Biotechnologist - 6320

Vor 4 Tagen


Visp, Schweiz CTC Resourcing Solutions AG Vollzeit

CTC are specialised industry experts who can help companies source the best talent and provide reliable HR and consulting services, support varied candidates in finding promising career opportunities and offer the latest in skill development training programmes.

Our client, a global leader in life sciences and biotechnology, is dedicated to advancing healthcare through high-quality products and cutting-edge innovations. They operate across multiple locations worldwide, maintaining the highest standards of compliance, efficiency, and customer satisfaction.

Job Overview

We are seeking a dedicated Manufacturing Specialist to join the Drug Product team at our client’s Visp site on a 12-month contract, with chances of extension. In this dynamic role, you will contribute to the production of liquid and freeze-dried drug forms, ensuring adherence to cGMP guidelines and supporting the seamless execution of manufacturing activities.

Key Responsibilities

  1. Execute manufacturing activities for Drug Product production in compliance with cGMP guidelines.
  2. Conduct batch execution, evaluate test results, troubleshoot equipment, and provide resolution recommendations.
  3. Collaborate with the manufacturing team to ensure batches are produced safely, on time, and meet quality standards.
  4. Prepare, execute, and review production documentation, including batch records and GMP-related documents.
  5. Support process investigations and assist in decision-making for production issues.
  6. Implement process changes and corrective actions (CAPAs) within defined timelines.
  7. Perform training for operators and support onboarding for new team members.
  8. Operate, set up, and clean production equipment and premises for liquid and freeze-dried drug forms (e.g., compounding, parts washing, autoclaving, filter integrity testing, and visual inspection).

Qualifications & Skills

  1. Experience: 2-4 years in a GMP environment, preferably in sterile Drug Product manufacturing.
  2. Languages: Fluent in English or German (proficiency in both is preferred).
  3. Knowledge: Familiarity with GMP requirements, quality procedures, and SOP execution. IT proficiency and experience with SAP/MES systems are advantageous.
  4. Competencies: Strong team orientation, communication skills, and the ability to interact across organizational interfaces.
  5. Attributes: Structured, focused, and highly motivated with a dynamic drive.
  6. Flexibility: Willingness to work flexible hours as needed.

How to Apply

Ready to take the next step in your career? Click the 'apply now' button or email your application to: vanessa.gilardoni@ctcresourcing.com

Seniority level

Associate

Employment type

Full-time

Job function

Science, Production, and Manufacturing

Industries

Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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