- Managing regulatory compliance activities and existing customer products and registrations as required and providing strategic planning for regulatory changes.
- Acting as the regulatory lead for site-specific activities (e.g., Quality Reviews, Change Committees, etc.)
- Co-ordinating and preparing regulatory documentation for clinical trial applications, Drug Master Files (DMFs), medical device technical documentation and registration CTD documents (where required).
- Managing or mentoring more junior staff as required to achieve the business and role goals and objectives.
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Medvacon Life Sciences Los Angeles, United StatesNO AGENCIES - pl do not submit. · Must be able to show proof of citizenship. · ***NOTE · If this opportunity interests you, please share a WORD resume that details your exp related to the job responsibilities and requirements. · Excellent opportunity to advance and grow your c ...
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Medical Director, Clinical Development
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Kite Pharma Santa Monica, United StatesFor Current Kite Pharma Employees and Contractors · Please log onto your Internal Career Site to apply for this job. · At Kite, we empower our leaders to step up, share ideas, listen, learn, and lead. We're welcoming bright, diverse, and imaginative minds; we're nurturing them ...
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Medical Director, Clinical Development
5 days ago
Gilead Sciences Santa Monica, United StatesMedical Director, Clinical Development - Hematology/Oncology · Medical Director, Clinical Development - Hematology/Oncology · United States - California - Santa Monica, United States Remote · Clinical Development & Clinical Operations · Regular · Job Description · At Gilead, were ...
Regulatory Affairs Pharma - Los Angeles, United States - Medvacon Talent Acquisition Llc
Description
NO AGENCIES - pl do not submit.W2 candidates only
***NOTE If this opportunity interests you, please share a WORD resume that details your exp related to the job responsibilities and requirements.
Scope
To support business in maintaining regulatory compliance of existing manufactured products for customers on a global basis.
Management and Mentoring (Approx. 10-20% of time):
Providing input and direction to the site on client's business on regulatory matters.
Providing regulatory support to team members as required on specific project issues ensuring alignment with global guidelines and legislation and the specific business needs of the client
Managing and/or mentoring members of the regulatory team as required.
Marketed Product and Manufacturing Site Support Duties and Responsibilities (Approx. 60 80% of Time):
Advising internal and external stakeholders of the likely regulatory requirements associated with planned and unplanned changes made within the site and organization.
Participating in technical reviews of data within technical teams to ensure alignment with current global guidelines and to ensure data is generated to meet regulatory needs, responding to regulatory questions from wider technical teams.
Managing regulatory authority meetings as required including preparing briefing documentation and presentations.
Membership of project teams, including estimating regulatory resource needs for incorporation into project plans and monitoring of regulatory activities versus the project plan; reporting of issues / delays to management.
Attending customer focused meetings and interfacing with identified regulatory contacts at the customer company including preparing and reviewing presentations.
Communication of regulatory learnings from other projects. E.g., IND feedback, MAA project feedback, Pre IND meeting outcomes to ensure continuous improvement.
Advising on CMC elements of variation / supplement packages as required.
Communicating expectations of approval timelines within the organization.
Other Duties and Responsibilities (Approx. 10-20% of Time):
Providing regulatory leadership for site-specific activities
Monitoring the developing and evolving global regulatory guidelines which impact the development and maintenance of medicinal products and providing assessments of the implications of the proposed legislation.
Recruiting, training, mentoring, motivating, and developing the team. Coaching and encouraging staff to be self-sufficient, to work actively with other departments and to become expert in their fields and where appropriate, to be active key members of project teams.
Ensuring continued personal development, identifying gaps, learning through doing and maintaining current knowledge of requirements for the
RequirementsGraduate in pharmacy or a life science (or equivalent).
12-15 years relevant experience of US, European or Global registration procedures (or significant experience in other areas of the pharmaceutical industry).
In-depth knowledge of the Global Regulatory Affairs environment Guidelines and legislation.
Deep practical knowledge of the drug regulatory processes in the US and background understanding of regulatory processes in other regions.
General understanding of drug development and pharmaceutical manufacturing from concept to launch including requirements for product development, manufacturing and marketing and the impact of regulatory changes on business goals/objectives.Broad understanding of the pharmaceutical business in general and of other relevant associated regulatory areas (e.g., Clinical Affairs, Medical Devices, Chemicals Regulations, etc.).
Regulatory Affairs Pharma professionals in Los Angeles
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RICH CHERRY
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