Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Manager, Regulatory Affairs- CMC

$127.28k - $190.92k

Daiichi Sankyo, Inc.

At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and the broader RA team. This position manages assigned developmental and post marketing projects with a high level of supervision. This position prepares content templates and supports the technical team in the preparation of submission documents (e.g., IND, BLA, IB, NDA, Amendments, Supplements, Briefing Books) for review by higher-level manager. This position demonstrates understanding of key regulatory guidances and their application during the development process. This position works with problems that are typically simple, straightforward and task driven. This position has a high level of supervision and is supportive in nature. Responsibilities Planning for Development and Post Marketing Projects: Manages CMC development and post marketing projects. Execution of Strategy and Submissions: Prepares content templates and supports the technical team in preparation of submission documents for review by higher-level manager. FDA Interactions: Leads FDA interactions with high level of supervision. Regulatory Knowledge: Demonstrates understanding of key US regulatory guidances and their application during the development process. Qualifications Education Qualifications Bachelors Degree in a scientific discipline required Masters Degree in a scientific discipline preferred Experience Qualifications 5-8 years of pharmaceutical industry experience with 2+ years of direct or related CMC regulatory experience preferred Travel Requirements Ability to travel up to 5% of the time. Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. Salary Range: USD$127,280.00 - USD$190,920.00 Download Our Benefits Summary PDF

Vacancy posted 1 day ago
Similar jobs that could be interesting for youBased on the Manager, Regulatory Affairs- CMC in Basking Ridge, NJ vacancy
  •  ...the Morris Plains, NJ area. Associate Director in the Regulatory Affairs CMC Department. The successful candidate may lead a small...  ...changes in regulatory information to project teams and senior management in a timely manner. Initiates local process... 
    Suggested
    Contract work
    Local area

    Fladger Associates

    Morris Plains, NJ
    3 days ago
  • $140k - $165k

     ...Job Title: Manager CMC Regulatory The role involves ensuring that CMC regulatory activities are conducted effectively to support both pre...  ...pharmaceutical industry experience, with at least 8 years in Regulatory Affairs focusing on CMC. Managerial experience is required.... 
    Suggested
    Permanent employment
    Temporary work

    Actalent

    Morristown, NJ
    3 days ago
  • $119.7k - $223.3k

    Novartis Farmacéutica is seeking a Senior Manager, Regulatory Affairs CMC in East Hanover, NJ, to lead global regulatory strategy and ensure compliance throughout the product lifecycle. Candidates should have over 5 years of experience in regulatory affairs, excellent organizational... 
    Suggested

    Novartis Farmacéutica

    Whippany, NJ
    3 days ago
  • $165k - $220k

     ...health in the future. The Director, Regulatory Affairs leads global regulatory strategy, reporting...  ...with Clinical, Nonclinical, CMC, Quality, Safety, and Regulatory Operations...  ...interactions, ensure highquality submissions, and manage regulatory risk across the product... 
    Suggested
    Temporary work
    Work visa

    Bausch + Lomb

    Morristown, NJ
    1 day ago
  •  ...YouTube. Job Description The Associate Director Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC) works with internal and external partners to deliver...  ...that enable first pass approvals. Develops and manages content strategy for regulatory submissions,... 
    Suggested
    Temporary work

    Allergan

    Florham Park, NJ
    3 days ago
  • $184.24k - $276.36k

     ...Job Title: Director, Regulatory Affairs Advertising and Promotion Job Requisition ID: 1531 Posting Start Date: 5/21/26 At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With... 
    Work at office

    Daiichi Sankyo, Inc.

    Basking Ridge, NJ
    2 days ago
  •  ...Responsibilities Act as the primary regulatory representative on, and...  ..., BLA submissions) Management of, and collaboration with, CRO...  ...Represent Regulatory Affairs with licensing partners Establish...  ...information Interface with CMC, nonclinical research and... 
    Worldwide
    Flexible hours
    Shift work

    ADC Therapeutics SA

    New Providence, NJ
    3 days ago
  •  ...Senior Manager Regulatory Affairs, Advertising and Promotion At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. This position requires the ability to apply clinical development knowledge in concert with... 
    Work at office

    Regeneron

    Warren, NJ
    2 days ago
  • $152.62k - $209.85k

     ...challenges us to be better every day, driven by our agile, performance-focused culture. About the Role This Senior Manager, Regulatory Affairs - OTC role is accountable for end-to-end regulatory activities for the OTC Category, owning and defending the full brand... 
    Work at office

    GSK Group of Companies

    Warren, NJ
    4 days ago
  • $122.25k - $176.58k

     ...Job Title: Senior Manager, Regulatory Affairs Advertising and Promotion Location: Morristown, NJ / Cambridge, MA About the Job As the Senior Manager, Regulatory Affairs Advertising and Promotion within our GRA Advertising and Promo Team, you will be responsible... 
    Work experience placement

    Sanofi Group

    Morristown, NJ
    5 days ago
  •  ...biopharmaceutical company focused on non-opioid pain management and regenerative health solutions,...  .... Position: The Senior Director, Regulatory Clinical Strategy, will lead the...  ...Clinical Development, Non-Clinical, CMC, Medical Affairs, Legal, and Commercial teams. Lead... 

    Kaye/Bassman International

    Parsippany, NJ
    2 days ago
  •  ...reports to the Functional Area Head, Global Regulatory Affairs and will be responsible for supporting...  ...review and submit regulatory documents, manage documentation systems and maintain...  ...all disciplines (nonclinical, clinical, CMC), as well as supporting regulatory interactions... 
    Full time
    Work at office

    Gan & Lee Pharmaceuticals

    Bridgewater, NJ
    more than 2 months ago
  • Senior Manager Regulatory Affairs US Advertising and Promotion-Immunology Combines knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet the required legislation. Develops and supervises regulatory... 
    Temporary work

    Allergan

    Florham Park, NJ
    4 days ago
  • $122.25k - $176.58k

    Job Title: Senior Manager, Regulatory Affairs Advertising and Promotion Location: Morristown, NJ / Cambridge, MA About the Job As the Senior Manager, Regulatory Affairs Advertising and Promotion within our GRA Advertising and Promo Team, you will conduct independent reviews... 

    Sanofi

    Convent Station, NJ
    5 days ago
  •  ...Senior Specialist, Regulatory Affairs CMC Qualifications: Education: Bachelor of Science degree (minimum) in science, engineering, or other...  ...independently and effectively with relevant functions to manage and prepare regulatory CMC dossiers, renewals/annual reports... 

    AA2IT

    Madison, NJ
    1 day ago
  • $126.11k - $152.81k

     ...and in their personal lives. Read more: careers.bms.com/working-with-us . The primary responsibility of a Senior Manager in Commercial Regulatory Affairs is to provide expert and strategic regulatory advice and risk assessment on promotional issues with guidance from... 
    Hourly pay
    Full time
    Temporary work
    Part time
    For contractors
    Fixed term contract
    Summer work
    Live in
    Work at office
    Local area
    Remote work
    Flexible hours
    Shift work

    Bristol-Myers Squibb

    Madison, NJ
    3 days ago
  • $122k - $212.75k

     ...Senior Manager, Government Contracting & Pricing Compliance Officer (GCCO) We are searching for the best talent for a Senior Manager, Government Contracting & Pricing Compliance Officer (GCCO) to be located in Titusville, NJ or Raritan, NJ. Your unique talents will... 
    Local area
    Immediate start
    3 days per week

    J&J Family of Companies

    Raritan, NJ
    3 days ago
  • $20 - $24 per hour

    TalentoHC is seeking a Legal Consultant II in Basking Ridge, NJ, to manage law enforcement legal requests in a hybrid role. The successful candidate will have 2+ years of experience in legal operations or compliance, with strong attention to detail and communication skills... 
    Hourly pay
    Flexible hours
    Night shift
    Weekend work

    TalentoHC

    Basking Ridge, NJ
    3 days ago
  • $141.5k

     ...and YouTube. ( Job Description The Associate Director, Regulatory Affairs US Advertising and Promotion is responsible for setting strategy...  .../plan, and leads initiatives. Assists in the management of the departmental budget, identifies and communicates budgetary... 
    Temporary work
    Work at office
    Local area

    AbbVie

    Florham Park, NJ
    1 day ago
  • $137.6k - $180k

     ...Regulatory Affairs Advertising Promotion Specialist This position is with Recordati Rare Diseases, Inc. (RRD), North America, an affiliate...  ..., Promotion, and Labeling Direct Report(s): None Areas Managed: Advertising & Promotion North America Overview This role... 
    Temporary work
    Night shift
    Weekend work

    Recordati Rare Diseases Inc

    Bridgewater, NJ
    2 days ago
  •  ...Associate Director, Regulatory Affairs (Advertising and Promotion) Job Location: Bridgewater, New Jersey, USA Job Requisition ID: 14896 Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes... 
    Temporary work
    Work at office
    Remote work
    Monday to Friday
    Flexible hours

    Bausch Health

    Bridgewater, NJ
    1 day ago
  • $190k - $200k

     ...Tonix is looking for a full-time Associate Director, Regulatory Affairs to effectively develop regulatory strategies and submission...  ...will report directly to the Co-Head of Regulatory Affairs, Management and Execution, and will be based out of a Tonix office or can... 
    Full time
    Temporary work
    Work at office
    Local area
    Remote work
    Flexible hours

    Tonix Pharmaceuticals

    Berkeley Heights, NJ
    4 days ago
  • $119.5k - $179k

     ...Title: Compliance Manager - Spinnaker Location: Austin, TX / Dallas, TX / San Jose, CA / Morristown, NJ (hybrid) Reports To: Director, Regulatory Compliance About Hippo Hippo was built on a promise: make homeownership effortless. Nearly a decade... 
    Temporary work
    Work at office
    Flexible hours

    Hippo Insurance

    Morristown, NJ
    2 days ago
  •  ...PSA Compliance Manager -Juntos 3 (3607) *Sign-On Bonus Take advantage of our new sign-on bonus! Center for Family Services is a place where you can be part of a dynamic, top workplace team dedicated to improving lives. When you apply and get hired, you are eligible... 
    Full time
    Interim role
    Local area
    Relocation package
    Flexible hours

    Center for Family

    Bridgewater, NJ
    5 days ago
  •  ...aligned professional to serve as Summer Employment Operations Manager. This seasonal leadership role (approximately May 1 - September...  ...100 % completion of onboarding requirements before Day 1. Regulatory Oversight Execute a comprehensive compliance checklist for all... 
    Hourly pay
    Full time
    Summer work
    Seasonal work
    Immediate start

    The Pingry School

    Basking Ridge, NJ
    4 days ago
  • A prestigious educational institution in Basking Ridge seeks a Summer Employment Operations Manager to ensure compliance and onboarding for seasonal staff. This role requires strong organizational skills and experience in managing large seasonal teams, ensuring staff safety... 
    Summer work
    Seasonal work

    The Pingry School

    Basking Ridge, NJ
    4 days ago
  •  ...Director Regulatory Affairs The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products...  ...skills, assertiveness, excellent negotiation and project management skills as evidenced by past performance on drug development... 
    Local area
    Relocation package

    Regeneron

    Warren, NJ
    3 days ago
  • $153.6k - $230.4k

     ...excellence and continuous improvement. Manage DSI's Strategic PV Partnerships and contracts...  ...Good Pharmacovigilance Practice and regulatory compliance in such arrangements. Oversees...  ..., Research & Development, Regulatory Affairs Facilitate operational meetings with CROs... 
    Contract work
    Local area

    Daiichi Sankyo, Inc.

    Basking Ridge, NJ
    1 day ago
  •  ...all Microsoft 365 services operate securely, remain aligned with regulatory and organizational requirements, and support Teva’s digital...  ...workloads to governance, legal, compliance, and privacy requirements. Manage Purview policies: sensitivity labels, retention, insider risk,... 
    Local area
    Flexible hours

    Tevapharm

    Parsippany, NJ
    4 days ago
  •  ...They will be identifying and assessing regulatory and quality risks during site GMP operations...  ...'s self-inspection program.  They will manage routine use of the Cellares Quality Management...  ...implementation plans Contribute to CMC sections of regulatory filings,... 
    Flexible hours

    Cellares

    Bridgewater, NJ
    8 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Manager, Regulatory Affairs- CMC. Be the first to apply!