Project Support Associate - Document writer — Thermo Fisher Scientific (Schweiz) AG

CHF 62'000 - 94'000

Thermo Fisher Scientific (Schweiz) AG · Allschwil, Switzerland (BL)

Categoria: Altro Contratto: full-time Salario: CHF 62'000 - 94'000

LohnCHF 62'000 - 94'000

Work Schedule Standard (Mon-Fri) Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale.

Work Schedule Standard (Mon-Fri) Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job Description
Key Responsibilities:
Partners with the internal project management team to help support the success of a study in any way possible.

Key Responsibilities:
Partners with the internal project management team to help support the success of a study in any way possible.
Assists in setting up and maintaining study filing systems and maintains accurate records for all work undertaken, working with appropriate quality management systems.
Collaborates with the Project Manager for ensuring that all Fisher Clinical activities come together in a timely manner to meet the customer and study requirements.
Gets results through the use of appropriate project planning tools to communicate achievements and critical path activities and responsibilities.
Creates and/ or supports creation of operational documentation using internal systems including but not limited to GMP operational documentation.
Build bill of materials and coordinates creation and review of billing packages.
Collects all information on a study design including; accurate label texts, coordination of primary, secondary packaging material and tools, coordination of label translation, producing all batch documentation for operations and check of documentation and GMP instructions. Applies GXP in all areas of responsibility As Demonstrated By: Project Management
General understanding of project plans and timeline management with a demonstrated track record for task delivery to enable achievement of goals.
Knowledge of general inventory, good documentation practices, and report generation.

REQUIREMENTS:• Bachelor's degree required, no prior experience required, preferably in clinical trials or pharmaceutical industry• Preferred Fields of Study: healthcare, supply chain management, life sciences, or related field• Strong understanding of GMP/GxP principles and quality management systems• Demonstrated project management skills with ability to handle multiple projects simultaneously• Advanced proficiency in Microsoft Office suite, especially Excel and Project• Strong analytical and problem-solving capabilities• Effective written and verbal communication skills• Detail-oriented with excellent organizational and documentation abilities• Demonstrated ability to work independently and as part of cross-functional teams• Fluent English required, additional languages beneficial• Experience coordinating with teams and managing stakeholder relationships• Ability to analyze data and generate clear, accurate reports• Focus on quality service and continuous improvement• Adaptable to changing priorities while maintaining attention to detail

Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office
You'll handle project planning, documentation management, and cross-functional coordination to meet timelines and client expectations. Your Role in that Mission:
Collects all information on a study design including; accurate label texts, coordination of primary, secondary packaging material and tools, coordination of label translation, producing all batch documentation for operations and check of documentation and GMP instructions. Applies GXP in all areas of responsibility As Demonstrated By: Project Management

Work Schedule
Standard (Mon-Fri)
Job Description
You'll handle project planning, documentation management, and cross-functional coordination to meet timelines and client expectations.
Your Role in that Mission:
Collects all information on a study design including; accurate label texts, coordination of primary, secondary packaging material and tools, coordination of label translation, producing all batch documentation for operations and check of documentation and GMP instructions.
Applies GXP in all areas of responsibility
As Demonstrated By:
Project Management

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