Job description

Engr 2, Validation

San Jose, CA

Duration: 12+ Months

Job Description:
Responsible for performing process, equipment, and software validation activities including, but not limited to, gathering historical data for product manufacture, analyzing data using statistical principles, writing validation protocols and reports, GDP review of data and reports, and final approval of validation protocols, reports, and deviations. May interact in cross-functional teams including Reagent Manufacturing Engineers and Chemists, Research and Development, and Quality Assurance Validation Engineers. May be responsible for leading teams to perform validation activities or perform as a member of the team. Will simultaneously work on multiple projects. Knowledge of general reagent manufacturing processes, antibody purification and conjugation, and flow cytometry, is preferred.

• Process, Test Method, Equipment, and Software Validations used in IVD product manufacture (IQ, OQ, PQ)
• Acts as Quality Assurance reviewer/approver or author for validation protocols, reports, and deviations.
• Provides and applies quality engineering direction to projects using quality engineering and statistical principles

 Root Cause Analysis
 FMEA
 Risk Management and Mitigation
 DOE
 Measurement Systems Analysis
 Sampling and Control Plans
 Post Market Surveillance Trend Review
 Process Capability

• Provides and applies scientific technical principles/concepts
• Follows company procedures
• Demonstrates working knowledge and application of applicable regulatory requirements
• Other duties as assigned.

Requirements:

• Education: bachelor’s degree

Experience (preferred):

• Experience in a quality related function in a medical device or other FDA regulated environment. Previous work with IVD reagent products under GMP conditions
• Process validation (IQ, OQ, PQ) and test method validation experience
• Software validation experience
• Knowledge of general reagent manufacturing processes, antibody purification and conjugation, flow cytometry
• Certified Quality Engineer
• Six Sigma Certification
• Knowledge of applicable regulatory requirements including ISO13485, ISO14971, ISO9001, quality systems regulations (21 CFR: 820)
• Training in statistics.
• Experience with Minitab or other statistical software, MS Excel, and MS Word required

- Weekend and off-shift support may be required.- Occasional lifting of heavy weights up to 25 to 35 lbs.TechData is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.

Job Types: Contract, Temporary

Pay: $74.80 per hour

Benefits:

• Dental insurance
• Health insurance

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday

Education:

• Bachelor's (Required)

Experience:

• antibody purification and conjugation: 1 year (Preferred)
• Certified Quality Engineer: 1 year (Required)
• Six Sigma Certification: 1 year (Required)
• Process validation (IQ, OQ, PQ) and test method validation: 1 year (Required)
• medical device or other FDA regulated environment: 1 year (Required)
• Software validation: 1 year (Required)

Work Location: In person

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