Engineer GMP Physical Test Methods - Hybrid JP13129
Engineer GMP Physical Test Methods - Hybrid JP13129
Posted on :
10-04-2025
Employer Active
1 Vacancy
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Hourly Salary
$ 38 - 42
Vacancy
1 Vacancy
Posted on :
10-04-2025
Job Description
Job Title: Engineer GMP Physical Test Methods Hybrid (JP13129
Location: Thousand Oaks CA. 91320 (Hybrid)
Business Unit:
Employment Type: Contract
Duration: 18 months with likely extensions and/or conversion to a permanent position.
Rate: $38 $42/hour W2
Posting Date: 8/23/2024.
Notes: Only qualified candidates need apply. Must be local to Thousand Oaks CA will work hybrid (typically onsite about twice per week sometimes more)
3 Key Consulting is hiring! We are recruiting an Engineer GMP Physical Test Methods for a consulting engagement with our direct client a leading global biotechnology company.
Job Description:
The Engineer in Physical Methods is responsible for engineering activities required for the development /
qualification / validation and transfer of physical GMP test methods for combination products devices
primary containers and secondary packaging parts. The Engineer shall have the ability to work on
multiple projects at one time that may involve changes or new product processes tooling or equipment
introduction to improve quality and reliability and reduce cost. Phases of projects include: developing
combination product test methods providing key experienced support for qualification validation transfer
and life cycle support of methods for manufacturing new product introduction training and production
support.
Top Must Have Skill Sets:
Day to Day Responsibilities:
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
Preferred Qualifications:
Why is the Position Open
Supplement additional workload on team
Interview Process:
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.
Location: Thousand Oaks CA. 91320 (Hybrid)
Business Unit:
Employment Type: Contract
Duration: 18 months with likely extensions and/or conversion to a permanent position.
Rate: $38 $42/hour W2
Posting Date: 8/23/2024.
Notes: Only qualified candidates need apply. Must be local to Thousand Oaks CA will work hybrid (typically onsite about twice per week sometimes more)
3 Key Consulting is hiring! We are recruiting an Engineer GMP Physical Test Methods for a consulting engagement with our direct client a leading global biotechnology company.
Job Description:
The Engineer in Physical Methods is responsible for engineering activities required for the development /
qualification / validation and transfer of physical GMP test methods for combination products devices
primary containers and secondary packaging parts. The Engineer shall have the ability to work on
multiple projects at one time that may involve changes or new product processes tooling or equipment
introduction to improve quality and reliability and reduce cost. Phases of projects include: developing
combination product test methods providing key experienced support for qualification validation transfer
and life cycle support of methods for manufacturing new product introduction training and production
support.
Top Must Have Skill Sets:
- Technical writing experience
- Strong communication skills
- CAD experience (modeling designing)
- Experience managing their own workload independently
Day to Day Responsibilities:
- Develop qualify and validate GMP physical test methods for vials prefilled syringes and injection devices.
- Work in teams to transfer new combination product test method and assembly requirements to manufacturing by developing six sigma processes and compiling documentation for manufacturing assembly requirements.
- Develop qualify validate and transfer new equipment software systems and methods.
- Implement projects per Final Product Technologies and company procedures to ensure projects are completed on schedule and within established budget.
- Provide experienced support for investigations as well as new process development required to improve manufacturing operations.
- Coordinate test method development and delivery with selected contractors.
- Ensure that qualification parameters are met for product assembly requirements.
- Support development of cost estimates for new processes gauges and equipment development used in generation of capital request documentation.
- Generate procedures necessary to support department and new process equipment.
- Provide experienced training to individuals in the operation and maintenance of processes test methods and equipment introduced to Quality Control and/or the manufacturing department (i.e. production operator mechanics process engineers).
- Participate in and assume responsibilities of team functions as assigned (i.e. Product Improvement Teams).
- Generate/author and be responsible for the Test Method documents.
- Gather test method requirements that result in equipment that operates safely and considers ergonomic factors in the design
- Perform other duties as required by the Group Manager
- Align with the requirements responsibilities and authority as required
- Maintains integrated timelines collecting appropriate multifunctional details and work which are aligned with the functional and project work
- Networks internally to ensure alignment commitment to project objectives and timelines as well as to ensure effective of projects
- Networks with manufacturing quality and regulatory organizations both internal and external to client
- Drives the multifunctional communication and integration of information to optimize decision making issue resolution and change management throughout project lifecycle
- Excellent verbal and written communication skills are applied to communicate project status and risks associated with integrated timelines to leadership
- Collaborates with other functional leaders to ensure project success momentum and commitment
- Proactively identifies issues and/or risks and develops mitigation options to resolve or increase efficiently
- Integrates partner/vendor timelines with client timelines as appropriate
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
Preferred Qualifications:
- M.S. in Mechanical Engineer Chemical or Biomedical Engineering or Chemistry
- Excellent written and verbal communication skills
- Ability to work in a highly matrixed team environment
- 2 years of experience in the biotechnology/pharmaceutical industry
- 2 years of experience in equipment method and mechanical design
- Technical writing experience
- Experience with SolidWorks (or other 3DCAD software)
- Experience with combination products and regulatory requirements
- Experience applying Minitab (or other statistical software packages)
Why is the Position Open
Supplement additional workload on team
Interview Process:
- Phone screen
- Video conference
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.
Regards
3KC Talent Acquisition Team
Required Experience:
Director
Employment Type
Hourly
Key Skills
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