Senior Specialist Regulatory Affairs Jobs at Vantive | Life Sciences Jobs | Apply Now
Are you seeking growth-oriented Senior Specialist regulatory affairs jobs in a mission-driven organization? Vantive Careers brings a compelling opportunity for regulatory professionals aiming to build long-term Life Sciences Jobs in global regulatory strategy, post-approval compliance, and marketing authorization support. This role blends scientific expertise, regulatory leadership, and cross-functional collaboration to drive meaningful impact on patient care.
- Job Title: Senior Specialist, Regulatory Affairs
- Req. ID: JR-191963
- Location: Bengaluru, India
- Job Category: General Regulatory Affairs
About the Company:
Vantive is a vital organ therapy company with a 70-year legacy of innovation in kidney care. As the organization expands into digital solutions and advanced therapies, Vantive remains committed to improving patient outcomes and supporting care teams worldwide. The company fosters a focused, courageous, and purpose-driven work culture.
Job Overview:
The Senior Specialist Regulatory Affairs role is a full-time position based in Bengaluru. The role focuses on implementing global regulatory strategies, maintaining marketing authorizations, supporting regulatory submissions, and advising project teams. The specialist collaborates with cross-functional stakeholders and regulatory authorities to ensure compliance across pharmaceutical and medical device portfolios.
Educational Requirements:
- Bachelor’s degree or Minimum of 2 years of regulatory or equivalent experience in a pharmaceutical, medical device, CRO, or similar organization
Key Responsibilities:
- Develop and execute regulatory project plans with guidance
- Identify and escalate regulatory risks
- Maintain awareness of global regulatory requirements
- Compile and submit regulatory documents within defined timelines
- Maintain and update regulatory authorizations
- Respond to regulatory authority queries
- Prepare, review, and approve labeling and SOPs
- Support regulatory activities across product portfolios
- Represent Regulatory Affairs in project teams
Skills Required:
- Knowledge of US and European post-approval regulations (CBE/PAS)
- Strong scientific and regulatory knowledge
- Project management and multitasking skills
- Ability to manage multiple deadlines
- Strong interpersonal, communication, and negotiation skills
- Proficiency in regulatory documentation systems and technical tools
- Ability to identify compliance risks and escalate appropriately
These Senior Specialist regulatory affairs jobs at Vantive offer a meaningful opportunity for professionals seeking impactful Life Sciences Jobs in a globally respected organization. If you are driven by compliance excellence and patient-centric innovation, this role provides a rewarding next step in your regulatory career.
