Validation Supervisor
Nashville, TN · On-site
The supervisor will manage validation projects and serve on validation project committees. Develop Validation Master Plans and provide guidance for best validation practices. The supervisor will also ...
Nashville, TN · On-site
The supervisor will manage validation projects and serve on validation project committees. Develop Validation Master Plans and provide guidance for best validation practices. The supervisor will also ...
Nashville, TN · On-site
The supervisor will manage validation projects and serve on validation project committees. Develop Validation Master Plans and provide guidance for best validation practices. The supervisor will also ...
Nashville, TN · On-site
The supervisor will manage validation projects and serve on validation project committees. Develop Validation Master Plans and provide guidance for best validation practices. The supervisor will also ...
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Nashville, TN · On-site
The supervisor will manage validation projects and serve on validation project committees. Develop Validation Master Plans and provide guidance for best validation practices. The supervisor will also ...
Nashville, TN · On-site
The supervisor will manage validation projects and serve on validation project committees. Develop Validation Master Plans and provide guidance for best validation practices. The supervisor will also ...
Nashville, TN · On-site
The supervisor will manage validation projects and serve on validation project committees. Develop Validation Master Plans and provide guidance for best validation practices. The supervisor will also ...
Charlotte, NC · On-site
Support audits, inspections, and validation project timelines Requirements: * Bachelor's degree in Engineering, Pharmacy, or related field * 5+ years of validation experience in the pharmaceutical ...
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Charlotte, NC · On-site
Support audits, inspections, and validation project timelines Requirements: * Bachelor's degree in Engineering, Pharmacy, or related field * 5+ years of validation experience in the pharmaceutical ...
This position requires experience with project management, good documentation practices, cGMP, & FDA validation methods and systems, ability to read engineering documents, set priorities, and work on ...
This position requires experience with project management, good documentation practices, cGMP, & FDA validation methods and systems, ability to read engineering documents, set priorities, and work on ...
Elgin, IL · On-site
$85K/yr
Participate in projects/program management, review new and existing drawings as received from customers and evaluate potential quality issues. * Develop and execute IQ, OQ, and PQ validation ...
Elgin, IL · On-site
$85K/yr
Participate in projects/program management, review new and existing drawings as received from customers and evaluate potential quality issues. * Develop and execute IQ, OQ, and PQ validation ...
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 ...
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 ...
Raleigh, NC · On-site
Lead validation project planning, scheduling, resource coordination, and execution tracking. * Support internal audits, client audits, and regulatory inspections by providing validation documentation ...
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Raleigh, NC · On-site
Lead validation project planning, scheduling, resource coordination, and execution tracking. * Support internal audits, client audits, and regulatory inspections by providing validation documentation ...
Maintain and update validation project plans and the Site Validation Master Plan. * Mentor and coach junior validation staff to build capability and consistency in execution. Support audits and ...
Maintain and update validation project plans and the Site Validation Master Plan. * Mentor and coach junior validation staff to build capability and consistency in execution. Support audits and ...
King Of Prussia, PA · On-site +1
Maintain and update validation project plans and the Site Validation Master Plan. * Mentor and coach junior validation staff to build capability and consistency in execution. Support audits and ...
King Of Prussia, PA · On-site +1
Maintain and update validation project plans and the Site Validation Master Plan. * Mentor and coach junior validation staff to build capability and consistency in execution. Support audits and ...
Bedford, NH · On-site
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 ...
Bedford, NH · On-site
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 ...
This position requires experience with project management, good documentation practices, cGMP, & FDA validation methods and systems, ability to read engineering documents, set priorities, and work on ...
This position requires experience with project management, good documentation practices, cGMP, & FDA validation methods and systems, ability to read engineering documents, set priorities, and work on ...
Chicago, IL · On-site
$70K - $100K/yr
Support commissioning & qualification (CQV) activities across projects * Contribute to GMP / GxP documentation and compliance efforts * Learn to lead validation workstreams and progress into a ...
Chicago, IL · On-site
$70K - $100K/yr
Support commissioning & qualification (CQV) activities across projects * Contribute to GMP / GxP documentation and compliance efforts * Learn to lead validation workstreams and progress into a ...
Mossville, IL · On-site
$128K - $192K/yr
You and your team will be performing Embedded software validation using a combination of SiL ... project milestones What You Will Have: * Analytical Thinking: Knowledge of techniques and tools ...
Mossville, IL · On-site
$128K - $192K/yr
You and your team will be performing Embedded software validation using a combination of SiL ... project milestones What You Will Have: * Analytical Thinking: Knowledge of techniques and tools ...
Nashville, TN · On-site
Plan, track, and perform validation projects; * Maintain current validation project schedules ... Provide training for contract validation personnel; * Review critical equipment drawings from a ...
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Nashville, TN · On-site
Plan, track, and perform validation projects; * Maintain current validation project schedules ... Provide training for contract validation personnel; * Review critical equipment drawings from a ...
Billerica, MA · On-site
Seeking a self-motivated Project Coordinator to coordinate validation testing on Biopharmaceutical/Pharmaceutical formulations of customer products and solutions. Candidate is responsible for being ...
Billerica, MA · On-site
Seeking a self-motivated Project Coordinator to coordinate validation testing on Biopharmaceutical/Pharmaceutical formulations of customer products and solutions. Candidate is responsible for being ...
$76K - $103K/yr
Project Lead - Validation (Supervisor) FLSA Classification : Full-Time, Exempt/Salary Professional Work Location : Fall River, MA Work Hours: General Shift: 8:30AM - 5:00PM (May very based on ...
$76K - $103K/yr
Project Lead - Validation (Supervisor) FLSA Classification : Full-Time, Exempt/Salary Professional Work Location : Fall River, MA Work Hours: General Shift: 8:30AM - 5:00PM (May very based on ...
Fall River, MA · On-site
$76K - $103K/yr
Project Lead - Validation (Supervisor) FLSA Classification : Full-Time, Exempt/Salary Professional Work Location : Fall River, MA Work Hours: General Shift: 8:30AM - 5:00PM (May very based on ...
Fall River, MA · On-site
$76K - $103K/yr
Project Lead - Validation (Supervisor) FLSA Classification : Full-Time, Exempt/Salary Professional Work Location : Fall River, MA Work Hours: General Shift: 8:30AM - 5:00PM (May very based on ...
Authors, executes and/or reviews validation documents such as validation project plans, validation protocols, validation reports, risk management tools, gap analysis, CAPA and validation exceptions ...
Authors, executes and/or reviews validation documents such as validation project plans, validation protocols, validation reports, risk management tools, gap analysis, CAPA and validation exceptions ...
Nashville, TN · On-site
Plan, track, and perform validation projects; * Maintain current validation project schedules ... Provide training for contract validation personnel; * Review critical equipment drawings from a ...
Nashville, TN · On-site
Plan, track, and perform validation projects; * Maintain current validation project schedules ... Provide training for contract validation personnel; * Review critical equipment drawings from a ...
$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
Reporting to the Senior Director of Validation and Metrology, the Validation Supervisor will be responsible for providing leadership and guidance in validation-related tasks to the validation team with up to 5 direct reports. The Supervisor independently directs and performs validation tasks to meet customer needs and comply with cGMPs. The supervisor will manage validation projects and serve on validation project committees. Develop Validation Master Plans and provide guidance for best validation practices. The supervisor will also represent the Validation Department on interdisciplinary facility teams and client meetings/visits. The Supervisor will be considered a subject-matter expert in certain validation methods and practices and will represent August Bio in both agency and customer audits.
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
August Bioservices is an equal opportunity employer and values diversity. All aspects of employment, including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. August Bioservices does not discriminate on the basis of any status protected under federal, state, or local law.
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Pharmaceutical and medicine manufacturing
51 - 200 Employees
Nashville, TN, US
2017