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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 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 Agilents Advanced Manufacturing Partnerships Division (AMPD), which also contains Agilents Nucleic Acid Solutions Division. Within AMPD, you will have the opportunity to work with cuttingedge 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. Key Responsibilities Lead investigations using structured tools: RCA, 5Why, fishbone, fault tree, data analysis, and interviews Assess product and equipment impact for deviations and contamination events Develop and document CAPAs, evaluating their effectiveness over time Analyze trends to support continuous process improvement Support change controls and revision of technical documentation (SOPs, batch records, forms) Participate in internal/external audits as the investigation SME Support cleanroom and contaminationrelated investigations, including personnel flow, material movement, gowning, and hygiene compliance Ensure safe, compliant operations consistent with Health Canada, FDA, EMA, and corporate standards Required Qualifications Bachelors degree in Science, Engineering, Biotechnology, or related field GMP manufacturing or quality experience, preferably in biologics. Desired Qualifications Strong technical writing skills and ability to lead crossfunctional teams Working knowledge of RCA tools and investigation methodologies Understanding of aseptic behavior, environmental monitoring, and utilities preferred Ability to manage multiple priorities and meet dispositioncritical timelines Proficiency with MS Office; experience in MasterControl, TrackWise, Veeva, or other QMS systems preferred Additional Details This job has a fulltime weekly schedule. The fulltime equivalent pay range for this position is $27.59 $48.29/hr 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 jobrelated 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: 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 Manufacturing #J-18808-Ljbffr