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Jobs or company...

Deviation Management Specialist

  • Full Time, onsite
  • Zachary Piper Solutions, LLC
  • On Site, United States of America
Salary undisclosed
Checking job availability...
Original
Simplified
Piper Companies is seeking a Deviation Management Specialist to fill an opportunity with a reputable Pharmaceutical company in Lansdale, PA.

Responsibilities for the Deviation Management Specialist
  • Investigate deviations by assessing product impact, identifying root causes, and implementing corrective/preventative actions.
  • Author and update GMP documentation, including SOPs, batch records, validation documents, and change controls.
  • Write quality incident and deviation reports, ensuring thorough analysis and compliance.
  • Collaborate with cross-functional teams to drive process improvements, resolve investigations, and maintain compliance.


Qualifications for the Deviation Management Specialist
  • 2-4 years of experience in deviation management and investigations within biologics, vaccines, or sterile manufacturing.
  • Proficient in Change Control processes and technical writing.
  • Strong communication, leadership, and teamwork abilities.
  • Skilled in managing projects and meeting deadlines.


Compensation for the Deviation Management Specialist
  • Salary Range is Commensurate with Experience
  • Long Term Contract (Possible Extension)
  • Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays

This job opens for applications on 4/23/2025. Applications for this job will be accepted for at least 30 days from the posting date.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job
Piper Companies is seeking a Deviation Management Specialist to fill an opportunity with a reputable Pharmaceutical company in Lansdale, PA.

Responsibilities for the Deviation Management Specialist
  • Investigate deviations by assessing product impact, identifying root causes, and implementing corrective/preventative actions.
  • Author and update GMP documentation, including SOPs, batch records, validation documents, and change controls.
  • Write quality incident and deviation reports, ensuring thorough analysis and compliance.
  • Collaborate with cross-functional teams to drive process improvements, resolve investigations, and maintain compliance.


Qualifications for the Deviation Management Specialist
  • 2-4 years of experience in deviation management and investigations within biologics, vaccines, or sterile manufacturing.
  • Proficient in Change Control processes and technical writing.
  • Strong communication, leadership, and teamwork abilities.
  • Skilled in managing projects and meeting deadlines.


Compensation for the Deviation Management Specialist
  • Salary Range is Commensurate with Experience
  • Long Term Contract (Possible Extension)
  • Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays

This job opens for applications on 4/23/2025. Applications for this job will be accepted for at least 30 days from the posting date.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job