What are the responsibilities and job description for the Engineer, Biopharma Medical Device Solid Modeling/Testing - Hybrid (JP13070) position at 3 Key Consulting?
Job Title: Engineer, Biopharma Container Closure Solid Modeling/Testing - Hybrid (JP13070)
Location: Thousand Oaks, CA. 91320 (Hybrid)
Business Unit: Physical Methods Development, Modelling and Emerging Methods
Employment Type: Contract
Duration: 18 months with possible extension or conversion to FTE
Rate: 36 - $42/hr with benefits
Posting Date: 2/7/2024.
Notes: Will be onsite at least 2x/ week. Candidate must be within commutable distance and must be able to come on site 5 days a week if needed.
3 Key Consulting is hiring! We are recruiting an Engineer for a consulting engagement with our direct client, a leading global biotechnology company.
Job Description:
Position involves support of senior staff in the initiation, design, and delivery of projects, particularly for container closure integrity testing (CCIT) related scope. Employ basic engineering skills and practices to gather user requirements and translate them into technical documentation for execution. Assist with project definition by performing engineering studies and assessment for CCIT system installations. Perform field evaluations of existing systems and provide engineering design recommendations and support development of CCIT technologies.
Biopharma or Biotech experience and/or Equipment Validation experience within another industry. Position is split between lab and office.
Equipment qualification- Equipment validation is a highly desired skillset. Will be working with other associates on testing and conducting testing themselves.
Day to day will include supporting development of technical documentation related to CCI testing, execution of protocols to support development, writing of technical documentation to support findings and results.
Heavy on documentation role
Top Must Have Skill Sets:
Solid modeling
Technical Writing
Working in a team
Day to Day Responsibilities:
Documentation writing (procedures, technical assessments, engineering drawings, etc)
Solid modeling (fixture development)
Meetings
Testing
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
Why is the Position Open?
Supplement additional workload on team.
Red Flags:
Less than a bachelors degree
A non-STEM bachelors degree
No work experience (internship okay)
Interview Process:
Initial phone call
Panel interview (2-3 people on call)
We invite qualified candidates to send your resume torecruiting@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 (Hybrid)
Business Unit: Physical Methods Development, Modelling and Emerging Methods
Employment Type: Contract
Duration: 18 months with possible extension or conversion to FTE
Rate: 36 - $42/hr with benefits
Posting Date: 2/7/2024.
Notes: Will be onsite at least 2x/ week. Candidate must be within commutable distance and must be able to come on site 5 days a week if needed.
3 Key Consulting is hiring! We are recruiting an Engineer for a consulting engagement with our direct client, a leading global biotechnology company.
Job Description:
Position involves support of senior staff in the initiation, design, and delivery of projects, particularly for container closure integrity testing (CCIT) related scope. Employ basic engineering skills and practices to gather user requirements and translate them into technical documentation for execution. Assist with project definition by performing engineering studies and assessment for CCIT system installations. Perform field evaluations of existing systems and provide engineering design recommendations and support development of CCIT technologies.
Biopharma or Biotech experience and/or Equipment Validation experience within another industry. Position is split between lab and office.
Equipment qualification- Equipment validation is a highly desired skillset. Will be working with other associates on testing and conducting testing themselves.
Day to day will include supporting development of technical documentation related to CCI testing, execution of protocols to support development, writing of technical documentation to support findings and results.
Heavy on documentation role
Top Must Have Skill Sets:
Solid modeling
Technical Writing
Working in a team
Day to Day Responsibilities:
Documentation writing (procedures, technical assessments, engineering drawings, etc)
Solid modeling (fixture development)
Meetings
Testing
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
Why is the Position Open?
Supplement additional workload on team.
Red Flags:
Less than a bachelors degree
A non-STEM bachelors degree
No work experience (internship okay)
Interview Process:
Initial phone call
Panel interview (2-3 people on call)
We invite qualified candidates to send your resume torecruiting@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.
Salary : $36 - $42
