Senior Specialist Regulatory Affairs - Nutrition - Columbus, OH or Abbott Park,
Abbott Laboratories, Columbus, OH, United States
Senior Specialist Regulatory Affairs
Location: Columbus, OH.
Benefits and Compensation
Career development with an international company where you can grow the career you dream of.
Employees can qualify for free medical coverage in the next calendar year.
An excellent retirement savings plan with a high employer contribution.
Tuition reimbursement, student debt program, and education benefit – an affordable and convenient path to getting a bachelor’s degree.
Company recognized as a great place to work and as one of the best big companies to work for in terms of diversity, working mothers, female executives, and scientists.
The base pay for this position is $78,000.00 – $156,000.00. In specific locations, the pay range may vary from the range posted.
The Opportunity
Our location in Columbus, OH, currently has an opportunity for a Senior Specialist Regulatory Affairs.
Specialist professional individual contributor with comprehensive knowledge in the area of Regulatory Affairs. Ability to execute highly complex or specialized projects. Adapts precedent and may make significant departures from traditional approaches to develop solutions.
What You’ll Do
Act as the Senior Specialist in the Regulatory Affairs Sub‑Function, acting as a highly experienced and knowledgeable resource within the organization in directing the development of product registration submissions, progress reports, renewals, amendments, or periodic experience reports.
Interact with country affiliates to compile and prepare registration and submission documentation.
Serve as regulatory liaison throughout the product lifecycle.
Participate in product plan development and implementation, and regulatory strategy.
Serve as regulatory representative to marketing, research teams and regulatory agencies.
Manage and evaluate product changes by assessing change scope, regulatory impact and international submission requirements.
Maintain annual food facility licenses.
Maintain strong communication and working relationships across business functions, third‑party manufacturers, and suppliers.
Required Qualifications
Bachelor’s Degree Preferred in science (biology, chemistry, microbiology, food science)
Minimum 3 years’ experience in a regulated industry (e.g., medicinal products, nutritionals)
MISC:
This is an on‑site role – not a remote role.
Applicants from all geographic locations are encouraged to apply for internal employees.
There’s no relocation assistance available for this role.
Certification is a plus (e.g., RD (Registered Dietician)).
Sponsorship: we will not provide sponsorship of any kind for this role (including OPT).
Abbott is an Equal Opportunity Employer, committed to employee diversity.
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Location: Columbus, OH.
Benefits and Compensation
Career development with an international company where you can grow the career you dream of.
Employees can qualify for free medical coverage in the next calendar year.
An excellent retirement savings plan with a high employer contribution.
Tuition reimbursement, student debt program, and education benefit – an affordable and convenient path to getting a bachelor’s degree.
Company recognized as a great place to work and as one of the best big companies to work for in terms of diversity, working mothers, female executives, and scientists.
The base pay for this position is $78,000.00 – $156,000.00. In specific locations, the pay range may vary from the range posted.
The Opportunity
Our location in Columbus, OH, currently has an opportunity for a Senior Specialist Regulatory Affairs.
Specialist professional individual contributor with comprehensive knowledge in the area of Regulatory Affairs. Ability to execute highly complex or specialized projects. Adapts precedent and may make significant departures from traditional approaches to develop solutions.
What You’ll Do
Act as the Senior Specialist in the Regulatory Affairs Sub‑Function, acting as a highly experienced and knowledgeable resource within the organization in directing the development of product registration submissions, progress reports, renewals, amendments, or periodic experience reports.
Interact with country affiliates to compile and prepare registration and submission documentation.
Serve as regulatory liaison throughout the product lifecycle.
Participate in product plan development and implementation, and regulatory strategy.
Serve as regulatory representative to marketing, research teams and regulatory agencies.
Manage and evaluate product changes by assessing change scope, regulatory impact and international submission requirements.
Maintain annual food facility licenses.
Maintain strong communication and working relationships across business functions, third‑party manufacturers, and suppliers.
Required Qualifications
Bachelor’s Degree Preferred in science (biology, chemistry, microbiology, food science)
Minimum 3 years’ experience in a regulated industry (e.g., medicinal products, nutritionals)
MISC:
This is an on‑site role – not a remote role.
Applicants from all geographic locations are encouraged to apply for internal employees.
There’s no relocation assistance available for this role.
Certification is a plus (e.g., RD (Registered Dietician)).
Sponsorship: we will not provide sponsorship of any kind for this role (including OPT).
Abbott is an Equal Opportunity Employer, committed to employee diversity.
#J-18808-Ljbffr