Senior Compliance Engineer, Process Engineering

Johnson & Johnson Innovation; Schaffhausen; Vor Ort; CHF 120.000 - 160.000; Vollzeit

Zusammenfassung

Johnson & Johnson Innovation in Schaffhausen, Switzerland, seeks a Compliance Engineer in Process Engineering to support GMP-compliant manufacturing, validation, and qualification activities in an aseptic environment.

The role focuses on process equipment, utilities, and systems, with emphasis on validation, change control, and collaboration across engineering teams to advance medical innovation. Fluency in German and English is required, with 4–6 years in pharma/chemical settings.

Qualifikationen

• Specifications & design of process equipment and systems in the aseptic environment.
• Troubleshoot equipment failures and define optimization and / or changes to existing equipment. Root-cause analyzation , definition of corrective actions and follow-up of implementations.
• Building experience in process & facility engineering, support GMP-compliance of facility, utilities and process equipment (e.g. COC, events, deviations, NC, qualification, support validation, ...)
• Write procedures, protocols, analyse data and write summary conclusions in reports.
• Building experience and knowledge of HVAC, certification, monitoring - Additional experience in the aseptic field is welcome
• Identify projects, create project plans and participate in their implementation. Perform evaluations to drive efficiency and business results.
• Overall understanding of project budgeting processes and systems.
• Understanding of the own role and the role of the department within the broader organization (CSC/DPDS/IMSC).
• Readiness to lead a project team.
• Provides an opportunity to explore process proof-of-principles to build up of knowlage for commercial process. Plans, coordinates and oversees validation operations, including scale up and optimization processes, equipment assembly, in process sample analysis, use of reactors, and preparation of compliance documents.
• Evaluate analytical results to maintain and improve the quality of batches.
• Propose and determine new or improved technologies to enhance product quality, manufacturing cost efficiencies, personnel safety and regulatory compliance.
• Strong knowledge of aseptic fill finish and Annex 1/FDA compliance with all related regulatory & guidelines to translate in a technical solution.
• Bilingual German & English
• 4-6 years’ of experience in the pharmaceutical/foot/chemical environment

Aufgaben

• Support the operation of the process equipment and production operation at the technical level in the Fill & Finish pilot plant.
• Troubleshooting, rectification and documentation (troubleshooting, non-conformance management) in collaboration with production personnel, equipment suppliers and quality assurance.
• Management of technical change and optimization processes (change control) systems and processes.
• Supervision of the technical order system in cooperation with mechanics and Technical Services.
• Instruction and training of employees on system and process level. Support in the evaluation and qualification of new technology-platforms/processes in the aseptic environment.
• Cross-cutting project collaboration with other engineering functions at the local campus level and in the global engineering environment

Kenntnisse

Agile Decision Making

Coaching

Critical Thinking

Engineering

Problem Solving

Process Control

Process Engineering

Product Costing

Product Improvements

Research and Development

SAP Product Lifecycle Management

Situational Awareness

Technical Research

Technical Writing

Technologically Savvy

Vendor Selection

Jobbeschreibung

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:

R&D Product Development

Job Sub Function:

R&D Process Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Schaffhausen, Switzerland

Job Description:

Compliance Engineer, Process Engineering (m/f)

Main Task

The Principal Engineer, Process Engineering is responsible for Engineering and Qualification; support Validation on process equipment, utilities & facilities and computerized systems in CM&T F2P2.

• Support the operation of the process equipment and production operation at the technical level in the Fill & Finish pilot plant
• Troubleshooting, rectification and documentation (troubleshooting, non-conformance management) in collaboration with production personnel, equipment suppliers and quality assurance
• Management of technical change and optimization processes (change control) systems and processes
• Supervision of the technical order system in cooperation with mechanics and Technical Services
• Instruction and training of employees on system and process level. Support in the evaluation and qualification of new technology-platforms/processes in the aseptic environment
• Cross-cutting project collaboration with other engineering functions at the local campus level and in the global engineering environment

Your profile

• Specifications & design of process equipment and systems in the aseptic environment.
• Troubleshoot equipment failures and define optimization and / or changes to existing equipment. Root-cause analyzation , definition of corrective actions and follow-up of implementations.
• Building experience in process & facility engineering, support GMP-compliance of facility, utilities and process equipment (e.g. COC, events, deviations, NC, qualification, support validation, ...)
• Write procedures, protocols, analyse data and write summary conclusions in reports.
• Building experience and knowledge of HVAC, certification, monitoring - Additional experience in the aseptic field is welcome
• Identify projects, create project plans and participate in their implementation. Perform evaluations to drive efficiency and business results.
• Overall understanding of project budgeting processes and systems.
• Understanding of the own role and the role of the department within the broader organization (CSC/DPDS/IMSC).
• Readiness to lead a project team.
• Provides an opportunity to explore process proof-of-principles to build up of knowlage for commercial process. Plans, coordinates and oversees validation operations, including scale up and optimization processes, equipment assembly, in process sample analysis, use of reactors, and preparation of compliance documents.
• Evaluate analytical results to maintain and improve the quality of batches.
• Propose and determine new or improved technologies to enhance product quality, manufacturing cost efficiencies, personnel safety and regulatory compliance.
• Strong knowledge of aseptic fill finish and Annex 1/FDA compliance with all related regulatory & guidelines to translate in a technical solution
• Bilingual German & English
• 4-6 years’ of experience in the pharmaceutical/foot/chemical environment

Required Skills:

Preferred Skills: Agile Decision Making, Coaching, Critical Thinking, Emerging Technologies, Engineering, Problem Solving, Process Control, Process Engineering, Process Improvements, Product Costing, Product Improvements, Research and Development, SAP Product Lifecycle Management, Situational Awareness, Technical Research, Technical Writing, Technologically Savvy, Vendor Selection