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Manufacturing Services Associate I (Days - B shift)

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Lonza logoLonza · Us - Portsmouth, NH
Full-timeOn-siteToday
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Requirements

  • High School Diploma or equivalent experience required; AS/BS preferred.
  • Prior experience in a manufacturing setting preferred.
  • Prior experience in a clean room or other similar sterile setting is preferred.
  • Validated logic and decision-making abilities, and critical thinking skills.
  • Strong written and verbal communication skills are required.
  • Join us at Lonza and be part of a team that values collaboration and contributes to life-changing solutions!
  • People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Benefits

Equity / stock options

Additional Information

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Discover an outstanding opportunity with Lonza as a Manufacturing Services Associate 1 in Portsmouth, New Hampshire. Join our premier team and contribute to bold projects that have a meaningful impact on millions of lives! The shift schedule is from 7am-7pm, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Key Accountabilities and Duties: Perform 6S and stock each suite daily, and clean soiled parts daily. Determine production needs for autoclaved assemblies and deliver them to suites. Perform daily and weekly maintenance activities on analytical equipment. Report all activities in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), and review documentation as appropriate. Attain qualification for all assigned tasks and maintain an individual training plan. Prepare materials for transport and delivery to manufacturing suites, and perform material movements into, out of, and across the production areas. Maintain facility and equipment through routine cleaning and sanitization. Support Site Data Integrity Plan by actively participating in projects, completing results, and attending training. Apply Data Integrity principles into routine tasks by following DI policies, guidelines, and procedures.


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