

New · posted Oct 13
Thermo Fisher Scientific · Biotechnology
QC Technician II
- Grand Island, NY
- On-site
- Full-time
- Associate & Specialist
Closes Nov 12, 2026 · 30 days left
The role
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Location/Division Specific Information:
3175 Staley Road, Grand Island NY
BioProduction Division
Position is for 1st shift, Monday - Friday
How Will You Make an Impact?:
The Finished Product Testing QC Technician II performs routine Quality Control testing of finished products to ensure they meet established specifications, customer requirements, and applicable regulatory requirements. Testing is performed using approved methods and SOPs in accordance with cGMP, Good Documentation Practices (GDP), data integrity expectations, and laboratory safety requirements.
We are seeking a self-motivated individual with strong communication, technical, and operational skills who can coordinate and execute laboratory testing with limited supervision or guidance. The successful candidate will demonstrate strong attention to detail, sound judgment, and the ability to work both independently and collaboratively within the Microbiology Quality Control Laboratories.
This position supports a variety of QC activities, including aseptic testing, sterility testing, finished-product testing, and other microbiological laboratory activities. The technician plays an important role in maintaining compliant laboratory operations and supporting the timely release of quality products to our customers.
A Day in the Life:
Perform finished-product Quality Control testing using approved procedures and aseptic techniques, including sterility, endotoxin, pH, osmolality, powder reconstitution, and other miscellaneous QC testing as required. Accurately document testing activities and results in accordance with cGMP and GDP requirements.
- Support laboratory inventory management and upkeep by monitoring testing supplies and materials, maintaining appropriate stock levels, identifying inventory needs, and helping ensure materials are available to support uninterrupted laboratory operations.
- Contribute to a culture of continuous improvement by supporting Lean and 5S principles, maintaining organized and efficient laboratory workspaces, identifying opportunities to reduce waste and improve workflow, and participating in team improvement initiatives.
- Demonstrate a positive, collaborative, and customer-focused attitude while working independently and with cross-functional teams. Communicate effectively, take ownership of assigned responsibilities, and contribute to timely, right-first-time testing that supports quality, operational excellence, and customer satisfaction.
Education:
High school diploma or equivalent required.
AAS degree preferred or 1-2 years of relevant lab experience
Experience:
Experience (2+ years) in MS Excel, Word, and Outlook, Microsoft Teams
Proficient oral and written communication skills are required to be effective in this role
Knowledge, Skills, Abilities:
Strong people skills, team focused.
- Strong written, verbal, and organizational skills, and the ability to work independently.
- Ability to work in a fast-paced environment and prioritize tasks as necessary
- Individual should be comfortable working a in a cGMP clean room environment for extended periods of time.
Physical Requirements / Work Environment:
Work within a Quality Control laboratory environment while adhering to applicable cGMP, safety, and laboratory requirements.
- Wear required Personal Protective Equipment (PPE) based on assigned laboratory activities and applicable safety procedures.
- Perform aseptic gowning and follow established gowning and contamination-control practices when working in designated areas.
- Ability to lift, carry, and safely handle materials weighing 20 pounds or more as required to support routine laboratory operations.
- Ability to perform laboratory activities requiring standing, walking, bending, reaching, and repetitive hand movements for extended periods.
- Safely handle laboratory samples, reagents, supplies, and equipment in accordance with established procedures.
- Maintain a clean, organized, and safe laboratory environment in accordance with 5S, contamination-control, and safety requirements.
What We Offer:
Compensation
Competitive Pay
Performance Related Bonus where eligible
Annual merit performance-based increase
Excellent Benefits
Medical benefits
Paid Time Off/Annual Leave
Employee Referral Bonus
Career Advancement Opportunities
What you need
Pay and benefits
$36,379 – $54,579 a year
Employer provided$17.49 – $26.24 an hour · yearly at 2,080 hours (40 a week)
How this comparesThe hourly pay range estimated for this position based in New York is $17.49–$26.24.
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 and dental plans
Paid time off and 10 paid holidays
Paid parental leave
401(k) retirement savings plan
Employee Stock Purchase Plan
Tuition reimbursement
Where you'll work
Grand Island, NYOn-siteOpen in Maps (opens in a new tab)
More jobs in Grand Island, NYSchedule and working conditions
Days
Standard (Mon-Fri)
Environmental Conditions
Laboratory Setting
Job intelligence
The context around this role
Live data · October 13, 2026
Salary intelligence
How the pay compares
This role's midpoint is 32% below the US median for Quality Control roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US57 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $36,379 | — | $54,579 |
| All US (middle half) | $51,500 | $66,500 | $80,000 |
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 13, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 205 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 21 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods12
- Collaboration and leadership6
- GMP and compliance4
- Documentation and SOPs4
- Data and digital systems2
- Quality systems and risk1
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 data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and Answers
- USPUSP compendial chapters(official source, opens in a new tab)Bioburden (USP <61>), endotoxin (USP <85>), TOC (USP <643>) and water testing
Company hiring pulse
Thermo Fisher on Regulatory Jobs
- 85
- Open roles
- 71
- Distinct roles
- 35
- Locations
By discipline
- Quality77 91%
- Regulatory6 7%
- Compliance & Safety2 2%
By level
- Senior & Principal35 41%
- Associate & Specialist28 33%
- Manager16 19%
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QC Technician II at Thermo Fisher
Applications close November 12. $36K–$55K a year, employer provided.

