JOB DESCRIPTION

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 production, 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 pharmaceutical and biotechnology manufacturing 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 Process Steward/Sanitation Production Technician will be responsible for executing routine production operations with the highest regard for safety, excellence and quality. The Process Steward will be required to provide assistance to the Production Technicians and Supervisors, as well as working with the manufacturing team to maximize production efficiency and meet departmental and company goals.
Shift: Monday to Thursday, 8:00 am to 5:00 pm/Friday 8:00 am to 4:30 pm

Sanitizing and cleaning of an industrial clean room environment where pharmaceuticals are manufactured to include, duct work, manufacturing equipment, floors, walls and outdoor areas.

• Operating manual and automated equipment.
• Handling of hazardous materials including acids, bases, solvents, potent compounds, and APIs safely and properly.
• Performing process sampling.
• Collaborating with other departments on process and equipment training for successful completion of manufacturing batches.
• Providing feedback to influence continuous improvements during the review and revision of Standard Operating Procedures and other process documentation.
• Participating in BIOVECTRA’s quality management system, focusing on the batch production records, work instructions, adherence to policies and standard operating procedures at all times
• Assisting with housekeeping, equipment cleaning, general warehousing, material staging and tanker operations as required.
• Will be required to wear PPE (Personal Protective Equipment) while performing duties.

QUALIFICATIONS

• High school diploma or equivalent required.
• 0 to 2+ years’ experience.
• Post secondary education with a diploma in an applicable area of study is considered an asset.
• Industrial experience in a pharmaceutical or food manufacturing FDA regulated environment would be considered a major asset.
• WHMIS certification (Workplace Hazardous Materials Information System) and First Aid, would be considered a major asset.
• Good Manufacturing Practices (cGMP) experience an asset.
• Ability to follow strict standard operating procedures and excellent attention to details is required.
• Ability to accurately weigh and measure chemical materials needed for the production of pharmaceutical products.
• Ability to work and communicate effectively in a dynamic team environment.
• Strong communicator, both written and oral.
  Ability to work independently with minimal supervision.

Please refer the Job description for details