Lonza · 1 day ago
QA Specialist III-Operations OTF
Lonza is a global leader in life sciences, dedicated to manufacturing the medicines of tomorrow. The QA Specialist III will ensure GMP compliance and operational excellence by providing real-time support on the manufacturing floor and reviewing GMP documentation.
BiotechnologyLife SciencePharmaceutical
Responsibilities
Provide real-time Quality Assurance support on the manufacturing floor
Review GMP documentation and observe operational practices
Offer guidance on routine and non-routine GMP issues
Respond to QA hotline calls and escalate complex issues
Authorize equipment release and manage quality tag-outs
Apply data integrity principles in all aspects of work
Represent QA in meetings and project teams
Qualification
Required
Bachelor's degree in a science-related field or equivalent experience
5–10 years of cGMP experience in a regulated environment
Strong understanding of GMP and ICH guidelines
Familiarity with systems such as TrackWise, SAP, LIMS, and Microsoft Office
Ability to identify and escalate quality issues promptly
Collaborative mindset and commitment to continuous improvement
Excellent communication and problem-solving skills
Benefits
Medical, dental, and vision insurance.
Company
Lonza
Lonza Group supplies products and services to pharmaceutical and agrochemical industries.
H1B Sponsorship
Lonza has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2024 (3)
2022 (1)
2021 (3)
2020 (2)
Funding
Current Stage
Public CompanyTotal Funding
$444.8M2023-11-06Post Ipo Debt· $444.8M
2020-12-07IPO
Recent News
2026-01-07
2026-01-05
Company data provided by crunchbase