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Regulatory and Scientific Affairs Manager Jobs

1,104 Jobs

  • 3.9
    QSpex Technologies – Alpharetta, GA
    $56k-$86k(Glassdoor est.)
    NEW
    Description Position Title: Manager, Quality Policy & RegulatoryAffairs Reports To: President & CEO Department… : Responsible for leading the Quality Policy and RegulatoryAffairs efforts within the organization. Incumbent will be responsible…
  • 3.5
    Vertex Pharmaceuticals – Boston, MA
    $89k-$123k(Glassdoor est.)
    11 days ago 11d
    pharmaceutical or biotech industry experience 3+ years of regulatoryaffairs CMC experience (or relevant experience), preferably in… and ambiguous situations, understanding the scientific principles and regulatory requirements. In-depth knowledge of cGMP, FDA…
  • 3.5
    Vertex Pharmaceuticals – Boston, MA
    $76k-$106k(Glassdoor est.)
    11 days ago 11d
    pharmaceutical or biotech industry experience 5+ years of regulatoryaffairs CMC experience (or relevant experience), preferably in… and ambiguous situations, understanding the scientific principles and regulatory requirements. In-depth knowledge of cGMP, FDA…
  • 3.0
    AlloSource – Centennial, CO
    $61k-$93k(Glassdoor est.)
    17 days ago 17d
    management of internal audits, regulatory audits, supplier audits). Bachelor’s degree RegulatoryAffairs Certification (RAC)… direct experience in all aspects of Quality Systems and RegulatoryAffairs, and indirect experience with related business functions…
  • 3.6
    Bausch & Lomb – Bridgewater, NJ
    $94k-$137k(Glassdoor est.)
    4 days ago 4d
    hope it will become. The RegulatoryAffairs – CMC Manager independently manages all regulatory CMC aspects of Valeant’s Pharmaceuticals… Provide regulatory support to other Valeant functions during Regulatory Authority inspections. Serve as RegulatoryAffairs representative…
  • 4.6
    EO Products – San Rafael, CA
    EASY APPLY
    NEW
    requests for information, such as product data, written regulatoryaffairs statements, surveys, or questionnaires. Coordinate recall… North Bay Business Journal four years in a row. The RegulatoryManager is a high impact role within our operations team, with…
  • 3.1
    Sanofi U.S. – Bridgewater, NJ
    $170k-$235k(Glassdoor est.)
    NEW
    Director, Global RegulatoryAffairs The RegulatoryAffairs Director is part of the Sanofi Global RegulatoryAffairs (GRA) team based… Represents Global RegulatoryAffairs (GRA) as a member of the cross functional project team and provides regulatory input for the…
  • 3.6
    Bausch & Lomb – Bridgewater, NJ
    $114k-$163k(Glassdoor est.)
    7 days ago 7d
    hope it will become. The Surgical RegulatoryAffairs Sr Manager is responsible for regulatory development of surgical devices.… product regulatory strategy and increase probability of regulatory approval Ability to critically review detailed scientific information…
  • 3.5
    Vertex Pharmaceuticals – Boston, MA
    $159k-$214k(Glassdoor est.)
    4 days ago 4d
    attention to detail and the ability to manage multiple projects Extensive experience using Regulatory information management systems… submissions and regulatory information practices The role drives the processes and standards for how Regulatory operates with…
  • 3.1
    Sanofi U.S. – Bridgewater, NJ
    $121k-$172k(Glassdoor est.)
    NEW
    Global Regulatory Team Lead (GRTL) and US regulatory lead is a dual role within the Sanofi Genzyme Global RegulatoryAffairs (GRA… industry experience in R&D, Regulatory or related functions, with at least 2 years working in regulatoryaffairs (regionally or globally…
  • 3.6
    Bausch & Lomb – Bridgewater, NJ
    $132k-$182k(Glassdoor est.)
    NEW
    hope it will become. The RegulatoryAffairs – CMC Manager independently manages all regulatory CMC aspects of Valeant’s Pharmaceuticals… Provide regulatory support to other Valeant functions during Regulatory Authority inspections. Serve as RegulatoryAffairs representative…
  • 3.6
    AbbVie – Waukegan, IL
    $125k-$196k(Glassdoor est.)
    8 days ago 8d
    Purpose: Provides specialist medical and scientific input into core medical affairs activities such as: health-care professional… preferred. Knowledge of clinical development, medical affairs and regulatory requirements. Interactions normally require the ability…
  • 3.6
    Bausch & Lomb – Bridgewater, NJ
    $114k-$163k(Glassdoor est.)
    22 days ago 22d
    specific pharmaceutical RegulatoryAffairs personnel for international submissions and registrations Manage interactions with other… product regulatory strategy and increase probability of regulatory approval Ability to critically review detailed scientific information…
  • 3.6
    Bausch & Lomb – Tampa, FL
    $99k-$144k(Glassdoor est.)
    17 days ago 17d
    will become. The RegulatoryAffairs – CMC Medical Devices Senior Manager independently manages all regulatory CMC post-approval… Provide regulatory support to other Valeant functions during Regulatory Authority inspections.  Serve as RegulatoryAffairs representative…
  • 3.6
    Bausch & Lomb – Bridgewater, NJ
    $114k-$163k(Glassdoor est.)
    23 days ago 23d
    Overview The Surgical RegulatoryAffairs Sr Manager handles all regulatory development aspects of surgical devices. The incumbent… country-specific surgical RegulatoryAffairs personnel for international submissions and registrations Manage interactions with other…
  • 3.5
    Vertex Pharmaceuticals – Boston, MA
    $81k-$116k(Glassdoor est.)
    19 days ago 19d
    biotech company 1 plus years of experience working in regulatoryaffairs CMC including understanding of post-approval changes for… global regulatory CMC requirement Minimum Qualifications Minimum Qualifications Bachelor’s degree in a scientific discipline…
  • 2.5
    Valeant Pharmaceuticals – Bridgewater, NJ
    $99k-$135k(Glassdoor est.)
    NEW
    hope it will become. The RegulatoryAffairs – CMC Manager independently manages all regulatory CMC aspects of Valeant’s Pharmaceuticals… Provide regulatory support to other Valeant functions during Regulatory Authority inspections. Serve as RegulatoryAffairs representative…
  • 4.5
    Advanced Clinical – San Francisco, CA
    $87k-$126k(Glassdoor est.)
    HOT
    professional to join a well-known clients team as Manager, RegulatoryAffairs. Their work will have a direct impact on not just… projects Drafts and reviews RegulatoryAffairs' SOPs. May participate in, and provide regulatory guidance to working teams (both…
  • 3.6
    Bausch & Lomb – Bridgewater, NJ
    $112k-$157k(Glassdoor est.)
    NEW
    Overview The RegulatoryAffairs – CMC Associate Director independently manages all regulatory CMC aspects of Valeant’s Pharmaceuticals… Provide regulatory support to other Valeant functions during Regulatory Authority inspections.  Serve as RegulatoryAffairs representative…
  • 3.9
    Salix Pharmaceuticals – Bridgewater, NJ
    $143k-$200k(Glassdoor est.)
    18 days ago 18d
    hope it will become. The RegulatoryAffairs – CMC Manager independently manages all regulatory CMC aspects of Valeant’s Pharmaceuticals… Provide regulatory support to other Valeant functions during Regulatory Authority inspections. Serve as RegulatoryAffairs representative…
  • 3.1
    Sanofi U.S. – Bridgewater, NJ
    $101k-$145k(Glassdoor est.)
    14 days ago 14d
    preparation of labeling for submission to regulatory agencies. Experience in regulatoryaffairs functions, alternatively adequate experience… than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe.…
  • 3.1
    Sanofi U.S. – Bridgewater, NJ
    $136k-$185k(Glassdoor est.)
    24 days ago 24d
    Sclerosis/Neurology Global Regulatory Team Lead (GRTL) is a role within the Sanofi Genzyme Global RegulatoryAffairs (GRA) organization… industry experience in R&D, Regulatory or related functions, with at least 5 years working in regulatoryaffairs (regionally or globally…
  • 3.5
    Vertex Pharmaceuticals – Boston, MA
    $195k-$261k(Glassdoor est.)
    19 days ago 19d
    working in regulatoryaffairs CMC including managing post-approval changes for commercial products Proficiency in regulatory (FDA,… Lead and manage GRA CMC team members Work collaboratively across functions and teams to develop and implement regulatory CMC strategies…
  • 3.5
    Vertex Pharmaceuticals – Boston, MA
    $81k-$174k(Glassdoor est.)
    19 days ago 19d
    be a strategic leader within RegulatoryAffairs, responsible for developing and executing regulatory plans for assigned programs… implementation of the global regulatory development plan for the project Represent Global RegulatoryAffairs (GRA) on cross-functional…
  • 3.6
    Bausch & Lomb – Tampa, FL
    $101k-$140k(Glassdoor est.)
    17 days ago 17d
    become. The RegulatoryAffairs – CMC Medical Devices Associate Director independently manages all regulatory CMC post-approval… Provide regulatory support to other Valeant functions during Regulatory Authority inspections.  Serve as RegulatoryAffairs representative…
  • 3.6
    Bausch & Lomb – Bridgewater, NJ
    $76k-$134k(Glassdoor est.)
    17 days ago 17d
    assigned brand products. Supports the RegulatoryAffairs Senior Manager for Brand and Generic submission timelines and liaises with the… it will become. The RegulatoryAffairs Senior Specialist executes on the pharmaceutical regulatory strategies for assigned…
  • 3.1
    Sanofi U.S. – Bridgewater, NJ
    $98k-$140k(Glassdoor est.)
    NEW
    years of RegulatoryAffairs or relevant industry experience Master's degree and at least 1 year of RegulatoryAffairs or relevant… RegulatoryAffairs CMC Biologics Associate/Senior Associate: This position is responsible for providing regulatory Chemistry…
  • 3.8
    Nektar Therapeutics – San Francisco, CA
    $88k-$124k(Glassdoor est.)
    HOT
    experience is required. A minimum of 1 year hands-on RegulatoryAffairs experience is preferred. Organizational, planning and… Requirements: A minimum of a Bachelors degree in a scientific discipline is required. Equivalent experience may be accepted…
  • 2.5
    Valeant Pharmaceuticals – Bridgewater, NJ
    $103k-$145k(Glassdoor est.)
    7 days ago 7d
    hope it will become. The RegulatoryAffairs – CMC Manager independently manages all regulatory CMC aspects of Valeant’s Pharmaceuticals… Provide regulatory support to other Valeant functions during Regulatory Authority inspections. Serve as RegulatoryAffairs representative…
  • 3.9
    NeoTract – Pleasanton, CA
    12 days ago 12d
    for on time delivery with the highest scientific value. Collaborate with medical affairs colleagues to develop CEC and DMC charters… more patients. About the Position The Senior Manager, Clinical Affairs is responsible for leadership and execution of clinical…
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