Regulatory Affairs Project Manager

Morton Grove  ‐ Onsite
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Keywords

Description

We seek a highly organized energetic individual to
  • Coordinate with cross functional members for initiating, planning, executing, monitoring, controlling of Exhibit batch at MGP
  • Act as the liaison with other line functions like Research & Development, Regulatory Affairs, Production, Quality Assurance, Quality Control, Purchase, Packaging Development, etc. to ensure smooth progress of the project.
  • Discuss the issues and problems with cross functional members, cut short the timelines, as and when possible
  • ANDA Deficiency response- executing, monitoring with stakeholders for solving the Deficiency
  • Manage detailed information using project tracking tools
  • Ensure continuous follow up advance preparation to avoid problems.
  • Forecast problems that may come during execution of project.


Qualifications:
  • A BS/MS Science degree or equivalent experience.
  • Strong interpersonal and problem-solving skills.
  • Self-starter expected to learn quickly and takes responsibility for deadlines.
  • Demonstrated computer literacy
  • Two years of pharmaceutical industry or related experience required with four or more years preferred.
  • Good Communication skills
  • Should be able to handle conflicts within group
  • Basic Project related technical knowledge
  • PMI. PMP certification is beneficial.


If you're interested, please apply today!

To find out more about Real please visit www.realstaffing.com
Start date
10/2013
From
Real Staffing
Published at
21.09.2013
Project ID:
602496
Contract type
Permanent
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