Compliance Specialist Operations

Johnson & JohnsonVerified source: this listing comes from the employer's official hiring system or a verified company · Schaffhausen, Switzerland · Onsite
Listed via Workday
Posted Jul 20, 2026 · Apply by Sep 18
Recently checked

Last checked active on Jul 20, 2026.

Position Overview

Compensation: Not disclosed
Position: Mid
Type: Job
Employment: Full time
Practice Area: Compliance
Remote: No
Company Size: 10000+ employees
Deadline: Sep 18, 2026

Job Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through 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 humanity. Learn more at jnj.com.

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 GMP‑compliant 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 two‑shift operation, with responsibility for target achievement and overall performance. 

  • Ensure on‑time 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/PAS‑X 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 two‑shift operation; project management experience is an advantage. 

  • Strong problem‑solving skills, effective cross‑functional 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)

Practice Area

Position

Mid

Industry

Healthcare

Application Deadline

September 18, 2026

Employment Type

Full time

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