Media & Buffer Technician (m/f/d)
Publication date:
11 April 2025Workload:
100%- Place of work:Corsier-sur-vevey
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Job summary
Join our DSD - Manufacturing team as a Media & Buffer Technician! You’ll enjoy a collaborative work environment and opportunities for growth.
Tasks
- Support large-scale preparation of Media & Buffer under GMP standards.
- Perform operational tasks and maintain documentation for compliance.
- Collaborate with cross-functional teams to enhance production efficiency.
Skills
- Technical diploma required; experience in pharmaceutical production is preferred.
- Proficiency in IT tools like SAP and LIMS is advantageous.
- Strong communication skills and teamwork abilities are essential.
Is this helpful?
/span data-teams="true"//p//strong/Your role://strong///p//p/Within the Drug Substance Development (DSD) - Manufacturing department, we are looking for a "Media&Buffer - Technician" who will support the preparation of Media&Buffer at large-scale (GMP).//p//p/You will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced from animal cells.//p//p/You will support the Media&Buffer activities from an operational and documentation point of view : Dispensing, Solution preparation, cleaning of vessels//p//p/As Media/ Buffer Technician, you will take part of the activities related to the Media&Buffer preparation for clinical production in our new building.//p//p/ //p//p//strong/As Media/ Buffer Technician,you will be responsible for://strong///p//ul//li/Performing operational Media/ Buffer preparation activities//li//li/Performing operational support activities//li//li/Carrying out the documentation related to your function (e.g. writing working instructions)//li//li/Supporting compliance activities (batch review, deviations, investigations...)//li//li/Participating in maintaining the functionality of the laboratories/clean rooms- Participating in the continuous improvement of the area and its activities by proposing and participating in the implementation of improvement projects.//li//li/Interacting with different stakeholders (e.g. Quality Assurance, Project Managers, or Operational team)//li///ul///span/
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qualifications
/span data-teams="true"//p//strong/Your profile//strong///p//ul//li/You have a technician diploma (CFC, HES, BTS, IUT...)//li//li/Language: French, English (written and reading comprehension is a plus)//li//li/Knowledge of /span style="font-size:inherit;"/of BPF, GLP and/or GMP//span///li//li//span style="font-size:inherit;"/- Knowledge of IT tools (Pack Office, Trackwise/ SAP, DeltaV, MES, LIMS) is a plus//span///li//li/You are able to work as part of a team and have good communication skills with all stakeholders (Managers, scientists and technicians) and stakeholders from other departments (Production, QC, QA...)//li//li/Ideally experience in the field of pharmaceutical production (Development, clinical or commercial)//li///ul///span/
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Andreia Lourenço
- Randstad Merck Aubonne
