Reference: Posted: Location: El Paso, TexasCompany: Planet Pharma GroupContact: ApplicationsEmail: may include the following and other duties may be assigned.
* Ensures that suppliers deliver quality parts, materials, and services.
* Qualifies suppliers according to company standards and may administer a Certified Supplier
Program in receiving inspection to ensure cost effectiveness.
* Monitors parts from acquisition through the manufacturing cycle and communicates and
resolves supplier-related problems as they occur.
* Evaluates suppliers’ internal functions to assess their overall performance and provides feedback
in assessment of their operation.
* Partners with cross functional teams (R&D, sourcing, engineering, operations, quality), to deliver
quality parts, materials, and services, prevent defects, and allow the company to provide customers
with the highest quality and reliable products.
* Provides technical guidance and quality compliance throughout the product lifecycle (with focus
on supplier changes) and implementing strategies for driving product quality and continuous
improvement, ensuring purchased products and components are manufactured and qualified in
accordance to applicable industry standards, regulatory requirements, and customer
requirements.
* Collaborates with cross functional teams to develop and deliver the Product Acceptance
Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and
Control Plans for new products.
Define Receiving Inspection requirements as required and associated test method validation for
all internal Test Methods.Requires advanced knowledge of job area combining breadth and depth, typically obtained
through advanced education combined with experience.
Bachelors degree (or for degrees earned outside of the United States, a degree which satisfies the
requirements of 8 C.F.R. § 214.2(h)( 4)(iii)(A)
Minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years
relevant experience.
Demonstrated experience on Medical Device Industry or Automotive part qualification
requirements
May have practical knowledge of project management.Experience using Agile and Trackwise would be a plus
Knowledge of ISO 13485 requirements
FDA QMSR
Geometric Tolerances
Supplier Development, quality and process improvement
* Ensures that suppliers deliver quality parts, materials, and services.
* Qualifies suppliers according to company standards and may administer a Certified Supplier
Program in receiving inspection to ensure cost effectiveness.
* Monitors parts from acquisition through the manufacturing cycle and communicates and
resolves supplier-related problems as they occur.
* Evaluates suppliers’ internal functions to assess their overall performance and provides feedback
in assessment of their operation.
* Partners with cross functional teams (R&D, sourcing, engineering, operations, quality), to deliver
quality parts, materials, and services, prevent defects, and allow the company to provide customers
with the highest quality and reliable products.
* Provides technical guidance and quality compliance throughout the product lifecycle (with focus
on supplier changes) and implementing strategies for driving product quality and continuous
improvement, ensuring purchased products and components are manufactured and qualified in
accordance to applicable industry standards, regulatory requirements, and customer
requirements.
* Collaborates with cross functional teams to develop and deliver the Product Acceptance
Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and
Control Plans for new products.
Define Receiving Inspection requirements as required and associated test method validation for
all internal Test Methods.Requires advanced knowledge of job area combining breadth and depth, typically obtained
through advanced education combined with experience.
Bachelors degree (or for degrees earned outside of the United States, a degree which satisfies the
requirements of 8 C.F.R. § 214.2(h)( 4)(iii)(A)
Minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years
relevant experience.
Demonstrated experience on Medical Device Industry or Automotive part qualification
requirements
May have practical knowledge of project management.Experience using Agile and Trackwise would be a plus
Knowledge of ISO 13485 requirements
FDA QMSR
Geometric Tolerances
Supplier Development, quality and process improvement
Supplier Quality Engineer in el paso at Unknown Company
This position is listed as full time and onsite.