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Ref. No. : 113506 Position: Senior Manufacturing Associate – BiopharmaceuticalLocation: Saint-LaurentSalary: Up to $70KDo 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 methodsYour 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 supervisorPlease 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