LivaNova logo

Operations Team Member I

LivaNova

Houston, TXOnsitePosted 22 days ago$17.00 - $22.00/hour
Full TimeEntry LevelManufacturing & CMCMedical Device
Original posting ↗

Summary

We are hiring an Operations | Manufacturing Team Member to join our operations team at our Houston site. In this role you'll be responsible for assembling and inspecting medical devices and related assemblies in compliance with company procedures and ensuring that production schedules and quality criteria are met. This position offers future opportunities for growth within the team and the company.

Job description

Primary Activities

  • Assemble, test and/or inspect medical devices in compliance with company procedures.
  • Works within one of the following specialty areas: SMT, Test and Screen, BBFT, Seam Welding, Header Attach, Helicals Welding, Helical Completions, Lead Finals, Wands, Tablets, Packaging, Labeling, Ancillaries, Repro.
  • Ensure that work orders are completed on a timely basis.
  • Ensure traceability compliance by maintaining accurate production documentation.
  • Maintain accurate material inventory.
  • Identify possible process or product improvements.
  • Ensure all production activities are in full compliance with all regulatory, Quality System and GMP requirements.
  • Perform other duties as may be required by management.

Minimum Qualifications

  • High School graduate or equivalent.
  • Must be able to read, comprehend and follow general work procedures.
  • Good listening and communication skills.
  • Basic computer skills.
  • Flexible working schedule.

Desired Skills & Qualifications

  • Experience in a manufacturing environment, preferably medical device.
  • Good initiative, self-reliance and professionalism a plus.
  • Experience working in an ISO 9001 or GMP manufacturing environment.
  • Clean room environment or soldering experience.
  • Ability to visually inspect or test components, assemblies or devices in accordance with written procedures and identify defects.
  • Familiar with basic measuring equipment, and a variety of manufacturing concepts, practices, and procedures.

Requirements

  • High School graduate or equivalent.
  • Must be able to read, comprehend and follow general work procedures.
  • Good listening and communication skills.
  • Basic computer skills.
  • Flexible working schedule.
  • Experience in a manufacturing environment, preferably medical device.
  • Good initiative, self-reliance and professionalism a plus.
  • Experience working in an ISO 9001 or GMP manufacturing environment.
  • Clean room environment or soldering experience.
  • Ability to visually inspect or test components, assemblies or devices in accordance with written procedures and identify defects.
  • Familiar with basic measuring equipment, and a variety of manufacturing concepts, practices, and procedures.

Benefits

  • Employee Recognition Program
  • Service Awards
  • Bonus Referral Program
  • Personal and Vacation Time
  • Flexible Work Schedules
  • Medical, Dental & Vision
  • HSA and FSA options
  • Life Insurance
  • On-site gym
  • 401(k) Matching
  • Employee Stock Purchase Plan
  • Training & Education Assistance

Company overview

LivaNova PLC is a global medical technology company with nearly five decades of experience in developing innovative medical solutions for neurological and cardiac conditions. Headquartered in London with operations in over 100 countries, the company employs approximately 2,900 professionals worldwide. LivaNova operates through two primary business segments: Cardiopulmonary and Neuromodulation. The Cardiopulmonary division focuses on perfusion systems, oxygenators, and autotransfusion devices, including the market-leading Essenz™ Perfusion System and world's number one heart-lung machine. The Neuromodulation segment specializes in VNS Therapy™ for treating drug-resistant epilepsy and difficult-to-treat depression. With annual revenues exceeding $1.25 billion, LivaNova has established itself as a leader in medical device innovation, having treated millions of patients globally. The company maintains manufacturing and R&D facilities across Europe and the United States, all ISO 13485 certified, and continues to advance clinical research in areas like obstructive sleep apnea and treatment-resistant depression.

Explore more jobs of your matchFind more biopharma roles with GetBioJob.