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Method Development Jobs in Massachusetts (NOW HIRING)

Nitto Denko Corp.

$84.40K - $103.30K/yr

Execute testing per method or protocol for development, qualification, verification, validation, and transfer of analytical methods * Analyze test samples, process data, and report results with ...

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Method Development information

See Massachusetts salary details

$31.7K

$58.3K

$88.5K

How much do method development jobs pay per year?

As of May 30, 2026, the average yearly pay for method development in Massachusetts is $58,339.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,400.00 and $65,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Method Development, and why are they important?

To excel in Method Development, you need a strong background in analytical chemistry, laboratory techniques, and scientific problem-solving, often supported by a degree in chemistry or a related field. Familiarity with analytical instruments such as HPLC, GC, and mass spectrometry, as well as knowledge of relevant regulatory guidelines and software for data analysis, is typically required. Attention to detail, critical thinking, and effective communication are crucial soft skills for designing robust methods and collaborating with cross-functional teams. These capabilities ensure the development of accurate, reliable methods that support research, quality control, and regulatory compliance.

What are some common challenges encountered in a Method Development role, and how are they typically addressed?

Professionals in Method Development often face challenges such as optimizing analytical techniques for complex samples, ensuring methods are robust and reproducible, and meeting stringent regulatory requirements. Addressing these challenges involves a systematic approach, including thorough literature review, iterative experimentation, and close collaboration with cross-functional teams (such as Quality Assurance and R&D) to validate and troubleshoot methods. Staying updated on industry best practices and regulatory guidelines is also crucial for success in this role.

What is method development in a laboratory setting?

Method development refers to the process of creating, optimizing, and validating analytical procedures or techniques used to identify, quantify, and analyze substances in various samples. This is crucial in industries like pharmaceuticals, environmental testing, and food safety to ensure accurate and reliable results. The process involves selecting appropriate instruments, developing sample preparation steps, and validating the method to meet regulatory and quality standards. Skilled professionals in method development help ensure that tests are robust, reproducible, and suitable for their intended purposes.

What is the difference between Method Development vs Analytical Chemist?

AspectMethod DevelopmentAnalytical Chemist
Primary FocusDesigning and optimizing new analytical methodsPerforming analysis using established methods
Work EnvironmentResearch labs, R&D departmentsQuality control labs, manufacturing facilities
Required CredentialsBachelor's or higher in Chemistry or related field; experience in method developmentBachelor's or higher in Chemistry; experience in analytical techniques

Method Development specialists focus on creating and refining new analytical procedures, while Analytical Chemists primarily perform routine analysis using existing methods. Both roles require strong chemistry knowledge, but Method Development involves more innovation and method optimization, often in research settings, whereas Analytical Chemists focus on quality control and routine testing in production environments.

What are popular job titles related to Method Development jobs in Massachusetts? For Method Development jobs in Massachusetts, the most frequently searched job titles are:
What job categories do people searching Method Development jobs in Massachusetts look for? The top searched job categories for Method Development jobs in Massachusetts are:
Method Development jobs near you
Sr. Development Quality Engineer

Sr. Development Quality Engineer

Generis TEK Inc.

Westford, MA

$46/hr

Other

Posted 21 days ago

Job description

Please Contact: To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Monu Karwasara at email address can be reached on # .
We have Contract role Sr. Development Quality Engineer for our client at Westford, MA. Please let me know if you or any of your friends would be interested in this position.
Position Details: Sr. Development Quality Engineer- Westford, MA Location: Westford, MA 01886 Duration: 12+ months Pay Rate: $46/hour on W2
Screening Questions:

  • Can you walk me through your experience supporting Design Controls in a medical device product development lifecycle (e.g., requirements, V&V, design transfer)?
  • What type of risk management activities have you led or contributed to (e.g., FMEA), and at what stages of product development?
  • What experience do you have with medical device regulations (FDA, ISO 13485, EU MDR) and test method validation or verification activities?


Description: The Sr. Development Quality Engineer will serve as a technical representative, providing design-quality expertise to a product development team. Responsible for maintaining a strong collaborative partnership with cross-functional team members to achieve patient/user safety, customer satisfaction, and organizational success.
Responsibilities:

  • Lead and/or support on-time completion of Design Control deliverables
  • Support the establishment of objective, measurable, and verifiable product requirements
  • Support Design Verification and Validation planning & execution, including any cross-functional investigation & resolution activities
  • Lead Risk Management activities from product concept through commercialization
  • Support test method development and lead test method validation activities
  • Support manufacturing process development & qualification for new products and design changes
  • Support the establishment of component specification definitions, supplied component sampling plan development, and vendor qualifications
  • Support biocompatibility and sterilization qualifications
  • Support audits and quality system improvement activities
  • Support Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and regulatory requirements.
  • Comply with Abbott, U.S. FDA, EUMDR, and other requirements, as applicable.
  • Maintain positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and suppliers.


Basic Qualifications:

  • Bachelor s degree in Engineering or Technical Field.
  • Minimum of 5 years of experience in R&D, Process/Manufacturing Engineering, and/or Quality with at least 2 years supporting product development.
  • Experience in medical devices and associated regulations/standards.
  • Experience in test method development and validation
  • Experience in preparing risk assessments, FMEA and other risk documents.


Preferred Qualifications:

  • Advanced Degree in Engineering/Technical Field
  • Experience in active implantable medical devices.
  • Knowledge of requirements management tools (e.g., DOORS) and use of problem reporting systems (e.g., JIRA).
  • Working knowledge of statistics and its application to verification and validation


To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Monu Karwasara at email address can be reached on # .

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