Job Title: Engineer GMP Test Methods Medical Device (JP10960 Location: Thousand Oaks CA. 91320 Employment Type: Contract Business Unit: Physical Testing Systems Development Duration: 18 months (with likely extensions and/or conversion to permanent) Posting Date: 10/25/22 Notes: Only qualified candidates need apply.
3 Key Consulting is hiring an Engineer for a consulting engagement with our direct client a leading global biopharmaceutical company.
Job Description: The Engineer will work under the team: Physical Science and Engineering CCI Container Closure Integrity) testing of syringes in the Device and Packaging Engineering lab. Research & Development. Lab Experiment. They will be 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 components. Position involves support of senior staff in the initiation design and delivery of projects particularly for Container Closure Integrity (CCI). Employ basic engineering skills and practices to gather user requirements and translate them into technical documentation for . Assist with project definition by performing engineering studies and assessment for CCI systems. Perform field evaluations of existing systems and provide engineering design recommendations.
Top Must Have Skills:
Bachelors must have (Engineering or BiomedicalSTEM)
Must have experience in work or laboratory settings (will consider new grads)
Experience with Statistical Software perferred
SolidWorks or Computer Aided Design (cad) experience perferred
MSA experience (Measurement System Analysis) training is a plus Our team uses this for measuring the abilities of the processes we design.
Day to Day Responsibilities:
Develop qualify and validate GMP physical test methods for vials prefilled syringes and injection devices.
Provide support of senior staff for delivery of Projects.
Coordinate test method development and delivery with selected contractors and vendors.
Ensure that qualification parameters are met for product requirements.
Generate procedures necessary to support department and new process equipment.
Maintains integrated timelines capturing appropriate cross functional details and deliverables which are aligned with the functional and project goals.
Participate in and assume responsibilities of team functions as assigned i.e. subject matter experts for test equipment
Generate/author and own the Test Method documents: Procedures engineering drawings specifications protocols reports etc.
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.
Comply with the requirements responsibilities and authority as required.
Communicate and collaborate internally to ensure alignment commitment to project objectives and timelines as well as to ensure effective of projects.
Network with manufacturing quality and regulatory organizations both internal and external to client.
Excellent verbal and written communication skills are utilized to communicate project status and risks associated with integrated timelines to leadership.
Basic Qualifications: Previous work experience is a plus. SolidWorks 3D CAD FEA. Minitab. JMP. Experience working in team.
Red Flags:
No Bachelors Degree
Degree not related to STEM or Biomedical
No mechanical aptitude no experience using tools building or designing and assembly or disassembly of equipment/components.
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