Pharma Deviation Management Specialist – Root Cause & CAPA

Pacer Group

Lansdale (Montgomery County)

Vor Ort

USD 117.096.000 - 130.872.000

Vollzeit

vor 34 Stunden
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

Pacer Group seeks a Deviation Management Specialist - I (Assistant) for a 12-month contract at its West Point, PA facility. Onsite role with pay rate $41/hr on W2. The position supports manufacturing and laboratory investigations in a cGMP environment within the Pharmaceuticals domain.

Responsibilities include leading deviations, implementing CAPA, and performing RCA with cross-functional teams. Qualifications include a science/engineering degree and 1–3 years of related experience.

Qualifikationen

  • B.S./M.S. in engineering or science field.
  • 1–3 years post-Bachelor's in a cGMP pharma/biotech environment; academic/internship accepted.
  • Experience writing investigations with root cause analysis and CAPA development.
  • Familiar with Lean Six Sigma and strong analytical/problem-solving skills.
  • Ability to work independently and in cross-functional teams.
  • Strong technical/scientific writing and verbal communication.

Aufgaben

  • Resolve deviations and implement corrective/preventive actions.
  • Lead manufacturing and laboratory investigations.
  • Provide on-floor technical/scientific support for manufacturing areas.
  • Develop working relationships with counterparts in aseptic manufacturing, testing, planning, and release.
  • Perform root cause analysis of laboratory test failures and deviations.

Kenntnisse

Root cause analysis
CAPA development
Lean Six Sigma
Analytical thinking
Verbal communication
Cross-functional teamwork

Ausbildung

B.S./M.S. in engineering/science

Jobbeschreibung

Pacer Group seeks a Deviation Management Specialist - I (Assistant) for a 12-month contract at its West Point, PA facility. Onsite role with pay rate $41/hr on W2. The position supports manufacturing and laboratory investigations in a cGMP environment within the Pharmaceuticals domain.

Responsibilities include leading deviations, implementing CAPA, and performing RCA with cross-functional teams. Qualifications include a science/engineering degree and 1–3 years of related experience.

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