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USA-Validation Specialist III (Engineering)

Ascent Services Group

Job Description

Validation Specialist III #21-02864
Swiftwater, PA
**Local Candidates
 
Job Description:
  • Experience in cleaning validation in the biologics or vaccine industry
  • Experience in authoring, reviewing, executing and approving validation documents
  • Interface with Quality organization and the ability to defend rationale in validation documents
  • Ability to review and analyze data
  • Cleaning Validation experience
  • Acceptance criteria determination
  • Sampling procedures, plans and sample size determination
  • Rinse and Swab sampling experience
  • Bracketing and worse case rating
  • QC testing requirements
  • Dirty hold times and clean hold times
     
Job Requirements:
  • BS/MS in Science (e.g. Chemistry, Biochemistry, Analytical Chemistry) or Engineering (Chemical or Biochemical)
  • 4+ total years of experience working in a biologic, vaccine or pharma industry
  • Experience utilizing Microsoft Word, Excel, and Outlook
  • Experience writing and revising documents (e.g. testing methods, protocols, reports)
  • Experience performing testing in a GMP setting
  • MS Project experience
  • Proficiency in utilizing documentation system to author protocols and reports
  • Experience participating in teams and collaborative work environments.
  • Good communication skills (verbal and written), math skills, general computer skills
  • Team environment a must
  • E Doc/GEODE+ experience with a working knowledge of templates, workflows and approval process
  • Strong root cause analysis with cGMP experience.
  • **This role will require some night and weekend work
     

  •  

Job Requirements

 
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Job Snapshot

Location US-PA-Swiftwater
Employment Type Contractor
Pay Type Hour
Pay Rate N/A
Store Type Clinical & Scientific

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Terms & Conditions
Snapshot
Ascent Services Group
Company:
US-PA-Swiftwater
Location:
Contractor
Employment Type:
Hour
Pay Type:
N/A
Pay Rate:
Clinical & Scientific
Store Type:

Job Description

Validation Specialist III #21-02864
Swiftwater, PA
**Local Candidates
 
Job Description:
  • Experience in cleaning validation in the biologics or vaccine industry
  • Experience in authoring, reviewing, executing and approving validation documents
  • Interface with Quality organization and the ability to defend rationale in validation documents
  • Ability to review and analyze data
  • Cleaning Validation experience
  • Acceptance criteria determination
  • Sampling procedures, plans and sample size determination
  • Rinse and Swab sampling experience
  • Bracketing and worse case rating
  • QC testing requirements
  • Dirty hold times and clean hold times
     
Job Requirements:
  • BS/MS in Science (e.g. Chemistry, Biochemistry, Analytical Chemistry) or Engineering (Chemical or Biochemical)
  • 4+ total years of experience working in a biologic, vaccine or pharma industry
  • Experience utilizing Microsoft Word, Excel, and Outlook
  • Experience writing and revising documents (e.g. testing methods, protocols, reports)
  • Experience performing testing in a GMP setting
  • MS Project experience
  • Proficiency in utilizing documentation system to author protocols and reports
  • Experience participating in teams and collaborative work environments.
  • Good communication skills (verbal and written), math skills, general computer skills
  • Team environment a must
  • E Doc/GEODE+ experience with a working knowledge of templates, workflows and approval process
  • Strong root cause analysis with cGMP experience.
  • **This role will require some night and weekend work
     

  •  

Job Requirements

 
USA-Validation Specialist III (Engineering) Apply now