Duration: 1+ years (with likely extensions and/or conversion to permanent)
Posting Date: 12/28/2021
Notes
3 Key Consulting is hiring an Risk Management Senior Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description
Position requires B.S. in Mechanical Engineering, Chemical or Biomedical Engineering, or Materials Science. The Engineer, in Final Product Technologies- Mechanical Engineering 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 components. 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 expert support for qualification, validation, transfer, and life cycle support of methods for manufacturing, new product introduction, training, and production support.
Why is the Position Open?
Supplement additional workload on team.
Top Must Have Skills
3D Design in CAD, SolidWorks.
Technical Writing Skills.
Qualification or Validation Experience with equipment, systems, software.
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 expert 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 expert 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 own 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
Comply with the requirements, responsibilities, and authority as required
Maintains integrated timelines capturing appropriate cross functional details and deliverables which are aligned with the functional and project goals
Networks internally to ensure alignment, commitment to project objectives and timelines as well as to ensure effective execution of projects
Networks with manufacturing, quality and regulatory organizations both internal and external to client
Drives the cross-functional communication and integration of information to optimize decision making, issue resolution and change management throughout project lifecycle
Excellent verbal and written communication skills are utilized 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 escalate efficiently
Integrates partner/vendor timelines with client timelines as appropriate
Employee Value Proposition
The person in this position will work to build test methods to determine if products are ready to go out to market. This team focuses mostly on device design, failure analysis.
Red Flags
No B.S. in Mechanical Engineering, Chemical or Biomedical Engineering, or Materials Science.
No 3D Design Software, CAD, SolidWorks.
No technical writing skills.
No communication skills.
Interview Process
Video Skype Panel Interview.
We invite qualified candidates to send your resume to [email protected]. 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.
Regards,
3KC Talent Acquisition Team
Seniority level
Entry level
Employment type
Full-time
Job function
Engineering and Information Technology
Industries
Biotechnology
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