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          Posted/Modified on: 02/06/2015 14:23 PDT
  Job Title:            
    Project Manager/Scheduler - Pharmaceutical Post OQ/IQ Validation  
                   
  Contact Name / Company:        
    Mark Raspotnik / The Spear Group, Inc.  
                   
  Contact e-mail:            
    mraspotnik@speargroup.com  
                   
  Contact Phone:            
    678-775-4489  
                   
  Industry:            
    Pharmaceutical/Biotech  
                   
  Location:            
    Elkton, VA  
                   
  Salary:            
    0  
                   
  Job Description:            
    Project Manager/Scheduler - Pharmaceutical Post OQ/IQ Validation

Elkton, VA

Posted: 2/6/2015
Category: Project Management
Job Type: Contractor

Minimum Experience: 7+
Required Education: BS Desired
Benefits: Dental
Medical

Job Description

Job #4021: Project Manager/Scheduler - Pharmaceutical Post OQ/IQ Validation



Industry: Pharmaceuticals (Vaccines Manufacturing)
Location: Elkton, VA
Duration: 2 years+


The Spear Group Inc. has an immediate need for a Pharmaceutical Project Manager/Scheduler working on Post Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ).

Responsibilities:
Manage Updates, Provide Monthly Reports, Confirm Completions, Outline/Highlight critical path per schedule
Meeting Note Scribe/Action list - update spreadsheets, participate in meetings
Drawing, Upload to team site - Organize and Assist with Drawing updates (IPS, Equipment, Process, PFDs, etc.)
Maintain and Coordinate updates to plan.
Organize, Manage protocol numbering, approval process for BSV and Tech Ops Studies
Manage Validation through licensing detailed schedule
Manage Action items
Facilitate Meetings
Will be using Primavera scheduling software
Managing construction schedules for underground construction projects
Work with the other members of the EPC contracting teams
Adjust schedules as necessary to model field­level constraints and potential changes to schedules due to field changes
Coordinate documentation to support PQ, stability and licensing.
** Projects will have 6 to 12 months on schedule with one project having 24+ months on its schedule.


Job Requirements

Requirements:

BS in Engineering or Science related field desireable.
5 + years of Experience in Pharmaceutical Manufacturing setting, dealing with Validation process.
5 + years of Experience in Project Management/Project Controls, Scheduling.
Advance knowledge of Primavera and Excel.
                   
       
           
   
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