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Job Title: Engineer - At-scale biologics purification (JP9826)
Location: Thousand Oaks, CA. 91320
Employment Type: Contract
Business Unit: ATO Process Engineering
Duration: 1+ years (with likely extensions and/or conversion to permanent)
Posting Date: 2/16/2022
Notes: Candidate will be required to be on site 4-5 days a week and may work remotely 1-2 days a week.
3 Key Consulting is hiring an Engineer for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Seeking a Process Development Engineer to join the Drug Substance Technology Engineering team at our client’s 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 purification 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. Under guidance of senior staff the engineer performs the following:
Why is the Position Open?
Supplement additional workload on team.
Top Must Have Skills:
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.
Basic Qualifications:
Master’s degree
OR
Bachelor’s degree
Associate’s degree and 7 years of Engineering or Operations experience
OR
High school diploma / GED and 8 years of Engineering or Operations experience
Preferred Qualifications:
Employee Value Proposition:
The person in this role will help manufacture clinical and commercial molecules. There are many unique opportunities to work on different programs.
Red Flags:
Interview process:
Video Skype Panel Interview
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 also welcome to share this opportunity with anyone you think might be interested in applying for this role.
Location: Thousand Oaks, CA. 91320
Employment Type: Contract
Business Unit: ATO Process Engineering
Duration: 1+ years (with likely extensions and/or conversion to permanent)
Posting Date: 2/16/2022
Notes: Candidate will be required to be on site 4-5 days a week and may work remotely 1-2 days a week.
3 Key Consulting is hiring an Engineer for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Seeking a Process Development Engineer to join the Drug Substance Technology Engineering team at our client’s 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 purification 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. Under guidance of senior staff the engineer performs the following:
- Transfer 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
Why is the Position Open?
Supplement additional workload on team.
Top Must Have Skills:
- At-scale biologics purification knowledge and 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.
Basic Qualifications:
Master’s degree
OR
Bachelor’s degree
Associate’s degree and 7 years of Engineering or Operations experience
OR
High school diploma / GED and 8 years of Engineering or Operations experience
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
- Purification process knowledge:
- Knowledge of purification processes/ equipment; scale up factors from, chromatography, UF/DF, process deviations, raw materials to growth and quality attributes
- 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:
The person in this role will help manufacture clinical and commercial molecules. There are many unique opportunities to work on different programs.
Red Flags:
- Multiple short duration jobs on resume.
- No purification experience.
Interview process:
Video Skype Panel Interview
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 also welcome to share this opportunity with anyone you think might be interested in applying for this role.