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Analytical Instruments Jobs in New Jersey (NOW HIRING)

Rice Industries LLC

QC Lab Technician

Moorestown, NJ

$20 - $21/hr

Proficiency in using measurement tools (calipers, micrometers, etc.) and analytical instruments. * Knowledge of cGMP, ISO standards, and quality control principles. * Strong attention to detail ...

Rice Industries

QC Lab Technician

Moorestown, NJ · On-site

$20 - $21/hr

Proficiency in using measurement tools (calipers, micrometers, etc.) and analytical instruments. * Knowledge of cGMP, ISO standards, and quality control principles. * Strong attention to detail ...

Anton Paar

Field Service Representative

Newark, NJ · On-site +1

$39.50 - $44.80/hr

Qualifications * 3 years experience in troubleshooting, repairing and maintaining complex analytical instruments. * Ability to work independently and a strong commitment to customer satisfaction.

Anton Paar

Field Service Representative

Newark, NJ

$39.50 - $44.80/hr

Qualifications * 3 years experience in troubleshooting, repairing and maintaining complex analytical instruments. * Ability to work independently and a strong commitment to customer satisfaction.

HORIBA, Ltd.

NJ · On-site

$80 - $100/hr

Strong expertise in Spectroscopy; experience with Raman spectroscopy is strongly preferred (expertise in microscopy, optics, or analytical instruments like Fluorescence, confocal microscopy, AFM, SEM ...

Integrated Resources INC

Chemist

Elizabeth, NJ

Experience with HPLC and GC analyses Good cGMP knowledge Performs testing of raw materials and drug products, maintenance and calibration of analytical instruments, prepares standard and sample ...

Actalent

Lab Technician

Bridgewater, NJ · On-site

$30 - $32/hr

Calibrate analytical instruments and laboratory equipment to ensure accurate measurements and consistent performance. * Troubleshoot analytical instrumentation and resolve routine technical issues to ...

Focus Laboratories

Senior Analytical Chemist

Cherry Hill, NJ · On-site

$65K - $85K/yr

... instruments; support audits and client technical discussions - Mentor junior analysts and improve lab efficiency Required qualifications: - BS in Chemistry (or related) and 4+ years in pharma/biotech ...

Focus Lab

Senior Analytical Chemist

Cherry Hill, NJ · On-site

$90 - $130/hr

Troubleshoot methods/instruments; support audits and client technical discussions * Mentor junior analysts and improve lab efficiency Required qualifications: * BS in Chemistry (or related) and 4+ ...

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Analytical Instruments information

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$29.9K

$102.2K

$196.4K

How much do analytical instruments jobs pay per year?

As of Sep 3, 2026, the average yearly pay for analytical instruments in New Jersey is $102,207.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,500.00 and $126,900.00 per year, depending on experience, location, and employer.

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 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 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 some analytical instruments careers?

Careers in analytical instruments include roles such as analytical chemist, laboratory technician, instrumentation specialist, and quality control analyst. These positions often require knowledge of laboratory equipment like spectrometers, chromatographs, and microscopes, along with relevant certifications or degrees in chemistry, biology, or related fields.

What are popular job titles related to Analytical Instruments jobs in New Jersey?

For Analytical Instruments jobs in New Jersey, the most frequently searched job titles are:

What job categories do people searching Analytical Instruments jobs in New Jersey look for?

The top searched job categories for Analytical Instruments jobs in New Jersey are:

Analytical Instruments jobs near you
Infographic showing various Analytical Instruments job openings in New Jersey as of August 2026, with employment types broken down into 88% Full Time, 7% Part Time, 2% Temporary, and 3% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $102,207 per year, or $49.1 per hour.

Quality Assurance Validation Manager

Thermo Fisher Scientific

Teterboro, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 24 days ago

Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 429 frontline employees who took The Breakroom Quiz

169th of 545 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Location: Ridgefield, New Jersey - Sterile Fill-Finish & Packaging Site
Our state-of-the-art sterile fill-finish and packaging facility in Ridgefield, NJ, is dedicated to meeting the growing needs of biotech and pharmaceutical drug developers. With expanded capabilities in pre-filled syringe and liquid vial manufacturing, the site increases U.S. capacity to manufacture the medicines patients rely on every day.
As part of Thermo Fisher Scientific's global network, Ridgefield complements our world-class contract development and manufacturing services and strengthens our sterile fill-finish footprint-now spanning seven sites worldwide, including three in the U.S. (Greenville, NC; Plainville, MA; and Ridgefield, NJ). Strategically located along the East Coast to streamline logistics and attract top talent, the 360,000 sq. ft. Ridgefield site plays a vital role in the global pharmaceutical supply chain, with products distributed to more than 67 countries across all continents.
Join Thermo Fisher Scientific and play a critical role in supporting the delivery of life-changing therapies and products to patients worldwide. As a Quality Assurance Validation Manager, you will lead validation activities that ensure product quality, operational excellence, and compliance with global regulatory requirements. Working in a highly collaborative environment, you will partner with Quality Assurance, Manufacturing, Engineering, Regulatory Affairs, and other cross-functional teams to maintain the validated state of systems and processes that support the manufacture of therapeutics and other critical products.
You'll have the opportunity to influence validation strategy, lead complex projects, and develop a high-performing team while contributing to a culture of quality, continuous improvement, and innovation.
Discover Impactful Work:
As a Quality Assurance Validation Manager, you will provide leadership and oversight for validation programs across equipment, utilities, facilities, computer systems, cleaning processes, analytical instruments, and manufacturing operations. You will ensure validation activities are executed in accordance with cGMP requirements, quality standards, and industry best practices while supporting business objectives, new product introductions, and technology transfer initiatives. In partnership with Quality Assurance and cross-functional teams, you will help maintain compliance and the validated state of critical systems and processes that support the manufacture of therapeutics and other life-changing products.
A Day in the Life:
  • Lead and manage validation activities across manufacturing, laboratory, utility, facility, computerized systems, and analytical instruments
  • Develop and maintain validation strategies, validation master plans, and project timelines
  • Oversee the planning, coordination, execution, review, and approval of validation protocols and reports
  • Partner with project managers and cross-functional stakeholders to establish priorities, monitor progress, and communicate project status
  • Ensure validation activities comply with FDA, EU, and applicable global regulatory requirements and Quality Assurance standards
  • Support equipment qualification, process validation, cleaning validation, utility qualification, computer system validation, and analytical instrument qualification programs
  • Apply risk assessment methodologies and statistical tools to support validation decisions
  • Drive continuous improvement initiatives to enhance validation processes and operational efficiency
  • Manage change control activities and assess validation impacts associated with process or system changes
  • Ensure adherence to data integrity requirements and governance standards across validation activities
  • Support regulatory inspections, customer audits, and quality assessments
  • Mentor, develop, and lead validation professionals while fostering a culture of accountability and excellence

Keys to Success:
Education
  • Advanced Degree with 8+ years of validation experience, or
  • Bachelor's Degree with 10+ years of validation experience
  • Preferred fields of study include Engineering, Chemistry, Biology, Life Sciences, or related technical disciplines

Experience
  • Significant experience in validation within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments
  • Experience coordinating, planning, executing, and approving validation activities across multiple disciplines
  • Demonstrated success managing complex validation projects, programs, and teams
  • Experience partnering with project managers to establish priorities and drive project execution
  • Experience participating in regulatory inspections and customer audits
  • Experience with validation master planning, change control systems, and quality management systems
  • Expertise in process validation and analytical instrument qualification
  • Proficiency in data integrity compliance, governance, and regulatory expectations related to data lifecycle management

Knowledge, Skills, Abilities
  • Strong knowledge of cGMP regulations, including FDA, EU, and global regulatory requirements
  • Expertise in equipment qualification, process validation, cleaning validation, computer system validation, utility qualification, and analytical instrument qualification
  • Strong understanding of ALCOA+ principles, data integrity requirements, and data governance practices
  • Proficiency in risk assessment methodologies and statistical analysis
  • Strong technical writing, documentation, and report review capabilities
  • Excellent leadership, communication, and interpersonal skills
  • Ability to influence stakeholders and collaborate effectively across functions and organizational levels
  • Knowledge of Lean Manufacturing and continuous improvement methodologies
  • Proficiency with Microsoft Office and standard business software applications
  • Strong organizational and problem-solving skills with the ability to manage multiple priorities

Relocation assistance is not provided
Must be legally authorized to work in the United States now or in the future without sponsorship
Must be able to pass a comprehensive background check, which includes a drug screening
Compensation and Benefits
The salary range estimated for this position based in New Jersey is $112,500.00-$168,750.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs
  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement
  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
  • Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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