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Regulatory Operations Associate Jobs in Rosedale, MD

Driver Associate Full-Time | Branch $15.00 - $28.84 / hr Hourly Pay Range Reports To: Branch ... regulations. CORE RESPONSIBILITIES Delivery & Route Operations * Prepare truck for operation by ...

Ensure compliance and maintenance of standards of overseeing regulatory agencies (AZA, APHIS/USDA ... operations * Coordinate animal acquisitions and dispositions, including record transfer and pre ...

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Regulatory Operations Associate information

See Rosedale, MD salary details

$10

$25

$51

How much do regulatory operations associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for regulatory operations associate in Rosedale, MD is $25.17, according to ZipRecruiter salary data. Most workers in this role earn between $17.07 and $29.04 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 cities near Rosedale, MD are hiring for Regulatory Operations Associate jobs?

Cities near Rosedale, MD with the most Regulatory Operations Associate job openings:

Infographic showing various Regulatory Operations Associate job openings in Rosedale, MD as of August 2026, with employment types broken down into 88% Full Time, 10% Part Time, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $52,357 per year, or $25.2 per hour.

Night Shift Supervisor Mfg. Operations (4PM-4AM)

Becton Dickinson

Hunt Valley, MD • On-site

Full-time

Re-posted 1 hour ago


BD rating

7.3

Company rating: 7.3 out of 10

Based on 143 frontline employees who took The Breakroom Quiz

314th of 495 rated machine equipment manufacturers


Job description

Company Description
Job Description
Be part of something bigger!BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.Responsibilities and Duties:Manages day to day manufacturing activities to ensure goals are accomplished and communication occurs within the group and across all functions/shifts. This includes providing leadership in day to day manufacturing operation activity, employee career development, and overall coaching support to the manufacturing team. Will also be responsible for the control of all material flows, manufacturing operations, and the supervision of the various teams.Identifies, troubleshoots, and resolves complex issues associated with manufacturing operations.Provides training to associates including on-boarding and/or new procedures.Leads continuous improvement recommendations and/or solutions to support overall operational efficiency.Leads and/or provides support on special projectsProvides coaching to associates on day-to-day activities and performanceResponsible for assigning and distributing workloadsDemonstrates the ability to follow established procedures according to Good Manufacturing Practices (GMP).Must follow all BD housekeeping, safety, policies and proceduresQualificationsMinimum Experience/Education:Bachelor's degree with 1 year experience manufacturing experience in Food, Pharma and Industrial production settings. Must have experience working in a regulated environment (FDA).Associate's degree with 5 years manufacturing experience in Food, Pharma and Industrial production settings. Must have experience working in a regulated environment (FDA).High school degree with 10 years manufacturing experience in Food, Pharma and Industrial production settings. Must have experience working in a regulated environment (FDA). Minimum 2 years team lead experience.Excellent interpersonal and communication skills and the ability to seek and accept feedback from others. Strong conflict resolution skills and the ability to share knowledge with others. Knowledge of regulatory requirements, process validations, safe work practices, and ISO 9000 requirements.Excellent organizational and communication skills. Must be capable of sharing knowledge and developing associates. Ability to work with all levels of personnel from company president to production associates. Ability to plan at a high level, but execute at the detail level. Understanding of SAP (PP/PE) preferred.Shift: ROTATING 12 HOUR WORK DAY (4PM- 4AM) (2 on, 2 off, 3 on, 2 off)For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.Why join us?A career at BD means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our associates can fulfill their life's purpose through the work that they do every day.You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth, and life balance components - is designed to support the varying needs of our diverse and global associates.To learn more about BD visit https://jobs.bd.com/Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.PDN
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About BD

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BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

Industry

Medical equipment and supplies manufacturing and manufacturing

Company size

10,000+ Employees

Headquarters location

Franklin Lakes, NJ, US

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