Jobs
>
Princeton

    Senior Regulatory Affairs - Princeton, United States - Diverse Lynx

    Diverse Lynx
    Diverse Lynx Princeton, United States

    1 week ago

    Default job background
    Description

    Hi,

    Welcome to Diverse Lynx We combine industry leading expertise and our personal dedication to help you find your next career opportunity. We are a Minority and Women Owned Business Enterprise (MWBE) certified by the State of New Jersey and Minority Business Enterprise (MBE) certified from National Minority Supplier Development Council.

    Established in 2002, we have helped thousands of candidates find their next role. Diverse Lynx is headquartered in Princeton, NJ and have exclusive job opportunities with Fortune companies in USA, Canada, United Kingdom, and India. We would love to speak with you and help get connected with the hiring team for this role.

    Benefits/Perks

    1. Competitive Compensation
    2. Flexible work models (Remote, Hybrid, Onsite)
    3. Career Growth Opportunities
    4. Exclusivity on all roles meaning your resume will be personally reviewed by hiring managers
    5. Long Term Contracts
    6. Medical Benefits
    Please go through below opening we have with one of our leading global professional services firm delivering outcomes that transform business and shape the future. Kindly review the details and let me know if you would like to apply and further discuss.

    Title: Senior Regulatory Affairs (RA) Manager
    Type: Contract
    Duration: 6 months
    Location: Los Angeles, CA, 90020(Onsite, atleast 3 day onsite)

    About the role:

    The Senior Regulatory Affairs Manager ensures regulatory compliance of clients cosmetic, OTC, dietary supplement, and device products from brief through launch in North America. Specifically, the Sr. Manager will assemble and review all product-related information including formulas, specifications, and quality/regulatory compliance documentation, and for approving claims, labeling, and advertising. Communicate emerging regulations to key stakeholders and their impact client's portfolio in NA.

    Required: 7-10 years' Experience Required

    Roles & Responsibilities
    Participate in project teams in assigned categories to ensure completion of appropriate documents during the development process through final formula approval and launch
    Maintain and ensure compliance with client ingredient policies and appropriate product regulations
    Ensure claims are compliant with client and local regulatory requirements and consistent across labels, advertising, and other consumer communications
    Review and approve NA artworks
    Responsible for US regulatory submissions, including FDA drug and establishment registrations, supplement notifications, WERCS and EPA and state pesticide registrations
    Assist monitoring US state and federal regulations impacting the cosmetic and personal care industry including OTC
    Support with upcoming changes in the regulations including any specific monitoring and implementation for states, e.g., California

    Preferred Qualifications
    Onsite 3 days per week

    Bilingual English/Korean preferred

    Minimum Qualifications
    Scientific degree
    Over 8 years of Regulatory Affairs experience within a regulated industry, preferably skin and personal care products including OTC
    Product development experience strongly preferred
    Skin and personal care including OTC claim review experience strongly preferred
    Track record adhering to compliance requirements (i.e. FDA, Health Canada, EPA, FTC, cGMP, ISO, etc.)
    Strong written communication skills, especially detail oriented and technical material
    Experience communicating with cross-functional teams and customers including verbal presentations
    Ability to work effectively both independently and as part of a team
    Ability to meet deadlines while being flexible to changes in priorities and interruptions
    Excellent organizational and analytical skills to complete assignments accurately
    Full usability of MS Office suite (Excel, Word, Outlook, PowerPoint)

    Diverse Lynx LLC is an Equal Employment Opportunity employer. All qualified applicants will receive due consideration for employment without any discrimination. All applicants will be evaluated solely on the basis of their ability, competence and their proven capability to perform the functions outlined in the corresponding role. We promote and support a diverse workforce across all levels in the company.


  • Novo Nordisk Plainsboro, United States

    **About the Department*** · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA ...


  • Freyr Princeton, United States

    Regulatory Affairs Analyst (Master's or equiv. degree w/1 yr. exp.) Princeton, NJ. Exp. in: manage & coordinate regulatory affairs team; implement regulations for preparation & submission of regulatory documentation; risk management planning & traceability matrix; submitting docu ...


  • BioPhase Princeton, United States

    Hybrid - 3 days a week in office - Princeton, NJ · The Associate Director of Regulatory Affairs Labeling will assist in the development of a cross-functional labeling strategy for products worldwide, including providing expert input on labeling requirements and strategic guidanc ...


  • TK-CHAIN LLC Princeton, United States

    SUMMARY OF POSITION The Director, Regulatory Affairs integrates and applies knowledge of US regulatory guidelines and federal regulations governing pharmaceutical drug development to all aspects of Our Client's 's drug development programs, policies and procedures; ensuring a com ...


  • Laboratoire Guerbet Princeton, United States

    At Guerbet, we build lasting relationships so that to enable people to live better . This is · Our Purpose. · We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventio ...


  • Laboratoire Guerbet Princeton, United States

    At Guerbet, we build lasting relationships so that to enable people to live better. This is Our Purpose. · We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional ...


  • TK-CHAIN LLC Princeton, United States

    Job Description · Job DescriptionSUMMARY OF POSITION · The Director, Regulatory Affairs integrates and applies knowledge of US regulatory guidelines and federal regulations governing pharmaceutical drug development to all aspects of Our Clients s drug development programs, polici ...


  • TK-CHAIN LLC Princeton, United States

    Job Description · Job Description · SUMMARY OF POSITION · Manages team and leads Regulatory Associates and/or Senior Regulatory Associates in regulatory activities associated with planning, authoring, compiling and submitting highest-quality regulatory submissions to the FDA with ...


  • Lynkx Staffing LLC Princeton, United States

    Job Description · Job DescriptionOur Pharmaceutical client is seeking a Director Regulatory Affairs Chemistry Manufacturing & Controls (CMC) to guide global teams through the development and execution of regulatory strategy and the design of CMC components of drug development pro ...


  • Dr. Reddy's Laboratories Inc. Princeton, United States OTHER

    At Dr. Reddy's "Good Health Can't Wait" · By joining Dr. Reddy's, you will contribute to making the breakthroughs of tomorrow a reality today From making medicines more affordable to discovering innovative treatment options to satisfy unmet medical needs, we are dedicated to help ...


  • Dr. Reddy's Laboratories Inc. Princeton, United States OTHER

    At Dr. Reddy's "Good Health Can't Wait" · By joining Dr. Reddy's, you will contribute to making the breakthroughs of tomorrow a reality today From making medicines more affordable to discovering innovative treatment options to satisfy unmet medical needs, we are dedicated to he ...


  • Novo Nordisk A/S Plainsboro, United States

    Provide proactive support and technical assistance to more experienced regulatory personnel. Identify issues and inform appropriate individuals. Ability to work with less supervision than Associate. Take initiative to assist with overflow in other ar Regulatory Affairs, Regulator ...


  • Novo Nordisk Plainsboro, United States

    About the Department · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to ...


  • Novo Nordisk Plainsboro, United States

    About the DepartmentThe Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to prov ...


  • Novo Nordisk Plainsboro, United States Full time

    About the Department · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to ...


  • Katalyst Healthcares & Life Sciences Inc Edison, United States

    **Responsibilities**: · - This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of international product registrations and related regulatory affairs activities, including execution of pr ...


  • Sun Pharma Princeton, United States

    Senior Director, Regulatory Affairs - GDP · Shionogi Inc. · posted 05/06/2024 · More... · front runner · Senior Director, Regulatory Affairs CMC · Meet · Philadelphia, PA 19117 · posted 05/09/2024 · More... · front runner · Senior Director Regulatory Affairs · Sun Pharma ...


  • Sun Pharma Princeton, United States

    The Brands and Innovative Medicines Global Regulatory Affairs organization is seeking a Senior Director, Global Regulatory Portfolio Leader. Working with leaders across the organization, this individual will provide leadership for the regulatory strategy of one or more in-line an ...


  • SUN PHARMA Princeton, United States

    The Brands and Innovative Medicines Global Regulatory Affairs organization is seeking a Senior Director, Global Regulatory Portfolio Leader. Working with leaders across the organization, this individual will provide leadership for the regulatory strategy of one or more in-line an ...


  • TK-CHAIN LLC Princeton, United States

    SUMMARY OF POSITION The Sr. Manager, Regulatory Affairs integrates and applies knowledge of US regulatory guidelines and federal regulations governing pharmaceutical drug development to all aspects of Our Client's 's drug development programs, policies and procedures; ensuring a ...