Senior Manufacturing Associate - Biopharmaceutical

Position : Senior Manufacturing Associate - Biopharmaceutical Location : Saint-Laurent Salary : Up to $70K Do you possess expertise in bioprocessing and downstream purification, particularly in the realm of blood protein purification?

If you have hands-on experience in this domain, we have an exciting opportunity awaiting you! Our esteemed partner in the pharmaceutical and research sector, located in Saint-Laurent, is actively seeking a Senior Manufacturing Associate to join their dynamic team.

This is your chance to apply your expertise and contribute to groundbreaking research in a cutting-edge environment. Don't miss this opportunity to take your career to the next level! Apply now and be a part of something extraordinary.

Our client offers : - 100% benefits paid by employer - Holiday period 2 weeks of vacation + an additional 2 weeks of vacation - 6 personal days - Group RRSP with contribution of 6.

5% Our client is looking for you : - Bilingualism required as bioresearch products are from the United States - Degree in life sciences - At least 3 years of experience in a biotechnology or industrial pharmaceutical environment (Bioprocessing and Purification) - Experience with AKTA liquid chromatography system, UNICORN Software with hands on experience in the operation of the purification equipment - Experience with protein purification and protein analysis methods Your role : - Program and operate AKTA liquid chromatography systems - Purify enzymes using the AKTA purification system and perform in-process analysis - Homogenize the cells and clarify the lysate using separation systems like continuous, batch centrifuges and / or depth filtration - Concentrate the process fluids using tangential flow filtration devices and formulates the reagents - Prepare the required buffers, reagents and solutions for downstream purification, formulation activities and in-process testing - Write Batch Production Records, Buffer Formulation Records, Standard Operating Procedures, Validation Protocols and Batch Summary Reports - Execute the processes according to the instructions in BPRs, BFRs, and SOPs and document the required production information contemporaneously with accuracy complying with good documentation practices - Identify the continuous improvement opportunities, present the opportunities to the line management and execute approved continuous improvement projects - Maintain a state of readiness for inspections and audits - Assist in the investigation of deviations and execute the investigation process - Execute additional project tasks as may be required from time to time by the supervisor Please send your resume to Cristina Bilbao at cristina.

[email protected]. REFER A PERM HIRE AND EARN UP TO $1,000! For more details, click here. OUR VIRTUAL DOORS ARE OPEN! We're also bringing the interviews to you by various web applications, virtually! Contact us today for your next opportunity.

CNESST permit number : AP-2000158