Validation experience jobs

Analyst 3 - Quality Assurance

Sunrise Systems Inc · Posted Sep 28, 2026

Open

Wilson, North Carolina, United States
On-site
Contract · Associate
18+ Months on W2 Contract
2–4 years

Analyst 3 - Quality Assurance

Sunrise Systems Inc · Posted Sep 28, 2026

Open

Wilson, North Carolina, United States
On-site
Contract · Associate
18+ Months on W2 Contract
2–4 years

Supplier Engineer III — Medical Device

Pharmavise Corporation · Posted Nov 5, 2026

Open

Maple Grove, Minnesota, United States
Hybrid
Contract · Senior
2–5 years

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Responsible for remediation activities for CAPA 7720 on contract manufactured medical device products.

Responsibilities

Review, remediate, and approve CM SFMD supplier’s process risk documentation (PFMEA) to newly defined criteria.
Review, remediate, and approve CM SFMD supplier’s process and inspection validations to client’s statistical requirements.
Perform change management activities to remediate gaps found in CM SFMD Supplier’s process risk documentation and process/inspection validations.
Collaborate with CM SFMD suppliers and client’s functional resources to complete all activities needed to approve supplier’s process risk documentation and process/inspection validations to the newly defined criteria.
Demonstrate a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.

Requirements

Bachelor’s degree in engineering
Nice to have: experience working with suppliers or in supply chain management
Nice to have: experience working in the Medical Device Field
Nice to have: experience with installation qualifications (IQ), operational qualifications (OQ), performance qualification (PQ), and test method validation (TMV)

Skills

manufacturing experience

Validation Lead

Danta Technologies · Posted Nov 5, 2026

Open

Secaucus, New Jersey, United States
Full-time
$45–$50 per hour
7–10 years

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Compensation

Rate - 45-50/hr on W2

Responsibilities

Validate and implement infrastructure systems and tools such as AWS, Azure, JIRA, ServiceNow
Manage multiple dispositions for J&J managers with limited supervision
Lead end-to-end validation activities from inventory to final dispositions
Write and execute documentation for validation deliverables
Review system test and UAT scripts, traceability matrix, and design specs

Skills

Validation experience AWS Azure JIRA ServiceNow CSV GxP Risk-based validation Documentation QA methodologies

Validation Engineer II

Alcami Corporation · Posted Nov 5, 2026

Open

Pepperell, Massachusetts, United States
On-site
Full-time · Associate
$38–$47 per hour
2+ years

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The Validation Engineer II performs validation equipment preparation, protocol execution, and final report generation for environmental chambers including cryo-freezers, cold rooms, incubators, depyrogenation ovens, stability chambers, warehouses, as well as sterilizers and CSV.

Compensation

The base hourly pay range for this position is $38.00 – $47.00 per hour.

Responsibilities

Perform pre- and post-validation verification on test equipment
Perform calibrations incidental to validation including controllers, gauges, recorders
Create and execute validation protocols, procedures, and final reports
Perform validation projects
Perform peer review of validation reports

Requirements

BA/BS in technical or science related field of study
HSD/GED
technical training
Associate’s degree
Nice to have: mechanical aptitude

Skills

validation experience validation of temperature-controlled units temperature mapping ISO 9001 ISO 17025

Senior QA Specialist - C&Q

Johnson & Johnson · Posted Nov 4, 2026

Open

Wilson, North Carolina, United States
On-site
Full-time · Senior
6+ years

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Seeking a highly qualified Senior QA Specialist to join a new Biotherapeutics Manufacturing facility in Wilson, NC, ensuring compliance with regulatory requirements and GMP policies throughout the C&Q validation lifecycle.

Responsibilities

Represents Quality Assurance on qualification teams and provides QA oversight of C&Q and validation execution across the capital project lifecycle—user requirements, design review, construction, FAT/SAT, commissioning, qualification and handover.
Supports development and maintenance of site validation program, Validation Master Plan, and project C&Q and validation plans.
Participates in risk assessments (FMEA, HACCP, HAZOP, ICH Q9(R1), CARA) for equipment, utilities and systems.
Reviews and approves commissioning and qualification documentation, including URS, FAT/SAT, IQ/OQ/PQ protocols, and reports.
Ensures Good Documentation Practice and data integrity of vendor, EPCM and CQV contractor documentation.

Requirements

Bachelor's degree in a scientific or engineering discipline
Master's degree in a scientific or engineering discipline
Nice to have: greenfield or start-up facility experience
Nice to have: ASQ certification (CQA, CQE)
Nice to have: Kneat

Skills

Quality Assurance Validation experience

Manufacturing Engineer III

Artech LLC · Posted Nov 3, 2026

Open

Maple Grove, Minnesota, United States
Hybrid
Contract · Senior
$50–$56 per hour
2–5 years

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Supplier Engineer responsible for remediation activities for contract manufactured medical device product, ensuring compliance and quality.

Compensation

Pay Rate: $50-56.35/hr. on w2

Responsibilities

Review, remediate, and approve CM SFMD supplier’s process risk documentation (PFMEA) to newly defined criteria.
Review, remediate, and approve CM SFMD supplier’s process and inspection validations to BSC’s statistical requirements.
Perform change management activities to remediate gaps found in CM SFMD Supplier’s process risk documentation and process/inspection validations.
Collaborate with CM SFMD suppliers and BSC functional resources to complete all activities needed to approve supplier’s process risk documentation and process/inspection validations to the newly defined criteria.
Maintain compliance to the Quality Policy and all other documented quality processes and procedures.

Requirements

Bachelor’s degree in engineering
Nice to have: Supply chain management
Nice to have: Medical Device Field
Nice to have: Installation qualifications (IQ)
Nice to have: Operational qualifications (OQ)

Skills

Problem solving Manufacturing experience

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