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Full Time Fda Inspector Jobs in Rochester, NY (NOW HIRING)

Full Time Fda Inspector information

See Rochester, NY salary details

$24.2K

$54.2K

$97.7K

How much do full time fda inspector jobs pay per year?

As of Jun 5, 2026, the average yearly pay for full time fda inspector in Rochester, NY is $54,207.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,000.00 and $62,700.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Full Time FDA Inspector, and why are they important?

To thrive as a Full Time FDA Inspector, you typically need a background in life sciences or a related field, strong analytical abilities, and knowledge of regulatory standards, often supported by a relevant bachelor's degree. Familiarity with inspection software, laboratory equipment, and FDA regulations, such as 21 CFR, is essential. Exceptional attention to detail, critical thinking, and effective communication skills help inspectors conduct thorough evaluations and collaborate with regulated entities. These skills ensure compliance with federal regulations, safeguarding public health and ensuring industry accountability.

What are some common challenges faced by Full Time FDA Inspectors during facility inspections?

Full Time FDA Inspectors often encounter challenges such as navigating complex manufacturing environments, ensuring compliance with evolving regulations, and effectively communicating findings to facility staff. Inspectors must balance thoroughness with efficiency, sometimes facing resistance or misunderstanding from inspected parties. Additionally, staying current on new product types and technologies can require ongoing training and adaptability, making collaboration with colleagues and subject matter experts essential.

What does a Full Time FDA Inspector do?

A Full Time FDA Inspector is responsible for ensuring that products regulated by the Food and Drug Administration (FDA)—such as food, drugs, medical devices, and cosmetics—comply with all applicable laws and regulations. They conduct inspections of manufacturing facilities, review processes for safety and quality, collect samples for laboratory analysis, and document their findings. Their work helps protect public health by identifying and addressing potential risks before products reach consumers.

What is the difference between Full Time Fda Inspector vs Part Time Fda Inspector?

AspectFull Time Fda InspectorPart Time Fda Inspector
CredentialsTypically requires a bachelor's degree in life sciences or related field, plus FDA inspector certificationSame as full-time, but may have more flexible certification requirements
Work EnvironmentFull-time, on-site inspections at manufacturing facilities, laboratories, and warehousesPart-time, often involves scheduled inspections or follow-ups
Employer & Industry UsageFDA, government agencies, regulated industriesFDA, contractors, or consulting firms

Full Time Fda Inspectors work primarily on-site, conducting regular inspections and ensuring compliance with FDA regulations. Part Time Fda Inspectors perform inspections on a flexible schedule, often supplementing full-time staff. Both roles require similar credentials but differ mainly in hours and scope of work.

What job categories do people searching Full Time Fda Inspector jobs in Rochester, NY look for? The top searched job categories for Full Time Fda Inspector jobs in Rochester, NY are:
Infographic showing various Full Time Fda Inspector job openings in Rochester, NY as of May 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $54,207 per year, or $26.1 per hour.
Manufacturing Associate III-ONSITE Job Fair-6/3/26-MULTIPLE OPENINGS! (EG)

Manufacturing Associate III-ONSITE Job Fair-6/3/26-MULTIPLE OPENINGS! (EG)

Bausch + Lomb

Rochester, NY • On-site

Full-time, Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 24 days ago


Bausch & Lomb rating

8.4

Company rating: 8.4 out of 10

Based on 37 frontline employees who took The Breakroom Quiz

49th of 515 rated manufacturers


Job description

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 every phase of life. Our mission is simple, yet powerful: helping you see better, to live better.
Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing, and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.
Experienced Manufacturing Talent Wanted!
Join Bausch + Lomb for an onsite job fair on Wednesday, June 3rd from 12:00 p.m. to 4:00 p.m. at 1400 North Goodman Street, Rochester, NY !
Hire type: Full-Time
Our team of Manufacturing Associates is growing, and we have openings available for people who've worked in manufacturing for at least 2 years. You'll be helping us make contact lenses and other eye-care products that people count on every day.
Work Schedule:
  • Day and Night Shifts available: 6:00 am - 6:00 pm and 6:00 pm - 6:00 am following a 2-2-3 schedule with built-in overtime and days off; Night Shift differential: $1.25/hr.

Here's what we're looking for:
  • At least 2 years of experience in a manufacturing environment
  • Experience in a regulated industry (like medical devices) is helpful, but not a must
  • You're comfortable using computers and can pick up new systems easily
  • You care about doing quality work, paying attention to detail, and keeping things running smoothly

Not sure if you check every box? That's okay, if you have a mix of the right experience, training, or certifications, we would still love to hear from you!
What to Expect:
• On-the-spot interviews
• Competitive compensation & benefits
• A chance to join a growing company setting the standard in eye health worldwide
This position is made for you if you love solving problems, the night shift fits your lifestyle, and being a part of a global vision care company interests you!
Ready to take the next step? Apply now!
Objective: Safely Operate highly automated and technical equipment and machines in all phases of the contact lens manufacturing process in accordance with all standard operating procedures and cGMP/FDA regulations and requirements.
Key Activities:
  • Safely operate highly automated and technical contact lens manufacturing equipment from multiple equipment vendors in all phases of the contact lens manufacturing process. May be responsible for any part of the manufacturing process including the manufacturing of the contact lens, packaging and inspection, in-process lens inspection and audit, sterilization etc.
  • Ensure work is performed in accordance with all established work instructions, SOP's, and procedures. May provide written input to the continuous improvement of procedures for troubleshooting and operation.
  • Independently identify, diagnose, correct, and document process trends, faults and problems. Utilize complex and detailed troubleshooting procedures to determine the best course of action for maximizing reliability of complex automation.
  • Responsible for proper communication of troubleshooting activities.
  • Perform in process quality inspections utilizing inspection tools, including visual inspection, to assess product quality.
  • Ensure all quality procedures are followed. Understand and accurately complete documentation to ensure compliant quality records.
  • Escalate issues to Team Leader/Group Leader, maintenance, or engineer. As needed, interface directly with support personnel regarding operational and technical issues.
  • Ensure compliance with established quality standards, test schedules maintenance schedules, and production schedules.
  • Provide feedback to Team Leader/Group Leader for daily production reports (shift logs) to include shift performance, shift accomplishments, and ongoing issues. As needed, responsible for coordinating the creation of shift logs, writing, and distributing.
  • Responsible for reviewing production reports and shift logs for understanding of process events that occur outside of assigned work hours.
  • As needed, perform corrective and preventative maintenance of equipment in cooperation with the plant maintenance team and other shifts.
  • Work independently as well as in a team environment. Support, encourage, and participate in team related activities (production meetings, in-service training, shift crossover, etc.).
  • Responsible for sharing job knowledge and helping train new and existing team members on manufacturing processes and safety protocols to ensure consistent quality and operational excellence.
  • Participate actively in cross-training initiatives across multiple production areas to enhance team flexibility and support continuous workflow improvement
  • Follow all safety procedures and practices.

Qualifications & Experience:
  • High school diploma or equivalent required. Associates degree or technical certifications in related field (electrical, mechanical, engineering preferred.
  • Minimum of 2 or more years related manufacturing experience. Equivalent combination of education, technical certifications/trainings, and experience will be considered.
  • Demonstrated understanding of troubleshooting.
  • Basic math skills including addition, subtraction.
  • Basic computer skills and willingness to learn new applications and programs.
  • Shift flexibility and the ability to work overtime.

We offer competitive salary & excellent benefits including:
  • Medical, Dental, Eye Health, Disability and Life Insurance begins on your hire date.
  • 401K Plan with company match and ongoing company contribution.
  • Paid time off - vacation (3 weeks - prorated upon hire), floating holidays and sick time.
  • Employee Stock Purchase Plan with company match.
  • Employee Incentive Bonus.
  • Tuition Reimbursement (select degrees).
  • Ongoing performance feedback and annual compensation review.

As required by New York State's pay transparency bill, Bausch + Lomb provides a good faith minimum and maximum salary range of compensation for roles that can or will be performed, in New York State. Actual compensation is influenced by a wide array of factors including but not limited to skill set, level of experience, and specific office location. For New York State, the range of starting hourly pay for this role is $18.00 - $24.00 per hour.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.
To learn more please read Bausch+Lomb's Job Offer Fraud Statement.
Our Benefit Programs: https://www.bausch.com/careers/benefits/
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

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About Bausch & Lomb

Sourced by ZipRecruiter

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 every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our nearly 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 12,500 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Bridgewater, NJ, US

Year founded

1853