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Fda Jobs in Michigan (NOW HIRING)

Medical Device Assembly

Wixom, MI ยท On-site

$16 - $17/hr

Document production activities, lot traceability, and quality records per FDA and ISO regulations * Identify and report non-conforming materials or process deviations to supervisors * Maintain a ...

Medical Device Assembly

Wixom, MI ยท On-site

$16 - $17/hr

Document production activities, lot traceability, and quality records per FDA and ISO regulations * Identify and report non-conforming materials or process deviations to supervisors * Maintain a ...

Medical Device Assembly

Wixom, MI ยท On-site

$16 - $17/hr

Document production activities, lot traceability, and quality records per FDA and ISO regulations * Identify and report non-conforming materials or process deviations to supervisors * Maintain a ...

Lab Technician

Novi, MI ยท On-site

$17.75 - $23.75/hr

Maintain NCIMS/FDA certifications.Ability to follow good lab practices.Detail oriented, organized, ability to multitask, and manages time well.Perform and maintain quality control testing records.

Delivery Driver - Medical Equipment

Big Rapids, MI ยท On-site

$15 - $18.50/hr

Maintain cleanliness and organization of delivery vehicle and warehouse, adhering to all FDA protocols * Work on-call rotation during evening and weekend hours to address any patient medical ...

Maintain cleanliness and organization of delivery vehicle and warehouse, adhering to all FDA protocols * Work on-call rotation during evening and weekend hours to address any patient medical ...

Maintain cleanliness and organization of delivery vehicle and warehouse, adhering to all FDA protocols * Work on-call rotation during evening and weekend hours to address any patient medical ...

Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...

Be Seen First

The technology originated from mitochondrial biology research at Wayne State University and the University of Michigan and has progressed through an active FDA Investigational Device Exemption (IDE ...

Showing results 21-40

Fda information

What does an FDA professional do?

An FDA professional works for the U.S. Food and Drug Administration, a federal agency responsible for protecting public health by ensuring the safety and efficacy of drugs, medical devices, food, cosmetics, and other products. Their roles can include reviewing and approving new drugs and medical devices, conducting inspections, enforcing regulations, and providing guidance to industries. FDA professionals may also work in research, policy development, and public outreach to ensure that products meet regulatory standards and are safe for consumer use.

What are the key skills and qualifications needed to thrive as an FDA Regulatory Affairs Specialist, and why are they important?

To thrive as an FDA Regulatory Affairs Specialist, you need a strong background in life sciences, regulatory guidelines, and compliance, usually supported by a relevant degree such as pharmacy, biology, or chemistry. Familiarity with regulatory submission systems, FDA regulations (such as 21 CFR), and certifications like RAC (Regulatory Affairs Certification) are highly beneficial. Attention to detail, strong analytical thinking, and effective communication skills help professionals navigate complex regulations and collaborate with cross-functional teams. These competencies ensure that products meet legal requirements and safety standards, facilitating successful approvals and market access.

What are some typical challenges faced by professionals working at the FDA, and how can they be managed?

Professionals at the FDA often navigate complex regulatory requirements, tight deadlines, and the need to balance public health priorities with industry innovation. Collaborating across multidisciplinary teams and staying updated on evolving scientific data are essential parts of the role. Adapting to frequent changes in policy and handling high volumes of submissions can be demanding, but leveraging strong communication skills and seeking mentorship within the agency can help manage these challenges effectively.

What is the difference between Fda vs Food Scientist?

AspectFdaFood Scientist
Required CredentialsTypically a degree in health, science, or related field; certifications varyBachelor's or master's in food science, microbiology, or related
Work EnvironmentRegulatory agencies, laboratories, inspection sitesFood manufacturing facilities, laboratories, research settings
Employer & Industry UsageU.S. Food and Drug Administration, government agenciesFood companies, research institutions, government agencies
Common Search & Comparison IntentUnderstanding regulatory roles, compliance, and enforcementFood safety, product development, research

While both Fda professionals and Food Scientists work within the food industry, Fda roles focus on regulation, compliance, and enforcement of food safety laws, often within government agencies. Food Scientists primarily engage in research, product development, and ensuring food quality in manufacturing settings. The two careers overlap in food safety knowledge but differ in their primary responsibilities and work environments.

What qualifications do you need to work for the Food and Drug Administration?

To work for the Food and Drug Administration (FDA), candidates typically need a bachelor's degree in a relevant field such as science, engineering, or public health. For certain positions, advanced degrees or specialized certifications may be required, along with relevant work experience and knowledge of regulatory processes and compliance standards.

What are the most commonly searched types of Fda jobs in Michigan?

The most popular types of Fda jobs in Michigan are:

What cities in Michigan are hiring for Fda jobs?

Cities in Michigan with the most Fda job openings:

Infographic showing various Fda job openings in Michigan as of August 2026, with employment types broken down into 93% Full Time, 5% Part Time, and 2% Contract. Highlights an 100% In-person job distribution.

Biopharmaceutical Inspector - 3rd shift (Entry Level)

Grand River Aseptic Manufacturing, Inc.

Grand Rapids, MI โ€ข On-site

$20/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 4 days ago


Job description

Description

Agility, Impact, Methodology. Do you exhibit these values and wish to be around others that do too? Do you thrive in fast-paced environments where agility, adaptability, and high standards go hand in hand? Are you driven to make a meaningful impact, whether through your work, your support of others, or your commitment to your community? Are you motivated by a disciplined, science-based approach that ensures consistent excellence, safety, and integrity in everything you do? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day!ย 


Overview of this Position:

As a Biopharmaceutical Inspector you'll play a crucial role in ensuring the quality and compliance of our products. You'll be responsible for visual inspections of our sterile liquid medication, along with some labeling, and packaging of products according to established procedures and cGMP regulations under the oversight of the FDA. With guidance from experienced technicians and supervisors, you'll help uphold our high standards and contribute to the success of our Finishing department.ย 


Non-Negotiable Requirements:

  • High School Diploma/GED
  • Proficiency in Microsoft Word, Excel, and Outlook
  • Ability to pass a vision screening and Visual Inspection Qualification testing (can wear glasses/contacts)

Preferred Requirements:

  • Associate degree or equivalent
  • Familiarity with QA principles and procedures in a pharma, biopharma, or biotech manufacturing environment
  • Knowledgeable about GMP standardsย 
  • Experience in an FDA-regulated environmentย 
  • Previous experience in pharmaceutical inspection OR packaging with a solid understanding of cGMP and FDA guidelines.

Responsibilities Include (but are not limited to):

  • Inspection along with some, labeling and package finished products (sterile liquid medicine)
  • Operate Finishing equipment
  • Adhere to finishing procedures and PDA guidelines
  • Accurately document data and complete any corresponding paperwork
  • Contribute to maintaining an FDA-compliant facility

Full job description available during formal interview process.


What Sets GRAM Apart from Other Employers:

MEDICAL BENEFITS starting day 1: Blue Cross Blue Shield medical and dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying for 75% of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well.ย 

Paid VOLUNTEERISM starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year!

PTO: Full-time employees accrue up to 17 days of time off per calendar year. You choose how to use this time for your vacation, sick, or mental health needs!

WELLNESS TIME OFF: We offer all employees one (1) paid day of Wellness Time Off (WTO) per quarter to invest in self-care, take some downtime, or whatever you choose.

PAID HOLIDAYS: We offer 10 paid holidays per calendar year with immediate eligibility!ย 

PAY: Depends on Experience and is discussed during the interview process. Shift differential available for second and third shift!

If you meet the required criteria listed above, GRAM welcomes you to apply today!