PHARMAFull-time
PV Process Excellence Specialist
BANGALORE (IN)ONSITEPOSTED: 9/18/2026
PHARMAFull-time
HIRING ORGANIZATIONNOVO NORDISKPharmaceuticals / Healthcare
ROLE OVERVIEW
PV Process Excellence Specialist supporting global pharmacovigilance governance, regulatory intelligence, process improvement, training oversight, and inspection readiness from Novo Nordisk Global Business Services in Bangalore.
ROLE DEFINITION & RESPONSIBILITIES
- •Facilitate governance board logistics including agendas, meetings, minutes, and action tracking
- •manage surveillance and assessment of emerging PV regulations, guidelines, and industry practices
- •support PV process maturity and inspection readiness
- •oversee completeness of PV system impact assessments
- •support training completeness, timeliness, and inspection readiness
- •deputise ownership of procedural documentation
- •coordinate with global patient safety, R&D, affiliates, health authorities, and partners
Reporting Hierarchy: Reports to/works closely with the Director of PV Process Excellence and collaborates with the EU QPPV, Deputy QPPVs, Global Patient Safety leadership, QPPV Office, R&D, affiliates, health authorities, and contractual partners.
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Bachelor's degree in life sciences and/or pharmaceutical sciences
- minimum 5 years of relevant pharmacovigilance experience
- significant experience in pharmacovigilance operations, quality systems, governance, compliance, or QPPV Office functions
- strong understanding of worldwide pharmacovigilance regulations
- strong strategic planning, governance, oversight, communication, and stakeholder management skills
- fluent written and spoken English
PREFERRED QUALIFICATIONS
- •Experience in PV regulatory intelligence, process governance, training, QPPV Office activities, inspection readiness, and large-scale complex assignments
- •experience translating regulatory requirements into practical compliant processes
- •continuous improvement and change-management experience
REQUIRED VERIFIED SKILLS
Pharmacovigilance
PV operations
PV regulations
regulatory intelligence
quality systems
governance
compliance
inspection readiness
process improvement
training oversight
impact assessment
stakeholder management
strategic planning
English communication
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Benefits may include professional development, employee wellbeing programs, learning opportunities, and standard corporate benefits; exact benefits vary by location and eligibility.
No salary or monetary bonus amount is disclosed in the supplied posting; compensation should be verified through the official application process.
ORGANIZATION CONTEXT & CULTURE
Novo Nordisk is a global healthcare and pharmaceutical company focused on developing medicines and solutions for serious chronic diseases, with more than a century of operations.
TEAM SIZE: 70,000+ employees globally
INDUSTRY: Pharmaceuticals / Healthcare
Culture: Global, collaborative, compliance-focused, patient-safety-driven culture emphasizing continuous improvement, mutual respect, operational excellence, and simplification without compromising compliance.
EXPECTED CAREER ROADMAP
Offers opportunities to deepen global pharmacovigilance governance and regulatory intelligence expertise, with potential progression into senior PV process excellence, quality, compliance, governance, or QPPV Office leadership roles.
APPLICATION ADVISORY
Emphasize 5+ years of pharmacovigilance experience, global PV regulatory knowledge, governance and quality-system exposure, inspection readiness, regulatory intelligence, process improvement, and stakeholder-management experience. Show examples of translating regulations into practical compliant processes.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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