IMP Quality Clinical Packaging Specialist
Job Summary:
A 12-month opportunity exists for an IMP Quality Clinical Packaging Specialist to support quality-relevant packaging processes and collaborate with stakeholders.
Key Responsibilities:
* Collaborate with packaging operations and interfaces on GMP topics, ensuring seamless delivery of company goals.
* Provide GMP support to stakeholders, reviewing and releasing manufacturing specifications and batch records.
* Actively manage deviations and changes, while coordinating local and global projects.
* Engage in optimization activities, improvements, and corrective measures within IMP Quality Clinical Packaging Switzerland.
* Build, verify, and implement standard documents, including SOPs.
Requirements:
* Mandatory proficiency in German and English.
* Master's degree in Life Sciences or Engineering, or a similar field.
* Minimum 3 years of experience in the pharmaceutical industry as a quality manager.
* Familiarity with cGMP and quality requirements for clinical development phases.
* Advantageous: experience in pharmaceutical development, packaging lines, master data management, quality control, or quality assurance.
* Proven track record of working towards outcomes and innovative problem-solving.
Work Details:
* Home office: 20%
* Seniority level: Associate
* Employment type: Contract
* Job function: Other
* Industries: Pharmaceutical Manufacturing and Biotechnology Research