventures in 2014, CPV pioneered Venture Capital-as-a-Service (VCaaS) for corporations ...

Ceritypartners

Investment Associate

San Francisco, CA

$100K - $115K/yr

CerityPartners Ventures (CPV) is hiring Investment Associates for our Built World team. Founded as Touchdown Ventures in 2014, CPV pioneered Venture Capital-as-a-Service (VCaaS) for corporations ...

Cerity Partners

Investment Associate

San Francisco, CA · On-site

$100K - $115K/yr

Cerity Partners Ventures (CPV) is hiring Investment Associates for our Built World team. Founded as Touchdown Ventures in 2014, CPV pioneered Venture Capital-as-a-Service (VCaaS) for corporations ...

Baxter

Quality Associate II

Mountain Home, AR · On-site

$88K - $110K/yr

As a Quality Associate II, you will have the outstanding opportunity to lead all aspects of critical systems, calibrations, continued process verification (CPV), pest control program, and visual ...

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How much do cpv jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for cpv in the United States is $37.09, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $44.71 per hour, depending on experience, location, and employer.

What is a CPV job?

A CPV (Certified Pharmacy Technician Verification) job typically involves verifying and validating prescriptions, ensuring accuracy in medication dispensing, and maintaining compliance with pharmacy regulations. CPV technicians often work in pharmacies, hospitals, or healthcare settings where they review prescriptions for errors and assist pharmacists in providing safe medication use. Strong attention to detail, knowledge of medical terminology, and certification may be required for this role.

What are the key skills and qualifications needed to thrive in the Cpv position, and why are they important?

To excel as a Construction Project Validator (CPV), you typically need a background in engineering, construction management, or a related field, with a strong grasp of project evaluation and quality assurance techniques. Familiarity with project management software, construction codes, and industry-standard compliance assessment tools is important, and certifications such as PMP or equivalent are often advantageous. Strong attention to detail, analytical thinking, and excellent communication skills help CPVs collaborate effectively across multidisciplinary teams. These competencies are essential to ensure that construction projects meet regulatory standards and client expectations throughout all phases.

What does a typical day look like for a Construction Project Validator (CPV)?

A CPV's day often involves conducting site inspections, reviewing project documentation, and verifying that construction work aligns with approved plans and regulatory standards. You’ll likely collaborate closely with project managers, engineers, and contractors to address discrepancies and provide recommendations for corrective actions. Regular meetings, report preparation, and the use of project management software are also commonplace. This role offers opportunities to see projects through various stages and ensures quality and compliance within dynamic construction environments.
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What states have the most Cpv jobs? States with the most job openings for Cpv jobs include:
What job categories do people searching Cpv jobs look for? The top searched job categories for Cpv jobs are:
Cpv jobs near you
Product Process Validation Manager

Product Process Validation Manager

Kindeva Drug Delivery

Bridgeton, MO • On-site

Full-time

Posted yesterday

Job description

Our Work Matters
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world
The Impact You Will Make
The is an exciting opportunity as Product Process Validation Manager is a key member of the Manufacturing Science & Technology (MS&T) organization, responsible for leading process validation strategy and execution across the product lifecycle. This role oversees the design, authorship, and facilitation of technology transfer activities, Process Performance Qualification (PPQ) protocols and reports, and supporting ongoing Continued Process Verification (CPV). The manager partners closely with Process Development, Quality, Manufacturing, and Regulatory Affairs to ensure robust, compliant, and efficient validation programs. This position reports directly to the Director of MS&T.
Role Responsibilities
Process Validation & PPQ
  • Lead the development, authorship, and execution of process validation strategies in alignment with regulatory expectations (e.g., FDA, EMA, ICH Q8-Q11).
  • Write, review, and approve PPQ protocols, sampling plans, risk assessments, and final reports.
  • Facilitate cross-functional PPQ readiness, including coordinating activities with Manufacturing, Quality Control, and Quality Assurance.
  • Ensure validation deliverables meet internal standards and external regulatory requirements.

Technology Transfer
  • Serve as the MS&T lead for technology transfer of new products, processes, or scale-up activities into manufacturing.
  • Develop and maintain tech transfer plans, process descriptions, and knowledge transfer documentation.
  • Drive process fit-gap assessments, risk analyses, and mitigation strategies.
  • Support equipment and facility readiness, including URS development and process capability assessments.

Continued Process Verification (CPV)
  • Partner with data analytics and quality teams to monitor process performance, identify trends, and drive data-based decision-making.
  • Lead investigations and corrective actions related to process performance deviations or CPV signals.

Cross-Functional Leadership
  • Collaborate with Process Development to translate laboratory-scale processes into robust, scalable manufacturing processes.
  • Support Regulatory Affairs with process validation content for submissions, responses to regulatory queries, and inspections.
  • Provide technical leadership during audits and regulatory inspections.
  • Mentor and guide junior MS&T staff in validation and tech transfer best practices.

Documentation & Compliance
  • Ensure all validation and tech transfer documentation is accurate, complete, and audit-ready.
  • Maintain strong alignment with internal quality systems, change control, and document management processes.
  • Champion continuous improvement initiatives to enhance validation efficiency and process robustness.

Basic Qualifications
  • Bachelor's or Master's degree in Engineering, Life Sciences, Biotechnology, or related field.
  • 7+ years of experience in biopharmaceutical or pharmaceutical manufacturing, MS&T, process validation, or related technical functions.
  • Demonstrated expertise in PPQ, CPV, and technology transfer.
  • Strong understanding of cGMP regulations and global validation guidelines.
  • Excellent technical writing, communication, and project management skills.

Preferred
  • Experience with biologics, cell therapy, gene therapy, or aseptic manufacturing.
  • Familiarity with statistical tools (e.g., JMP, Minitab) for process analysis.
  • Prior leadership or team management experience.
  • Experience supporting regulatory inspections.

#LI-Onsite
California residents should review our Notice for California Employees and Applicants before applying.
Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees-regardless of format-without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.
Equal Opportunity Employer:
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
Do you see yourself as part of the Kindeva mission? Click Apply Now Today!

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