Senior Manufacturing Associate – Biopharmaceutical

Ref. No. : 114703

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 .

REFER A PERM HIRE AND EARN UP TO $1,000! For more details, .

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