Regulatory Affairs Director jobs in Poughkeepsie, NY

Regulatory Affairs Director oversees regulatory matters and executes the strategy to ensure the organization complies with applicable regulations. Develops processes and systems to ensure that all necessary licensing, filings, certifications, and permits are processed and monitored. Being a Regulatory Affairs Director establishes monitoring policies and procedures to ensure compliance with existing regulations. Anticipates new or changing regulations and coordinates with internal stakeholders to develop strategies to address changes in product, operations, or testing requirements. Additionally, Regulatory Affairs Director investigates and addresses any reported issues of non-compliance. Requires a bachelor's degree. Typically reports to a director. The Regulatory Affairs Director typically manages through subordinate managers and professionals in larger groups of moderate complexity. Provides input to strategic decisions that affect the functional area of responsibility. May give input into developing the budget. To be a Regulatory Affairs Director typically requires 3+ years of managerial experience. Capable of resolving escalated issues arising from operations and requiring coordination with other departments. (Copyright 2024 Salary.com)

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Regulatory Affairs Specialist II – Diabetes Care (on-site)
  • 1024 Abbott Diabetes Care Sales Corporation
  • Amenia, NY FULL_TIME
  • Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. JOB DESCRIPTION: Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of. Free medical coverage for employees* via the Health Investment Plan (HIP) PPO An excellent retirement savings plan with high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree. A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. The Opportunity This Regulatory Affairs Specialist II position will work on-site out of our Austin, TX location in the Abbott Diabetes Care Division. This role supports change control for manufacturing/operations activities as well as provides regulatory direction on cross functional projects. This new team member will apply basic regulatory understanding to support products and teams and will prepare U.S. regulatory submissions and/or registration documents for international affiliates and government agencies worldwide. This individual contributor will handle regulatory activities involved in ensuring quality of documentation to support a variety of product and process changes, with a particular focus on those relating to the manufacturing environment. Additionally, will apply regulatory and technical knowledge to a focused area of work assignments. This new hire will understand, implement, and maintain the quality policy, along with ensuring compliance to and demonstrating knowledge of site and division level policies and procedures. What You’ll Work On Verifies with supervisory staff and executes regulatory deliverables in relation to product development, submissions, product maintenance, and project plans. Implements Division Regulatory Strategy as they apply to specific product related activities. Leverage basic understanding of laws and regulations to ensure compliance. Obtains supervisory input for interpretation of regulations leading to the solution of issues, and to product development and support. Analyzes the input of cumulative product changes to current product submissions. Shares knowledge with others in department and on cross functional teams. Provides solutions to a variety of problems where analysis requires moderate degree of evaluation. Prepares and aligns impact goals with department goals. Establishes and executes against project goals and implements plans. Provides input to establishing group plans and implementation of those plans. Follows GMP guidelines and procedures. Writes Effectively: Prepares written information in a clear and concise fashion, appropriately designed for varying target audiences. Responsible for implementing and maintaining the effectiveness of the quality system. For products division-wide: Advises and communicates to project, group, or venture regarding basic regulatory strategies. Signs-off at team level within delegated parameters for change control. Release authority for labeling materials. Official correspondence with outside regulatory agencies as guided by supervisory staff. Conducts basic negotiations on routine product related issues with government agencies. Follows through on submission related activities to secure product approval/clearance. Directs own daily activities in alignment with team goals and division regulatory priorities. Provides support to Regulatory Affairs management when working towards resolution of compliance issues, assuring these resolutions comply with site and division level policies and procedures and are aligned with the appropriate quality system. Obtains supervisory regulatory review on submission documents prior to submission to government agencies. Interface with Abbott’s third party manufacturing partners and suppliers to ensure efficient collaboration and compliant resolution of issues. Required Qualifications Bachelor’s Degree or an equivalent combination of education and experience Preferred Qualifications Bachelor’s degree in a technical discipline such as biology, chemistry, microbiology, immunology, medical technology, etc. 1-2 years of regulatory experience. Effectively communicate, prepare, and negotiate both internally and externally with various regulatory agencies. Communicate effectively verbally and in writing. Able to follow scientific arguments, identify regulatory scientific data needs and solve regulatory issues. Think analytically with good problem-solving skills. 510(k), PMA, or other international regulatory submission experience. RAPS Certification. Apply Now * Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $64,000.00 – $128,000.00 In specific locations, the pay range may vary from the range posted. JOB FAMILY: Regulatory Operations DIVISION: ADC Diabetes Care LOCATION: United States > Texas > Austin : 12501B Research Boulevard ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Yes, 5 % of the Time MEDICAL SURVEILLANCE: No SIGNIFICANT WORK ACTIVITIES: Awkward/forceful/repetitive (arms above shoulder, bent wrists), Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans. EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf Abbott is about the power of health. For more than 135 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions — across the spectrum of health, around the world, for all stages of life. Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health. The people of Abbott come to work each day with relentless energy, enthusiasm and a promise to enhance the health and well-being of millions of people. They push the boundaries to help manage and treat some of life’s greatest health challenges. We invite you to explore opportunities at Abbott, to see if your talents and career aspirations may fit with our openings. An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce. Follow Us: Facebook LinkedIn YouTube Twitter
  • 2 Days Ago

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Regulatory Affairs Specialist II – Diabetes Care
  • 1024 Abbott Diabetes Care Sales Corporation
  • Amenia, NY FULL_TIME
  • Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and ...
  • 26 Days Ago

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Maintenance Supervisor 4
  • Military and Naval Affairs, Division of
  • Newburgh, NY FULL_TIME
  • This position is not in the Classified Service of New York State, but is covered under New York State Military Law. If selected, current Civil Service employees will lose their seniority within the Cl...
  • 21 Days Ago

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TEMPORARY SEASONAL - Maintenance Helper - Kingston FMS - Anticipated duration of employment thru 4/26/23
  • Military and Naval Affairs, Division of
  • Kingston, NY TEMPORARY
  • This position is not in the Classified Service of New York State, but is covered under New York State Military Law. If selected, current Civil Service employees will lose their seniority within the Cl...
  • 1 Day Ago

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Airport Firefighter 2
  • Military and Naval Affairs, Division of
  • Newburgh, NY FULL_TIME
  • THIS PROMOTION OPPORTUNITY IS OPEN ONLY TO QUALIFIED PERMANENT EMPLOYEES OF THE DIVISION OF MILITARY AND NAVAL AFFAIRS This position is not in the Classified Service of New York State, but is covered ...
  • 22 Days Ago

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Psychologist-Outpatient
  • Department of Veteran's Affairs
  • Wappingers Falls, NY FULL_TIME
  • Please apply by copy/pasting to your browser the below link, which will take you directly to the position on USA Jobs. If you do not apply using the links, your application WILL NOT be considered. htt...
  • 10 Days Ago

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0 Regulatory Affairs Director jobs found in Poughkeepsie, NY area

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Executive Director, US Regulatory Affairs CREA (CNS, Retinopathies & Emerging Areas) Product Group
  • Boehringer Ingelheim
  • Ridgefield, CT
  • Description The Executive Director of the US Regulatory Affairs CREA Product Group serves on the US Regulatory Leadershi...
  • 4/24/2024 12:00:00 AM

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Trauma Operations Coordinator
  • Nuvance Health
  • Danbury, CT
  • Nuvance Health has a network of convenient hospital and outpatient locations - Danbury Hospital, New Milford Hospital, N...
  • 4/22/2024 12:00:00 AM

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Associate Director Market Research
  • eTeam
  • Ridgefield, CT
  • Job title: Associate Director Market Research Competitive Intelligence Duration: 6+ months Location: Ridgefield, CT (Rem...
  • 4/22/2024 12:00:00 AM

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Associate Director Market Research
  • TalentBurst, an Inc 5000 company
  • Ridgefield, CT
  • Minimum Requirement of 10 years working within a large product marketing corporation specifically in the role of market ...
  • 4/22/2024 12:00:00 AM

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Program Director
  • ADAPT of the Hudson Valley
  • Middletown, NY
  • Summary of Position: Responsible for oversight of several group homes. Participates in development and writes plans of s...
  • 4/20/2024 12:00:00 AM

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Section Manager 3L - OR Customer Meter Operations
  • ConEdison
  • Middletown, NY
  • Section Manager 3L - OR Customer Meter Operations Job Info 112141 Posting Expiration Date:May 4, 2024 Schedule Type:Full...
  • 4/20/2024 12:00:00 AM

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Program Director
  • Adapt Of The Hudson Valley
  • Middletown, NY
  • Summary of Position: Responsible for oversight of several group homes. Participates in development and writes plans of s...
  • 4/20/2024 12:00:00 AM

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Associate Director Market Research
  • Talentburst An Inc 5000 Company
  • Ridgefield, CT
  • Minimum Requirement of 10 years working within a large product marketing corporation specifically in the role of market ...
  • 4/20/2024 12:00:00 AM

Poughkeepsie (/pəˈkɪpsi/ pə-KIP-see), officially the City of Poughkeepsie, is a city in the state of New York, United States, which is the county seat of Dutchess County. As of the 2010 census it had a population of 32,736. Poughkeepsie is in the Hudson Valley midway between New York City and Albany, and is part of the New York metropolitan area. The name derives from a word in the Wappinger language, roughly U-puku-ipi-sing, meaning "the reed-covered lodge by the little-water place", referring to a spring or stream feeding into the Hudson River south of the present downtown area. Poughkeepsie...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Regulatory Affairs Director jobs
$181,027 to $257,825
Poughkeepsie, New York area prices
were up 1.5% from a year ago

Regulatory Affairs Director in Spartanburg, SC
There can be no guarantees with respect to pipeline products that the products will receive the necessary regulatory approvals or that they will prove to be commercially successful.
December 13, 2019
Regulatory Affairs Director in New Brunswick, NJ
The apprenticeship programme lasts 30 months and provides a combination of Masters-level training in regulatory affairs and paid work experience.
February 12, 2020
Regulatory Affairs Director in Syracuse, NY
They often advise project teams on subjects such as premarket regulatory requirements, export and labeling requirements, or clinical study compliance issues.
January 18, 2020