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Fda Inspector Jobs in Pittsburgh, PA (NOW HIRING)

Supply Specialist

Pittsburgh, PA · On-site

$19.60 - $30.25/hr

Unload equipment, inspect verifies, accept or reject supplies and materials from delivery trucks ... The items can contain FDA legend medication under the supervision of the Director of Pharmacy. Will ...

Supply Specialist

Pittsburgh, PA · On-site

$19.60 - $30.25/hr

Unload equipment, inspect verifies, accept or reject supplies and materials from delivery trucks ... The items can contain FDA legend medication under the supervision of the Director of Pharmacy. Will ...

Supply Specialist

Pittsburgh, PA · On-site

$19.60 - $30.25/hr

The items can contain FDA legend medication under the supervision of the Director of Pharmacy. Will ... Unload equipment, inspect verifies, accept or reject supplies and materials from delivery trucks ...

Unload equipment, inspect verifies, accept or reject supplies and materials from delivery trucks ... The items can contain FDA legend medication under the supervision of the Director of Pharmacy. Will ...

Warehouse Lead (Friday-Sunday 7am-7pm)

Burgettstown, PA · On-site

$17.50 - $22.25/hr

Ensure facility is inspection ready at all times for SQFI, FDA, and customer needs. * Communicate and report any incidents to supervisor * Ensure product rotation procedures are followed. * Review ...

Warehouse Lead (9am-7pm Mon-Thur)

Burgettstown, PA · On-site

$17.50 - $22.25/hr

Ensure facility is inspection ready at all times for SQFI, FDA, and customer needs. * Communicate and report any incidents to supervisor * Ensure product rotation procedures are followed. * Review ...

Showing results 41-60

Fda Inspector information

See Pittsburgh, PA salary details

$23.8K

$53.3K

$96.1K

How much do fda inspector jobs pay per year?

As of Aug 22, 2026, the average yearly pay for fda inspector in Pittsburgh, PA is $53,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,400.00 and $61,600.00 per year, depending on experience, location, and employer.

What does an FDA inspector do?

An FDA Inspector is responsible for ensuring that companies comply with federal regulations related to food, drugs, medical devices, and other products overseen by the U.S. Food and Drug Administration. They conduct inspections, review records, collect samples, and assess manufacturing practices to ensure public health and safety. Inspectors may also investigate complaints, issue compliance notices, and recommend enforcement actions if violations are found.

What skills and qualifications are needed to be an FDA inspector?

To thrive as an FDA Inspector, you need a solid background in science or public health, attention to detail, and thorough knowledge of regulatory standards, often supported by a relevant degree. Familiarity with inspection protocols, laboratory testing equipment, and digital reporting systems is commonly required, along with potential USDA or FDA certifications. Strong analytical thinking, effective communication, and integrity are important soft skills for this role. These competencies ensure accurate inspections, compliance with safety regulations, and clear reporting essential to public health and organizational accountability.

What types of facilities or products do FDA inspectors review, and what does a typical inspection process involve?

FDA Inspectors routinely examine a variety of facilities, such as food processing plants, pharmaceutical manufacturers, medical device companies, and cosmetic production sites, to ensure compliance with federal safety and quality regulations. A typical inspection involves reviewing operational procedures, examining production environments, sampling products, and interviewing staff to identify potential violations or risks. Inspectors often work onsite, sometimes with travel required to cover multiple locations within their region, and collaborate closely with facility management to explain findings and recommend corrective actions. This role offers the opportunity to make a significant impact on public health and provides clear advancement pathways into specialized inspection or supervisory roles within regulatory agencies.

How do you become an FDA inspector?

To become an FDA inspector, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or food science, along with experience in food safety, pharmaceuticals, or related areas. They must pass a written exam and a background check, and often undergo specialized training at the FDA's training center. Certification or licensing is not required but can enhance prospects in the field.

What are popular job titles related to Fda Inspector jobs in Pittsburgh, PA?

For Fda Inspector jobs in Pittsburgh, PA, the most frequently searched job titles are:

What cities near Pittsburgh, PA are hiring for Fda Inspector jobs?

Cities near Pittsburgh, PA with the most Fda Inspector job openings:

Infographic showing various Fda Inspector job openings in Pittsburgh, PA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $53,336 per year, or $25.6 per hour.

Quality Control Laboratory Analyst (Raw Materials)

Krystal Biotech

Pittsburgh, PA • On-site

$23.25 - $31.25/hr

Full-time

Re-posted 22 days ago


Job description

About Krystal Bio: At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs.
Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient's end-to-end experience.
Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology.
Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values.
Position Overview:
Krystal Biotech, Inc is seeking a highly motivated Quality Control Analyst who will be responsible for in-house raw materials and product testing for the use in the manufacture of clinical and commercial drug products.
Primary Responsibilities:
  • Perform cGMP material inspection for all materials utilized for drug product manufacturing.
  • Perform cGMP material testing for all materials needed for further use in manufacturing process.
  • Review analytical data for compliance with regulations, methods and other specifications or criteria and collaborate with management when data does not meet acceptance criteria.
  • Participate in laboratory investigations, quality event investigations, protocol and report development.
  • Initiate and update quality control documentation, such as SOPs, material monographs (specification and testing documents), and test methods.
  • Support activities for Document Control and Record Retention.
  • Implementation of USP Quality Standards and verification of USP Methods.
  • Maintain equipment in the QC Lab by performing and coordinating equipment qualification, calibration, and preventive maintenance.
  • Other duties as assigned.
Requirements and Preferred Qualifications:
  • Bachelor's degree in life sciences or equivalent.
  • Experience with pH, Osmo, Endotoxin, Appearance, customized media, cell culture, and FBS testing, preferred.
  • Demonstrated experience in laboratory environment and ability to follow SOPs.
  • A demonstrated self-starter who is highly motivated and able to address changing priorities.
  • Ability to take a proactive approach on the job with the ability to work with a dynamic team.
  • Excellent scientific writing, other written and oral communication skills are required.
  • Proficient in Microsoft Word, Excel and PowerPoint.

Krystal Biotech, Inc. is an Equal Employment Opportunity and Affirmative Action Employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this Web site or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc. will not pay fees to any third-party agency or company that does not have a signed agreement with Krystal Biotech, Inc.