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Gmp Quality Control Jobs in Rochester, NY (NOW HIRING)

Manufacturing Supervisor A Shift

Rochester, NY · On-site

$59K - $81K/yr

Maintains a management presence in the productionareas through the monitoring and control of ... GMP Audit Programs. Will halt process and immediately notify QA and Manager of any concerns for ...

Custodian II

Rochester, NY · On-site

$16 - $18/hr

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through ...

Facilities Manager

Rochester, NY · On-site

$85K - $90K/yr

Ensure OSHA, NEC, GMP, Lockout/Tagout, and safety compliance. * Manage vendors, budgets ... Establish high standards for maintenance quality, urgency, accountability, and equipment care.

Assemble custom electrical and mechanical control panels using stock components and detailed job ... Test, inspect, and verify electrified assemblies to ensure proper functionality and quality ...

Assemble and wire electrical systems, motors, and control panels according to schematics and ... Completed accurate testing documentation, maintained quality standards, and supported additional ...

Showing results 21-40

Gmp Quality Control information

See Rochester, NY salary details

$11

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$32

How much do gmp quality control jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for gmp quality control in Rochester, NY is $21.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.07 and $23.70 per hour, depending on experience, location, and employer.

Is GMP quality control inspection a good career?

GMP quality control inspection is a stable career in the pharmaceutical and biotech industries, focusing on ensuring products meet regulatory standards. It often requires attention to detail, knowledge of Good Manufacturing Practices, and certifications such as GMP training. The role offers opportunities for advancement and consistent employment in regulated environments.

What is the role of quality control in GMP?

In GMP, quality control (QC) is responsible for testing and verifying raw materials, in-process samples, and finished products to ensure they meet specified quality standards. QC helps prevent contaminated or substandard products from reaching consumers and maintains compliance with regulatory requirements through proper documentation and testing procedures.

What is the difference between Gmp Quality Control vs Gmp Quality Assurance?

AspectGmp Quality ControlGmp Quality Assurance
Primary FocusTesting and inspecting products to ensure compliance with standardsDeveloping and maintaining quality systems and processes
ResponsibilitiesSampling, testing, and documenting product qualityAuditing, process validation, and quality system oversight
CertificationsGMP training, laboratory skillsGMP knowledge, quality management system training
Work EnvironmentLaboratories, manufacturing sitesQuality departments, compliance offices

Gmp Quality Control focuses on testing products to verify they meet quality standards, while Gmp Quality Assurance involves establishing and maintaining systems to prevent defects. Both roles are essential in ensuring product safety and compliance in the pharmaceutical and biotech industries.

Is GMP Quality Control a good career?

GMP Quality Control is a vital role in the pharmaceutical and biotech industries, focusing on ensuring products meet regulatory standards through testing and documentation. It often requires attention to detail, knowledge of Good Manufacturing Practices, and certifications such as GMP training. The career offers stability, opportunities for advancement, and the chance to work in regulated environments that prioritize quality and safety.
What cities near Rochester, NY are hiring for Gmp Quality Control jobs? Cities near Rochester, NY with the most Gmp Quality Control job openings:
Infographic showing various Gmp Quality Control job openings in Rochester, NY as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $44,073 per year, or $21.2 per hour.

Manufacturing Supervisor - 2nd shift

Thermo Fisher Scientific

Rochester, NY • On-site

$59K - $81K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 days ago


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 422 frontline employees who took The Breakroom Quiz

196th of 537 rated manufacturers


Job description

Work Schedule
Second Shift (Afternoons)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
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 day by enabling 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 take science a step beyond. Together, we develop solutions for some of the world's toughest challenges-from protecting the environment and ensuring food safety to advancing life-saving therapies and helping find cures for cancer.
Position Summary
Thermo Fisher Scientific is seeking a Manufacturing Supervisor to lead day-to-day manufacturing operations while driving excellence in safety, quality, delivery, and cost performance. In this role, you will lead, coach, and develop a team of approximately 10-20 manufacturing operators within a GMP-regulated environment.
The Manufacturing Supervisor plays a critical role in fostering a culture of operational excellence and continuous improvement through Lean and Practical Process Improvement (PPI) methodologies. This is an opportunity to make a meaningful impact by supporting the production of life-changing products while growing your leadership career with a global industry leader.
Key Responsibilities
  • Lead daily manufacturing operations to achieve safety, quality, delivery, and cost objectives.
  • Supervise, coach, and develop a team of 10-20 manufacturing operators to drive engagement and performance.
  • Promote a culture of continuous improvement using Lean and PPI methodologies to improve productivity, quality, and customer satisfaction.
  • Oversee production planning, scheduling, and workflow optimization to ensure efficient operations.
  • Analyze operational data and performance metrics to identify opportunities for process improvements.
  • Ensure compliance with GMP, ISO, quality systems, SOPs, and applicable regulatory requirements.
  • Lead manufacturing investigations, CAPAs, and change control activities.
  • Implement and sustain standard work, 5S, and other Lean manufacturing practices.
  • Partner cross-functionally with Quality, Engineering, Supply Chain, and other teams to resolve issues, drive improvements, and build consensus.
  • Support manufacturing floor activities and cleanroom operations as needed.
Minimum Qualifications
  • Advanced degree with 3+ years of manufacturing operations experience, or Bachelor's degree with 5+ years of manufacturing operations experience, including 2+ years in a leadership role.
  • Experience in a GMP, ISO, or other regulated manufacturing environment.
  • Experience leading and developing high-performing teams.
  • Strong understanding of Lean manufacturing and continuous improvement methodologies.
  • Expertise in production planning, scheduling, and workflow optimization.
  • Ability to analyze data and metrics to drive process improvements.
  • Experience with quality systems, SOPs, and regulatory compliance.
  • Proficiency with ERP systems and Microsoft Office Suite.
  • Excellent verbal and written communication skills.
  • Strong analytical and problem-solving abilities.
  • Flexibility to work varying shifts and schedules as business needs require.
  • Physical ability to perform manufacturing floor activities and work in cleanroom environments.
  • Experience leading investigations, CAPAs, and change control processes.
  • Ability to collaborate effectively across functions and build consensus.
  • Experience implementing standard work and 5S practices.
Preferred Qualifications
  • Bachelor's or advanced degree in Engineering, Science, Business, or a related field.
  • Lean and/or Six Sigma certification.

Compensation and Benefits
The salary range estimated for this position based in New York is $68,200.00-$95,000.00.
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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