Johnson & Johnson
Compliance Specialist Operations
Schaffhausen · SH
- Berufsfeld
- Chemie, Pharma & Labor
- Ausbildung
- Berufslehre
- Erfahrung
- 2 bis 5 Jahre
- Sprachkenntnisse
- Deutsch · Englisch
- Lohn
- Geschätzt CHF 80’000–110’000 pro Jahr (100 %)
- Schätzung von jopp, nicht aus dem Inserat.
- Erstmals gesehen
- 26. September 2026
- Zuletzt gesehen
- 26. September 2026
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at .
As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Supply Chain Manufacturing
Job Sub Function:
Manufacturing Pharmaceutical Process Operations
Job Category:
Business Enablement/Support
All Job Posting Locations:
Schaffhausen Switzerland
Job Description:
Compliance Specialist / Teamlead Operations (m/w) CM&T F2P2
This role is responsible for implementing and ensuring compliance with new regulatory requirements supporting other production team leaders in GMPcompliant manufacturing leading a team that produces clinical products (compounding filling visual inspection and device assembly) and supporting projects within CM&T production.
Responsibilities (summary)
Support and implement measures to ensure compliance with Annex 1 requirements.
Lead and schedule a production team in a twoshift operation with responsibility for target achievement and overall performance.
Ensure ontime delivery of clinical and commercial batches in coordination with global and local planning.
Ensure EHS GMP and regulatory compliance including audit readiness.
Manage and execute NPI and operational projects; support qualification and validation activities.
Contribute to MES/PASX adjustments MBR/ESP management and document maintenance.
Coach and develop team members and promote continuous improvement (Lean).
Provide role coverage during absences deputising for other team leads or department management.
Your profile
Completed vocational training in the pharmaceutical field or a BSc in Pharmaceutical Biochemical Chemical sciences or equivalent.
Minimum of 2 years experience in a GMP environment.
Production leadership experience in a twoshift operation; project management experience is an advantage.
Strong problemsolving skills effective crossfunctional collaboration and clear communication.
Excellent German and English skills both written and spoken.
#DPDS
Required Skills:
Preferred Skills:
Agile Manufacturing Analytics Dashboards Chemistry Manufacturing and Control (CMC) Communication Data Compilation Data Savvy Empowering People Execution Focus Gap Analysis Give Feedback Good Manufacturing Practices (GMP) Operational Excellence Plant Operations Proactive Behavior Problem Solving Process Optimization Project Administration Resource Allocation Standard Operating Procedure (SOP)
Required Experience:
IC
Employment Type : Full-Time
Experience: years
Vacancy: 1