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Fda Inspector Jobs in Grand Rapids, MI (NOW HIRING)

... FDA, USDA) and industry standards. Facilitate the GFSI audit at each facility. * Assure that QA/QC ... Conduct regular audits and inspections of the production process, raw materials, and finished ...

Coach, train, and mentor QA Technicians in inspection procedures, documentation accuracy, and GMP ... Support preparation and execution of customer, regulatory (FDA), and third-party (SQF/BRC) audits.

The environment emphasizes adherence to cGMP standards, FDA and ICH requirements, and internal quality procedures, with a strong focus on inspection readiness, audit support, and continuous ...

Help with audits and inspections (internal, customer, or regulatory) * Participate in cross ... Exposure to regulatory and customer requirements (e.g., FDA, USDA, SQF, BRC) * Root cause analysis ...

Help with audits and inspections (internal, customer, or regulatory) * Participate in cross ... Exposure to regulatory and customer requirements (e.g., FDA, USDA, SQF, BRC) * Root cause analysis ...

Technician, Quality

Walker, MI · On-site

$17.25 - $23.25/hr

Programs and operates automated inspection equipment. Prepares shipping documentation ... Knowledge and experience with FDA and ISO Quality Systems to include SPC and calibrations systems.

Technician, Quality

Walker, MI · On-site

$17.25 - $23.25/hr

Programs and operates automated inspection equipment. Prepares shipping documentation ... Knowledge and experience with FDA and ISO Quality Systems to include SPC and calibrations systems.

Quality Engineer

Grand Rapids, MI · On-site

$69K - $89K/yr

Understanding and experience in AQL inspection, control plans and interpretation of spec and ... Exposure to the FDA, medical device or medical manufacturing is a strong plus. * Experience in ...

Quality Engineer

Grand Rapids, MI · On-site

$69K - $89K/yr

Understanding and experience in AQL inspection, control plans and interpretation of spec and ... Exposure to the FDA, medical device or medical manufacturing is a strong plus. * Experience in ...

Ensure compliance with all regulatory requirements, including FDA, USDA (if applicable), and third ... Oversee product quality testing, inspections, and release processes * Monitor key quality metrics ...

Showing results 21-40

Fda Inspector information

See Grand Rapids, MI salary details

$23.5K

$52.8K

$95.1K

How much do fda inspector jobs pay per year?

As of Sep 4, 2026, the average yearly pay for fda inspector in Grand Rapids, MI is $52,765.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,000.00 and $61,000.00 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 job categories do people searching Fda Inspector jobs in Grand Rapids, MI look for?

The top searched job categories for Fda Inspector jobs in Grand Rapids, MI are:

Infographic showing various Fda Inspector job openings in Grand Rapids, MI as of August 2026, with employment types broken down into 87% Full Time, 10% Part Time, 2% Contract, and 1% Nights. Highlights an 97% Physical, and 3% Remote job distribution, with an average salary of $52,765 per year, or $25.4 per hour.

Sr. Quality Compliance Manager

Hearthside Food Solutions LLC

Kentwood, MI • On-site

Full-time

Re-posted 11 hours ago


Key responsibilities

  • Ensure sites are audit-ready and support QAMs during inspections and visits.

  • Oversee and ensure the timely execution of validation programs, audit programs, and compliance responses.

  • Lead or support site audits, non-conformance investigations, and drive CAPA completion.


Hearthside Food Solutions rating

5.9

Company rating: 5.9 out of 10

Based on 34 frontline employees who took The Breakroom Quiz

351st of 443 rated food and drinks producers


Job description

Job Summary:
The Senior Quality Compliance Manager is a strategic leadership role responsible for driving and sustaining compliance across multiple USDA- and FDA-regulated facilities. This position ensures designated sites consistently meet regulatory, customer, and corporate requirements through oversight of audit readiness, validation programs, compliance responses, and continuous improvement efforts. The role supports and collaborates with local QAMs, provides training, and acts as a key resource during high-profile visits or regulatory inspections.
Job Duties:
Duties may include, but are not limited to the following:
  • Ensure defined sites are audit-ready at all times, supporting QAMs in managing internal, customer, third-party, and regulatory inspections (USDA-FSIS, FDA).
  • Act as site liaison during regulatory or high-level customer visits in the absence of the QAM, supporting Regional QAMs or Directors as needed.
  • Ensure timely and complete execution of validation programs, including allergen validations, oven validations, SOP/SSOP validations, and annual Food Safety Plan reviews.
  • Ensure site management is following internal audit program, and monitor and track performance, escalate violations or when program is not in compliance.
  • Monitor allergen controls to ensure sites maintain a state of allergen readiness, with validated procedures, updated records, and compliant practices.
  • Support the development, review, and update of SOPs, SSOPs, HACCP, and Food Safety Plans in coordination with site as part of annual validation and improvement cycles.
  • Lead or support site audits, non-conformance investigations, and drive CAPA completion and effectiveness verification.
  • Ensure all compliance responses (internal, customer, or regulatory) are completed on time, and assist with drafting, reviewing, and submitting responses to ensure accuracy and alignment.
  • SQF Program management, including executing gap assessments, tracking and trending compliance.
  • Track training compliance and escalate gaps on critical job specific compliance gaps, such as CCP certifications training needs.
  • Issue and communicate updates related to policies, procedures, and regulatory changes, ensuring sites implement them effectively through training and documentation.
  • Partner with Procurement and Corporate QA on supplier compliance, ingredient risk evaluations, and resolution of supplier non-conformances.
  • Foster and support Food Safety Culture, providing ongoing compliance training and coaching to QA teams and broader plant personnel.
  • Understanding of Environmental program management and how Non conformances are tracked.
  • Customer Complaint Management across multiple sites
  • Execute and manage meetings to show progress.
  • Lead site management base trainings, such as CAPA training for managers.
  • Other duties as assigned by RQAM, FSQA Director or QA VP.

Required Competencies & Knowledge:
Knowledge of:
  • Makers Pride procurement, products and production processes.
  • Knowledge and experience with SAP, Master Data, Trace Gain, Alchemy a plus!
  • Microsoft Knowledge a must (Outlook, Word, Excel etc.)

Skilled in:
  • Demonstrated proficiency in advanced quality statistics, measurement systems analysis
  • and continuous improvement required.
  • Strong understanding of SQF/BRC and its implementation is required.
  • Experience w/ Quality systems and knowledge of pre-requisite programs required.
  • Knowledge of Customer Expectation management, including audit preparation and
  • program management.
  • Maintaining harmonious relationships and effectively communicating with all customers, suppliers, local, site and corporate-wide MP employees.

Ability to:
  • Strong written and verbal communication skills, analytical ability, leadership strength and ability to effectively work with all levels of the organization.
  • Strong self-starter and can work with minimal direction.

Proficiency in: MS Office Suite, Excel, Power Point (SAP, Trace Gain a plus)
Certifications:
  • HACCP Certified (USDA-compliant) (Must unless has PCQI Certificate)
  • PCQI (Preventive Controls Qualified Individual) (Must unless has HACCP Certificate)
  • SQF Practitioner or BRC Internal Auditor (preferred)

Work Environment:
  • Work is primarily done in an office setting.
  • Infrequent production environment exposure, which includes noise, dust, moving machinery, fork lifts and fluctuations in temperature.
  • Travel up to +30%

Physical Requirements:
  • Sitting at a work station for extended periods of time.
  • Stand, walk and climb stairs on an infrequent basis.
  • Must be able to lift 25 pounds on an infrequent basis.

Minimum Qualifications:
  • Bachelor's degree in business/science-related field is preferred but will consider years of experience; post-graduate degree a plus.
  • Five (5) - Seven (7) years of related work experience, including experience managing and leading a Quality and food safety / sanitation staff in a related food manufacturing environment (i.e., baked bar, granola manufacture, bread, cold form bar, cookies, crackers, RTE etc).
  • Dual site FDA and USDA Experience preferred.
  • American Society for Quality Certification, such as CQE, CQM status is a plus.
  • Must be detailed-oriented, have strong self-confidence and leadership skills and have excellent oral and written communication skills.
  • Must be able to uphold Makers Pride's mission, vision and values on a daily basis.

Maker's Pride is an Equal Opportunity Employer.

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