Great opportunity for Project Management Manager @ SunGlow Life Science- M.Pharm, B.Pharm Apply

  • Full Time
  • CHENNAI

Website SunGlow

SunGlow is a company that was incorporated in January 2010 and founded by a group of experienced industry professionals. The corporate office is situated in Chennai, India. SunGlow has two manufacturing facilities, each serving different markets.

The first facility is located in Puducherry, a small state in southern India, approximately 145 kilometers south of Chennai. This facility is focused on manufacturing products for the domestic market, catering to customers within India.

The second facility is situated in Chengalpattu, a town around 80 kilometers southwest of Chennai. This facility is dedicated to manufacturing products for the global market, targeting customers worldwide.

Job Title: Manager – Project Management Location: Chennai, India Email: hr_admin@sunglowlifescience.com Application Deadline: June 10th, 2023

Job Description: We are currently seeking a qualified individual for the position of Manager – Project Management. The responsibilities and qualifications for this role are as follows:

Responsibilities:

  • Project planning and project initiation.
  • Knowledge in formulation development, technology transfer, and manufacturing for higher regulatory markets.
  • Expertise in end-to-end project planning, implementation, and execution.
  • Planning various project-related activities, including manufacturing slots and analytical activities.
  • Planning and coordinating with CRO (Contract Research Organization) for BE studies and monitoring the activity.
  • Coordinating the timely delivery of documents required for dossier preparation.
  • Providing cross-functional forecasting, tracking, and reporting to management.
  • Managing cross-functional project timelines and conducting frequent follow-ups with project team members to ensure timely completion.
  • Resolving conflicts within the project team.
  • Proactively identifying and managing project opportunities, risks, and issues.
  • Logistics management, licensing, RLD (Reference Listed Drug) sourcing, etc.
  • Conducting regular status meetings with internal stakeholders.

Candidate Profile:

  • Qualification: B.Pharmacy / M.Pharmacy
  • Experience: 8-12 years in the pharmaceutical industry with extensive knowledge in oral solid dosage form development and manufacturing, along with exposure to higher regulatory markets.

If you meet the qualifications and are interested in this position, please submit your resume to hr_admin@sunglowlifescience.com before the application deadline of June 10th, 2023.

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To apply for this job email your details to hr_admin@sunglowlifescience.com