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Regulatory Operations Associate Jobs in Alabama (NOW HIRING)

The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution ... Works across business units and regional RA operations teams to harmonize key processes, escalate ...

... branch operations. Associate MSOs perform routine branch duties and follow standard branch ... and regulatory requirements. Ensure all member information remains confidential and members ...

... branch operations. Associate MSOs perform routine branch duties and follow standard branch ... and regulatory requirements. Ensure all member information remains confidential and members ...

... branch operations. Associate MSRs perform routine branch duties and follow standard branch ... and regulatory requirements. Ensure all member information remains confidential, and members ...

Operations Supervisor - Distribution

AL ยท On-site

$62K - $70K/yr

Your leadership will be vital in guiding our frontline associates, fostering a safe and productive ... Take proactive measures to consistently uphold compliance with health and safety regulations ...

Your leadership will be vital in guiding our frontline associates, fostering a safe and productive ... Take proactive measures to consistently uphold compliance with health and safety regulations ...

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Regulatory Operations Associate information

See Alabama salary details

$10

$23

$48

How much do regulatory operations associate jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for regulatory operations associate in Alabama is $23.79, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $27.45 per hour, depending on experience, location, and employer.

What is a regulatory operations associate?

Regulatory Operations Associates are professionals who support the preparation, submission, and management of documents required by regulatory agencies for product approvals, especially in industries like pharmaceuticals, biotechnology, and medical devices. They ensure that submissions comply with legal and regulatory standards, track submission timelines, and often use specialized software for document management. Their work is crucial for maintaining compliance and facilitating smooth communication between their company and regulatory authorities. Additionally, Regulatory Operations Associates may coordinate with cross-functional teams to gather necessary documentation and maintain up-to-date records.

How does a regulatory operations associate typically collaborate with cross-functional teams within an organization?

Regulatory Operations Associates frequently work alongside regulatory affairs, quality assurance, clinical, and legal teams to ensure that all submissions and documentation comply with industry standards and governmental regulations. They coordinate the collection, formatting, and timely submission of regulatory documents, often acting as a liaison between departments to resolve any discrepancies or gather necessary information. Effective communication and organization are key, as the role requires balancing multiple deadlines and adapting to evolving requirements set by regulatory authorities.

What are the key skills and qualifications needed to thrive as a regulatory operations associate, and why are they important?

To excel as a Regulatory Operations Associate, you generally need a background in life sciences or a related field, strong attention to detail, and experience with regulatory documentation processes. Familiarity with electronic document management systems (EDMS), eCTD publishing tools, and knowledge of regulatory submission standards are typically required. Excellent organizational skills, communication, and the ability to manage multiple deadlines help candidates stand out. These competencies ensure accurate, timely regulatory submissions and compliance, which are critical for product approvals and organizational success.

What is the difference between Regulatory Operations Associate vs Regulatory Affairs Specialist?

AspectRegulatory Operations AssociateRegulatory Affairs Specialist
Required CredentialsBachelor's degree, familiarity with regulatory processesBachelor's degree, often with certifications in regulatory affairs
Work EnvironmentSupportive regulatory teams, administrative tasksStrategic planning, compliance management
Employer & Industry UsagePharmaceutical, biotech, healthcare companiesPharmaceutical, medical device, biotech sectors
Common Search & ComparisonYesNo

The Regulatory Operations Associate typically handles administrative and operational support within regulatory teams, focusing on document management and submission processes. In contrast, the Regulatory Affairs Specialist is more involved in strategic compliance, ensuring products meet regulatory standards. Both roles are essential in regulated industries like pharma and biotech, but they differ in scope and responsibilities.

What are the most commonly searched types of Regulatory Operations jobs in Alabama?

The most popular types of Regulatory Operations jobs in Alabama are:

What are popular job titles related to Regulatory Operations Associate jobs in Alabama?

For Regulatory Operations Associate jobs in Alabama, the most frequently searched job titles are:

What job categories do people searching Regulatory Operations Associate jobs in Alabama look for?

The top searched job categories for Regulatory Operations Associate jobs in Alabama are:

What cities in Alabama are hiring for Regulatory Operations Associate jobs?

Cities in Alabama with the most Regulatory Operations Associate job openings:

Infographic showing various Regulatory Operations Associate job openings in Alabama as of August 2026, with employment types broken down into 89% Full Time, 9% Part Time, 1% Temporary, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $49,478 per year, or $23.8 per hour.

Operations Associate - CleanPac

Hoover, AL โ€ข On-site

BIOHORIZONS IMPLANT SYSTEMS
201 - 500 employees

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 14 days ago


Job description

*************************Work Schedule: Monday - Thursday 10 hr. days*************************

The Operations Associate will support proper cleanroom operations, policies, procedures, and work instructions. This role must maintain and ensure Regulatory Compliance in every work task. This position is primarily responsible for ensuring product integrity, traceability and proper labeling and packaging through the accurate documentation of each aspect of their job function. Tasks may include operating automated machinery, product assembly, preventative maintenance, and cleanroom monitoring. Other duties may develop over time based on business needs and availability. 

Essential Duties and Responsibilities:

  • Perform routine cleaning, maintenance, and monitoring of cleanroom and controlled area operations.
  • Operate process equipment, such as automated machinery, measurement tools, label printers, etc.
  • Perform assembly and packaging of medical devices.
  • Maintain product integrity and traceability through proper documentation of Manufacturing Orders.  
  • Perform and be actively engaged in shutdowns, and other events that adversely affect operational status.
  • Assist engineering team in troubleshooting efforts and other tasks that affect operations.
  • Maintain a Safe work environment and adherence to regulated products in a regulated environment. 
  • Adhere to the Quality Management System and support all quality initiatives.
  • Maintain regulatory batch records as required for each operational task and assigned equipment.
  • Assist in cleanroom inventory control as necessary. 

Qualifications:

  • Must be detail oriented, able to follow directions and adhere to work instructions and procedures in a structured work environment.
  • Ability to complete tasks independently without constant supervision.
  • Experience with Microsoft Office Suite Required including Excel. 
  • Must be able to work in a cleanroom environment utilizing required garments and PPE.

Education:

  • High School Diploma and/or combination of experience.
  • Minimum 2 years’ experience in a production or shop environment is preferred.
  • Medical Device manufacturing preferred.
  • Cleanroom manufacturing experience preferred.

Benefits:

  • 2 comprehensive medical plan options to choose from available the first of each month following your date of hire
  • Flexible Spending Account or HSA Account available
  • Vision Benefits
  • Company paid Dental Insurance for employee and dependents
  • Wellness Plan
  • 401k with 5% matching
  • Generous PTO plan including 11 paid holidays, 2 Floating Holidays and Community Service Hours
  • Company paid Short Term Disability
  • Long Term Disability
  • Company provided Life Insurance
  • Paid Parental Leave
  • Casual Dress Code
  • Social events for employees and family

 

 

Henry Schein, Inc.  is an Equal Employment Opportunity Employer and does not discriminate against applicants or employees on the basis of race, color, religion, creed, national origin, ancestry, disability that can be reasonably accommodated without undue hardship, sex, sexual orientation, gender identity, age, citizenship, marital or veteran status, or any other legally protected status.

 

Please note that any offer of employment made by BioHorizons is contingent upon the successful completion of a pre-employment background investigation to include a pre-employment drug screen.