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Fill/Finish Tech Mid Level

Posted 23 January by Lonza Ended
At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success. Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia. Our vision: We strive to be the leading supplier using science and technology to improve the quality of life.Our mission: We work with passion, using advanced technologies, to transform life science into new possibilities for our customers.
Do you want to help us as we shape the future of this great organization?

Job Description Summary

Responsible for performing production functions in the Class 100 cleanroom (core)
and Finishing area according to company and departmental SOP’s. Individual will
set up and operate production equipment. Individual will maintain records to
comply with Good Manufacturing Practices and Standard Operating Procedures.
Individual will work in a fast-paced, safety-oriented, team environment.

Primary Role Responsibilities1. Responsible for executing aseptic processing in a clean room environment adhering to

Standard Operating Procedures

2. Complete documentation concurrently with completion of manufacturing processes

3. Responsible for completing assigned tasks (for example, cleaning, lab setup etc.) related to

departmental functions

4. Perform preventative maintenance and general upkeep on equipment and facilities including

environmental monitoring

5. Responsible for reviewing SOPs, MBRs and other associated forms for revision

6. Review and sign manufacturing batch records

7. Responsible for keeping current on all job relevant trainings

8. Assist in writing deviations and supporting investigations

9. Assist in training entry level staff members

10. Being available for business necessitated overtime is required

  • A.A in biological sciences with 1-5 years in a cGMP production environment is desirable. College education can be substituted for years of experience.
  • Ability to read, understand and follow the production schedule, DMRs (Devive Master Records) and SOPs (Standard Operating Procedures).
  • Ability to understand the importance of compliance with Good Manufacturing Practices and ISO requirements.
  • Must be able to use aseptic technique.
  • Computer software skills including Microsoft (Outlook, Word, Excel). SAP and Trackwise.
  • Must be able to manage time and maintain regular attendance is mandatory
  • Neat and accurate record keeping.
  • Written and oral communication skills, team oriented, attention to detail, independent working skills, strong work ethic.
  • Must be able to work a flexible schedule with overtime and weekend work requiredWorking conditions:

    A majority of the work is done in a laboratory environment. While working in the area the minimal gowning requirements are safety glasses, hairnet, steel toe shoes and lab coat. Additional responsibilities require entrance into a cleanroom environment. While working in the cleanroom additional gowning requirements are shoe covers, hood, gown, mask boots, and two pair of gloves. Working conditions can include standing for long periods of time.

    Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

    Lonza. The place to Go, Stay and Grow.
  • Reference: 34294256

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