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Manager Regulatory Affairs CMC (Small Molecules) - Remote / Telecommute for our client in Jersey City, NJ Job Title: Manager Regulatory Affairs CMC (Small Molecules) - Remote / TelecommuteJob Location: Jersey City, NJ Job Type: ContractJob Description:Pay Range $55hr - $60hr- Inviting applications for the role of Senior Manager (SM) Regulatory Affairs CMC (Small molecules).
- SM of Regulatory Affairs CMC, small molecules, is responsible for developing and implementing CMC regulatory strategies for all assigned products with the intention of achieving successful registration and life-cycle management.
- Deliver regulatory CMC strategic leadership to support development and regulatory approval of multiple innovative products, mainly small molecules, for a wide variety of therapeutic areas and dosage forms.
- Lead project related regulatory CMC activities in a matrix structure.
- Manage and implement planning, preparation, and submission of high-quality CMC related applications with a focus on the US and EU/EMEA regions.
- Ensure that CMC-related applications and/or sections, including IMPDs/INDs, investigator brochures, scientific advice requests, agency briefing documents, and MAAs are complete, well written, and meet all relevant requirements.
- In collaboration with the Regulatory Strategy Leads, coordinate negotiations on CMC topics with regulatory agencies to resolve CMC issues.
- Effectively communicate regulatory CMC strategy to Regulatory Strategy leads and other internal stakeholders.
- Drive adherence to CMC regulatory guidelines relevant for the development of biologics.
- Assess proposed manufacturing process changes and provide strategic regulatory guidance to enable global implementation.
- Assess the impact of new regulations, guidance and directives and advise the regulatory organization on requirements to maintain compliance with regulatory operations activities.
- Manage post approval changes where needed.
- Prior experience and a successful track record within the biotechnology and/or pharmaceutical industry in successful preparation and submission of IMPDs/INDs, Scientific Advice, MAAs, post-approval life cycle management for mainly small molecule products.
- Experience with medical device and combination products would be advantageous.
- Strong knowledge of current Good Manufacturing Practices (GMP), drug (and biologics) development regulations and guidelines including ICH, EMA and FDA guidelines.
- Strong leadership qualities including strategic thinking, innovation, people management, project management and excellence in communication.
- This position requires a self-motivated and organized individual with the ability to exercise flexibility, and solution focused decision making.
- The successful candidate should be self-motivated and well organized.
- Master’s degree in life sciences in biochemistry, chemistry, biology, or related pharmaceutical fields; higher degree, such as a PhD is desirable.
- At least 12 years of relevant biopharmaceutical industry experience, with at least 10 years’ experience in the regulatory CMC area (mainly dealing with small molecules).
- Prior experience in big (or mid-size) Pharma companies.
- Proven project management delivery
- Robust communication and presentation skills.
- Proven track record in working cross-culturally.
Vacancy caducado!