Production Technician

BIOVECTRA, now a part of Agilent, is recognized as a leader in the contract development and manufacturing space of active pharmaceutical ingredients specializing in clinical-to-commercial scale production for microbial fermentation, synthetic small molecules including ADC, HPAPI, plasmid DNA, mRNA, LNP and sterile filling capabilities. With over 650 employees at both the Windsor, NS and Charlottetown, PEI sites, BIOVECTRA supports over 100 clients, including over 20 top pharma and biotech companies.

BIOVECTRA joined Agilent in 2024 and is part of Agilent’s Advanced Manufacturing Partnerships Division (AMPD), which also contains Agilent’s Nucleic Acid Solutions Division. With BIOVECTRA, Agilent aims to align advanced manufacturing capabilities, expertise, and resources to foster greater innovation and operational excellence. Within AMPD, you will have the opportunity to work with cutting-edge technologies and collaborate with a team of dedicated professionals committed to revolutionizing advanced manufacturing, making a significant impact in the industry and, most importantly, improving patient care through the manufacture of better therapeutics. 

• →Work a 12-hour rotating shift schedule, including days and nights.
• →Comply with GMP, GDP, and Standard Operating Procedures (SOPs) while performing production and assembly processes in a manufacturing environment.
• →Operate production, filling, and packaging equipment.
• →Weigh, measure, and verify raw materials to ensure batches contain the correct ingredients and quantities.
• →Assist with the validation of processes and equipment related to filtration, cleaning, and sterilization.
• →Maintain accurate documentation to meet regulatory requirements and assist with in-process testing to ensure batches meet established specifications.

• High school diploma or equivalent.
• Ability to lift up to 25 kg (55 lbs).
• Strong written and verbal communication skills.

• Manufacturing experience.
• Experience maintaining documentation in a regulated environment.
• Experience working in a cGMP-regulated environment.