Top 10769 Manager process validation Jobs

Product Process Validation Manager
Kindeva Drug Delivery Careers —Bridgeton, MO
- Full-time
- 7 years
- Engineering
- Analysis skills
Quick Apply
Process Manager
Pinnaql —Barceloneta, PR
- Extended hours
- Engineering
- Travel
- Senior level
Quick Apply
Manager, GMP Quality
SimulStat —Remote
- Contract
- Bachelor's degree
- Senior level
- Communication skills
Validation, Quality & Compliance Lead
BULLFROG AI MANAGEMENT LLC —Gaithersburg, MD
- $130,000 - $160,000 a year
- Full-time
- Remote
- 5 years
- US work authorization
- Senior level
- Paid holidays
- Disability insurance
Quick Apply
Manager, Validation
ImmunityBio —Dunkirk, NY
- $144,000 - $160,000 a year
- Full-time
- Ability to lift 50 pounds
- Bachelor's degree
- Mentoring
- AD&D insurance
- Disability insurance
Senior Manager, Reference Standards & Reagents
Vera Therapeutics, Inc. —Remote
- $125,000 - $185,000 a year
- Remote
- Bachelor of Science
- 3 years
- Bachelor's degree
- Paid holidays
- Health insurance
Manager, QA Validation (Sterile Manufacturing)
MannKind Corporation —Danbury, CT
- $116,000 - $174,000 a year
- Engineering
- 3 years
- Project management
Quick Apply
Computer System Validation Manager
Ofni Systems —Raleigh, NC
- Computer science
- Computer Science
- Bachelor of Science
Senior Project Manager, Clinical Trials
Cogstate —Remote
- $125,000 - $135,000 a year
- Full-time
- Remote
- Nursing
- 7 years
- Computer Science
- Paid holidays
- Disability insurance
Quick Apply
Validation Team Manager (Raleigh, NC)
Eupry —Raleigh, NC
- Full-time
- Engineering
- English
- Office
Quick Apply
Business Process Manager
Cornerstone Building Brands —Remote
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Bachelor's degree
Quick Apply
Packaging Manager
Epiq Infotech LLC —Manassas, VA
- $100,000 - $135,000 a year
- Full-time
- Mid-level
- Supervising experience
- Mentoring
- Health insurance
- Paid time off
Quick Apply
8d
Sr. Manager, GMP Quality Assurance
Deciphera Pharmaceuticals —Waltham, MA
- $138,000 - $190,000 a year
- Full-time
- Remote
- 8 years
- Bachelor's degree
- Travel
- Health insurance
- Dental insurance
Quick Apply
Release Manager
Fortress Information Security —Remote
- $110,228 - $135,000 a year
- Full-time
- Remote
- Pass drug screening
- Mid-level
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
Manager, Regulatory Labeling and Operations
LivaNova —Remote
- $120,000 - $145,000 a year
- Full-time
- 8 years
- Bachelor's degree
- Travel
- Employee stock purchase plan
- Health insurance
10d
Validation Specialist & Project Manager (12-18mo Contract)
Eckert & Ziegler Radiopharma Inc —Wilmington, MA
- $90 - $120 an hour
- Contract
- Mid-level
- Communication skills
Quick Apply
Validation Manager
Biosimilar Sciences PR LLC —Aguadilla, PR
- Extended hours
- Management
- 5 years
- Engineering
- Health insurance
- Dental insurance
Quick Apply
Computer System Validation Lead / Program Manager
Veeva Systems —Remote
- $85,000 - $120,000 a year
- Full-time
- Remote
- Engineering
- 3 years
- Product management
- Paid holidays
- Health insurance
Senior Manager - Business Process
S & C Electric Company —Chicago, IL
- $151,140.00 - $200,318.80 a year
- Full-time
- Inventory management
- Engineering
- Organizational skills
- Paid parental leave
- Health savings account
Manager, Quality Assurance GMP
CG Oncology Inc —Remote
- $123,000 - $145,000 a year
- Full-time
- Remote
- 5 years
- Bachelor of Science
- Bachelor's degree
- Health savings account
- Disability insurance
Quick Apply
8d

I want to receive the latest job alert for manager process validation

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

manager process validation jobs near

Product Process Validation Manager

Kindeva Drug Delivery Careers -
Bridgeton, MO

Quick Apply

Job Details

Full-time

Qualifications

Content creation for technical audiences
Project management experience in technology
Technical writing experience within manufacturing
GMP
Project management experience in manufacturing
Manufacturing facility experience
Production validation processes
Pharmaceutical company experience
Technology transfer (scale-up process)
Bioprocessing
Pharmaceutical manufacturing facility experience

Full 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!

Quick Apply

Refine Your Search

manager process validation jobs

Product Process Validation Manager

Process Manager

Manager, GMP Quality

Validation, Quality & Compliance Lead

Manager, Validation

Senior Manager, Reference Standards & Reagents

Manager, QA Validation (Sterile Manufacturing)

Computer System Validation Manager

Senior Project Manager, Clinical Trials

Validation Team Manager (Raleigh, NC)

Business Process Manager

Packaging Manager

Sr. Manager, GMP Quality Assurance

Release Manager

Manager, Regulatory Labeling and Operations

Validation Specialist & Project Manager (12-18mo Contract)

Validation Manager

Computer System Validation Lead / Program Manager

Senior Manager - Business Process

Manager, Quality Assurance GMP

I want to receive the latest job alert for manager process validation

Related Searches

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected