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Regulatory Affairs Jobs in Delaware (NOW HIRING)

Perform account reconciliations. Assist in the preparation of reports for Regulatory Affairs. Assist in preparation of depreciation studies. Respond to data requests from Regulatory Commissions, the ...

Supports distribution operations in regulatory affairs and facility design. Evaluates, plans, and designs major construction projects. Secures regulatory approvals to complete project installations.

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Regulatory Affairs information

See Delaware salary details

$19

$39

$62

How much do regulatory affairs jobs pay per hour?

As of May 28, 2026, the average hourly pay for regulatory affairs in Delaware is $39.60, according to ZipRecruiter salary data. Most workers in this role earn between $31.78 and $46.92 per hour, depending on experience, location, and employer.

What Is Regulatory Affairs?

Regulatory affairs employees focus on meeting local, national, and international requirements for products. These jobs are particularly common in food, cosmetics, and companies that produce medicine or medical devices. With a position in regulatory affairs, you may be asked to ensure a medicine meets all safety regulations, prepare documents for submission to regulators, monitor translators to ensure the accurate translation of materials as needed, and ensure that records and reports are submitted in line with inspection standards. Regulatory affairs employees also provide support for currently-marketed products and may work with engineering drawings, technical files, or design history files to note required changes.

What are the key skills and qualifications needed to thrive as a Regulatory Affairs professional, and why are they important?

To thrive as a Regulatory Affairs professional, you need a strong understanding of regulatory guidelines, compliance standards, and scientific or technical documentation, often supported by a degree in life sciences, pharmacy, or a related field. Familiarity with regulatory submission systems, document management tools, and certifications like RAC (Regulatory Affairs Certification) are commonly required. Excellent attention to detail, project management, and effective communication skills help professionals navigate complex regulations and collaborate with cross-functional teams. These competencies ensure timely product approvals, minimize compliance risks, and facilitate successful market access for products.

What are some typical challenges faced by professionals in Regulatory Affairs, and how can they be managed?

Regulatory Affairs professionals often navigate complex and ever-changing regulations across different regions, which can be challenging when managing multiple submissions or product lines. Staying up-to-date with regulatory updates and effectively communicating requirements to cross-functional teams is essential. Building strong relationships with regulatory agencies and leveraging robust internal processes can help streamline submissions and respond quickly to compliance issues. Proactive planning and regular professional development are key strategies for managing these challenges successfully.

What are Regulatory Affairs?

Regulatory Affairs is a field focused on ensuring that companies comply with all of the regulations and laws pertaining to their business, particularly in industries such as pharmaceuticals, biotechnology, medical devices, and food. Professionals in Regulatory Affairs help guide products through the approval process by preparing and submitting required documentation to regulatory agencies like the FDA or EMA. They also monitor changes in regulations, advise on compliance strategies, and help organizations maintain market access for their products. This role is crucial for minimizing legal risks and ensuring the safety and efficacy of products.

What is the difference between Regulatory Affairs vs Quality Assurance?

AspectRegulatory AffairsQuality Assurance
Primary FocusEnsuring compliance with regulations and submitting documentation to authoritiesMaintaining product quality and implementing quality systems
Required CredentialsDegree in life sciences, regulatory certifications often preferredDegree in sciences or engineering, quality management certifications
Work EnvironmentRegulatory agencies, corporate compliance teamsManufacturing plants, quality departments
Industry UsagePharmaceuticals, biotech, medical devicesPharmaceuticals, manufacturing, medical devices

While Regulatory Affairs focuses on navigating regulatory requirements and submissions, Quality Assurance emphasizes maintaining product quality standards. Both roles are essential in ensuring products meet industry and legal standards, often collaborating closely within regulated industries.

What are the most commonly searched types of Regulatory Affairs jobs in Delaware? The most popular types of Regulatory Affairs jobs in Delaware are:
What are popular job titles related to Regulatory Affairs jobs in Delaware? For Regulatory Affairs jobs in Delaware, the most frequently searched job titles are:
What cities in Delaware are hiring for Regulatory Affairs jobs? Cities in Delaware with the most Regulatory Affairs job openings:
Regulatory Affairs Specialist

Regulatory Affairs Specialist

Dentsply Sirona, Inc

Milford, DE • On-site, Remote

Other

Posted 7 days ago


Dentsply Sirona rating

6.2

Company rating: 6.2 out of 10

Based on 9 frontline employees who took The Breakroom Quiz


Job description

Requistion ID: 83371 

 

Dentsply Sirona is the world's largest manufacturer of professional dental products and technologies, with over a century of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands.

Dentsply Sirona's products provide innovative, high-quality, and effective solutions to advance patient care and deliver better and safer dental care. Dentsply Sirona's headquarter is located in Charlotte, North Carolina. The company's shares are listed in the United States on NASDAQ under the symbol XRAY. Visit www.dentsplysirona.com for more information about Dentsply Sirona and its products.

Summary:

We are seeking an experienced and highly motivated Regulatory Affairs Specialist who will be a contributing member of a cross-functional team in support of regulatory market access activities for US, Canada, EU, and other countries.

This postion can be located in one of the following DS facilities: Sarasota, FL; Charlotte, NC; Johnson City, TN; Milford, DE; York, PA; Waltham, MA

Key Responsibilities:

  • Prepares and submits international regulatory submissions to obtain and maintain regulatory approvals for medical devices, including 510(k) submissions and technical files for CE Marking
  • Maintains regulatory files and databases to ensure compliance with regulatory requirements
  • Reviews and interprets regulatory requirements and guidance documents to ensure compliance  
  • Coordinates regulatory activities with internal teams and external regulatory agencies
  • Supports regulatory audits and inspections as SME for questions related to market access
  • Stays current with regulatory requirements and updates affecting medical devices
  • Fosters professional interactions with internal and external stakeholders through various communication channels, enhancing business relationships
  • Complies with company and departmental policies and administrative requirements
  • Performs other duties as assigned or as needed

Education:

  • Bachelor's degree in a relevant field, such as life sciences, regulatory affairs, or a related discipline

Years and Type of Experience:

  • 1-5 years of experience in regulatory affairs, preferably in the medical device industry
  • Experience with regulatory submissions and documentation, including 510(k) submissions and CE marking
  • Knowledge of FDA regulations and international standards (e.g., ISO 13485, MDSAP, EU MDR)

 

Required Computer / Software Skills:

  • Proficiency with Microsoft Office Suite
  • Proficiency with Regulatory software

 

Key Required Skills, Knowledge, and Capabilities:

  • Strong attention to detail and organizational skills
  • Excellent communication (both written and verbal) and interpersonal skills
  • Ability to work effectively in a team environment
  • Knowledge of regulatory affairs principles and practices
  • Ability to critically review detailed scientific information and assess whether technical arguments are presented clearly, and conclusions are adequately supported
  • Willingness to learn and adapt to new processes and technologies
  • Regulatory registration experience within med device organizations
  • Prior technical writing experience and proven track record with FDA and EU regulatory submissions preferred

Equal Opportunity Employer: Dentsply Sirona is an Equal Opportunity Employer. All qualified applicants will be considered without unlawful discrimination or regard for race, color, religion, sex, sexual orientation, sexual or gender identity, national or ethnic origin, age, marital status, disability, genetic factors, military and veteran status, or any other characteristics protected by applicable local law.

Eligibility: All successful applicants must be eligible to work in the country the position is based.

Assistance: If you need assistance with completing the online application due to a disability, please send an accommodation request to accommodationrequest@dentsplysirona.com.

Agencies: Please note that Dentsply Sirona does not accept or respond to unsolicited requests or applications submitted by Recruitment Agencies/ Search Firms.

Notice on Fraudulent Job Offers: Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following information: careers.dentsplysirona.com.