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Regulatory Operations Associate Jobs in Alabama (NOW HIRING)

NC SECU

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

Ferguson Enterprises, LLC

Operations Manager

Arab, AL ยท On-site

$4.54K - $7.26K/mo

Our associates' growth and development are shown in the long tenure of our team. Ferguson ... Ferguson complies with all wage regulations. The starting wage may be higher in certain locations ...

HP Products

Operations Manager

Arab, AL

$4.54K - $7.26K/mo

Our associates' growth and development are shown in the long tenure of our team. Ferguson ... regulations and procedures set by the organization * Maintain documents according to record ...

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Regulatory Operations Associate information

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$10

$23

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How much do regulatory operations associate jobs pay per hour?

As of Jun 1, 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 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.

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 Regulatory Operations Associates?

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.

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:
Regulatory Operations Associate jobs near you
Operations Associate

Operations Associate

Career Personnel Services

Birmingham, AL

Contractor

Posted 4 days ago

Job description

Position Summary
We are seeking a Contract to Hire Cleanroom Operations Associate. The Cleanroom Operations Associate supports manufacturing operations in a regulated medical device environment. This role ensures product integrity, traceability, accurate documentation, and regulatory compliance while operating equipment, assembling products, and maintaining cleanroom standards.

Responsibilities

  • Perform routine cleaning, maintenance, and monitoring of cleanroom and controlled areas
  • Operate automated machinery, measurement tools, label printers, and related equipment
  • Assemble and package medical devices
  • Assist with shutdowns and operational events
  • Support engineering with troubleshooting and process improvements
  • Maintain product integrity and traceability through accurate documentation of Manufacturing Orders
  • Complete and maintain regulatory batch records
  • Follow Quality Management System (QMS) requirements
  • Maintain a safe work environment in a regulated setting
  • Assist with cleanroom inventory control

Requirements

  • Detail-oriented and able to follow structured procedures and work instructions
  • Able to work independently with minimal supervision
  • Proficient in Microsoft Office (Excel required)
  • Comfortable working in a cleanroom environment with required garments and PPE
  • High School Diploma or equivalent
  • 2+ years in production or manufacturing environment preferred
  • Medical device manufacturing experience preferred
  • Cleanroom experience preferred