AM/DM - Project Management - Pharma - CDMO Hyderabad

SAI Life Sciences

Hyderabad

On-site

INR 1,500,000 - 2,500,000

Full time

6 days ago
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Job summary

SAI Life Sciences is seeking a Project Management professional in Shameerpet, Hyderabad, to lead complex CDMO projects from kickoff through closure. The role requires strong cross-functional collaboration with R&D, tech transfer, QA/QC, and production teams, along with rigorous schedule tracking and customer updates.

Candidates should have a 6-year track record in science-based projects, PMP or MBA is preferred but not mandatory, and at least 4 years as a Program Manager in a CDMO environment. //

Qualifications

  • M.Sc. (Chemistry) or Chemical Engineering; minimum 6 years in cross-functional settings.
  • PMP certification and/or MBA preferred but not mandatory.
  • At least 4 years as Program Manager in a reputed CDMO.

Responsibilities

  • Kick off the awarded project on time.
  • Prepare and update a comprehensive Gantt chart for delivery schedule.
  • Coordinate with cross-functional teams (R&D, AR&D, Technology Transfer, Process Engineering, Production or Outsourcing) through meetings.
  • Prepare and update action trackers for project activities.
  • Send scheduled updates to the customer and BD.
  • Schedule telcons/VC with customer and facilitate technical discussions.
  • Highlight and escalate roadblocks to senior management.
  • Ensure complete and timely project closure documentation and invoicing updates.

Job description

Department: Project Management


Location: Shameerpet


About Us: Sai Life Sciences is one of the fastest-growing Contract Research, Development, and Manufacturing Organizations (CRDMOs). As a pure-play, full-service partner, we collaborate with over 300 global innovator pharma and biotech companies to accelerate the discovery, development, and commercialization of their NCE programs. We have over 3000 employees across our facilities in India, the UK, and the USA, working together to deliver scientific excellence and customer success. We are a Great Place to Work certified organization with a culture of openness, mutual respect, and inclusivity. We embrace diversity and follow equal opportunity practices across all levels.


Key Responsibilities:

  • To timely kick off the awarded project
  • To timely prepare and update, comprehensive Gantt chart for the project delivery schedule
  • Regularly coordinate with CFT comprising of PR&D, AR&D, PE, QA, QC, Production etc, through daily meetings as well as issue-based meetings
  • To prepare and update the comprehensive action tracker for the project activities
  • To send the prescheduled updates to the customer and BD
  • To schedule the telcons / VC with customer and facilitate discussion between technical teams
  • To highlight and escalatethe roadblocks or anticipated roadblocks to the senior management team
  • To ensure complete and timely documentation on project closure
  • To timely raise the invoice and update finance and BD of the same

Performance Indicators

  • QUOTIF as per commitment
  • Overall management of projects, project creeps and communications

Job specifications / pre-requisites:(Qualification, experience, any other specifications)

M.Sc. (Chemistry) or Chemical Engineering, with minimum 6 years experience working along with CFTs (PR&D, AR&D, Technology Transfer, Process Engineering, Production or Outsourcing) PMP certification and / or MBA desired but not must. Additionally, minimum 4 years experience as Program Manager with a reputed CDMO. Ideally API CDMO but can also be from formulation CDMO or least preferred from Clinical Research Organization.

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