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. 

The responsibilities will include:

•         12 hour rotating shift work. Days and nights

•         Being in compliance with GMP, GDP and standard operating procedures, performs production and assembly processes in a production environment

•       Operating production/filling/packaging equipment

•        Weighing, measuring and checking raw materials to ensure batches manufactured contain proper ingredients and quantities

•      Helping in validating processes and equipment that are directly related to filtration, cleaning and sterilization

•       Maintaining records to comply with regulatory requirements and may assist with in-process testing to ensure batches meet specifications

·        High School Diploma

·        Lift up to 25 kg

·        Communication Skills both written and oral

·        Manufacturing experience

·        Experience with documentation in a regulated environment

·        cGMP experience