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Technical Project Manager

Actively Reviewing the Applications

Biocon

India Full-Time
Posted 1 day ago Apply by June 30, 2026

Job Description

Global Quality & Corporate IT – Technical Manager


Location: Bengaluru, Karnataka


Department: Information Technology – Quality and Corporate IT.


Purpose

Responsible for end-to-end support, technical architecture oversight, vendor, stakeholder management and compliance of GxP-regulated Quality & Corporate IT Systems (QMS, DMS, Artwork. CLMS, GRC Digital platform etc.) within a Life Sciences / Pharmaceutical environment. Ensures availability, validation, data integrity, and audit readiness of Quality applications, with exposure to technical management of assigned IT applications.


Key Responsibilities


IT Application management

  • Support Veeva QMS, DMS - document management system, Artwork and other regulated global Quality platforms
  • Manage incidents, problems, changes, and releases as per ITIL
  • Ensure system uptime, performance, and data integrity
  • Coordinate releases, upgrades, and validation impact assessments of the assigned IT systems

Technical management

  • Own application architecture, integrations, APIs, and data flows
  • Perform architectural impact and validation assessments
  • Ensure scalability, security, and compliance
  • Ensure all systems adhere to IT security guidelines and standards.
  • Support entire Global Quality & Corporate IT team for all technical requirements.

Stakeholder & Vendor Management

  • Act as primary IT point of contact for Quality, Compliance and Business stakeholders for all technical-related questions.
  • Manage and coordinate vendors, SaaS providers, and system integrators
  • Lead service reviews, SLA tracking, and vendor performance management
  • Communicate effectively with global stakeholders and leadership

GxP / GMP / Validation/ QMS Governance

  • Ensure compliance with GxP, GMP, 21 CFR Part 11, EU Annex 11
  • Support CSV (IQ, OQ, PQ)
  • Participate in audits and inspections
  • Work closely with QA and Compliance teams
  • Maintain SOPs, validation documents, and system review artifacts


Skills and Experience


Mandatory

  • Experience in support/maintenance of Quality Management Systems in Life Sciences
  • ITIL-based application support
  • GxP, GMP, CSV, QMS knowledge
  • Application architecture exposure with in-depth knowledge of integration to other systems.

Soft Skills and Competencies

  • Strong verbal and written communication skills
  • Proven stakeholder engagement and relationship management abilities
  • Vendor management and negotiation skills
  • Ability to work cross-functionally with IT, Quality, Regulatory, and Business teams
  • High ownership, accountability, and problem-solving mindset

Preferred

  • QMS, Veeva Quality, DMS
  • SAP, LIMS, MES integrations
  • ITIL certification
  • Good understanding of release management
  • Expert in GxP understanding

Experience

  • 7-12 years overall IT experience
  • 4-6+ years in Life Sciences Quality IT

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