At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success.
Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia.
Our vision :
We strive to be the leading supplier using science and technology to improve the quality of life.
Our mission :
We work with passion, using advanced technologies, to transform life science into new possibilities for our customers.
Do you want to help us as we shape the future of this great organization?
Support day-to-day Quality Assurance activities in accordance with approved SOPs / Policies for a large scale, multi-product, GMP biotech contract manufacturing facility.
Able to plan for future activities and coordinate with other departments to complete this.
Develops skills to be Qualified Trainer in area of expertise.
In depth awareness of entire process; identifying operational factors which influence the process.
Participates in Regulatory and Customer Audits.
Able to participate actively or lead in deviation investigations, change controls, CAPA plans and closure of discrepancy reports.
Makes real-time decisions on process events on the floor based on knowledge of defined SOPs & policies.
Develops good working relationships with internal & external customers.
A competent Reviewer and Approver of SOPs, protocols, reports or records.
Leads a small team and provides supervision to QA Coordinators, interns or QA Specialists I and II.
Any other tasks as and when assigned by supervisor.
Diploma with 5 7 years’ experience in a similar type of industry or a similar job role
Degree from recognized institution with 3 to 5 years’ experience in a similar type of industry or a similar job role.