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

Regulatory CMC Manager Cell and Gene Therapy

Syneos Health, Inc.

Regulatory CMC Manager Cell and Gene Therapy Updated: Yesterday Location: Remote, DC, Colombia Job ID: 25108926-OTHLOC-7352-2DR Description Regulatory CMC Manager Cell and Gene Therapy Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities General Position Summary The Chemistry Manufacturing Controls Manager will supportthe execution of cell and gene therapy global regulatory CMC strategies for marketed and development products. This role contributes to the preparation and submission of regulatory CMC documentation. This role also provides regulatory support and guidance to various cross functional teams to ensure all applicable global regulatory requirements are considered and appropriately incorporated into development and commercial programs. Key Duties & Responsibilities Reviews CMC sections of regulatory submissions, as well as the interactions and responses with regulatory agencies Contributes to the development of global regulatory CMC strategies for commercial products Works with regulatory colleagues in development of global regulatory CMC strategies and Submissions Providesregulatory CMC guidance to cross-functional teams and key stakeholders Supports regulatory assessment and guidance on product compliance topics including change controls, deviations, and GMP investigations Required Education Level & Experience Strong interpersonal skills to exchange complex information with others and to guide others Proficiencyin regulatory (FDA, EMA, HealthCanadaand ICH) guidelines Experience in the preparation, including writing, of CMC submissions Strategic thinking and strongproblem solvingskills Ability to collaborate and communicate in an open, clear, complete,timelyand consistent manner Strong senseof planning and prioritization, and the ability to work with all levels of management Capable of strategic thinking with ability to resolve complex and ambiguous situations Sound knowledge of cGMP, FDA, EMA, ICH Bachelor's degree, with a preference in Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics or Medical Devices, or another related life-science field Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Summary CMC expertise in small molecule experience with support to Regulatory team with Global expansion on multiple markets. Veeva RIM authoring is required. Discover what our more than 29,000 employees already know: work here matters everywhere. We work hard,and smart, all in the name of getting much-needed therapies to thosewho need them most. A career with Syneos Health means your everyday work improvespatients’ lives around the world. Selecting us as an employer secures a career inwhich you’re guaranteed to: Syneos Health ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. #J-18808-Ljbffr Syneos Health, Inc.

Vacancy posted 4 days ago
Similar jobs that could be interesting for youBased on the Regulatory CMC Manager Cell and Gene Therapy in Washington DC vacancy
  • $268.2k - $402.2k

    Job DescriptionGeneral Summary:The Executive Director, Regulatory Strategy will serve as a seasoned regulatory leader with expert technical...  ...of programs within the T1D portfolio. This position will manage a group of global/regional regulatory professionals with program... 
    Suggested
    Full time
    Summer work
    Local area
    Remote work
    Flexible hours
    2 days per week

    Vertex Pharmaceuticals

    Washington DC
    5 days ago
  • Vertex Pharmaceuticals is seeking an Executive Director, Regulatory Strategy in the Washington, D.C. area to lead global regulatory strategies for Type 1 Diabetes programs. This role oversees a team of regulatory professionals across regions and is responsible for strategic... 
    Suggested

    Vertex Pharmaceuticals

    Washington DC
    3 days ago
  •  ...patients worldwide. It's time for a career you can be proud of. Regulatory Affairs Senior Manager Regional Regulatory Lead Job Description How might you...  .... Let's change the world. The Regulatory Affairs Manager CMC contributes to product teams and acts as product lead or... 
    Suggested
    Ongoing contract
    Local area
    Worldwide
    Flexible hours

    Initial Therapeutics, Inc.

    Washington DC
    2 days ago
  • $135.3k - $376.8k

     ...commercialization, offering expertise in regulatory strategy, clinical trial...  ...and responsibilities include managing the development of regulatory...  ...and leading or expanding new therapy ideas, as applicable. The...  ...regulatory discipline (e.g., CMC); MS or PhD preferred.... 
    Suggested
    Full time
    Part time
    Work experience placement
    Immediate start
    Worldwide

    IQVIA

    Washington DC
    4 days ago
  •  ...Innovative company designing & developing gene therapeutic products Industry...  ...Pharmaceuticals Genetics Specialties gene therapy adeno-associated virus...  ...will be responsible for the operational management of GxP Compliance Audit and Supplier Quality... 
    Suggested
    For contractors

    Confidential

    Washington DC
    4 days ago
  • $160.8k - $201k

     ...diseases. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We're...  ...of the Role The Associate Director, Regulatory Labeling and Disclosures, will be...  ...results posting on Health Authority-managed databases worldwide (e.g., Clinicaltrials... 
    Work at office
    Local area
    Immediate start
    Worldwide

    Sarepta Therapeutics

    Washington DC
    5 days ago
  • $125k - $165k

    The Pharmaceutical Care Management Association (PCMA) is the national association representing...  ...The Director, Federal Regulatory Affairs, will participate in PCMA’s engagement...  ...AFFAIRS Director, Regulatory Affairs - CMC (Cell Therapy) Washington, DC $170,000.00-$215,000.0... 
    Full time
    Work at office
    3 days per week

    Pharmaceutical Care Management Association (PCMA)

    Washington DC
    3 days ago
  •  ...Consultant | Military Spouse Are you a regulatory affairs professional with a deep...  ...meetings and industry events. Issues Management Serve as an internal subject matter expert...  ...Gaithersburg Director, Regulatory Affairs - CMC (Cell Therapy) Senior Director, Nuclear Regulatory... 
    Full time
    Work at office

    TalentRemedy

    Arlington, VA
    3 days ago
  •  ...Consultant | Military Spouse Are you a regulatory affairs expert with a strong background...  ...strategic priorities. The Director will manage complex issues, frame narrative, and...  ...Arlington, VA . Director, Regulatory Affairs - CMC (Cell Therapy) Washington, DC $170,000.00-$215,000.00... 
    Full time
    Temporary work
    Work at office

    TalentRemedy

    Arlington, VA
    3 days ago
  •  ...Therapeutics seeks a senior Biostatistics/ Biometrics leader to oversee statistical leadership across DMD programs and gene therapy platforms. You will guide regulatory-grade deliverables, drive rapid data exploration, and mentor a team of biostatisticians and programmers. The... 

    Sarepta Therapeutics

    Washington DC
    19 hours ago
  •  ...Radical Ventures and NVIDIA. Learn more about our vision, team, and backers at About the Role We’re looking for a Policy & Regulatory Affairs Manager to help shape and execute our policy and regulatory strategy at a critical moment of growth. As demand accelerates and... 
    Work from home
    Flexible hours
    2 days per week

    emerald-ai

    Washington DC
    3 days ago
  • $189k - $246k

    Department: 107000 Regulatory Location: San Diego, USA- Remote Position...  ...Affairs, Biostatistics, CMC, Quality, Nonclinical, Commercial...  ...procedures, Breakthrough Therapy Designation, Fast Track, PRIME...  ...programs. Demonstrated success managing interactions with FDA and... 
    Temporary work
    Local area
    Remote work
    Weekend work

    Travere Therapeutics

    Washington DC
    3 days ago
  •  ...-better products that reach over 10 million patients worldwide. Its time for a career you can be proud of. United States Regulatory Senior Manager Obesity and Related Conditions Live What You Will Do Lets do this! Lets change the world! Amgen is seeking a United States... 
    Worldwide
    Flexible hours

    BioSpace

    Washington DC
    19 hours ago
  •  ...patients while transforming your career. Regulatory Affairs Director - Inflammation and Rare...  ..., registration, and life cycle management of all Amgen molecules. In this vital,...  ...marketing applications, label extensions, CMC changes) Ensure consistency of evidence... 
    Worldwide
    Flexible hours

    Amgen SA

    Washington DC
    3 days ago
  • Google is seeking a Program Manager to lead complex, multi-disciplinary projects across Global Affairs, Product Areas and Regulatory teams. You’ll coordinate requirements, schedules, risks, and cross-functional communication across offices, time zones, and hemispheres... 

    Google

    Washington DC
    5 days ago
  • $210.38k - $272.25k

     ...cancer – working relentlessly to develop therapies that help improve lives and to ensure...  ...objective assessments of compliance with global regulatory requirements, internal quality policies,...  ...Duties and Responsibilities: Manage and develop an auditing team, including... 
    Full time
    Contract work
    For contractors
    Local area

    Gilead Sciences

    Washington DC
    13 days ago
  • Consumer Brands Association in Arlington, VA is seeking a Manager, Regulatory & Technical Affairs to support regulatory and technical initiatives, respond to federal and state actions, and help implement association policies while engaging members. The role requires a bachelor... 

    Consumer Brands Association

    Arlington, VA
    4 days ago
  • $110k - $125k

     ...Position Objective The Scientific Program Manager will provide support to the National...  ...Health (NIH). Responsibilities Serve as a regulatory affairs management expert. Responsible for...  ...objectives, chemistry manufacturing and control (CMC) documents, and nonclinical study report... 
    Full time
    Contract work
    Work at office
    Shift work

    GAP SOLUTIONS INC

    Bethesda, MD
    1 day ago
  • $109.44k - $244.8k

     ...organization expands rapidly and becomes more complex, so too does the regulatory and legal environment. We are therefore expanding the Trust &...  ...part within the team, with responsibility for programme management and the ongoing monitoring of relevant regulatory obligations.... 
    Temporary work

    TikTok

    Washington DC
    5 days ago
  • Tundra Technical Solutions is seeking an experienced Project/Program Manager to coordinate cross-functional programs in a highly regulated environment in Washington, DC. You will manage reporting, testing workstreams, and ensure deliverables are completed on schedule. Responsibilities... 
    Shift work

    Tundra Technical Solutions

    Washington DC
    3 days ago
  • $252k - $351k

     ...government, in-house, or at a law firm. 7 years of experience with legal, regulatory and litigation matters, including addressing, minimizing, and avoiding regulatory risk. Experience managing teams. Admitted to the bar and in good standing or otherwise authorized to... 
    Temporary work
    Shift work

    Google

    Washington DC
    4 days ago
  • $232k - $348k

    Job DescriptionThe Regulatory Strategy Senior Director is a regulatory leader with expert technical and tactical experience in regulatory...  ...teams and GRA leadership. Counsels and advises senior management on status of global Regulatory Affairs strategies and tactics,... 
    Full time
    Summer work
    Work at office
    Local area
    Remote work
    Flexible hours
    2 days per week
    3 days per week

    Vertex Pharmaceuticals

    Washington DC
    5 days ago
  • $186.75k - $311.25k

     ...institutional adoption, formulary, and on-label access to our therapies. This role requires fluency across clinical science, real-world...  .../biotech commercial roles working in OncologyAccount management experience in complex settings (E.G., Academic, IDN Accounts,... 
    Full time
    Contract work
    Local area
    Remote work

    GSK

    Washington DC
    4 days ago
  • $142.5k - $256.5k

     ...changing the biotech industry.Reporting to the Director, Regulatory Information Management (RIM), the Associate Director, Regulatory Data Management...  ...partner closely with Regulatory Affairs, Regulatory Operations, CMC, Labeling, Quality, Enterprise Data, Digital, and external... 
    Permanent employment
    Full time
    For contractors
    Work at office
    Work from home

    Moderna Therapeutics

    Bethesda, MD
    5 days ago
  • Company DescriptionProSidian is a Management and Operations Consulting Services firm that delivers value to clients through tailored solutions...  ...at DescriptionProSidian Seeks a Engineering Services Regulatory Commissioning Manager | Compliance / Risk / Regulatory: Risk,... 
    Full time
    Contract work
    Temporary work
    For contractors
    Work at office
    Remote work
    Flexible hours

    Prosidian Consultng

    Washington DC
    1 day ago
  • $110k - $160k

     ...enabling human life on Mars. SATELLITE POLICY MANAGER (STARLINK MOBILE) SpaceX is developing a...  ...directly from satellites to existing cell phones, with the goal of providing coverage...  .... In this role, you will drive SpaceX’s regulatory and policy strategy to enable this ground... 
    Permanent employment
    Temporary work
    Remote work
    Worldwide
    Weekend work

    SpaceX

    Washington DC
    2 days ago
  • $110k - $160k

     ...human life on Mars. SATELLITE POLICY MANAGER (STARLINK MOBILE) SpaceX is developing...  ...service directly from satellites to existing cell phones, with the goal of providing...  ...In this role, you will drive SpaceX’s regulatory and policy strategy to enable this ground... 
    Permanent employment
    Temporary work
    Remote work
    Worldwide
    Weekend work

    SpaceX

    Washington DC
    4 days ago
  • Jobtailor in Washington, DC is seeking an experienced data analyst to analyze regulatory intelligence data, identify trends and risks, and translate findings into actionable insights for stakeholders. You will prepare recurring and ad hoc reports, dashboards, and executive... 

    Jobtailor

    Washington DC
    2 days ago
  • $76.08k - $98.9k

     ...from all forms of violence. We won’t stop until we are all equal. The Compliance Manager manages core compliance operations for Plan International USA, including regulatory filing coordination, policy and template management, records retention, data privacy... 
    Work at office
    Local area

    Plan USA

    Washington DC
    20 days ago
  •  ...Job title: Manager, Regulatory Training Department: Training & Technology Services Reports to: Director, Training & Technology Services Location of job: Headquarters Work schedule: Full time, 40 hours/5 days per week FLSA status: Exempt Position... 
    For contractors
    Work experience placement

    American Association Of Airport Executives

    Arlington, VA
    7 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Regulatory CMC Manager Cell and Gene Therapy. Be the first to apply!