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.
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.
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.