Job Description

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.bilbao@quantum.ca.

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CNESST permit number: AP-2000158

Services de Gestion Quantum Lt\xc3\xa9e

Founded in 1968 in Montr\xc3\xa9al, Quantum has established a strong reputation as the full-service human resource partner of choice for providing unique and effective recruitment solutions that meet our clients complex staffing needs. Our unwavering...

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