Role overview

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.

This role supports GMP production of biologics and small-molecule APIs. The position shapes manufacturing strategy, evaluates technologies, improves processes, and develops capital projects. Using deep expertise in process systems, equipment, automation, quality, and lifecycle management, the incumbent translates complex business and technical requirements into practical solutions that improve compliance, quality, capacity, reliability, cost, and long-term manufacturing performance.

Role Responsibilities:

Provide technical leadership, coaching, and mentorship to engineering and project teams
Guide process scale-up, technology transfer, facility modifications, and lifecycle optimization
Develop the three- to five-year manufacturing and capital plan in partnership with Finance and aligned with corporate growth objectives
Evaluate facility expansions, acquisitions, outsourced manufacturing, technology transfers, and strategic partnerships
Assess manufacturing programs, products, and technologies that improve quality, throughput, flexibility, profitability, and cost efficiency.
Lead enterprise-wide manufacturing initiatives and advise executives on technology options, risks, and opportunities
Lead major capital projects from concept through commissioning and qualification, delivering within approved scope, schedule, budget, risk, and value targets
Develop business cases and financial models that assess ROI, payback, total cost of ownership, and expected operational benefits
Resolve complex, enterprise-level engineering challenges and recommend initiatives that advance corporate objectives

Qualifications

Required:

Bachelor’s degree in engineering, biotechnology, biopharmaceutical sciences, chemistry, or a comparable discipline
Ten years in pharmaceutical manufacturing, with substantial biologics and/or API experience
Experience successfully leading complex capital projects and strategic initiatives
Thorough knowledge of GMP, Annex 1, ICH guidance, and regulatory expectations from the FDA, EMA, and Health Canada
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Desired:

Master’s degree and/or MBA
Professional Engineer (P.Eng.) designation, or an equivalent credential
Expertise in biologics production and small-molecule API production

Additional Details

This job has a full time weekly schedule. It includes the option to work remotely.

The full-time equivalent pay range for this position is $121,644.00 - $190,069.00/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:
10% of the Time

Shift:
Day

Duration:
No End Date

Job Function:
Manufacturing