drjobs Associate Engineer - Biopharma GMP Background JP10606

Associate Engineer - Biopharma GMP Background JP10606

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Job Location drjobs

Thousand Oaks, CA - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Job Title:Associate Engineer Biopharma GMP Background (JP10606
Location:Thousand Oaks CA. (hybrid remote and onsite)
Employment Type: Contract to Hire
Business Unit:
U.S. FPT Process Engineering
Duration:18 months with likely extension or conversion to permanent
Posting Date:08/02/2022

3 Key Consulting is hiring anAssociate Engineerfor a consulting engagement with our direct client a leading global biopharmaceutical company.

Job Description:
This Associate Engineer position is in the Thermal Engineering Systems (TES) group at client. The individual will lead TES project management and documentation. Under supervision by senior personnel the individual will apply engineering principles and follow current SOPs to help execute the design qualification and implementation of thermal packaging systems. In addition the individual will assist transportation lab test conduct experimental studies and document the results following SOPs.

Why is the Position Open
Staff Augmentation


Top MustHave Skill Sets:
  • Knowledge of cGMPBio/Pharma background
  • Project management and documentation
  • Proven written and oral communication skills

Day to Day Responsibilities:
  • Lead weekly team meetings to get project updates and discussion from TES team
  • Update group dashboard and manage Smartsheet (Project Management) to track project updates
  • Maintain TES SharePoint site and organize the group documents
  • Participate in shipping qualification projects and trouble shootings
  • Assist lab test and perform thermal experiments; conduct data analysis and generate report
  • Author and revise controlled documents (SOPs PCSs TPC SOPs) in CDOCS and PLM system
  • Collaborate with crossfunctional teams (i.e. Research and Development QA/QC Supply Chain Maintenance Manufacturing Regulatory) on protocol review testing preparation change control process and deviation & CAPA
  • Excels in MS Office Suit (Excel Word Visio PowerPoint etc.


Basic Qualifications:
  • Engineering or Science degree biotechnology chemical or mechanical bachelors degree preferred. recent graduates welcome to apply
  • Prior lab experience/knowledge on pharmaceutical GMP
  • Prior project management & documentation experience
  • Good oral/written communication skills

Employee Value Proposition:
The person in this position will work with a team to qualify shipping solutions for products to ensure they are maintained during transportation.

Red Flags:
  • Candidates who lack relevant skills
  • Candidates who do not meet the qualification requirements
  • Candidates who were separated from previous employment due to unethical behaviors

Interview process:
Phone screening followed by inperson interview.

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


Required Experience:

Director

Employment Type

Full Time

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