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QC Analyst I - Microbial Control

Lonza - USA
Portsmouth, NH Full Time
POSTED ON 3/13/2025 CLOSED ON 3/30/2025

What are the responsibilities and job description for the QC Analyst I - Microbial Control position at Lonza - USA?

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.

The Quality Microbial Control Analyst 1 will act as a team member of the

Quality Microbial Control department to support production of in-process and

final product drug lots for customers. Also participate in quality testing for

ongoing customer stability studies. Provide on-time, high quality results to meet

Manufacturing demands

*This position is a 2nd shift role that reports to work Wednesday to Saturday 1:00PM-11:30PM*

Training will be conducted during 1st shift for a few weeks

Key Responsibilities:

  • Applies job skills and company's policies and procedures to complete a variety of tasks.

  • Running test samples for In-Process, Lot Release and Stability studies.

  • Support Utility and HVAC monitoring and sampling throughout the facility.

  • Use of Microsoft Suites (Word, Excel, PowerPoint).

  • Use of Laboratory computer systems.

  • Works on assignments that are semi-routine in nature where ability to

  • recognize deviation from accepted practice is required.

  • Works on problems of moderate scope in which analysis of situation or

  • data requires a review of identifiable factors.

  • Apply Data Integrity principles in all aspects of work, in compliance with

  • Lonza DI policies, guidelines and procedures.

  • Perform other duties as assigned.

Key Requirements:

  • High School Diploma or equivalent. An Associate's Degree is preferred in Microbiology, Biochemistry or Related Science fields.

  • 0-4 years industry experience, preferably in a cGMP environment.

  • Strong ability to interpret data both alone and with guidance.

  • Perform assigned, complex and/or varied tasks.

  • Prioritization and problem solving.

  • Comprehend and follow instructions.

  • Strong ability to communicate in both written and verbal format.

  • Exercises judgment within defined procedures and practices to determine appropriate action.

  • Self-motivated team player.

  • Completes assignments on-time and accurately.

  • Displays commitment to quality and performs job functions to the best of his/her ability.

  • Relate to others in a team setting.

  • Maintain a positive attitude in a team environment.

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