Manufacturing Associate - AM Shift

Zimmer Biomet Holdings Inc

Norfolk, VA

JOB DETAILS
SKILLS
Banking Services, Check Processing, Cleanroom, Communication Skills, Corporate Policies, Current Good Manufacturing Practice (cGMP), Customer Relations, Documentation, Electronics Manufacturing, FDA Requirements, Healthcare Quality, High School Diploma, ISO (International Organization for Standardization), ISO 9001, Inventory Management, Laboratory, Laboratory Equipment, Labware, Logistics, Manufacturing, Manufacturing Operations, Manufacturing Systems, Medical Equipment, Operations, Operations Processes, Organizational Skills, Plan Meetings, Presentation/Verbal Skills, Problem Solving Skills, Process Improvement, Process Quality, Production Planning, Production Schedule, Production Support, Profit & Loss, Quality Management, Record Keeping, SAP, Safety Compliance, Safety Training, Standard Operating Procedures (SOP), Team Building, Technical Leadership, Time Management, Writing Skills
LOCATION
Norfolk, VA
POSTED
30+ days ago

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 talented 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 inspired, invested, cared for, valued, and have a strong sense of belonging.

What You Can Expect

This position is responsible for the production of quality medical devices. This position supports Production and Logistics by performing and documenting daily manufacturing operations that involves operation of various process equipment and other tasks in support of the production schedule. This person will comply with safety requirements, current Good Manufacturing Practices and Standard Operating Procedures and coordinate the cleaning, assembly and preparation of equipment and final products according to written instructions. The manufacturing specialist will further support P&L by maintaining raw material stock, cleanroom readiness and final product inventory.

How You'll Create Impact

  • Responsible for performing the daily manufacturing steps required to produce medical devices.
  • Maintain the integrity of ISO class 7 & 8 Cleanrooms by performing proper gowning, entry and cleaning procedures.
  • Perform in-process quality checks on sub-assemblies and finished products.
  • Responsible for inspection, labeling, packaging and shopping of final products.
  • Perform daily equipment, labware and manufacturing areas in accordance with SOPs.
  • Responsible for maintaining raw material inventory and performing incoming inspections.
  • Assist in ongoing process improvement and subsequent validation activities.
  • Participate in line and production planning meetings as needed.
  • Work with engineers, technicians and management to resolve line issues and suggest improvements.
  • Maintain accurate records and documentation related to quality, work in progress, test results and special projects.
  • May interact with external customer contacts including participating in tours for visitors including VIPs and may be questioned and/ or observed during audits.
  • Adhere to general safety rules, manufacturing procedures, company policies and procedures, ISO and FDA regulations.

What Makes You Stand Out

  • Experience working with laboratory chemicals and equipment including pipettes, balances, sealers and vacuum ovens.
  • Ability to follow SOPs, work instructions, and maintain daily records in a timely and reliable fashion.
  • Must be a highly organized individual who works independently with minimum supervison in a fast-paced environment.
  • Must have a high level of hand-eye coordination.
  • Excellent communication skills both written and verbal.
  • Comfortable working under an ISO 13485 or 9001 Quality Management System

Your Background

  • High school diploma or equivalent
  • Minimum 2 years working in a manufacturing environment, preferably within the medical device or tissue banking industry.
  • Minimum 2 years working with an electronic manufacturing and inventory system such as SAP.

EOE

About the Company

Z

Zimmer Biomet Holdings Inc

Do you find pride and purpose in helping millions of people around the world renew their lives? If so, career opportunities at Zimmer facilities worldwide will be an excellent fit for you. We're looking for remarkable people who can be catalysts for change, collaborate globally and push the boundaries of innovation so that we can continue to make the world a more mobile place. We've found that when you're working to improve others' lives, you start to feel incredibly proud and excited about what you do. Join us and find your fit in a company with passion.

INDUSTRY
Medical Devices and Supplies
FOUNDED
1927
WEBSITE
http://www.zimmer.com/