drjobs Engineer Process Development hybrid JP13072

Engineer Process Development hybrid JP13072

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1 Vacancy
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Job Location drjobs

Thousand Oaks, CA - USA

Hourly Salary drjobs

$ 38 - 42

Vacancy

1 Vacancy

Job Description

Job Title: Engineer Process Development hybrid (JP13072
Location: Thousand Oaks CA. 91320 (hybrid)
Business Unit: Drug Substance Technology and Engineering
Employment Type: Contract
Duration: 1 year(s) with likely extensions and/or conversion to permanent.
Rate: $38 $42/hour W2
Posting Date: 8/6/2024.
Notes: Only qualified candidates need apply. Onsite 34 days a week at Thousand Oaks CA. campus. Standard business hours with some after hour support. On site minimum 3 days per week. Must have biotech background/experience plus must have cell culture and/or purification experience


3 Key Consulting is hiring! We are recruiting a Engineer Process Development for a consulting engagement with our direct client a leading global biotechnology company.

Job Description:
Our ideal candidate will have 24 years of relevant experience working in drug and animal cells; and strong process knowledge. Experience purifying cells (biologics purifications) drug substance GMP manufacturing.

We are seeking a Process Development Engineer to join the Drug Substance Technology Engineering team at our clients Thousand Oaks CA. facility. Providing process engineering support for human therapeutic products in clinical development through commercial production our clients mission is to translate developmental processes to commercial reality for patients through scientific expertise and engineering innovation.

The Engineer will apply cell culture and/or purification process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing in an innovative manufacturing suite using singleuse technology. Will partner with manufacturing quality analytical and bench scientists to support a highly dynamic manufacturing facility.

Top Must Have Skill Sets:
  • Drug substance biologics process development pilot plant or manufacturing technical support
  • Purification of monoclonal antibodies
  • Experience in GMP environment (preferably in drug substance)

Day to Day Responsibilities:
The Engineer will apply cell culture and/or purification process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing in an innovative manufacturing suite using singleuse technology. Will partner with manufacturing quality analytical and bench scientists to support a highly dynamic manufacturing facility.

Basic Qualifications:
  • Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience
  • Must have biotech background/experience plus must have cell culture and/or purification experience

Why is the Position Open
Backfill.

Red Flags:
  • Short duration stints in prior jobs
  • Resume does not accurately reflect true experience
  • Cultural fit manager described the team as easy going growth motivated organized and respectful.
  • Too senior or experienced for the position (not looking for more than 5 years of experience)


Interview Process:
  • Phone interview
  • Panel interview with 34 individuals in the team (with manager and director)

We invite qualified candidates to sendyour resume to. Ifyou decide that youre not interested in pursuing this particular position please feel free to take a look at the other positions on our websitewww.3keyconsulting/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.

Employment Type

Hourly

About Company

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