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 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 Technical Investigations Lead leads the site investigation program for manufacturing, environmental, contamination, and process-related events. The role ensures timely, compliant, scientifically sound investigations and drives the effectiveness of CAPAs that impact Windsor biologics operations. Key Responsibilities: Provide daily leadership to site investigators supporting Manufacturing, QC, and Engineering Ensure investigations meet CGMP, ICH, Health Canada, and corporate standards Oversee and improve deviation, CAPA, and change-control lifecycle management Establish investigation workflow, team goals, and RCA capability across the site Represent the Windsor site during internal and external audits for deviations and CAPAs Trend site nonconformance to identify systemic issues and improvement opportunities Drive consistency, training, and technical coaching for investigators and SMEs Partner cross-functionally to eliminate recurrence of contamination and process failures Qualifications Required: Bachelor’s degree in Science or Engineering 6+ years of experience in GMP manufacturing environment Desired: Advance degree in applicable field of study Experience in methodology, quality, engineering, or investigations Expertise in RCA, CAPA effectiveness, and deviation management Strong communication, facilitation, teamwork, presentation and technical writing skills Ability to lead cross-functional teams and manage competing priorities Experience supporting regulatory inspections (FDA, Health Canada, EMA) Knowledge of biologics, upstream/downstream operations, utilities, and contamination control preferred Additional Details This job has a full time weekly schedule. The full-time equivalent pay range for this position is $81,022.00 - $126,596.00/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 Graduate and Student Career Site Visit our career site and learn more about Agilent Watch our video playlist to get a glimpse of life at Agilent! As a global leader in laboratory and clinical technologies, we are passionate about bringing great science to life. Our commitment to quality and innovation supports cutting-edge life science research, patient diagnostics, and ensures the safety of water, food, and pharmaceuticals. As scientists and clinicians pursue small, everyday advances and life-changing discoveries, we provide trusted answers to their most critical questions and challenges. Leveraging more than 50 years of expertise, we create advanced instruments, software, and consumables supported by teams of highly skilled and knowledgeable people. With 18,000 employees around the world, our global reach and comprehensive solutions provide the most reliable and accurate results, as well as optimal scientific, economic, and operational outcomes. We work collaboratively with our customers on their journey to make a real difference in human lives. Our culture is founded on trust, respect, and uncompromising integrity, and we pride ourselves on being a dynamic and inclusive workplace that celebrates diversity and fosters innovation. We can’t wait for you to join us as we continue our mission to improve the world around us. Information about Agilent is available at Agilent.com.