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. 

• Providing guidance and oversight to direct or indirect reports including QC microbiology and environmental monitoring staff. Responsible for human resources services for direct or indirect reports; including pay, attendance management, and employee performance management.

• Administering the environmental monitoring program throughout the facility encompassing the compliance of the program, the functionality of the equipment and conduct of the personnel.

• Ensuring that the training of all members of the microbiology and environmental monitoring programs are up to date and the procedures they follow are compliant.

• Taking a lead role in designing, outlining and executing investigation plans and the execution of any associated work to determine root causes including identifying contaminants and environmental isolates associated with quality events (non-conformances, CAPAs, etc.)

• Designing and reviewing the validation and verification of microbiology methods and periodically reviewing departmental and interdepartmental SOPs to ensure compliance with current guidelines including but not limited to USP, ICH, FDA, Health Canada, ISPE and Ph. Eur.

• Acting as the Biosafety officer for the BSL2 microbiology and lab in the facility and ensure compliance with PHAC guidelines if required.

• Providing information and presentations on the environmental monitoring program and microbiological lab activities to internal stakeholders and our clients.

• Reviewing of QC records and data for completeness, correctness and compliance with GMP.

• Providing training and support for instrumental and bench techniques for the microbiology lab.

• Maintaining accurate, real-time records of all laboratory activities and ensuring all team members are maintaining accurate, up-to-date, compliant records.

Qualifications

• Bachelor of Science degree in Microbiology or related discipline.
• Master of Science or PhD is considered an asset.
• 5 + years of relevant work experience in a GMP or GLP environment.
• 7+ years of Microbiology experience or relation experience in a life sciences field; or equivalent combination of education and experience.
• Previous supervision and mentorship of junior staff members is required.
• Proficiency in microbiological techniques employed in a regulatory environment:
  • Sterility per USP <71>
  • Bioburden per USP <61>
  • Microbial identification
  • Subculturing
  • Media Preparation
  • Methodology for handling/testing materials inside a BSC
• Experience leading environmental monitoring investigations in sterile manufacturing environments is considered an asset.
• Tracking/trending environmental monitoring data.
• Ability to lead a project within QC, including collaborating with internal and external clients, auditors and presenting data and results clearly and concisely.
• Knowledge of cGMP regulations/guidelines (Health Canada, FDA, EU Annex as well as international regulations (i.e. International Committee on Harmonization (ICH Q &, USP, EP, ISO Standards) pertaining to the microbiology, environmental monitoring, and cleaning validation programs to support production of drug products.
• Robust technical writing skills, with experience in writing and reviewing SOP's and reports.
• Proficient communicator, both written and oral.
• Knowledge of current Good Manufacturing Practices (cGMP).
• Ability to work independently with minimal supervision or informally leading people, projects and/or programs.

Additional Details

This job has a full time weekly schedule.

The full-time equivalent pay range for this position is $88,536.00 - $138,338.00/yr CAD plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations

Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.

Travel Required:

Occasional

Shift:

Day

Duration:

No End Date

Job Function:

Quality/Regulatory