Director, Validation
Bedford, NH · On-site
As a member of the Validation organization, the Validation Director will lead pharmaceutical and medical device validation operations and staff across all PCI sites. The scope of responsibility ...
Director, Validation
Bedford, NH · On-site
As a member of the Validation organization, the Validation Director will lead pharmaceutical and medical device validation operations and staff across all PCI sites. The scope of responsibility ...
As a member of the Validation organization, the Validation Director will lead pharmaceutical and medical device validation operations and staff across all PCI sites. The scope of responsibility ...
As a member of the Validation organization, the Validation Director will lead pharmaceutical and medical device validation operations and staff across all PCI sites. The scope of responsibility ...
Active pharmaceutical ingredient (API) manufacturing equipment * Filling operations * Device ... Direct-hire applicants only. C2C, 1099, and third-party agency submissions will not be considered
Quick apply
Active pharmaceutical ingredient (API) manufacturing equipment * Filling operations * Device ... Direct-hire applicants only. C2C, 1099, and third-party agency submissions will not be considered
Active pharmaceutical ingredient (API) manufacturing equipment * Filling operations * Device ... Direct-hire applicants only. C2C, 1099, and third-party agency submissions will not be considered
Active pharmaceutical ingredient (API) manufacturing equipment * Filling operations * Device ... Direct-hire applicants only. C2C, 1099, and third-party agency submissions will not be considered
Active pharmaceutical ingredient (API) manufacturing equipment * Filling operations * Device ... Direct-hire applicants only. C2C, 1099, and third-party agency submissions will not be considered
Active pharmaceutical ingredient (API) manufacturing equipment * Filling operations * Device ... Direct-hire applicants only. C2C, 1099, and third-party agency submissions will not be considered
The Director of Commissioning, Qualification, and Validation (CQV) is responsible for leading the ... and commercial pharmaceutical manufacturing operations, including aseptic processing ...
The Director of Commissioning, Qualification, and Validation (CQV) is responsible for leading the ... and commercial pharmaceutical manufacturing operations, including aseptic processing ...
... pharmaceutical/GMP-regulated environment. * Strong knowledge of GAMP 5 methodology, V-model ... Direct experience validating JCI Metasys, Honeywell, Siemens, or similar BMS platforms.
... pharmaceutical/GMP-regulated environment. * Strong knowledge of GAMP 5 methodology, V-model ... Direct experience validating JCI Metasys, Honeywell, Siemens, or similar BMS platforms.
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Quick apply
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Quick apply
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Quick apply
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Quick apply
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Quick apply
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Quick apply
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Quick apply
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Quick apply
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Quick apply
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Quick apply
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Quick apply
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Quick apply
PR · On-site
Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...
Pharmaceutical Validation Director information
See salary details
$22.60 - $27.64
2% of jobs
$27.64 - $32.69
6% of jobs
$32.69 - $37.74
13% of jobs
$39.32 is the 25th percentile. Wages below this are outliers.
$37.74 - $42.79
13% of jobs
$42.79 - $47.84
11% of jobs
The median wage is $50.36 / hr.
$47.84 - $52.88
12% of jobs
$52.88 - $57.93
9% of jobs
$61.82 is the 75th percentile. Wages above this are outliers.
$57.93 - $62.98
13% of jobs
$62.98 - $68.03
13% of jobs
$68.03 - $73.08
6% of jobs
$73.08 - $78.13
3% of jobs
$22
$51
$78
How much do pharmaceutical validation director jobs pay per hour?
As of Jul 18, 2026, the average hourly pay for pharmaceutical validation director in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.
What is the difference between Pharmaceutical Validation Director vs Quality Assurance Manager?
| Aspect | Pharmaceutical Validation Director | Quality Assurance Manager |
|---|---|---|
| Credentials | Typically requires advanced degrees in life sciences or engineering, with validation certifications | Requires degrees in related fields, often with QA certifications |
| Work Environment | Oversees validation processes across manufacturing and R&D facilities | Manages QA systems, audits, and compliance within manufacturing sites |
| Industry Usage | Commonly found in pharmaceutical and biotech companies focusing on validation of processes and equipment | Widely used in pharmaceutical companies ensuring product quality and regulatory compliance |
The Pharmaceutical Validation Director focuses on validating manufacturing processes and equipment, ensuring compliance with industry standards. In contrast, the Quality Assurance Manager oversees overall quality systems, audits, and compliance. Both roles are essential in maintaining product safety and regulatory adherence, but they differ in scope and specific responsibilities within the pharmaceutical industry.
More about Pharmaceutical Validation Director jobs
What cities are hiring for Pharmaceutical Validation Director jobs? Cities with the most Pharmaceutical Validation Director job openings:
What are the most commonly searched types of Pharmaceutical Validation jobs? The most popular types of Pharmaceutical Validation jobs are:
What states have the most Pharmaceutical Validation Director jobs? States with the most job openings for Pharmaceutical Validation Director jobs include:
What job categories do people searching Pharmaceutical Validation Director jobs look for? The top searched job categories for Pharmaceutical Validation Director jobs are:
PCI Pharma Services rating
6.7
Based on 42 frontline employees who took The Breakroom Quiz
437th of 528 rated manufacturers
Job description
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
We are PCI.
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
Summary of Objective:
As a member of the Validation organization, the Validation Director will lead pharmaceutical and medical device validation operations and staff across all PCI sites. The scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including computer systems, in a CMO aseptic fill finish environment and ensure the proper validation of all equipment and processes. The Validation Director will also schedule the appropriate resources for assistance with validation, to meet the established production schedule, vendor/contract activities in the cleanrooms, maintain a state of control within the cleanroom environment, and support facilities and other operations, development and maintenance of validation program documents including SOPs, Validation Project (VPP) and Validation Master (VMP) Plans. This individual should be able to manage tasks and responsibilities with minimal guidance and demonstrate outstanding multi-tasking, problem solving and communication skills, in a dynamic and challenging contract manufacturing environment.
Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned.
Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
#LI-AL1
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future
Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.
We are PCI.
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
Summary of Objective:
As a member of the Validation organization, the Validation Director will lead pharmaceutical and medical device validation operations and staff across all PCI sites. The scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including computer systems, in a CMO aseptic fill finish environment and ensure the proper validation of all equipment and processes. The Validation Director will also schedule the appropriate resources for assistance with validation, to meet the established production schedule, vendor/contract activities in the cleanrooms, maintain a state of control within the cleanroom environment, and support facilities and other operations, development and maintenance of validation program documents including SOPs, Validation Project (VPP) and Validation Master (VMP) Plans. This individual should be able to manage tasks and responsibilities with minimal guidance and demonstrate outstanding multi-tasking, problem solving and communication skills, in a dynamic and challenging contract manufacturing environment.
Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned.
- Provide strategic and operational leadership to the Validation function, ensuring continuous, compliant execution of validation activities in alignment with established procedures, schedules, and business objectives.
- Evaluate process, equipment, and systems validation capabilities across Operations and develop short- and long-term improvement strategies to support corporate and regulatory goals.
- Guide the strategy for development, execution, review, and approval of all validation documentation, including IQ, OQ, and PQ protocols and reports.
- Ensure effective oversight of change control, deviations, investigations, and CAPAs related to validation activities; provide leadership in Quality Management System (QMS) integration and inspection readiness.
- Partner with senior leadership to define and implement validation strategies for new and existing processes, equipment, utilities, and systems, translating strategy into compliant protocols and SOPs.
- Direct and manage all aseptic and non-aseptic validation activities, including process validation, cleaning validation, sterilization validation, and equipment qualification.
- Maintain ownership and accountability for the site Master Validation Plan, ensuring alignment with regulatory expectations and business needs.
- Serve as a primary client and internal stakeholder interface for assigned validation projects, ensuring alignment on scope, timelines, and compliance requirements.
- Provide strategic leadership for validation-related regulatory inspections and third-party audits, including timely and effective closure of observations and commitments.
- Interface with regulatory agencies during inspections and technical discussions, representing the organization's validation strategy, rationale, and compliance posture.
- Lead project planning, prioritization, and resource allocation for validation teams to ensure timely execution of validation initiatives.
- Mentor, develop, and evaluate validation staff, fostering a culture of collaboration, technical excellence, and sustained cGMP compliance.
- Perform additional duties as assigned in support of operational excellence and evolving business needs.
Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- Bachelor's degree in science or engineering required.
- A master's degree is a plus, preferred.
- 15+ years of progressive leadership of operational validation experience in Pharmaceutical or Biotechnology industry, required.
- Sound industry knowledge of pharmaceutical and medical device facilities, lyophilization technology, cleanrooms, facilities clean utilities. WFI, purified water, process gasses, HVAC and industry processes and utilities
- Experience in successful management of complex technical issues using structured analysis, methodology and articulates clear and concise direction to other operations staff
- Strong experience with project and people management, particularly for large validation projects or programs
- Experience in Facility, Equipment and Utility or Cleaning validation is a must (preferably in a multi-product CMO facility). Experience with Process Validation as a plus.
- Demonstrate SME level knowledge of process/equipment validation, computer systems, standards and GxP regulations. Strong technical experience in the successful management of complex validation is required
- Able to effectively lead and coordinate multiple, complex requests/projects and allocate resources effectively, across multiple sites, managing both local and remote based staff
- Advanced understanding of applicable regulatory requirements (FDA, EMA, international regulatory)
- Audit experience is strongly preferred
- Advanced understanding of industry standards for commissioning and validation of facilities, utilities and process equipment for cGMP manufacturing
- Strong oral and written (reports) communication, organization and leadership skills
- Responsible for the activities and schedules to meet designated timelines as well as communicating with the technical team on technical aspects of the processes, if needed.
- Responsible for communicating the status of validation activities with Operational Management, Project Management, MTS, Facilities, Engineer, Material Management, EHS and Quality teams.
- The Director will participate in audits from clients and Regulatory agencies, as appropriate.
- Responsible for directing activities of Validation team members
- Responsible for the staff's development and preparation of staff evaluations
- Must be able to provide hands-on leadership, coaching and coordination of needed actions with a focus on achieving production goals.
#LI-AL1
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future
Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.
What PCI Pharma Services employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom