GMP Inspector

The Siegfried Group is a Swiss-based worldwide life science company that develops and manufactures active pharmaceutical ingredients, intermediates, standard controlled substances, and ready-formulated drugs. Forming part of the Siegfried group, Siegfried Malta Limited specialises in a high-value and innovative generic portfolio in the solid dosage form range, from bulk to final packaging including capsule filling and highly potent FDA-approved products.

The chosen candidate will be responsible for:

• Support the production operations to ensure that GMP guidelines and internal procedures are abided by at all times (e.g. cGMP, ICH, PIC-GMP, 21CFR) and provide support during any issues that might arise within the production operations;

• Online executed batch record quality review to ensure that each batch has been manufactured as per predefined instructions and GMP;

• Issue batch records for use in production in accordance with the Production plan;

• Support in sampling activities and ensure that the correct procedures are followed;

• Support on-the-floor quality issues in a timely manner, monitoring systems and procedures to ensure compliance in accordance with company-industry standards, and identify areas of opportunity and quality improvements;

• Support in quality investigation / deviations arising from production.

The ideal candidate should possess:

• A post-secondary level of education in Life Sciences or a related field;

• Previous experience working in a GMP-regulated manufacturing environment, preferably in the pharmaceutical industry;

• Strong interpersonal and communication skills;

• Excellent organizational abilities with an eye for detail;

• Proactive problem-solver with a commitment to maintaining high-quality standards.

Join our team and experience a dynamic 4-shift work schedule, designed to provide flexibility and ensure a balanced approach to meeting operational needs.