Katalyst CRO
Responsibilities
Manage assigned projects to ensure thoroughness, accuracy, and timeliness of CMC dossiers and responses. Partner with RA CMC Project Leads and develop module 3 content and project timelines. Collaborate with diverse functional groups to ensure file-ability and acceptance of CMC sections. Skills for running review meetings for submission documents. Understand CMC expectations including CTD content, structural and formatting requirements. Maintain awareness of and utilize current best practices for use of regulatory business systems within the group. Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval. Authoring and submitting PMA supplements (30-day Notice, Real-Time Reviews, 180-Day Supplements, Annual Reports). Review/approval of engineering study protocols/reports and validation study protocols/reports. Review and approval of manufacturing changes for Class III implantable medical devices. Manage, compile, and author CMC sections of marketed product variations including CTD content, structural and formatting requirements are being met for assigned projects with minimal management oversight. Independently facilitate project team meetings. Familiarity with US and other international regulatory requirements for dossiers. Superior oral and written communication skills. Ability to work cooperatively with all levels and types of global personnel required. Experience working with electronic document management systems. Ability to work independently. Manage multiple projects simultaneously. Stay attuned to shifts in project scope, business objectives, and team feedback, adjusting priorities and strategies as necessary. Detail/accuracy oriented, collaborative, and willing to learn. Requirements
Minimum of a BA/BS Degree in Chemical, Biological Sciences, or relevant discipline. 3+ years pharmaceutical experience. 1-3 years cross-functional project management. 4 years pharmaceutical experience including 1-2 years in regulatory affairs, R&D, or Manufacturing (CTD Module 3). May require an advanced degree and 2 to 5 years of direct experience in the field. Recent experience with Class III implantable medical devices; Proven successful track record of authoring/submission/approval of Class III implantable PMA supplements; knowledge of FDA PMA guidance documents and CFR regulations. Performs a variety of tasks. May lead and direct the work of others.
#J-18808-Ljbffr
Manage assigned projects to ensure thoroughness, accuracy, and timeliness of CMC dossiers and responses. Partner with RA CMC Project Leads and develop module 3 content and project timelines. Collaborate with diverse functional groups to ensure file-ability and acceptance of CMC sections. Skills for running review meetings for submission documents. Understand CMC expectations including CTD content, structural and formatting requirements. Maintain awareness of and utilize current best practices for use of regulatory business systems within the group. Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval. Authoring and submitting PMA supplements (30-day Notice, Real-Time Reviews, 180-Day Supplements, Annual Reports). Review/approval of engineering study protocols/reports and validation study protocols/reports. Review and approval of manufacturing changes for Class III implantable medical devices. Manage, compile, and author CMC sections of marketed product variations including CTD content, structural and formatting requirements are being met for assigned projects with minimal management oversight. Independently facilitate project team meetings. Familiarity with US and other international regulatory requirements for dossiers. Superior oral and written communication skills. Ability to work cooperatively with all levels and types of global personnel required. Experience working with electronic document management systems. Ability to work independently. Manage multiple projects simultaneously. Stay attuned to shifts in project scope, business objectives, and team feedback, adjusting priorities and strategies as necessary. Detail/accuracy oriented, collaborative, and willing to learn. Requirements
Minimum of a BA/BS Degree in Chemical, Biological Sciences, or relevant discipline. 3+ years pharmaceutical experience. 1-3 years cross-functional project management. 4 years pharmaceutical experience including 1-2 years in regulatory affairs, R&D, or Manufacturing (CTD Module 3). May require an advanced degree and 2 to 5 years of direct experience in the field. Recent experience with Class III implantable medical devices; Proven successful track record of authoring/submission/approval of Class III implantable PMA supplements; knowledge of FDA PMA guidance documents and CFR regulations. Performs a variety of tasks. May lead and direct the work of others.
#J-18808-Ljbffr