Headquartered in Basel, Switzerland, Lonza is one of the world's leading suppliers to the pharmaceutical, healthcare and life science industries. Its products and services span its customers’ needs from research to final product manufacture. Lonza is the global leader in the production and support of active pharmaceutical ingredients both chemically as well as biotechnologically. Biopharmaceuticals are one of the key growth drivers of the pharmaceutical and biotechnology industries. Lonza has strong capabilities in large and small molecules, peptides, amino acids and niche bioproducts, which play an important role in the development of novel medicines and healthcare products. Lonza is a leader in cell-based research, endotoxin detection and cell therapy manufacturing. Lonza is also a leading provider of value chemical and biotech ingredients to the nutrition, hygiene, preservation, agro and personal care markets.

The company's successes stem from excellence as a sustainable competitive advantage: continuously improving best practices by retaining the talent vital for the competencies required. In an environment that fosters personal and professional growth, this is where you could realise your potential.

Position: QA Supervisor
Work Location: Across Singapore

Responsibilities:
You will provide leadership in leading team to achieve high quality and in compliance with current Good Manufacturing Practices.

• Responsible for ensuring quality process are in compliance.
• Ensure cGMP compliance oversight for operational areas.
• Review and approve documents, process, procedures, changes and reports.
• Working closely with various departments to ensure compliance.
• Participate in review, assessment, investigation and impact assessment of deviations and ensure appropriate corrective/preventive actions are implemented.
• Participate in Customer and Regulatory Inspection Management.
• Ensure day to day operations are effective to meet site needs.
• Lead, train and motivate the team to achieve quality goals.
• Responsible for resource planning and execution of projects.
• Participate in the GMP Readiness Program.

Requirements:

• University Degree in relevant science discipline.
• At least 7 years of relevant experience in the biopharmaceutical or related industry.
• Extensive and working knowledge of cGMP requirements and working knowledge of GMP systems.
• Strong planning and supervisory skills.
• Excellent interpersonal and communication skill.
• A person who is thorough, meticulous, analytical and a team player.

To Apply:
Please, use the following "Apply Online" link below and apply via our recruiting system. (Note: browse with latest Mozilla Firefox or Google Chrome to get the best view).

We regret that only shortlisted candidates will be notified

Closing Date: 3 February 2012

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