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Analytical Instruments Jobs in Massachusetts (NOW HIRING)

Perform analytical testing using instruments such as ICP-MS, GC-MS, LC-MS, and related platforms. * Perform sample preparation for ICP-MS analysis, including microwave digestion and ashing. * Conduct ...

Operate and maintain variety of optical, test and analytical instruments * Test all aspects of optical components, critical for laser development and manufacturing * Participate in design and ...

Operate and maintain variety of optical, test and analytical instruments * Test all aspects of optical components, critical for laser development and manufacturing * Participate in design and ...

Experience using analytical instruments/methods such as chromatography (HPLC/UPLC), electrophoresis (CE, cIEF), spectroscopy (UV/Vis) and ELISA. * Experience using or developing methods to determine ...

Associate Scientist I

Woburn, MA ยท On-site

$28/hr

Experience using analytical instruments/methods such as chromatography (HPLC/UPLC), electrophoresis (CE, cIEF), spectroscopy (UV/Vis) and ELISA. * Experience using or developing methods to determine ...

Operate and maintain variety of optical, test and analytical instruments * Provide reports and presentations * Provide assistance and training to internal personnel Location: * 75% of the position is ...

Showing results 21-40

Analytical Instruments information

See Massachusetts salary details

$32.2K

$109.9K

$211.3K

How much do analytical instruments jobs pay per year?

As of Aug 8, 2026, the average yearly pay for analytical instruments in Massachusetts is $109,948.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,700.00 and $136,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the analytical instruments position, and why are they important?

To thrive in an Analytical Instruments role, you need a solid background in chemistry, physics, or engineering, with experience in laboratory procedures and instrumentation. Proficiency in operating, calibrating, and troubleshooting tools such as spectrometers, chromatographs, or mass spectrometers, along with certifications like ASCP or relevant manufacturer training, is often required. Strong analytical thinking, attention to detail, and effective communication make someone stand out in this field. These combined skills ensure accurate data collection, dependable instrument maintenance, and meaningful reporting for research and industrial projects.

What are the typical daily responsibilities for someone working with analytical instruments?

Professionals working with analytical instruments typically spend their days preparing and analyzing samples, maintaining and calibrating laboratory equipment, recording and interpreting data, and ensuring compliance with safety and quality standards. They often collaborate with researchers, engineers, or production teams to solve technical issues and optimize test protocols. Daily tasks can also include troubleshooting instrument malfunctions, documenting results for reports, and participating in team meetings to discuss project goals and findings. This variety of responsibilities helps ensure accurate, timely results that support scientific and industrial objectives.

What is an analytical instruments job?

An Analytical Instruments job involves working with precision instruments used for scientific analysis, measurement, and quality control in industries like pharmaceuticals, biotechnology, environmental science, and manufacturing. Professionals in this field may install, maintain, calibrate, and troubleshoot instruments such as spectrometers, chromatographs, and microscopes. They also ensure compliance with industry standards and regulatory requirements. Strong technical knowledge, problem-solving skills, and attention to detail are essential for success in this role.

What are popular job titles related to Analytical Instruments jobs in Massachusetts? For Analytical Instruments jobs in Massachusetts, the most frequently searched job titles are:
What job categories do people searching Analytical Instruments jobs in Massachusetts look for? The top searched job categories for Analytical Instruments jobs in Massachusetts are:
Infographic showing various Analytical Instruments job openings in Massachusetts as of July 2026, with employment types broken down into 88% Full Time, and 12% Contract. Highlights an 100% In-person job distribution, with an average salary of $109,948 per year, or $52.9 per hour.

6445 - Lead CQV SME / Lead Validation Engineer

Verista, Inc.

Devens, MA โ€ข On-site

$114K - $150K/yr

Full-time

Re-posted 1 hour ago


Job description

Description

Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values:

  • We empower and support our colleagues
  • We commit to client success at every turn
  • We have the courage to do the right thing
  • We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
  • We constantly acquire new skills and learn from our experiences to enhance our collective expertise

Job Overview: We are seeking a Lead Validation Engineer to provide senior technical governance across the C&Q lifecycle for a mixed portfolio of facility, utility, process equipment, analytical instrument, automation, and room qualification scope. This role is the technical backstop for strategy, deliverable quality, risk-based qualification rationale, protocol comments, deviation handling, and execution readiness.

Lead Validation Engineer Responsibilities:

  • Provide senior technical governance for commissioning, qualification, and validation activities across facilities, utilities, process equipment, analytical instruments, automation systems, and cleanroom qualifications. Ensure qualification strategies align with regulatory expectations, industry best practices, project objectives, and quality requirements
  • Mentor and provide technical oversight to system leads and CQV engineers, offering guidance on qualification execution, risk-based decision making, protocol development, technical problem solving, and regulatory compliance while promoting consistency across multiple workstreams
  • Review and approve system qualification strategies including Commissioning Plans, Qualification Plans, Validation Master Plans (VMPs), and lifecycle deliverables to ensure appropriate application of risk-based commissioning and qualification methodologies in accordance with ASTM E2500, ISPE Baseline Guides, and GAMP 5 principles
  • Provide technical leadership in resolving complex protocol execution, deviation, and investigation issues, evaluating technical impact, determining appropriate corrective actions, and ensuring timely closure of deviations while maintaining project schedules and compliance with cGMP requirements
  • Support vendor leveraging and risk-based qualification approaches by evaluating vendor documentation, Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), and commissioning packages for qualification suitability. Develop and review Quality Risk Assessments (QRA), Design Qualifications (DQ), Installation/Operational Qualification (IOQ) strategies, Qualification Summary Reports (QSR), and Traceability Matrices (TM) to optimize testing while ensuring complete regulatory compliance
  • Review and guide QP, QRA, data integrity risk assessment, ERES assessment, configuration specification, traceability matrix, commissioning protocol/report, IOQ/PQ, blue tag, and QSR strategy
  • Own technical escalation for protocol exceptions, discrepancies, punch items, deviations, and test evidence gaps
  • Support family/grouping rationale where systems can be qualified efficiently while maintaining traceability and defensibility
  • Partner with PM and document manager to keep 5-business-day review and approval cycles realistic and clean

Job Requirements:

  • Bachelor's Degree or equivalent required
  • 15+ years in GMP CQV, ideally across biologics, viral vector, cell therapy, gene therapy, aseptic manufacturing, or complex sterile facilities
  • Strong risk-based qualification judgment: can decide when to leverage vendor FAT/SAT packages, when to write project-specific testing, and how to defend the rationale to quality stakeholders
  • Experience reviewing direct impact systems, computerized/automation interfaces, analytical instruments, utilities, cleanrooms, and process equipment without becoming a bottleneck
  • Able to mentor system leads, normalize document quality, resolve comments, and prevent drift across parallel system deliverables
  • Deep knowledge of GMP validation lifecycle.
  • Extensive experience with ASTM E2500, ISPE, GAMP 5, FDA, and EU Annex 15.
  • Strong technical writing and problem-solving abilities
  • ValGenesis experience a plus

This role requires the ability to be on-site, full-time in Devens, MA.

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.

*Verista is an equal opportunity employer.

National (US) Range
$87,780—$161,654 USD

Benefits

Why Choose Verista?

  • High growth potential and fast-paced organization with a people-focused culture
  • Competitive pay plus performance-based incentive programs
  • Company-paid Life, Short-Term, and Long-Term Disability Insurance.
  • Medical, Dental & Vision insurances
  • FSA, DCARE, Commuter Benefits
  • Supplemental Life, Hospital, Critical Illness and Legal Insurance
  • Health Savings Account
  • 401(k) Retirement Plan (Employer Matching benefit)
  • Paid Time Off (Rollover Option) and Holidays
  • As Needed Sick Time
  • Tuition Reimbursement
  • Team Social Activities (We have fun!)
  • Employee Recognition
  • Employee Referral Program
  • Paid Parental Leave and Bereavement

Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.

For more information about our company, please visit us at Verista.com