We are currently supporting our top client, a global leader in plasma-derived therapies, in their search for an Engineering Data Support Specialist (m/w/d) based in Bern. In this role, you will support the Manufacturing Science & Technology (MS&T) and Validation teams by contributing to data management, analysis, process improvement, documentation, and compliance activities. Your work will play a key role in ensuring efficient operations, maintaining data integrity, and supporting compliance with quality and regulatory requirements. You will collaborate closely with engineering, validation, and production teams to drive operational excellence and support critical business processes.
Your Responsibilities
Safety & Compliance
Adhere to all company safety policies, procedures, and regulatory requirements.
Participate in mandatory safety training and use all required safety equipment correctly.
Consistently wear personal protective equipment (PPE) where required and ensure defective equipment is replaced promptly.
Proactively identify and eliminate hazards where possible, or elevate risks immediately to your supervisor.
Actively contribute to a strong safety culture and support continuous improvement initiatives related to workplace safety.
Data Management & Analysis
Support the setup, maintenance, and validation of STATISTICA workspaces for the automated analysis of data from systems such as LIMS and MES.
Verify data integrity and ensure the accuracy and reliability of data analyses and reporting.
Assist with data extraction, processing, analysis, and reporting activities to support MS&T and Validation projects.
Documentation & Archiving
Coordinate and support document archiving activities, including the preparation, organization, and transfer of records to the Scan Competence Center.
Update and maintain SOPs, work instructions, forms, and other controlled documentation within the MS&T and Validation departments.
Ensure documentation remains accurate, compliant, and aligned with quality standards.
Project Support
Provide operational support for validation and MS&T initiatives.
Assist with sample handling and related project activities.
Collaborate with cross-functional stakeholders to ensure projects are completed on time and in compliance with regulatory requirements.
Your Profile
Degree in a scientific discipline such as Pharmacy, Pharmaceutical Technology, Biology, Chemistry, or a related field (Bachelor's, Master's, or PhD). Equivalent industry experience will also be considered.
2-5 years of experience in engineering data management, maintenance systems, or pharmaceutical manufacturing environments.
Strong experience working with LIMS and MES systems
Advanced proficiency in Microsoft Excel and familiarity with data visualization tools such as Power BI or Tableau.
Good understanding of GMP/cGMP requirements and quality systems within regulated industries.
Excellent analytical, problem-solving, and organizational skills.
Strong attention to detail and the ability to communicate effectively with stakeholders across different functions.
Comfortable working in a collaborative, fast-paced environment.
What We Offer
Opportunity to work with cutting-edge systems and contribute to high-impact projects within a leading global biopharmaceutical company.
Exposure to innovative manufacturing, validation, and data-driven improvement initiatives.
Collaborative and supportive international working environment.
Start date: 01.09.2026. Temporary project assignment with the potential for extension
Location: Bern, Switzerland with home office option
#J-18808-Ljbffr
Your Responsibilities
Safety & Compliance
Adhere to all company safety policies, procedures, and regulatory requirements.
Participate in mandatory safety training and use all required safety equipment correctly.
Consistently wear personal protective equipment (PPE) where required and ensure defective equipment is replaced promptly.
Proactively identify and eliminate hazards where possible, or elevate risks immediately to your supervisor.
Actively contribute to a strong safety culture and support continuous improvement initiatives related to workplace safety.
Data Management & Analysis
Support the setup, maintenance, and validation of STATISTICA workspaces for the automated analysis of data from systems such as LIMS and MES.
Verify data integrity and ensure the accuracy and reliability of data analyses and reporting.
Assist with data extraction, processing, analysis, and reporting activities to support MS&T and Validation projects.
Documentation & Archiving
Coordinate and support document archiving activities, including the preparation, organization, and transfer of records to the Scan Competence Center.
Update and maintain SOPs, work instructions, forms, and other controlled documentation within the MS&T and Validation departments.
Ensure documentation remains accurate, compliant, and aligned with quality standards.
Project Support
Provide operational support for validation and MS&T initiatives.
Assist with sample handling and related project activities.
Collaborate with cross-functional stakeholders to ensure projects are completed on time and in compliance with regulatory requirements.
Your Profile
Degree in a scientific discipline such as Pharmacy, Pharmaceutical Technology, Biology, Chemistry, or a related field (Bachelor's, Master's, or PhD). Equivalent industry experience will also be considered.
2-5 years of experience in engineering data management, maintenance systems, or pharmaceutical manufacturing environments.
Strong experience working with LIMS and MES systems
Advanced proficiency in Microsoft Excel and familiarity with data visualization tools such as Power BI or Tableau.
Good understanding of GMP/cGMP requirements and quality systems within regulated industries.
Excellent analytical, problem-solving, and organizational skills.
Strong attention to detail and the ability to communicate effectively with stakeholders across different functions.
Comfortable working in a collaborative, fast-paced environment.
What We Offer
Opportunity to work with cutting-edge systems and contribute to high-impact projects within a leading global biopharmaceutical company.
Exposure to innovative manufacturing, validation, and data-driven improvement initiatives.
Collaborative and supportive international working environment.
Start date: 01.09.2026. Temporary project assignment with the potential for extension
Location: Bern, Switzerland with home office option
#J-18808-Ljbffr
Engineering Data Support (m/w/d) Arbeitgeber: LHH
Als Arbeitgeber bieten wir eine dynamische und flexible Arbeitsumgebung in der Schweiz, die es Ihnen ermöglicht, Ihre Fähigkeiten im Bereich E-Learning voll auszuschöpfen. Wir fördern eine Kultur der Zusammenarbeit und Innovation, in der Sie nicht nur Ihre beruflichen Fähigkeiten weiterentwickeln können, sondern auch aktiv zur Verbesserung unserer digitalen Lernlösungen beitragen. Mit einem wettbewerbsfähigen Gehalt und einem umfassenden Leistungspaket sind wir bestrebt, unseren Mitarbeitern ein bedeutungsvolles und erfüllendes Arbeitsumfeld zu bieten.
