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Process Development Engineer

In California / United States

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Process Development Engineer   

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JOB TITLE:
Process Development Engineer
JOB TYPE:

JOB SKILLS:
JOB LOCATION:
Thousand Oaks California / United States

JOB DESCRIPTION :

Title: Process Development Engineer

Location: Thousand Oaks, CA

Here they want person to be onsite 25% of the time in California

Experience in development/characterization and tech transfer of aseptic fill/finish unit operations (freeze/thaw, mixing, sterile filtration, filling, stoppering, visual inspection, etc.) to define critical process parameters (3-5 years of experience)

MS in Chemical/Biomedical Engineering, Pharmaceutical Sciences, Chemistry/Biochemistry or Biotechnology

3+ years of experience within the pharmaceutical/biotechnology industry

Experience in development/characterization of aseptic fill/finish unit operations (freeze/thaw, mixing, sterile filtration, filling, stoppering, visual inspection, etc.) to define critical process parameters

Familiarity with Design of Experiments (DOE) and Quality by Design (QbD) principles

Familiarity with cGMPs, regulatory filings, and compliance issues for sterile injectable products manufactured by aseptic processing

Experience in a matrix team environment and interacting with Analytical Sciences, Process Development, Project Management, Manufacturing, Regulatory, Compliance, and/or Quality

Organizational, technical problem solving, communication (written and verbal) skills, and regular interactions

Position Details

S16174660767202928
California / United States
Thousand Oaks
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Process Development Engineer    Apply

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Title: Process Development Engineer

Location: Thousand Oaks, CA

Here they want person to be onsite 25% of the time in California

Experience in development/characterization and tech transfer of aseptic fill/finish unit operations (freeze/thaw, mixing, sterile filtration, filling, stoppering, visual inspection, etc.) to define critical process parameters (3-5 years of experience)

MS in Chemical/Biomedical Engineering, Pharmaceutical Sciences, Chemistry/Biochemistry or Biotechnology

3+ years of experience within the pharmaceutical/biotechnology industry

Experience in development/characterization of aseptic fill/finish unit operations (freeze/thaw, mixing, sterile filtration, filling, stoppering, visual inspection, etc.) to define critical process parameters

Familiarity with Design of Experiments (DOE) and Quality by Design (QbD) principles

Familiarity with cGMPs, regulatory filings, and compliance issues for sterile injectable products manufactured by aseptic processing

Experience in a matrix team environment and interacting with Analytical Sciences, Process Development, Project Management, Manufacturing, Regulatory, Compliance, and/or Quality

Organizational, technical problem solving, communication (written and verbal) skills, and regular interactions