Development, process and engineering technician
ExternalFull-timeHybrid1d ago
ComplianceHTML
Prepare for this interview
EliteAI-generated questions, company research, and talking points tailored to this role
Responsibilities
- Support RD&production department manager to plan and execute medical device customers' semi-finished product CDMO projects (note: 90% of target end medical implants belong to Class III).
- Carry out development and production activities for semi-finished products of medical implants, and assure execution in the ESH and quality system complianced and know-how protected way.
- Draft SOPs for production and process management when required by RD&production department manager.
- Support RD&production department manager to manage cleanroom in good way, including cleanliness maintaining, related equipment and utillities routinely monitoring, maintenance reporting, monitoring and feedback.
Requirements
- University (First degree)
- Experience of R&D and production in medical device company (who produce Class III medical implants device) is preferred.
- Good experience and skills in processing medical polymers based mainly on bio-resorbable polymers.
- Good experience ad skills in operating and trouble shooting for the process, e.g. single screw extrusion, twin screw extrusion, injection molding etc.
- Good experience ad skills in producing monofilament, tube, membrane , composite, molding part is preferred
- Experienced practitioner able to work unsupervised in project management and execution including evaluating project feasibility and providing technical suggestion, make execution plan, carry out development and production activities including trouble-shooting etc.
- Good skills and experience of coordinating, communicating with others in the teamwork.
- Good skills and experience of coordinating, communicating with external customer and suppliers.
- Works without supervision and provides work related data, report and records to business objectives under complianced, quality system required, know-how protection regulated way.
- Good knowledge about cleanroom and lab utilities engineering and management
- Good knowledge about ISO 13485 and medical device laws and regulations
- Works without supervision when required on achieving full compliance with applicable rules and regulations in management and/or operations.
- Your Application
- To ensure that your application is proceeded as quickly as possible and to protect the environment, please apply online via our careers portal . Further information about Evonik as Employer can be found at www.evonik.com/en/careers.html .
- Please address your application to the Talent Acquisition Manager, stating your earliest possible starting date and your salary expectations.
- Your Talent Acquisition Manager:
- Angelica Wen (闻鹃)
- Company is
- Ev(Shanghai)InvMan
Benefits
Click on the link below to learn what our employees have to say about Evonik:https ://careers.evonik.com/en/about/meet-the-team/Health insuranceVision insuranceFlexible schedule
Your Match
How well this role fits your profile.
Company Intel
What employees say
Worked at Evonik? Share your experience