Not specified; not specified; benefits available a...
Not specified (potentially hybrid or onsite based on industry norms).
5+ years pharmaceutical engineering experience
Fractionation and aseptic processing expertise
Gmp compliance and contamination control knowledge
CSL Behring is seeking a Senior Production Engineer specializing in fractionation to provide engineering support for pharmaceutical manufacturing operations. The role focuses on equipment reliability, compliance with GMP standards, and continuous improvement initiatives while collaborating with various teams
Job Summary
The Senior Production Engineer provides technical leadership to ensure optimal asset performance and compliance throughout the pharmaceutical asset lifecycle.
This role drives risk-based asset management strategies aligned with ISO 55000 principles and GMP requirements while partnering with production and maintenance teams.
CSL Behring is a global biotherapeutics leader committed to saving lives through innovative therapies derived from plasma fractionation and recombinant protein technology.
Matching Summary
Match Score: 85
CSL Behring is seeking a Senior Production Engineer specializing in fractionation to provide engineering support for pharmaceutical manufacturing operations. The role focuses on equipment reliability, compliance with GMP standards, and continuous improvement initiatives while collaborating with various teams.
Salary
Not specified; Not specified; Benefits available as per CSL policy
Skills & Requirements
Must-have
5+ years pharmaceutical engineering experience
Fractionation and aseptic processing expertise
GMP compliance and contamination control knowledge
Root cause analysis and CAPA implementation
SAP CMMS data analysis skills
ISO 55000 asset management alignment
Nice-to-have
Six Sigma or Lean principles knowledge
Mentoring junior engineers and technicians
Cross-functional collaboration with quality teams
Experience with capital project execution
Key Requirements
Bachelor's degree in Engineering (Mechanical, Chemical, Biomedical)
Master's degree preferred
Proven experience in cGMP environments
Strong technical problem-solving abilities
Ability to lead projects within budget and timeline