Regulatory Affairs Specialist
Milford, DE · On-site +1
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 ...
Milford, DE · On-site +1
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 ...
Milford, DE · On-site +1
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 ...
Milford, DE · On-site +1
Manages day to day activities for less senior Regulatory Affairs professionals, including but not limited to mentoring, coaching, performance reviews, developmental plans, succession planning.
Milford, DE · On-site +1
Manages day to day activities for less senior Regulatory Affairs professionals, including but not limited to mentoring, coaching, performance reviews, developmental plans, succession planning.
Wilmington, DE · On-site
$145.60K - $192.10K/yr
As Director of Promotional Regulatory Affairs, you will set the regulatory guardrails that enable confident brand execution and speed. You will partner closely with Medical, Legal, Commercial, and ...
Wilmington, DE · On-site
$145.60K - $192.10K/yr
As Director of Promotional Regulatory Affairs, you will set the regulatory guardrails that enable confident brand execution and speed. You will partner closely with Medical, Legal, Commercial, and ...
Job Summary (Primary function) The Associate Director, International Regulatory Affairs works in collaboration with International Regulatory Affairs Lead to develop regulatory strategies with multi ...
Job Summary (Primary function) The Associate Director, International Regulatory Affairs works in collaboration with International Regulatory Affairs Lead to develop regulatory strategies with multi ...
IFF is seeking an Associate Manager, Regulatory & Scientific Affairs to provide regulatory support across North America (United States and Canada) for the Health & Biosciences business unit, with a ...
IFF is seeking an Associate Manager, Regulatory & Scientific Affairs to provide regulatory support across North America (United States and Canada) for the Health & Biosciences business unit, with a ...
IFF is seeking an Associate Manager, Regulatory & Scientific Affairs to provide regulatory support across North America (United States and Canada) for the Health & Biosciences business unit, with a ...
IFF is seeking an Associate Manager, Regulatory & Scientific Affairs to provide regulatory support across North America (United States and Canada) for the Health & Biosciences business unit, with a ...
IFF is seeking an Associate Manager, Regulatory & Scientific Affairs to provide regulatory support across North America (United States and Canada) for the Health & Biosciences business unit, with a ...
IFF is seeking an Associate Manager, Regulatory & Scientific Affairs to provide regulatory support across North America (United States and Canada) for the Health & Biosciences business unit, with a ...
Millsboro, DE · Hybrid
$39/hr
Regulatory Affairs US Biologicals labeling specialist Minimum Education: Associate degree. Preferred Education: Bachelor/Master's degree in Life Science. Required Experience and Skills: • With ...
Millsboro, DE · Hybrid
$39/hr
Regulatory Affairs US Biologicals labeling specialist Minimum Education: Associate degree. Preferred Education: Bachelor/Master's degree in Life Science. Required Experience and Skills: • With ...
Millsboro, DE · Hybrid
$39/hr
Regulatory Affairs US Biologicals labeling specialist Minimum Education: Associate degree. Preferred Education: Bachelor/Master's degree in Life Science. Required Experience and Skills: • With ...
Millsboro, DE · Hybrid
$39/hr
Regulatory Affairs US Biologicals labeling specialist Minimum Education: Associate degree. Preferred Education: Bachelor/Master's degree in Life Science. Required Experience and Skills: • With ...
Wilmington, DE · Remote
$145.50K - $192.10K/yr
Stay current on a wide range of regulatory and policy issues, including K‐12, workforce ... Proven record of effective and successful government affairs and government relations work ...
Wilmington, DE · Remote
$145.50K - $192.10K/yr
Stay current on a wide range of regulatory and policy issues, including K‐12, workforce ... Proven record of effective and successful government affairs and government relations work ...
Wilmington, DE · On-site
$145.50K - $192.10K/yr
A leading global education technology firm is seeking a Senior Director, State Government Affairs, based anywhere in the U.S. The ideal candidate will promote and protect company interests and lead ...
Wilmington, DE · On-site
$145.50K - $192.10K/yr
A leading global education technology firm is seeking a Senior Director, State Government Affairs, based anywhere in the U.S. The ideal candidate will promote and protect company interests and lead ...
Newark, DE · On-site +1
$22/hr
... Regulatory Affairs, Science and Strategy team by managing documentation activities for third-party product registrations. This role reports to the Global Regulatory Documentation Manager.
Newark, DE · On-site +1
$22/hr
... Regulatory Affairs, Science and Strategy team by managing documentation activities for third-party product registrations. This role reports to the Global Regulatory Documentation Manager.
Dover, DE · On-site +1
$160K - $210K/yr
Senior Manager, Government & Industry Affairs Operations VGW is an interactive entertainment ... The ability to read complex regulatory, legislative, or legal materials and translate the practical ...
Quick apply
Dover, DE · On-site +1
$160K - $210K/yr
Senior Manager, Government & Industry Affairs Operations VGW is an interactive entertainment ... The ability to read complex regulatory, legislative, or legal materials and translate the practical ...
... Development, Clinical Operations, Regulatory Affairs, Biostatistics, and Drug Safety ... Pharmacovigilance Department, Sales Training). * Participate in the design, conduct, analysis, and ...
... Development, Clinical Operations, Regulatory Affairs, Biostatistics, and Drug Safety ... Pharmacovigilance Department, Sales Training). * Participate in the design, conduct, analysis, and ...
Newark, DE · On-site
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 ...
Newark, DE · On-site
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 ...
They will lead legislative and regulatory engagement; manage contract lobbyists where appropriate ... Government Affairs * Serves as the company's primary representative at the assigned state capitols ...
They will lead legislative and regulatory engagement; manage contract lobbyists where appropriate ... Government Affairs * Serves as the company's primary representative at the assigned state capitols ...
Wilmington, DE · Remote
Lead cross-functional teams across Clinical Operations, Regulatory Affairs, Data Management, Biostatistics, Medical Affairs, Pharmacovigilance, and QA. * Act as the primary liaison with clients ...
Wilmington, DE · Remote
Lead cross-functional teams across Clinical Operations, Regulatory Affairs, Data Management, Biostatistics, Medical Affairs, Pharmacovigilance, and QA. * Act as the primary liaison with clients ...
Lead the development and execution of medical affairs strategy to support successful product launch ensuring alignment with commercial, clinical development, regulatory teams and internal ...
Lead the development and execution of medical affairs strategy to support successful product launch ensuring alignment with commercial, clinical development, regulatory teams and internal ...
The US State Government Affairs Lead is one of the most consequential roles in our US business ... Carries enterprise-wide responsibility for all state legislative and regulatory strategy across all ...
The US State Government Affairs Lead is one of the most consequential roles in our US business ... Carries enterprise-wide responsibility for all state legislative and regulatory strategy across all ...
$19.01 - $22.97
3% of jobs
$22.97 - $26.92
6% of jobs
$26.92 - $30.88
13% of jobs
$31.40 is the 25th percentile. Wages below this are outliers.
$30.88 - $34.84
20% of jobs
The median wage is $36.38 / hr.
$34.84 - $38.80
19% of jobs
$38.80 - $42.76
9% of jobs
$44.74 is the 75th percentile. Wages above this are outliers.
$42.76 - $46.72
10% of jobs
$46.72 - $50.68
6% of jobs
$50.68 - $54.64
5% of jobs
$54.64 - $58.60
5% of jobs
$58.60 - $62.55
3% of jobs
$19
$39
$62
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.
| Aspect | Regulatory Affairs | Quality Assurance |
|---|---|---|
| Primary Focus | Ensuring compliance with regulations and submitting documentation to authorities | Maintaining product quality and implementing quality systems |
| Required Credentials | Degree in life sciences, regulatory certifications often preferred | Degree in sciences or engineering, quality management certifications |
| Work Environment | Regulatory agencies, corporate compliance teams | Manufacturing plants, quality departments |
| Industry Usage | Pharmaceuticals, biotech, medical devices | Pharmaceuticals, 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.
Other
Posted 7 days ago
6.2
Based on 9 frontline employees who took The Breakroom Quiz
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:
Education:
Years and Type of Experience:
Required Computer / Software Skills:
Key Required Skills, Knowledge, and Capabilities:
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.