Job Title: Quality Engineer (Temporary/Part-Time)
Hours: Up to 20 Hours per week (three 8-hour shifts per week)
Duration: 90 days
Pay: Up to$75.00
Department: Quality
Reports to: Quality Director
POSITION OVERVIEW
The primary responsibility of the quality engineer is to maintain, and support compliance activities associated with product manufacturing, non-conformance reports (MRB), customer complaints, product acceptance and release through active involvement & presence in the assembly operations. Continual improvement of methods & systems towards full compliance and world class manufacturing.
The position requires a high level of innovative thought and problem-solving skills. Multiple tasks will need to be prioritized and responsibilities delegated to ensure department success. In addition to the above responsibilities, the quality engineer is required to interact with multiple departments within the Adagio Medical organization to ensure compliance to the Quality Management System (QMS).
ESSENTIAL DUTIES
- Daily support of production requirements and issues through active involvement & presence in the assembly operations and clean rooms.
- Maintain and support compliance activities associated with the Quality Management System (QMS) to comply with international and domestic regulations.
- Maintain the CAPA system and files. Coordinate CAPA activities including investigations, root cause analysis, and implementation of corrective actions with effectivity analysis.
- Develop quality assurance specifications, test devices & methods, inspection procedures, sampling plans and related written procedures.
- Support new product launch, Risk Management Activities (FMECA), Master validation plans, product V&V, Process Validations, and Design Transfer into manufacturing.
- Implement and review changes to existing products, SOPs, DOPs, Test Methods, Process Changes, Design Changes, Labeling/Labels, and Field issues to define the requirements for regulatory submissions and notifications.
- Support Internal Audit process and follow-up on Audit findings.
- Manage the Supplier Evaluation and Qualification process. Work with purchasing to manage the qualification process of new suppliers and re-evaluation of existing suppliers.
- Support & develop quality metrics and monitor production/product non-conformance trends in order to alert senior management of these trends so corrective actions can be implemented.
- Recommends modifications of existing quality or production standards to achieve optimum quality and compliance.
- Provide quality engineering support to quality control and provide guidelines on inspection methods and equipment used including measuring systems capabilities.
- Complete projects in a manner consistent with corporate objectives.
- Work with Manufacturing and Engineering teams to coordinate pilot production of new process validations and risk analysis activities.
QUALIFICATIONS
- Bachelor's degree (B.S.) from four-year College or University.
- Three (3) years minimum experience in quality engineering and quality assurance.
- Current knowledge of FDA Quality System Regulations and Guidelines, ISO 13485, and standards applicable to company products.
- Knowledge and understanding of Quality and Regulatory concepts and application
- Strong analytical, planning and organizational skills
- Strong interpersonal and communications skills (oral & written)
- Self-starter with ability to work independently under pressure and react quickly to changing priorities
- Proficient in MS Office products.
PHYSICAL REQUIREMENTS
This position is based in an office and manufacturing environment with low to moderately high noise levels. Ability to sit or stand for extended periods while performing repetitive assembly tasks. Occasional standing with the ability to traverse confined spaces and maneuver up to 25lbs required.
This employer participates in E-Verify, a federal program to confirm the employment eligibility of new hires. If you have any questions about the E-Verify process or your rights, please visit the E-Verify website or contact Human Resources.
Consistent with the Americans with Disabilities Act (ADA), CDPA, and FEHA, it is the policy of Adagio Medical to provide reasonable accommodation when requested by a qualified applicant or candidate with a disability, unless such accommodation would cause an undue hardship for the company. The policy regarding requests for reasonable accommodation applies to all aspects of the hiring process. If reasonable accommodation is required, please contact [email protected].
Adagio Medical is committed to creating an inclusive and equitable workplace where all individuals are valued and receive equal opportunities for employment and advancement, regardless of their race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected status or characteristic.
Pay: Up to $75.00 per hour
Application Question(s):
- Do you now or in the future require sponsorship to accept or remain employed in the United States (ie. F1, OPT, CPT, H-1B)?
Location:
- Laguna Hills, CA 92653 (Preferred)
Ability to Commute:
- Laguna Hills, CA 92653 (Required)
Work Location: In person
