
Senior Regulatory Affairs Manager
4 days ago
Graduate of any four (4) year course.
• Bachelor's degree in Life Sciences or a related field; advanced degree preferred.
• Extensive experience in regulatory affairs, including drug development, manufacturing, and commercialization.
• Proven leadership and project management capabilities.
• Experience working across multiple regulatory functions and strong partnerships with FDA.
• Knowledgeable with Permits and Licenses, Liaison, Effective Internal and External Communication, Strong Leadership, Emotional Intelligence, Delegation, Organizational and Management Skills.
• Goal Oriented, highly motivated, organized and with keen eye for detail
• Have succeeded leadership roles over the last 10-12 years with 3 years in the same capacity or level
• Work with leadership to deliver quality output, monitor and communicate status and progress towards the goals.
• Excellent and professional communicator across written, verbal and presentations
• Communicates, builds and maintains good working relationship between the team, different departments, stakeholders, top level executives and various government offices
• Delegates tasks effectively.
• Sets schedule, timeline and target among team members and concerned departments to deliver quality output/ results within the agreed time frame.
• Provides support, motivation, assistance and mentoring among team members to improve process, to avoid possible setbacks and to deliver quality results/output.
• Plans and identifies seminars, trainings, workshops, etc. that will be of help to the team members in order improve their skills, knowledge, etc. That may also help them and the team to meet the goal and deliverables.
Salary Budget: 90k to 120k
Type of employment: Regular/Contractual: Regular
Work location: Pasig
Work arrangement: Hybrid
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