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Method Validation Jobs in Massachusetts (NOW HIRING)

Artius Solutions

Analytical QA Supervisor

Fall River, MA · On-site

$78K - $99K/wk

Oversee and verify method validation reports, comparisons, and study documentation. * Monitor laboratory operations for cGLP compliance and ensure SOPs are followed. * Review and assess standard ...

Moderna, Inc.

Sr. Specialist, Bioanalytics

Cambridge, MA · On-site

$89K - $143K/yr

Engage with CROs and manage method transfer, method validation, bioanalysis, and troubleshooting of nonclinical bioanalytical methods such as Pharmacokinetics (PK) and Ligand Binding Assay (LBA)

RPMGlobal

Director, Quality Assurance

Lexington, MA · On-site

$170 - $218/hr

Support validation activities including equipment qualification, process validation, analytical method validation, technology transfer, and associated quality oversight. * Support Quality ...

Emergent BioSolutions

Sr Engineer, Validation

Canton, MA · On-site

$129 - $156/hr

Determining methods and procedures on complex assignments and providing technical direction and guidance to engineers within the Validation department. * Demonstrate strong leadership and management ...

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Showing results 21-40

All JobsMethod Validation JobsMethod Validation Jobs in Massachusetts

Method Validation information

See Massachusetts salary details

$24

$56

$85

How much do method validation jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for method validation in Massachusetts is $56.79, according to ZipRecruiter salary data. Most workers in this role earn between $43.08 and $69.04 per hour, depending on experience, location, and employer.

What is a method validation?

A Method Validation job involves assessing and verifying analytical methods to ensure they produce reliable, accurate, and reproducible results. Professionals in this role typically work in pharmaceutical, biotechnology, or chemical industries, following regulatory guidelines such as ICH, USP, or FDA requirements. Their responsibilities include designing validation protocols, performing experiments, analyzing data, and documenting results. Method validation ensures compliance with industry standards and guarantees product quality and safety.

What does a method validation do?

As a Method Validation professional, you will design, conduct, and document experiments to confirm that laboratory methods produce accurate and reproducible results under specified conditions. Typical daily tasks include preparing protocols, running validation samples, analyzing data, and preparing comprehensive validation reports for internal or regulatory review. You’ll work closely with scientists, quality assurance teams, and regulatory specialists to ensure compliance with industry standards. This collaborative environment provides opportunities to contribute to critical product development stages and to build expertise that supports career progression into quality management, regulatory affairs, or advanced analytical roles.

What are the key skills and qualifications needed for method validation?

To excel in Method Validation, a strong background in analytical chemistry, laboratory techniques, and scientific data analysis is typically required, often supported by a degree in chemistry, biochemistry, or a related field. Familiarity with validation protocols, industry regulations (such as GLP, GMP, or ISO standards), and analytical instrumentation (e.g., HPLC, GC, MS) is essential. Strong attention to detail, problem-solving skills, and effective collaboration and documentation abilities help professionals thrive in this position. These skills are vital to ensure that laboratory methods are reliable, regulatory-compliant, and suitable for their intended purposes.

What are popular job titles related to Method Validation jobs in Massachusetts?

For Method Validation jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Method Validation jobs in Massachusetts look for?

The top searched job categories for Method Validation jobs in Massachusetts are:

Method Validation jobs near you
Infographic showing various Method Validation job openings in Massachusetts as of August 2026, with employment types broken down into 50% Full Time, 7% Part Time, and 43% Contract. Highlights an 100% In-person job distribution, with an average salary of $118,116 per year, or $56.8 per hour.

Sr. Supplier Quality Engineer (ONLY W-2 role)

APN Software Services, Inc

Bedford, MA • On-site

Other

Posted 26 days ago

Job description

Position Title: Sr. Supplier Quality Engineer (PHIAJP00004186)
Location:  Bedford MA
Duration: 12 months
Positions Requested: 2
Hours per Week: 40 (8 hrs/day)

Notes from the manager:

Major focus in experienced Process Validation, Verification across plastic, metal and electronics along with problem solving for candidates to support +700 parts for part qualification for Spectrawave products. The product contains Catheter and Console (System) products. Manufacture engineering, Product Quality, and/or SQE with this hands-on experience in Process Validation, Verification and TMV (Test Method Validation) would be right fit to this role.

In this role you

Responsible for achieving a state of high-quality performance at our Supplier partners through the application and practice of Advanced Product Quality Planning ‘APQP’ , Supplier Qualification (Audit, Quality Agreement/Change Notice Agreement), and continuous monitoring the performance supplier to drive zero defect through Supplier Corrective Actions and notification. You will fill a high-profile, cross functional position and play an integral role enabling development and production flow of Philips IGTD’s critical supply base. You will work in close coordination with Product Engineering, Supply Chain and Production and Suppliers to execute effective, creative and smart supply chain strategies to achieve production goals.

Your role:

• Perform Process Validation and Verification across Spectrawave IGTD portfolios for Consoles and Catheter parts.

•           Collaborate with R&D and Quality Design Assurance in Design for Manufacturability and Part Risk management per DFMAE and PFMEA.

•           Perform Process Validation , Verification, Test Method Validation, and assess CTS/CTQ criteria per APQP requirement for +700 parts.

•           Support Supplier Qualification including Audit, Quality Agreement and Change Notice Agreement.

•           Perform Problem solving in the case of FAI and APQP failure.

•           Deep dive Value Stream mapping across process.

•           Conducts thorough investigations of defects to determine if they are supplier-caused and implement corrections using the SCAR process.

•           Proactively manage, monitor, and troubleshoot supplier-related issues for quality of components, sub-assemblies, and assemblies including monitoring trends and managing Supplier Improvement and Supplier Quality Performance Monitoring.

•           Providing Quality oversight of product/process change requests from suppliers (SICRs: Supplier Initiated Chage Requests), ensuring appropriate regulatory review and adequate validation to support requested changes including following our APQP process and leading process validation, as necessary.

•           Develop and oversee process validation plans, including equipment qualifications, with suppliers and lead continuous improvement projects based on process/product trends, customer complaints, industry standards and government regulations.

You''re the right fit if:

• Bachelor Degree engineering (Master Degree is plus). 3+ years of engineering experience (Manufacturing Engineer and/or Product Quality is plus).

• In-depth product manufacturing and quality experience in process validation and verification

•           Subject Matter in IQ, OQ, PQ

•           ISO 13485 Lead Auditor certified is plus.

•           Experienced in plastic , metal, electronics commodities.

•           Strong written, oral and interpersonal skills to be able to effectively interface interdepartmentally and complete assignments with accuracy and a high attention to detail

•           Min 20% travel time

Thanks,
Amit Sehdev
APN Software Services Inc.
Direct: | Fax: |
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