Menu

Senior Supplier Development Quality Engineer

Location: Pleasanton, California

Category: Labour/Helper Jobs

Job highlights

Identified by Google from the original job post

Qualifications

Education Level Major/Field of Study

Bachelor's degree in engineering or Technical Field

Minimum 5 years Related experience

Engineering experience and demonstrated use of Quality tools/methodologies

Detailed knowledge of FDA, GMP, ISO 13485, and ISO 14+71

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 leverage and/or engage others to accomplish projects

Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization

Ability to travel approximately 10-40%, including internationally

ISO Audit Certifications for performing Supplier Auditing (ISO 13485 and +001)

Benefits

The base pay for this position is $83,600.00 – $167,200.00

In specific locations, the pay range may vary from the range posted

Responsibilities

Supplier Development Quality Engineer responsible for activities related to supplier selection and evaluation, material qualification, supplier performance and receiving inspection

Contributes to the development, establishment and maintenance of supplier quality engineering methodologies, systems and practices which meet company and regulatory requirements

Contributes to the development, maintenance and improvement of division supplier development quality program policies, procedures and forms

May provide coaching, and mentoring for technical team personnel

Provides guidance and training to Purchasing, R&D, Manufacturing and Quality engineers in applying program requirements

Reviews and approves all supplied product drawings and component quality plans

Manages development of supplied product inspection procedures and first article requirements

Provides engineering guidance to division Receiving Inspection including statistical analysis, measurement techniques, Gage R&R studies and inspection procedures

Assesses supplier capabilities through direct visits, technical discussions, directed testing and quality system audits

Proactively communicates quality issues to suppliers as needed through supplier quality system audits, supplier corrective action requests and technical discussions

Participates and provides engineering ownership for all supplied product Non-Conforming Material Reviews

Contributes and participates in supplier performance reviews

Evaluates and develops Supplied Data Agreement partnerships with suppliers

Applies sound engineering analysis and judgment to reduce the need for inspection in accordance to program policies

Works with Manufacturing engineering to assess and address purchased product issues

Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues

Design and conduct experiments for process optimization and/or improvement

Participate in or lead teams in supporting Supplier Development Quality program requirements (e.g., represent the Supplier Development Quality function as a Core Team Member)

Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments

Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors

Job 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.

MAIN PURPOSE OF ROLE

Supplier Development Quality Engineer responsible for activities related to supplier selection and evaluation, material qualification, supplier performance and receiving inspection. Contributes to the development, establishment and maintenance of supplier quality engineering methodologies, systems and practices which meet company and regulatory requirements.

MAIN RESPONSIBILITIES

• Contributes to the development, maintenance and improvement of division supplier development quality program policies, procedures and forms.

• May provide coaching, and mentoring for technical team personnel.

• Provides guidance and training to Purchasing, R&D, Manufacturing and Quality engineers in applying program requirements.

• Reviews and approves all supplied product drawings and component quality plans.

• Manages development of supplied product inspection procedures and first article requirements.

• Provides engineering guidance to division Receiving Inspection including statistical analysis, measurement techniques, Gage R&R studies and inspection procedures.

• Assesses supplier capabilities through direct visits, technical discussions, directed testing and quality system audits.

• Proactively communicates quality issues to suppliers as needed through supplier quality system audits, supplier corrective action requests and technical discussions.

• Participates and provides engineering ownership for all supplied product Non-Conforming Material Reviews.

• Contributes and participates in supplier performance reviews.

• Evaluates and develops Supplied Data Agreement partnerships with suppliers.

• Applies sound engineering analysis and judgment to reduce the need for inspection in accordance to program policies.

• Works with Manufacturing engineering to assess and address purchased product issues.

• Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues

• Design and conduct experiments for process optimization and/or improvement

• Participate in or lead teams in supporting Supplier Development Quality program requirements (e.g., represent the Supplier Development Quality function as a Core Team Member)

• Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.

• Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

QUALIFICATIONS

Education

Education Level Major/Field of Study

Bachelor's degree in engineering or Technical Field

Advanced degree preferred

Experience/Background

• Minimum 5 years Related experience. Prior medical device experience preferred.

• Demonstrated supervisory experience preferred. Engineering experience and demonstrated use of Quality tools/methodologies.

• Detailed knowledge of FDA, GMP, ISO 13485, and ISO 14+71.

• 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). ASQ CQE or other certifications preferred.

• Experience working in a broader enterprise/cross-division business unit model preferred.

• 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. Ability to travel approximately 10-40%, including internationally.

Preferred Skills:

ISO Audit Certifications for performing Supplier Auditing (ISO 13485 and +001)

The base pay for this position is $83,600.00 – $167,200.00. In specific locations, the pay range may vary from the range posted.

Apply on Company Website You will be redirected to the employer’s website