×
Register Here to Apply for Jobs or Post Jobs. X

Deviation Management Specialist Assistant

Job in West Point, Montgomery County, Pennsylvania, 19486, USA
Listing for: Spectraforce Technologies
Full Time position
Listed on 2026-07-19
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Manufacturing Engineer, Validation Engineer
Salary/Wage Range or Industry Benchmark: 70000 - 90000 USD Yearly USD 70000.00 90000.00 YEAR
Job Description & How to Apply Below
Position: Deviation Management Specialist - I (Assistant)
Location: West Point

Position Title:
Deviation Management Specialist - I (Assistant)

Work Location:
West point, PA 19486

Assignment Duration: 12 months

Work Arrangement:
Onsite

Position Summary

Primary responsibilities include day-to-day technical support to manufacturing operations, including resolution and reduction of process deviations, development and implementation of corrective/preventative actions, and leading manufacturing investigations.

Background & Context

This individual will be responsible for providing scientific support for manufacturing areas within our organization's Manufacturing Division (MMD).

Key Responsibilities
  • Primary responsibilities include day-to-day technical support to manufacturing operations, including resolution and reduction of process deviations, development and implementation of corrective/preventative actions, and leading manufacturing investigations
  • This individual will be responsible for providing scientific support for manufacturing areas within our organization's Manufacturing Division (MMD)
  • This Individual will also develop working relationships with counterparts in other areas supporting aseptic manufacturing, testing, planning, and release and is required to utilize sound scientific and engineering principles to investigate process deviations
  • Troubleshooting and root cause analysis of manufacturing atypical events, development of corrective/preventative actions is required
  • Analysis of complex problems through critical analytical thinking
  • Off-shift work may be required.
Qualification & Experience
  • B.S./M.S. degree in appropriate engineering/scientific field
  • Minimum of 0-3 years post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Technical Services or related field) in pharmaceutical/biotech industry
  • Previous experience in writing investigations for atypical events in a manufacturing environment
  • Familiar with Lean Six Sigma Methodologies and proven analytical/problem solving capabilities
  • Demonstrated ability to work both independently and as a part of a cross-functional team
  • Excellent written and verbal communication skills
#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary