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Posted: Tuesday, September 5, 2017 10:15 AM

Sr. Specialist CMC Regulatory Affairs (Medical Device and Combination Products):REG003100
Merck and Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck's success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
Merck is on a quest for cures and is committed to being the world's premier, most research:intensive biopharmaceutical company. Today, we're doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck's leading discovery capabilities and world:class small molecule and biologics R and D expertise to create breakthrough science that radically changes the way we approach serious diseases.
Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.
Reporting to the Director, the Sr. Specialist is responsible for implementing Medical Device and Combination Product CMC regulatory strategies for Mercks products in accordance with global regulations and guidances, and is responsible for the preparation and submission of CMC dossiers for pipeline and commercial products. Primary responsibilities include, but are not limited to:
Regulatory Responsibilities:
: The Medical Device and Combination Product CMC Lead is accountable for the delivery of all regulatory milestones for less complex products through the product lifecycle in which responsible including assessment of the probability of regulatory success together with risk mitigation measures.
: Lead the development, communication, lifecycle management and review of the Medical Device and Combination CMC Regulatory Strategy Document for smaller:scoped projects.
: Lead execution of Medical Device and Combination CMC documentation including support of IND/CTA, NDA/BLA/MAA, post:approval supplements, annual reports, registration renewals and responses to health authority questions per established business processes and systems.
: Conduct all activities with an unwavering focus on compliance.
Education Requirement:
: B.S. in a biological science, engineering, or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, Biomedical Engineering or Biochemistry.
Required Experience:
: Technical Skills:
: Experience in reviewing scientific information and assessing whether technical arguments are presented clearly and conclusions are adequately supported by data.
: Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills.
: Demonstrated understanding of related fields (e.g., manufacturing, analytical, quality assurance, medical devices).
: Leadership Skills:
: Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders.
: Demonstrated flexibility in responding to changing priorities or dealing with unexpected events.
: Demonstrated effective leadership, communication, and interpersonal skills.
: Required:
: At least two (2) years of relevant experience, including biological/pharmaceutical/ medical devices; manufacturing, testing, or licensure of biological


• Location: Staten Island

• Post ID: 127900933 newyork is an interactive computer service that enables access by multiple users and should not be treated as the publisher or speaker of any information provided by another information content provider. © 2017