Quality Engineer II
at Abbott Laboratories
Santa Clara, California, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 27 Dec, 2024 | USD 65900 Annual | 01 Oct, 2024 | 2 year(s) or above | Interpersonal Skills,Leadership Skills,Computer Skills,Project Teams,Gmp,Iso | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
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OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
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Contract to Hire – Corp 2 Corp |
Description:
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
REQUIRED QUALIFICATIONS
- BS degree in Engineering or Technical Field or equivalent experience; 2-5 years’ experience
- Engineering experience and demonstrated use of Quality tools/methodologies
- Detailed knowledge of FDA, GMP, ISO 13485, and ISO 14971
- Solid communication and interpersonal skills
- Strong project management and leadership skills, including the demonstrated ability to lead multi-departmental project teams and resolve quality-related issues in a timely and effective manner
- Advanced computer skills, including statistical/data analysis and report writing skills
- Experience implementing various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing)
- Ability to work in a highly matrixed and geographically diverse business environment
- Ability to work within a team and as an individual contributor in a fast-paced, changing environment
- Ability to leverage and/or engage others to accomplish projects
- Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization
- Multitasks, prioritizes and meets deadlines in timely manner
- Strong organizational and follow-up skills, as well as attention to detail
- Ability to travel approximately 10%
- Ability to maintain regular and predictable attendance
PREFERRED QUALIFICATIONS
- Advanced degree
- Demonstrated supervisory experience
- ASQ CQE or other certifications
- Prior medical device experience
- Experience working in a broader enterprise/cross-division business unit model
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:2.0Max:5.0 year(s)
Information Technology/IT
Engineering Design / R&D
Other
BSc
Engineering
Proficient
1
Santa Clara, CA, USA