Senior Aseptic Process Compliance Engineer

Johnson & Johnson Innovation

Schaffhausen

Vor Ort

CHF 120.000 - 160.000

Vollzeit

14 Tage+
Bewerbungsgenerator

Hebe dich für diese Rolle von der Masse ab — erstelle in etwa einer Minute einen maßgeschneiderten Lebenslauf und ein Anschreiben.

Schaffe es an den ATS-Filtern vorbei

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

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.

Hol dir deinen kostenlosen, vertraulichen Lebenslauf-Check.

oder ziehe deine Datei hierhin.

Similar jobs

Ähnliche Jobs, die dir auch gefallen könnten

Senior Compliance Engineer, Process Engineering
Senior Compliance Engineer, Process Engineering

Johnson & Johnson Innovation • Schaffhausen

Vor Ort
CHF 120.000 - 160.000
Staff Process Engineer, Parenteral Manufacturing & NPI
Staff Process Engineer, Parenteral Manufacturing & NPI

jj • Schaffhausen

Vor Ort
CHF 110.000 - 150.000
Pharma Manufacturing Operator & Process Support (Schaffhausen)
Pharma Manufacturing Operator & Process Support (Schaffhausen)

Johnson & Johnson Innovation • Schaffhausen

Vor Ort
CHF 65.000 - 90.000
Staff Process Engineer, Parenterals NPI & LCM
Staff Process Engineer, Parenterals NPI & LCM

8562-Cilag AG Legal Entity • Schaffhausen

Vor Ort
CHF 120.000 - 150.000
Senior Project Engineer, Aseptic Fill Finish (Pharma)
Senior Project Engineer, Aseptic Fill Finish (Pharma)

8562-Cilag AG Legal Entity • Schaffhausen

Vor Ort
CHF 120.000 - 160.000
Quality Process & Qualification Manager - Compliance
Quality Process & Qualification Manager - Compliance

8525-Cilag GmbH International Legal Entity • Zug

Vor Ort
CHF 120.000 - 160.000
Senior Project Engineer, Pharmaceutical Manufacturing
Senior Project Engineer, Pharmaceutical Manufacturing

8562-Cilag AG Legal Entity • Schaffhausen

Vor Ort
CHF 120.000 - 160.000
Staff Process Engineer PAR NPI/LCM
Staff Process Engineer PAR NPI/LCM

Johnson & Johnson Innovation • Schaffhausen

Vor Ort
CHF 115.000 - 140.000
Regulatory Affairs Specialist — Swissmedic & GMP Compliance
Regulatory Affairs Specialist — Swissmedic & GMP Compliance

8562-Cilag AG Legal Entity • Schaffhausen

Vor Ort
CHF 90.000 - 130.000
Regulatory Affairs Specialist — Swiss GMP, Health Authority
Regulatory Affairs Specialist — Swiss GMP, Health Authority

jj • Schaffhausen

Vor Ort
CHF 110.000 - 140.000