LocationSchaffhausen (hybrid working: 3 days onsite / 2 days home office)
Contract DurationUntil 31st December 2026.
Essential QualificationsFull professional proficiency in both English and German.3+ years experience in a GMP environment (Pharma, Bio‑Tech, or Food industry).Mandatory previous experience with batch record systems.Proven experience with Manufacturing Execution Systems (MES).Completed apprenticeship or scientific degree (University/College).
Project OverviewImagine your next project supporting the digital transformation of life‑saving medicine production. We are seeking a highly skilled QA MES specialist to strengthen the QA Parenterals Team. This role is at the heart of our challenging journey to digitalise batch records, offering the opportunity to work with cross‑functional teams on exciting projects where quality is always the North Star.
Roles and ResponsibilitiesOwn compliance‑relevant project tasks within the MES implementation, define framework conditions and approve relevant procedures.Approve and release MES relevant data within the project implementation.Review and approve MES relevant non‑conformities and corrective actions (NC & CoC) records.Take over the QA MES role during Dry Run, Verification and Wet testing.Maintain compliance with all company policies and procedures.Work in a hybrid model (3 days onsite in Schaffhausen, 2 days home office).
Qualifications and How to SucceedWe are looking for a quality‑minded professional who thrives at the intersection of traditional GMP standards and modern digital systems. You will bring:
Professional experience in a GMP environment (Pharma, Bio‑Tech, or Food industry).Full professional proficiency in both German and English (mandatory).Proven experience with MES and digital batch records.Completed apprenticeship or scientific degree (University/College).Excellent computer proficiency (MS Office, MES).Excellent analytical skills to identify gaps and root causes of issues.Ability to work independently to meet tight deadlines while maintaining a positive attitude.
BenefitsThis role offers a very competitive hourly rate. The contract runs until 31st December 2026.
Application ProcessWe are looking to process the first round of applications within the next two working days. Please do not submit applications via email.
Diversity, Equity & InclusionJohnson & Johnson is working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued. Everyone belongs and can reach their potential.
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