Inserat online seit: 15 Juni
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Ensure the highest quality standards in pharmaceutical packaging with us!
Adherence to strict GMP guidelines is the foundation of our success and the safety of patients worldwide. For our packaging department, we are seeking a dedicated and detail-oriented individual to oversee operational processes and ensure compliance with our quality standards. From managing the SOP system and conducting GMP walkthroughs to supporting regulatory inspections, you will assume significant responsibility. Contribute your quality awareness and strengthen our team as a Production Support Compliance Specialist (m/f/d).
Here's what we offer
Attractive salary and long-term job security through affiliation with a large corporation.Up to 30 days of vacation per yearCompany pension scheme contribution after the end of the probationary periodExtensive social benefits, including Christmas and holiday payReimbursement of travel expensesUsually an open-ended employment contractGood opportunities for acquisition with our business partnersTailored professional development opportunities and free language coursesA wide range of employee benefits Your tasks
The focus of this position is on ensuring smooth operational processes and compliance with quality standards in the area of pharmaceutical packaging under GMP conditions.
Your responsibilities include contributing to the content and technical aspects as well as coordinating the company's internal SOP system.They participate in the training and continuous education of production staff with regard to GMP requirements, including the documentation of relevant training certificates and support in the planning and implementation of training measures based on existing guidelines.Furthermore, you will collaborate on the electronic documentation of training courses in the relevant system (LOS).They assist in conducting GMP inspections to ensure GMP-compliant drug packaging.Furthermore, you will be involved in the preparation, coordination, execution and follow-up of internal and external (official) inspections.Your responsibilities also include conducting the logbook review in accordance with the applicable process guidelines. Your profile
Completed vocational training in natural sciences or pharmaceuticals with many years of relevant professional experienceExcellent knowledge of the GMP environment , especially with regard to quality requirements and regulatory specifications in the pharmaceutical industry.Experience in the manufacture and/or packaging of pharmaceuticals is an advantage.Excellent German skills and basic English skillsStrong quality awareness, structured and meticulous work methods, reliability, and a high degree of responsibility.Strong team orientation and communication skills in an interdisciplinary environmentHigh flexibility, quick comprehension, and the ability to work in a structured and goal-oriented manner even under time pressure.
