Job Summary

To customize| implement and support quality processes for multiple projects with objective towards improving product/project quality| reducing the rework and improving customer satisfaction

Key Responsibilities

1. To facilitate project for process piloting| process tailoring| progress reviews
2. To do process audits for the processes assigned in a particular project
3. To do process trainings for the new incumbents
4. To define process for the project assigned as per the quality standards

Skill Requirements

SCAR Implementation and Closure:

• Open SCARs must be taken through formal closure- Implement corrective actions and formally close all open SCARs with appropriate evidence by 30 September.
• Detailed review of open SCAR records to understand current status and gaps. Categorization of SCARs by supplier, product family, age, and severity.

• Supplier follow-ups and coordination, Documentation completeness, Verification of implemented actions and Closure readiness aligned with FDA QSR expectations

• Establish an inspection-ready supplier control framework through procedure gap assessment, ASL validation, and need-based supplier requalification.

• Supplier follow-ups to obtain:
• Containment evidence. Root cause analysis documentation
• Corrective action implementation details

• Verification and documentation of implementation evidence
• Support for effectiveness checks, as defined by client procedures
• Preparation of complete SCAR closure documentation aligned to the client QMS and FDA QSR requirements

Supplier Controls and ASL Remediation

• Gap assessment of the global purchasing & supplier management procedure against actual practices at the El Paso site
• Documentation of identified gaps across process, roles, records, and controls
• Validation of approximately ASL suppliers, including:
• Classification as active or inactive
• Mapping to products and supplier criticality
• Execution of need-based supplier requalification, including:

• • Updated supplier qualification forms
  • Risk assessment and supporting documentation review.
• Support for supplier record migration readiness into Teamcenter (as per client-defined scope and rules).

Basic Qualifications:

• Proven ability to lead multiple SCAR Implementation and Supplier Controls projects.
• Proficiency in the use of Microsoft Word, Excel, PowerPoint, Access, Microsoft Project.
• Full time Degree in a relevant engineering field is required (i.e., Mechanical) with 5-6 years in supplier quality function.
• Candidates with prior experience in Medical Devices will be required.
• Strong written and verbal communications skills.  Ability to write and independently manage the required technical documentation.
• Knowledge of the following standards: 21 CFR Part 820, ISO 13485, and ISO 14971.

Other Requirements

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