A day in the life:

• Goods receipt inspection: Checking delivered materials for completeness, integrity and conformity with order and customer specifications.
• Outgoing goods inspection: Final inspection of study medications and customer-specific shipments packaged for dispatch; ensuring that all specifications are met.
• Secondary packaging: QC startup and release of secondary packaging orders; monitoring of the correct implementation of all packaging steps.
• Prevention of quality deviations: Identifying and reporting potential deviations, initiating appropriate corrective and preventive actions.
• Sample collection / Sampling: Execution and monitoring of sample collection as well as proper storage of the samples.
• Monitoring of destruction: Accompanying the destruction of bulk material, study medication and packaging material in compliance with legal and internal requirements.
• Quarantine management: Quarantining materials in case of suspected quality deviations or pending tests.
• Documentation & Deviation Management: Precise and complete processing of all quality-relevant deviations, documentation according to internal SOPs.
• SOP Management: Participation in the creation and revision of standard operating procedures (SOPs).
• Training & Meetings: Determining one's own training needs, participating in regular coordination meetings, and informing the supervisor in a timely manner about significant difficulties.

The key to success:

Education:

• Completed vocational training in the pharmaceutical, technical or logistics field (e.g. PTA, PKA, CTA, druggist, pharmacy assistant) or comparable experience.

Experience:

• Prior professional experience in QA/QC, warehouse processes or secondary packaging is an advantage.

Knowledge, skills, abilities:

• Knowledge of GMP/GDP is desirable, but not a mandatory requirement.
• High sense of responsibility
• Careful, structured work methods.
• Attention to detail & strong documentation skills

What we offer:

• A temporary position in a 2-shift system with an innovative, forward-thinking employer, with the possibility of extension and subsequent permanent employment.
• Excellent development and career prospects in a globally growing company. 
• Attractive company pension scheme. 
• A corporate culture in which integrity, involvement, intensity and innovation are practiced.

A day in the life:

• Goods receipt inspection: Checking delivered materials for completeness, integrity and conformity with order and customer specifications.
• Outgoing goods inspection: Final inspection of study medications and customer-specific shipments packaged for dispatch; ensuring that all specifications are met.
• Secondary packaging: QC startup and release of secondary packaging orders; monitoring of the correct implementation of all packaging steps.
• Prevention of quality deviations: Identifying and reporting potential deviations, initiating appropriate corrective and preventive actions.
• Sample collection / Sampling: Execution and monitoring of sample collection as well as proper storage of the samples.
• Monitoring of destruction: Accompanying the destruction of bulk material, study medication and packaging material in compliance with legal and internal requirements.
• Quarantine management: Quarantining materials in case of suspected quality deviations or pending tests.
• Documentation & Deviation Management: Precise and complete processing of all quality-relevant deviations, documentation according to internal SOPs.
• SOP Management: Participation in the creation and revision of standard operating procedures (SOPs).
• Training & Meetings: Determining one's own training needs, participating in regular coordination meetings, and informing the supervisor in a timely manner about significant difficulties.

The key to success:

Education:

• Completed vocational training in the pharmaceutical, technical or logistics field (e.g. PTA, PKA, CTA, druggist, pharmacy assistant) or comparable experience.

Experience:

• Prior professional experience in QA/QC, warehouse processes or secondary packaging is an advantage.

Knowledge, skills, abilities:

• Knowledge of GMP/GDP is desirable, but not a mandatory requirement.
• High sense of responsibility
• Careful, structured work methods.
• Attention to detail & strong documentation skills

What we offer:

• A temporary position in a 2-shift system with an innovative, forward-thinking employer, with the possibility of extension and subsequent permanent employment.
• Excellent development and career prospects in a globally growing company. 
• Attractive company pension scheme. 
• A corporate culture in which integrity, involvement, intensity and innovation are practiced.