Robin Snyder

linkedin.com/in/robin-snyder-***a***4

Summary

Detail-Oriented and Communicative Quality Leader with 18 Years' Experience Roy, UT

Hard working, innovative self starter with 18 years experience being part of, or leading a Quality team in multiple manufacturing industries.

Dynamic leader of a high paced teams performing quality activities in a complex settings including manual, semi- automated and automated manufacturing. Versed in auditing, investigations and Lean Manufacturing. Experience

Quality Supervisor

Autoliv

Apr 2022 - Present (1 year 3 months)

• Led team of 10 Quality Engineers and support functions in the Driver and Side airbag group to ensure product quality, drive continuous improvement, streamline processes, solve customer quality concerns and comply with regulatory agencies including ISO and AITF

• Spearheaded engineering change teams for product improvements in my department, performed complex root cause analysis using 8D format, and corrective action plans for quality concerns addressing systemic issue.

• Organized and drove cross functional teams to address plantwide issues across multiple departments and disciplines.

• Reviewed drawings, prototype builds and development testing to ensure the quality of launching products. Developed testing to ensure quality of new designs, performed gap analysis and reaction or improvement plans for changes needed pre-launch.

• Recognized by upper management four times in the last year for projects spearheaded to completion, team leadership and proactive solutions.

Quality Supervisor

ARUP Laboratories

Nov 2018 - Present (4 years 8 months)

Led a diverse Quality and Compliance team of 13 individuals servicing the internal product needs of a large reference laboratory suppling a catalog of over 3000 products. Responsible for workflow, budgeting

and employee retention.

• Actively involved with the development, writing and review of departmental technical procedures, SOPs, validations and audits. Maintained an in-depth knowledge of production, regulatory, testing techniques and principles along with Lean Manufacturing.

• Spearheaded the performance of all internal and external audits, maintaining compliance for multiple regulatory requirements CAP, NY and ISO 15189

• Strengthened Quality Management Processes. Identified gaps, improved transparency, streamlined processes, performed CAPAs. Presenting quality indicators and improvement presentations to higher management and staff

• Interpreted and correlated complex data sets to establish trends, set product specifications and predict Robin Snyder - page 1

future changes.

Quality Lead

ARUP Laboratories

Nov 2009 - Nov 2018 (9 years 1 month)

Generated and evaluated quality control statistics for assays and/or product(s) in relation to accuracy, reproducibility, precision, and validity of assay methods and materials. Assisted in the development of new quality requirements for products.

• Responded to special requests relating to product troubleshooting and development. Identified non- conformances and performed investigations using Root Cause Analysis and 5 Whys

• Improved validation processes, monitored all performance check systems and preventative maintenance programs for instruments and equipment. Performed some maintenance and repairs of equipment.

Quality Control Scientist

Protherics Salt Lake City, Inc.

Nov 2007 - Jul 2009 (1 year 9 months)

Performed sampling and analysis of raw materials, in-process materials and final polymer product using a wide variety of analytical test methods: HPLC, GPC, FTIR, TOC, dissolution, gravimetric analysis,

conductivity, pH, lyophilization and other methods.

• Executed AQL testing following ANSI requirements. Generated documentation of all analyses following

GLP, GMP, and GCP guidelines. Custody tracking and disposal of all samples.

• Documented of all out of specification results and incidents fully, correctly and in a timely manner. Performed CAPA investigations on out of specification, out of testing, incidents and deviations as needed

following PathWise™.

Quality Assurance Manager

Mineral Resources International, Inc.

Nov 2006 - Dec 2007 (1 year 2 months)

Managed and coordinated personnel working in the Quality Laboratory and each subunit of the Quality Unit, including GMP Team, Quality Control, Quality Assurance, Quality Engineering, and the Material Review Board.

• Interpreted data, predicted patterns, performed statistical analysis and created study profiles. Responsible for product quality including ongoing implementation and management of standard operating procedures and quality testing.

• Maintained the GMP manual and verified all procedures to be GMP compliant. Performed both internal and external audits

Chemist, Quality Control

Mineral Resources International, Inc.

Aug 2004 - Nov 2006 (2 years 4 months)

Collected samples and performed physical, microbial, and mineral analyses of ingredients, intermediates, and finished products to verify they meet company standards with the use of (FLAA), wet Robin Snyder - page 2

chemistry techniques, titrations, potentiometer, calipers, dissolution, (TLC).

• Designed and performed experiments for new products and studies. Perform shelf life studies of products to predict future potency.

• Trained personnel on testing procedures, developed a on site food handlers class and gave appropriate

testing for state compliance. Improved current facilities to become GMP certified. Education

Weber State University

BS, Chemistry

Skills

documentation • gmp • iso • materials management • Validation (Drug Manufacture) • Calibration • Auditing • Corrective and Preventive Action (CAPA) • Team Leadership • Lean Manufacturing Robin Snyder - page 3

Contact this candidate