The scope of work for this role is to provide QA Validation support to validation activities associated with Quality Control (QC) Laboratory instruments. The main responsibility is review and ...
The scope of work for this role is to provide QA Validation support to validation activities associated with Quality Control (QC) Laboratory instruments. The main responsibility is review and ...
Qa Specialist II- Validation
Bedford, NH · On-site
No The QA Specialist II - Validation is a member of the Quality Assurance department and partners with other members of the QA, Operations, QC and Validation organization to work and perform an array ...
Qa Specialist II- Validation
Bedford, NH · On-site
No The QA Specialist II - Validation is a member of the Quality Assurance department and partners with other members of the QA, Operations, QC and Validation organization to work and perform an array ...
QA Validation Specialist 3
Portsmouth, NH · On-site
$80 - $84.41/hr
Provide Subject Matter Expert support to Quality Control, Manufacturing and other departments for the design, operation and troubleshooting of equipment. * Drive/own the validation plans and ...
QA Validation Specialist 3
Portsmouth, NH · On-site
$80 - $84.41/hr
Provide Subject Matter Expert support to Quality Control, Manufacturing and other departments for the design, operation and troubleshooting of equipment. * Drive/own the validation plans and ...
Sr. Manager Quality Assurance Validation Computerization Systems The incumbent will be responsible for supporting the Computerized System project teams in the review and QA approval of system ...
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Sr. Manager Quality Assurance Validation Computerization Systems The incumbent will be responsible for supporting the Computerized System project teams in the review and QA approval of system ...
Provide QA oversight and assurance that all GxP computerized system implementation and validation activities are executed in accordance with internal procedures and standards and meet all regulatory ...
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Provide QA oversight and assurance that all GxP computerized system implementation and validation activities are executed in accordance with internal procedures and standards and meet all regulatory ...
... validation reports, cleaning verification reports, analytical reports and manufacturing records ... Provides guidance and training for other Quality Assurance staff in the accomplishment of Quality ...
... validation reports, cleaning verification reports, analytical reports and manufacturing records ... Provides guidance and training for other Quality Assurance staff in the accomplishment of Quality ...
... method validation, and troubleshooting. Assumes responsibility for the QC portion of projects ... Performs other tasks as assigned by the Manager, QA, and/or QA Team Lead. * Holds a Bachelor ...
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... method validation, and troubleshooting. Assumes responsibility for the QC portion of projects ... Performs other tasks as assigned by the Manager, QA, and/or QA Team Lead. * Holds a Bachelor ...
Specialist QA
Juncos, PR · On-site
Approve process validation protocols and reports for manufacturing processes. * Participate in incident triage teams and provide QA oversight. * Approve Environmental Characterization reports.
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Specialist QA
Juncos, PR · On-site
Approve process validation protocols and reports for manufacturing processes. * Participate in incident triage teams and provide QA oversight. * Approve Environmental Characterization reports.
Senior Manager IT Quality Assurance Validation Computerization Systems Allendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical ...
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Senior Manager IT Quality Assurance Validation Computerization Systems Allendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical ...
Senior Manager IT Quality Assurance Validation Computerization Systems Allendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical ...
Quick apply
Senior Manager IT Quality Assurance Validation Computerization Systems Allendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical ...
Execute scheduled quality improvement testing and activities to generate statistical data for reporting and QA validation or issues identification. Determine the resources required for quality ...
Execute scheduled quality improvement testing and activities to generate statistical data for reporting and QA validation or issues identification. Determine the resources required for quality ...
Maintaining Ocular's QA Validation Program in a state of compliance and inspection readiness. * Participating as the SME during regulatory/internal inspections for QA Validations topics. QMS:
Maintaining Ocular's QA Validation Program in a state of compliance and inspection readiness. * Participating as the SME during regulatory/internal inspections for QA Validations topics. QMS:
The Validation Manager, Quality Assurance ensures all validation lifecycle activities comply with global regulatory requirements for radiopharmaceuticals, sterile manufacturing, and ...
The Validation Manager, Quality Assurance ensures all validation lifecycle activities comply with global regulatory requirements for radiopharmaceuticals, sterile manufacturing, and ...
NIH Quality Assurance Manager
Bethesda, MD · On-site
Execute scheduled quality improvement testing and activities to generate statistical data for reporting and QA validation or issues identification. * Determine the resources required for quality ...
NIH Quality Assurance Manager
Bethesda, MD · On-site
Execute scheduled quality improvement testing and activities to generate statistical data for reporting and QA validation or issues identification. * Determine the resources required for quality ...
The Validation Manager, Quality Assurance is responsible for leading and overseeing the qualification and validation program supporting existing and new cGMP radioligand therapy (RLT) manufacturing ...
The Validation Manager, Quality Assurance is responsible for leading and overseeing the qualification and validation program supporting existing and new cGMP radioligand therapy (RLT) manufacturing ...
The Validation Manager, Quality Assurance ensures all validation lifecycle activities comply with global regulatory requirements for radiopharmaceuticals, sterile manufacturing, and ...
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The Validation Manager, Quality Assurance ensures all validation lifecycle activities comply with global regulatory requirements for radiopharmaceuticals, sterile manufacturing, and ...
PR · On-site
The QA Lead will work cross-functionally with Fintech, IT/Solutions, Product, and Compliance to validate system changes, reduce production issues, and support scalable platform growth. This is a ...
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PR · On-site
The QA Lead will work cross-functionally with Fintech, IT/Solutions, Product, and Compliance to validate system changes, reduce production issues, and support scalable platform growth. This is a ...
The Position Validation Lead (Project Quality) for IFP expansion projects. Provides comprehensive validation subject matter expertise (i.e., equipment, facility, cleaning, sterilization, product ...
The Position Validation Lead (Project Quality) for IFP expansion projects. Provides comprehensive validation subject matter expertise (i.e., equipment, facility, cleaning, sterilization, product ...
... validation. * The QA Manager will delegate responsibilities to direct reports (QA Associate I, II, and III) to achieve the requisite business needs, while providing ongoing support to Manufacturing ...
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... validation. * The QA Manager will delegate responsibilities to direct reports (QA Associate I, II, and III) to achieve the requisite business needs, while providing ongoing support to Manufacturing ...
... QA Engineer for their gaming team. The role involves executing testing and validation activities across PC and cloud gaming platforms, performing system-level testing, and collaborating with ...
... QA Engineer for their gaming team. The role involves executing testing and validation activities across PC and cloud gaming platforms, performing system-level testing, and collaborating with ...
Qa Validation information
See salary details
$10.34 - $18.36
4% of jobs
$18.36 - $26.38
0% of jobs
$26.38 - $34.40
8% of jobs
$40.68 is the 25th percentile. Wages below this are outliers.
$34.40 - $42.42
16% of jobs
$42.42 - $50.44
17% of jobs
The median wage is $52.56 / hr.
$50.44 - $58.46
18% of jobs
$58.46 - $66.48
8% of jobs
$68.34 is the 75th percentile. Wages above this are outliers.
$66.48 - $74.50
15% of jobs
$74.50 - $82.52
9% of jobs
$82.52 - $90.54
3% of jobs
$90.54 - $98.56
1% of jobs
$10
$56
$98
How much do qa validation jobs pay per hour?
What are some common challenges faced by QA Validation professionals in regulated industries?
What are QA Validation professionals?
What is the difference between Qa Validation vs Qa Analyst?
| Aspect | Qa Validation | Qa Analyst |
|---|---|---|
| Certifications | GMP, GxP, Validation certifications | GMP, GxP, Quality assurance certifications |
| Work Environment | Regulated industries like pharma, biotech | Pharmaceutical, biotech, manufacturing |
| Primary Focus | Validating processes, systems, equipment | Analyzing quality data, audits, process improvements |
| Employer Usage | Quality validation teams in regulated industries | Quality assurance departments across industries |
Qa Validation specialists focus on validating systems and processes to ensure compliance with industry standards, often working on equipment and software validation. Qa Analysts primarily analyze quality data, perform audits, and support process improvements. While both roles ensure product quality, Qa Validation emphasizes validation activities, whereas Qa Analysts focus on ongoing quality analysis and reporting.
What are the key skills and qualifications needed to thrive as a QA Validation professional, and why are they important?
- Quality Validation Manager
- Full Time Csv Validation
- Quality Validation
- Internship Quality Assurance Biotech
- Remote Quality Assurance Biology
- Temporary International Manual Qa Tester
- Overnight Accenture Qa Tester
- Jr Quality Assurance Engineer
- Pharmaceutical Quality Assurance Specialist
- Director Quality Assurance Gmp

Job description
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
The scope of work for this role is to provide QA Validation support to validation activities associated with Quality Control (QC) Laboratory instruments. The main responsibility is review and approval of validation documentation including specifications, executed protocols, summary reports, deviations, periodic reviews, procedures, and change controls. In addition, this role may provide support to the site's data integrity initiative
Successful candidate requires a strong working knowledge of global GMPs with an emphasis on validation lifecycle including computer system validation, 21 CFR Parts 210 and 211, and Part 11, Electronic Records and Electronic Signatures.
Candidate requires strong interpersonal, oral and written communication skills as there is a high degree of collaboration required between members of QA Validation, Instrument Validation and QC personnel.
Candidate must be detail oriented as the main job responsibility is review and approval of validation documentation.
Candidate must have at a minimum a BS in biology, engineering or related sciences with at least 3 years of pharmaceutical or biopharmaceutical experience in a quality assurance and/or validation role.
Past experience working with QC instrumentation, Labware, Trackwise, and/or Documentum in the pharma/biopharmaceutical field is preferred but not required.
Minimum BS in biology, engineering or related sciences with at least 3 years of pharma/biopharma experience in a QA or validation role
Strong working knowledge of global GMPs with emphasis on validation, including computer validation
Strong interpersonal, oral and written skills
We do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job.
Thanks & Regards,
Jasmine Jogewar
Sr. Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
(Direct) 732-844-8720| (F) 732-549-5549
www.irionline.com , www.linkedin.com/in/Jasmine-Jogewar
Gold Seal JCAHO Certified for Health Care Staffing
"INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996