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Manager, Planning & Administration

Astellas
Astellas
3-7+ years
Not Disclosed
Bengaluru, India
10 Feb. 19, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Manager, Planning & Administration

Location: Bengaluru, India
Company: Astellas Pharma Inc.
Industry: Pharmaceutical / Regulatory Affairs / Pharmacovigilance
Employment Type: Full-Time
Experience Required: Minimum 7 years

ThePharmaDaily.com presents an excellent leadership opportunity with Astellas Pharma Inc., a global pharmaceutical organization operating in more than 70 countries. The company is focused on transforming innovative science into meaningful medical solutions that address unmet patient needs worldwide.

This role is best suited for experienced professionals in regulatory operations, pharmacovigilance, portfolio management, and pharmaceutical project governance who are looking to contribute within a Global Capability Centre (GCC) environment.

About Astellas Global Capability Centres (GCCs)

Astellas’ Global Capability Centres are strategically located in India, Poland, and Mexico. These centres consolidate key capabilities across the pharmaceutical value chain, improving operational efficiency, resilience, and innovation while supporting global business priorities.

The Bengaluru GCC plays a vital role in regulatory, pharmacovigilance, and portfolio oversight functions.

Role Purpose

The Manager, Planning & Administration collaborates with global stakeholders to execute major Planning & Administration (P&A) programs and continuous improvement initiatives.

The position contributes to RAPV (Regulatory Affairs & Pharmacovigilance) Portfolio/PMO oversight, manages selected non-drug project initiatives, and leads operational oversight of:

  • Training Management (Learning Management Systems including GVP compliance)

  • Records Information Management (RIM)

  • Budget planning and forecasting cycles

  • Business continuity coordination

This is a strategic and operational role within a highly regulated pharmaceutical environment.

Key Responsibilities

  • Contribute to RAPV Portfolio/PMO governance and maintain oversight of non-drug project portfolios

  • Serve as Project Manager for selected cross-functional initiatives

  • Support business process design, implementation, and ongoing monitoring

  • Lead annual, mid-term, and long-term business planning including budget and resource forecasting

  • Prepare financial analyses and scenario planning reports

  • Oversee Training Management operations (LMS implementation, compliance tracking, remediation planning)

  • Maintain RIM procedures, documentation controls, and audit readiness

  • Support inspections, audits, and corrective/preventive action plans

  • Coordinate global cross-functional stakeholders to ensure timely delivery

  • Support Business Continuity Planning (BCP) activities

  • Drive process improvement and organizational transformation initiatives

Required Qualifications

  • Bachelor’s degree (Science or Technology preferred)

  • Minimum 7 years of experience in regulatory operations or similar regulated pharmaceutical processes

  • Experience in pharmaceutical portfolio or PMO environments

  • Strong project management and stakeholder coordination skills

  • Demonstrated change management and process improvement experience

  • Strong analytical skills in budgeting and resource planning

  • Excellent written and verbal communication skills in English

  • Ability to manage multiple priorities across regions and time zones

  • High integrity in handling confidential and proprietary information

  • Ability to perform effectively under pressure

Preferred Qualifications

  • Bachelor’s degree in Pharmacy, Life Sciences, or Technology

  • 7+ years of pharmaceutical industry experience

  • 3+ years of project or program leadership experience

  • Experience in Training Management (LMS, Good Pharmacovigilance Practices compliance)

  • Experience in Records Information Management (RIM)

  • RA/PV operations exposure

  • Project management certification (PMBOK, PRINCE2, or equivalent)

  • Experience with portfolio and project management tools

  • Additional language skills depending on region

Working Model

Astellas offers a hybrid working model aligned with Responsible Flexibility Guidelines, enabling a balance between office collaboration and remote work.

Equal Opportunity Statement

Astellas is committed to equal opportunity in all aspects of employment and fosters an inclusive workplace environment.