

New · posted Oct 27
Thermo Fisher Scientific · Biotechnology
Senior Quality Control Technician
- Bedford, MA
- On-site
- Full-time
- Senior & Principal
The role
The Senior Quality Control (QC) Technician performs inspection, testing, and documentation activities to ensure raw materials, components, and finished goods meet established quality requirements and specifications. The role conducts visual, dimensional, functional, and analytical testing in accordance with approved procedures and supports the identification and resolution of quality issues.
The Senior QC Technician is expected to work with a high degree of independence, demonstrate strong knowledge of quality systems and inspection practices, and provide technical guidance and support to other QC personnel.
What you need
Minimum Qualifications
- High school diploma or equivalent required; associate degree or technical certification in a scientific, engineering, manufacturing, or quality-related discipline preferred.
- Typically 1-2 + years of experience in Quality Control, inspection, laboratory testing, manufacturing, or a related technical environment.
Knowledge, Skills & Abilities
- Strong attention to detail and commitment to product quality.
- Sound technical judgment and problem-solving skills.
- Ability to independently prioritize and execute inspection and testing activities.
- Effective written and verbal communication skills.
- Ability to work collaboratively across functions.
- Ability to recognize potential quality or compliance risks and escalate issues appropriately.
- Strong organizational and documentation skills.
- Ability to follow established procedures while identifying opportunities for process improvement.
Preferred Qualificationsnice to have
- Experience performing incoming, in-process, and/or finished-goods inspection.
- Experience using inspection and measurement equipment such as calipers, micrometers, gauges, balances, or other applicable instrumentation.
- Experience performing analytical or laboratory testing according to established methods and specifications.
- Ability to read and interpret specifications, drawings, procedures, test methods, and other technical documentation.
- Strong documentation skills and attention to detail.
- Ability to identify quality issues, evaluate results against established acceptance criteria, and appropriately escalate concerns.
- Basic computer skills and experience using electronic quality, laboratory, ERP, or manufacturing systems.
- Experience working in a regulated manufacturing environment such as medical devices, diagnostics, pharmaceuticals, biotechnology, or other life-science industries.
- Working knowledge of applicable quality-system requirements and Good Manufacturing Practices (GMP).
- Experience with nonconformance investigations, CAPA, deviations, or out-of-specification investigations.
- Experience with sampling plans and statistical inspection techniques.
- Familiarity with laboratory instrumentation and analytical test methods relevant to the products or materials being evaluated.
- Experience training or mentoring junior QC personnel.
What you'll do
- Perform incoming inspection and testing of raw materials, components, and supplies against approved specifications, drawings, procedures, and acceptance criteria.
- Perform final inspection and release testing of finished goods to verify compliance with established product and quality requirements.
- Conduct visual, dimensional, functional, and analytical testing using approved methods and calibrated equipment.
- Perform routine laboratory or analytical testing, which may include physical, chemical, or other product-specific test methods.
- Accurately document inspection and test results in accordance with applicable procedures and Good Documentation Practices (GDP).
- Review inspection and testing data for completeness, accuracy, and compliance with specifications.
- Identify, document, and escalate nonconforming materials, products, or test results in accordance with established procedures.
- Support investigations of nonconformances, deviations, out-of-specification results, complaints, and other quality issues as appropriate.
- Assist with root-cause investigations and implementation of corrective and preventive actions (CAPA).
- Ensure inspection and laboratory equipment is appropriately maintained, calibrated, and suitable for use.
- Maintain QC records, samples, retain samples, and laboratory or inspection areas in accordance with applicable procedures.
- Support material and finished-goods disposition activities by providing accurate and timely inspection and testing results.
- Provide technical guidance and on-the-job training to QC Technicians and other personnel as needed.
- Assist in developing, reviewing, and improving inspection procedures, test methods, work instructions, and related quality documentation.
- Participate in continuous improvement activities focused on quality, efficiency, compliance, and reduction of defects.
- Support internal and external audits and regulatory inspections as needed.
- Collaborate with Manufacturing, Quality Assurance, Engineering, Supply Chain, and other functions to resolve quality-related issues.
- Follow applicable safety, environmental, quality-system, and regulatory requirements.
- Travel to our Framingham facility is required
Pay and benefits
$49,920 – $66,560 a year
Employer provided$24.00 – $32.00 an hour · yearly at 2,080 hours (40 a week)
How this comparesThe hourly pay range estimated for this position based in Massachusetts is $24.00–$32.00.
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
Medical, dental and vision plans
Paid time off and 10 paid holidays
Paid parental leave
401(k) retirement plan
Employee Stock Purchase Plan
Tuition reimbursement
Where you'll work
Bedford, MAOn-siteOpen in Maps (opens in a new tab)
More jobs in Bedford, MAWorking conditions
First Shift (Days)
Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Warehouse, Will work with hazardous/toxic materials
Work is primarily performed in manufacturing, warehouse, inspection, and/or laboratory environments. The position may require standing for extended periods, handling materials and samples, use of personal protective equipment (PPE), and lifting or moving materials within established safety limits. Work schedules may vary based on manufacturing and business requirements.
Job intelligence
The context around this role
Live data · October 28, 2026
Salary intelligence
How the pay compares
This role's midpoint is 39% below the US median for Quality Control roles at this level.
This roleEmployer provided
Senior & Principal roles in Massachusetts11 roles publishing pay
Senior & Principal roles in the US61 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $49,920 | — | $66,560 |
| Massachusetts (middle half) | $85,750 | $97,500 | $116,250 |
| All US (middle half) | $78,500 | $95,500 | $115,500 |
This role: Thermo Fisher Scientific's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 28, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 341 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Thermo Fisher's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 44 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance19
- Lab testing and methods19
- Documentation and SOPs10
- Collaboration and leadership5
- Investigations and CAPA4
- Quality systems and risk3
- Data and digital systems1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticals
- FDAFDA OOS guidance(official source, opens in a new tab)Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production
From Regulatory News
Manufacturing and quality coverage for this professionCompany hiring pulse
Thermo Fisher on Regulatory Jobs
- 81
- Open roles
- 70
- Distinct roles
- 34
- Locations
By discipline
- Quality73 90%
- Regulatory6 7%
- Compliance & Safety2 2%
By level
- Senior & Principal35 43%
- Manager21 26%
- Associate & Specialist21 26%
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Senior Quality Control Technician at Thermo Fisher
Open until filled. $50K–$67K a year, employer provided.

