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From Home Fda Compliance Jobs (NOW HIRING)

Harlan Bakeries LLC

Compliance Coordinator II

Avon, IN · On-site

Overview The Compliance Coordinator II is responsible for document compliance with FDA regulations ... Job Requirements * Associates or bachelor's degree from an accredited college or university ...

Aerotek

Clean Room Operator

Twinsburg, OH

$18.50/hr

Follow Good Manufacturing Practice (GMP) guidelines and FDA-compliance procedures at all times ... Team members benefit from a supportive culture that celebrates successes through holiday luncheons ...

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SharkNinja

Compliance Engineer

Needham, MA · On-site

The candidate will support certification projects from product concept to mass production, ensuring ... FDA-regulated medical devices and products subject to EU MDR 2017/745. Assist in preparing ...

Restaurant Company

Warehouse Supervisor

Union City, CA · On-site

$75K - $80K/yr

... of materials -- from the development of forecasted replenishment needs to the delivery of the ... Working knowledge of USDA & FDA compliance Company Description Warehouse Distribution/ Logistics

SharkNinja

Compliance Engineer

Needham, MA · On-site

... lives in homes around the world. Powered by two trusted, global brands, Shark and Ninja , the ... The candidate will support certification projects from product concept to mass production, ensuring ...

Gehl Foods LLC

Process Engineer

Germantown, WI · On-site

Lead capital projects from concept through commissioning, including equipment validation (IQ/OQ/PQ) and FDA compliance. * Support new product development, process design, and commercialization ...

Certified Group

FDA Sampling Supervisor

Melville, NY · On-site

Schedule and coordinate all FDA sample collection activities from public warehouses, client ... Training & Compliance * Maintain training records and qualification requirements for all FDA ...

Shehadey Family Foods LLC

SQF Coordinator

Fairfield, CA · On-site

$30 - $33/hr

... SQF and FDA compliance, and continual monitoring of production for compliance * Assist the QA ... Request and review documents from vendors/suppliers * Maintain document control * Review food ...

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Senior Regulatory Affairs Specialist -FDA Medical, Cosmetics, Dietary Supplements

Wacker Chemie AG

Ann Arbor, MI • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 25 days ago

Job description

Job Title: Senior Regulatory Affairs Specialist -FDA Medical, Cosmetics, Dietary Supplements
Job Location (Short): Ann Arbor, MI, USA, 48108
Posting Start Date: 6/19/26
Do you want to take responsibility and make a difference with your work? With your expertise, we can achieve great goals together. We are WACKER - Reliable. Determined. Ambitious. As one of the world's most research-intensive chemical companies, we've been making countless products that are an integral part of your everyday life possible for over 100 years. From vegan food to resource-efficient buildings to solar cells, we develop sustainable solutions that change the future.
To strengthen our team in Ann Arbor,
we are looking for you as a(n) Senior Regulatory Affairs Specialist -FDA Medical, Cosmetics, Dietary Supplements.
Senior Regulatory Affairs Specialist-FDA Medical
  • Responsible for managing Wacker Chemical Corporation's corporate compliance program for Medical and Drug applications per the requirements of the 21 CFR regulations
  • Responsible for refining Wacker's corporate procedures and strategy regarding FDA compliance toward medical device components, drugs, ad healthcare applications.
  • Evaluates and responds to incoming internal and external customer product compliance requests and will review and access the chemical composition of Wacker product formulas and incoming raw material chemicals used in medical device, drug, and healthcare applications such as wound care
  • Prepars and submits forms and applications for Wacker FDA Drug and Device Master Files. Prepare portions of Drug Master File (DMF) packages, establishing project work as needed with outside consultation and preparing and submitting Medical Device Master File (MAF) packages and updates.
  • Experience in Natural Health Products, as well as in the process for filing new drug ingredient notifications and the technical data required by the agency, even if the customer is doing the actual filing.
  • Awareness of drug facility registration requirements would be useful. For medical devices, working knowledge of biocompatibility testing (USP Class VI & ISO 10993) and their applicability to different types of products.
  • Recognition of the differences between US and Canadian regulations. Familiarity with Canadian Medical Device regulations, Drug regulations, and Cosmetic regulations and serving as the liaison between Wacker and our Canadian Regulatory Agent
  • Work with other departments to ensure compliance to Good Manufacturing (GMP), FDA-CFR, ISO, Responsible Care standards and regulations.
  • Will interpret FDA regulations and utilizing government and 3rd party databases such as the FDA Electronic Submission Gateway (ESG). Familiarity with appropriate FDA cGMP or other applicable guidance such as the USP Good Manufacturing Processes for Bulk Pharmaceutical Excipients and FDA Active Pharmaceutical Ingredient (API) regulatory approval process.

Requirements:
  • Bachelor of Science Degree in Biology, Chemistry, Toxicology, or Pharmacology. Master's Degree is preferred.
  • 7+ years of experience preferred.
  • Strong organizational and professional skills with extensive knowledge of FDA regulations and reading and interpreting legal documents.
  • Knowledge and experience in 21 CFR regulations on Drugs (API, OTC, Excipient), Veterinary products, Medical Devices, and products which can cross categories, like transdermal patches.
  • Strong leadership, interpersonal and problem-solving skills.
  • Experience working in cross-functional teams.
  • Experience working with leadership and team members to ensure a safety, quality and environmentally conscience culture.
  • Experience in polymer chemistry is preferred.

What do we offer?
WACKER is an equal opportunity employer committed to diversity, equity, inclusion, and sustainability. We are innovators, researchers, and pioneers and we believe that our individual differences are our collective strength. We foster an inclusive environment that promotes individuality, celebrates diversity, and builds cohesive teams. Together, we create exceptional value for our employees, our customers, and our communities by creating a culture of inclusion and equity that enables, empowers, and values our diverse contributions.
WACKER strives to reward its employees in a fair and equitable manner. Our Total Rewards Package considers employee wellbeing and is comprised of compensation, benefits, work-life balance, performance & recognition, and career development.
  • Compensation and Incentive plans
  • Medical, Dental, and Vision Insurance effective day 1
  • Paid Time Off in addition to personal days and holidays
  • Paid parental leave
  • Wellbeing fund
  • Flexible hybrid work arrangements
  • 401(k) with company match
  • Education Assistance Program
  • Career development and advancement opportunities
  • Support for Community Involvement

We are looking forward to your online application at www.wacker.com.
Reference Code: 31073
#LI-LGI
The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job.
A minimum requirement for this US-based position is the ability to work legally in the United States on a permanent unrestricted basis. Visa sponsorship is not available for this position, including for any type of US permanent residency (e.g., for a green card).
WACKER is proud to be an Equal Opportunity/Affirmative Action Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class.

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