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QA Specialist III-Lot Review

Lonza
Posted 2 months ago, valid for 18 days
Location

Portsmouth, NH 03801, US

Salary

$28,000 - $33,600 per year

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Contract type

Full Time

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Sonic Summary

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  • The QA Specialist III – Lot Review position is located onsite at the Portsmouth, NH facility and focuses on ensuring the integrity and compliance of manufacturing processes.
  • Candidates should have a Bachelor's degree in Science or a related field and 5–10 years of experience in cGMP environments.
  • The role involves reviewing and closing manufacturing batch records, resolving issues, and training junior staff on record review processes.
  • The position offers a dynamic working culture, competitive compensation, and a comprehensive benefits package including medical, dental, and vision insurance.
  • Lonza values collaboration and innovation, seeking individuals who are ready to contribute to the development of life-changing therapies.

 

QA Specialist III – Lot Review

Location: Onsite at our Portsmouth, NH facility

Join our Quality Assurance team in Portsmouth, NH, where you’ll play a critical role in ensuring the integrity and compliance of our manufacturing processes. This is an exciting opportunity to contribute to the release of life-changing therapies while developing your skills in a collaborative environment.
 

What you will get:

  • An agile career and dynamic working culture

  • An inclusive and ethical workplace

  • Compensation programs that recognize high performance

  • Medical, dental, and vision insurance

  • Opportunities for professional growth and leadership development

  • Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits 


What you will do:

  • Review and close manufacturing batch records and related documentation for API release

  • Resolve issues and escalate complex cases when needed

  • Participate in daily lot release meetings and routine QA activities

  • Train junior staff on record review processes

  • Apply data integrity principles in all aspects of work

  • Support process improvement projects and quality initiatives

  • Collaborate with QA, QC, and Manufacturing teams to maintain compliance
     

What we are looking for:

  • Bachelor’s degree in Science or related field

  • 5–10 years of experience in cGMP environments

  • Strong knowledge of quality systems and good documentation practices

  • Excellent attention to detail and critical thinking skills

  • Effective written and verbal communication skills

  • Ability to work independently and within a team environment

  • Proficiency in Microsoft Office; experience with Trackwise and SAP preferred
     

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.




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