Quality Engineer I

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

What You Can Expect

• Responsible for gathering relevant, factual information and data in order to solve quality related problems.
• Resolve issues by identifying and applying solutions from acquired technical experience and guided precedents.
• Plan and lead projects by identifying and organizing activities into time dependent sequencing with realistic timelines. Work effectively/ productively with all departments by developing a
• team atmosphere.
• Interacts with many different functional departments, suppliers, and experts outside Zimmer to implement Zimmer Quality goals.
  
  

Work Mode: 2 days WFH, 3 days WFO.

Location: Bengaluru

How You'll Create Impact

Gather, organize, analyze and present data from various quality sub-processes:

• Works with other functions within the company to obtain SME feedback.
• Leads the change implementation of required amendments to the QMS.
• Formulates procedures, specifications, requirements and standards for acceptance of Zimmer products and processes.
• Develops and implements corrective/preventative action plans
• Provides technical support during audits.
• Support front room and backroom by producing supporting documents.
• Work with the audit response team in implementing corrective actions and verifying effectiveness.
  
  

What Makes You Stand Out

• Ability to work within a team environment and build relationships outside of the department as well as outside the company (suppliers, regulatory agencies, etc.).
• Facilitates team efforts on quality engineering projects.
• Ability to deliver, meet deadlines and have results orientation.
• Able to communicate both orally and in written form to multiple levels of the company.
• Microsoft Office Suite, expert knowledge of blueprint reading and geometric dimensioning and tolerancing, understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods, and are able to use optical comparators and CMMs.
• Knowledge of statistics, process control, and process capability
  
  

Your Background

• Stated experience must include experience in medical device industry with ISO 13485 and 21 CFR part 820standards; using verification and validation concepts; using IQ/OQ/PQ in manufacturing, using project management techniques.
• Prefer certification as a quality engineer (e.g. CQE) or the Reliability Engineer Certification (CRE) or Supplier
• Quality Profession (CSQP) granted through the American Society of Quality (ASQ), or Certified in Project Management (e.g. CAPM, APM).
• Combination of education and experience may be considered (in evaluating experience relative to requirements).
• Proficient in English - written and spoken B2.
  
  

Physical Requirements

Travel Expectations

Up to 5% travel.

EOE/M/F/Vet/Disability