Lonza
Pharmaceutical
Intern-QASpecialistBatchRecordReview
Neural analysis suggests this role is
optimal for Entry candidates.
“Intern - QA Specialist Batch Record Review at Lonza. Skills: Batch Record Review, Quality Assurance, GMP. Review Executed Batch Records. Review comments added to Executed Batch Records”
What You'll Achieve.
Ensure timely and accurate batch record processing
Industry & Context.
What They're Looking For.
Must Have
Bachelor degree or relevant work/ internship experience in Biology, Chemistry, Biotechnology, Life Science or other related field, Ability to identify non-compliance and gaps from quality standards, Structured, precise and well-organized working, English: Fluent
Nice to Have
Previous experience in GMP regulated pharmaceutical / API industry is an advantage, German: Good to have
What You'll Do.
Review Executed Batch Records
Review comments added to Executed Batch Records
Clarify with operations team
Evaluate with responsible QA Manager
Support initiation of deviations
Support investigations for Batch Record review related observations
How You'll Work.
Team & Collaboration
Work closely with QA specialists; Work with cross-functional teams
Full Job Description
The Batch Record Review Intern supports the Quality Assurance team (QA OPS) by assisting in the review, verification, and organization of electronic GMP manufacturing documentation. This role provides hands‑on exposure to regulated industry practices, including data integrity, documentation control, and compliance with internal procedures and regulatory standards. The intern will work closely with QA specialists and cross‑functional teams to ensure timely and accurate batch record processing. This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. ****What you will get:**** * An agile career and a dynamic work culture. * An inclusive and ethical workplace. * Compensation programs that recognize high performance. **What you will do:** * Review of the Executed Batch Records (e.g. cleaning logs, production documentation review, temperature reports, test procedures, raw data, logbooks) * Review comments added to the Executed Batch Records, clarify with the operations team and evaluate with the responsible QA Manager * Support the initiation of deviations and investigations for Batch Record review related observations **What we are looking for:** * Bachelor degree or relevant work/ internship experience in Biology, Chemistry, Biotechnology, Life Science or other related field * Previous experience in GMP regulated pharmaceutical / API industry is an advantage * Ability to identify non-compliance and gaps from quality standards * Structured, precise and well-organized working attitude; open-minded for new ideas and suggestions; agile, highly motivated and dynamic drive * English: Fluent. German: Good to have. ****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
Applying for this Intern - QA Specialist Batch Record Review role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Workday
- Workday has a multi-step form — save your progress after every section.
- "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
- Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
- Job requisition numbers are useful when following up with HR by email.
ANONYMOUS · UNFILTERED
What do employees actually say about Lonza?
Real rants from real employees. Read before you apply.