Senior QC Analyst

Lonza•Portsmouth, NH

3d•Onsite

About The Position

Senior QC Microbial Analyst – Cell Therapy Location: Portsmouth, NH. The shift schedule is from 7:00 am-3:30 pm (Monday to Friday). The Sr. QC Microbial Analyst supports drug production by performing quality testing on in-process and final product lots, as well as ongoing stability studies. In this role, you will deliver high-quality, timely results to meet manufacturing demands while following all company policies and procedures. The position involves handling semi-routine tasks and moderate-scope problems that require strong data analysis and the ability to identify deviations. Additionally, you may assist with special projects and provide leadership support in the absence of a supervisor. What you will get: Competitive salary and comprehensive benefits package Opportunities for career development and advancement Supportive and collaborative team environment Access to cutting-edge technology and tools Commitment to employee well-being and safety Inclusive workplace culture Recognition and reward for your contributions Access to our full list of global benefits: https://www.lonza.com/careers/benefits What you will do: Run test samples for in-process, lot release and stability studies. Writing quality records (Deviations, CAPA, Change Control) and test methods. Applies job skills and company's policies and procedures to complete a variety of tasks. Reviewing assays. 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. What we are looking for: Bachelor's or Associate's Degree preferably in Microbiology, Biochemistry, or related science discipline. 5-10 year’s of GMP industry experience; aseptic experience is preferred. Use of Microsoft Suites (Word, Excel, PowerPoint) and Laboratory computer systems. Experience using GMP Quality Systems such as: TrackWise, LIMS preferred. Perform assigned, complex and/or varied tasks. Exercises judgment within defined procedures and practices to determine appropriate action. Self-motivated team player. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.

Requirements

Bachelor's or Associate's Degree preferably in Microbiology, Biochemistry, or related science discipline.
5-10 year’s of GMP industry experience; aseptic experience is preferred.
Use of Microsoft Suites (Word, Excel, PowerPoint) and Laboratory computer systems.
Experience using GMP Quality Systems such as: TrackWise, LIMS preferred.
Perform assigned, complex and/or varied tasks.
Exercises judgment within defined procedures and practices to determine appropriate action.
Self-motivated team player.

Responsibilities

Run test samples for in-process, lot release and stability studies.
Writing quality records (Deviations, CAPA, Change Control) and test methods.
Applies job skills and company's policies and procedures to complete a variety of tasks.
Reviewing assays.
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.