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Our client is rapidly seeking to hire a motivated individual for the position of Technician in Downstream Manufacturing. This exciting role is a stepping stone into the multi-product biopharmaceutical industry.

Temporary contract for 5 months

As a Downstream Manufacturing Technician, you will perform a variety of technical activities under Good Manufacturing Practices. You will play a key role in supporting safety, compliance, quality, and scheduling in a fast-paced environment. Your enthusiasm to learn and contribute will make a difference.

Your role:

• Responsibility for technical activities related to GMP Manufacturing Operations.

• Supporting safety, compliance, quality, scheduling, and production process execution.

• Contributing to equipment onboarding, process improvement projects and manufacturing training.

• Assisting in tech transfer and new project integration activities for manufacturing.

• Managing daily and mid-term schedule planning and being the primary point of contact for daily issue escalation.

• Ensuring strict accordance with SOPs and Good Manufacturing Practices. You will also be responsible for overwatching cross-functional operations that are both reliable and successful. This requires a drive for continuous improvement and simplicity and looking for opportunities to ensure equipment operation is reliable. 

• This proven and qualified candidate will use their past experiences, depth, and knowledge from fundamentals, like media/buffer preparation, USP or DSP operations to teach, troubleshoot and continuously improve the production operations.

• Driving process improvement initiatives, troubleshoot issues, trend and track metrics and author, review and approve procedures, deviations, CAPAs, and change controls as needed 

• Ensuring staff maintain a high level of compliance to procedures and quality expectations. 

Your profile:

We're seeking candidates who are ready to hit the ground running. Here are the qualifications we're looking for:

• A Bachelor's degree in a related scientific or engineering discipline.

• At least 4 years' experience in related GMP manufacturing operations.

• Demonstrated knowledge of purification unit operation.

• Experience in single-use platform technology is preferred.

• Excellent written and verbal communication skills.

• Fluency in French (both reading and writing). English communication abilities are a plus.

• Proficiency in MS Office, ERP, EDMS, production equipment software.

• Open to work on on-call activities /Shifts 2x8

If you are ready to join our dynamic team, we are looking forward to receiving your application.