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Associate Tech Ops Biotech Manufacturing West Point PA month contract

In Pennsylvania /

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Associate Tech Ops Biotech Manufacturing West Point PA month contract   

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JOB TITLE:

Associate Tech Ops Biotech Manufacturing West Point PA month contract

JOB TYPE:

JOB SKILLS:

JOB LOCATION:

West Point Pennsylvania /

JOB DESCRIPTION:

Title: Associate Tech Ops - Biotech Manufacturing

Location: West Point, PA (12-month contract)

Qualifications:

  • Bachelor's Degree in Science/Engineering
  • 2+ years of experience in biopharmaceutical/chemical manufacturing
  • 6+ months of cGMP experience in vaccine manufacturing
  • Knowledge of Change Control, CFR, and regulations
  • Experience with TrackWise, MS Project, and Excel
  • Strong problem-solving and communication skills
  • Familiarity with aseptic vaccine manufacturing and process changes

Responsibilities:

  • Provide technical support for commercial manufacturing projects
  • Manage project schedules and resources
  • Engage stakeholders and manage communications
  • Develop and execute change control protocols and regulatory filings
  • Author/update technical and manufacturing documents
  • Design and conduct experimental protocols
  • Identify and resolve root causes of issues
  • Apply standardized work, engineering, and process tools
  • Provide technical support for manufacturing investigations and process improvements

Note: This role requires a proactive and collaborative mindset, and the ability to work both independently and as part of a team

Position Details

POSTED:

Apr 21, 2023

EMPLOYMENT:

INDUSTRY:

Others

SNAPRECRUIT ID:

S3047-9767-03232023-304802

LOCATION:

Pennsylvania /

CITY:

West Point

Job Origin:

CEIPAL_ORGANIC_FEED

A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Associate Tech Ops Biotech Manufacturing West Point PA month contract    Apply

Click on the below icons to share this job to Linkedin, Twitter!

Title: Associate Tech Ops - Biotech Manufacturing

Location: West Point, PA (12-month contract)

Qualifications:

  • Bachelor's Degree in Science/Engineering
  • 2+ years of experience in biopharmaceutical/chemical manufacturing
  • 6+ months of cGMP experience in vaccine manufacturing
  • Knowledge of Change Control, CFR, and regulations
  • Experience with TrackWise, MS Project, and Excel
  • Strong problem-solving and communication skills
  • Familiarity with aseptic vaccine manufacturing and process changes

Responsibilities:

  • Provide technical support for commercial manufacturing projects
  • Manage project schedules and resources
  • Engage stakeholders and manage communications
  • Develop and execute change control protocols and regulatory filings
  • Author/update technical and manufacturing documents
  • Design and conduct experimental protocols
  • Identify and resolve root causes of issues
  • Apply standardized work, engineering, and process tools
  • Provide technical support for manufacturing investigations and process improvements

Note: This role requires a proactive and collaborative mindset, and the ability to work both independently and as part of a team


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