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Process Engineer - Biotech (JP7381)

Thousand Oaks, California · Biotech/Pharmaceutical
Job Title:  Process Engineer - Biotech (JP7381)
Location: Thousand Oaks, CA
Employment Type:  Contract
Business Unit: Process Engineering
Duration: 12+ months (with likely extensions)
Posting Date: 6/17/20
 
3 Key Consulting is hiring an Engineer for a consulting engagement with our client, a leading global biopharmaceutical company.
 
Job Description:
Seeking a Process Development Engineer to join the Drug Substance Process Engineering team at our Thousand Oaks facility. Providing process engineering support for human therapeutic products in clinical development through commercial production, our mission is to translate developmental processes to commercial reality for patients through scientific expertise and engineering innovation.

The Engineer will apply cell culture process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing in an innovative manufacturing suite using single-use technology. Will partner with manufacturing, quality, analytical, and bench scientists to support a highly dynamic manufacturing facility.
 
Top Must-Have Skill Sets:
  • At-scale biologics cell culture or purification experience
  • Strong understanding of data analysis tools
  • Excellent communication and troubleshooting. 
     
Day to Day Responsibilities:
Staff will perform tech transfer of early clinical candidate molecules. In addition, staff will support all processes (clinical and commercial) executed in the facility, performing process monitoring and responding to issues as appropriate.
 
JOB RESPONSIBILITIES:
Under guidance of senior staff, the Engineer performs the following:
  • Transfer cell culture or purification drug substance processes and performs process improvements from the laboratory into the manufacturing facility
  • Provide technical support for successful scale-up, transfer of process technology, and for clinical and/or commercial manufacturing operation
  • Offer process validation support for late stage commercial processes
  • Provide routine process monitoring and troubleshooting
  • Execute data trending and statistical process analysis
  • Support technical direction for process related deviations, CAPAs and change controls
  • Identify and support process related operational excellence opportunities
  • Represent process development and collaborates with other functions such as Manufacturing, Quality, and Regulatory
 
BASIC QUALIFICATIONS:
Master’s degree OR Bachelor’s degree


PREFERRED QUALIFICATIONS:
  • Master’s Degree in Chemical or Biochemical Engineering
  • 1+ years of Process Engineering experience preferably related to scale-up principles and commercial cGMP manufacturing facilities
  • Background in biologics tech transfer into commercial facilities
  • Upstream process knowledge:
    o Knowledge of cell culture or purification processes/ equipment; scale up factors from, mass oxygen transfer capabilities impact of metabolism, chromatography, UF/DF, process deviations, raw materials to growth and quality attributes OR
  • Strong capability of analysis, troubleshooting and problem solving
  • Ability to develop and follow detailed protocols
  • Independently motivated with ability to multi-task and work in teams
  • Excellent written and verbal communication skills with technical writing and presentation experience  
 
Employee Value Proposition:
High level technical exposure to cross functional teams within company.
 
Red Flags:
Multiple short duration jobs on resume. 
 
Interview process:
Phone screen, followed by teleconference
 
We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are welcome to also share this opportunity with anyone you think might be interested in applying for this role.
 
 
 
Regards,
 
3KC Talent Acquisition Team
 
 
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