Manager, Manufacturing Science and Technology

CA03 BioVectra Inc.

Windsor

On-site

CAD 108,000 - 168,000

Full time

14 days+
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Job summary

BIOVECTRA, now part of Agilent, is seeking a senior Process Engineer to lead design from bench to scale, determine equipment, flows, and lifecycle alignment to client needs. You will drive technology transfer, evaluate cycle times and risks, coordinate with Process Science and transfer teams, and mentor staff to deliver robust, compliant commercial manufacturing processes.

The role requires a Bachelor of Science and extensive experience in biologics and regulated pharmaceutical manufacturing.

Qualifications

  • Bachelor of Science degree in a relevant field.
  • Two years of leadership experience.
  • Experience with drug substance projects (Biologics).
  • Six years’ experience in a pharmaceutical manufacturing or similarly regulated environment.

Responsibilities

  • Lead process design from bench to scale up and map equipment and flows.
  • Drive technology transfer and enforce best practices.
  • Perform process engineering analysis to assess cycle time and risks.
  • Coordinate with Process Science and transfer teams on technology transfer plans.
  • Mentor staff and manage cross-functional project deliverables.

Skills

Leadership
Biologics experience
Pharmaceutical manufacturing

Education

Bachelor of Science

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 candidate will be responsible for:
  • Leading process design from bench to scale up, determining appropriate and available process equipment, process flows and ensuring end of view to product life cycle to meet client needs
  • Leading and enforcing best practices for technology transfer
  • Performing process engineering analysis to determine cycle time, equipment fit, required technologies, scale up risk, etc
  • Ensuring detailed review of the process science/CMC for incoming projects and coordinating with Process Science and process transfer team for the technology transfer plan
  • Ensuring robust systems are used throughout the technology transfer exercise to ensure all risks are identified and mitigated
  • Technical evaluating and modelling of alternative manufacturing plans related to new scales, flows, costs and risks
  • Showcasing BIOVECTRA’s technical expertise in Business Development interactions
  • Participating as a member of the evaluation team for new projects and products
  • Collaborating with cross-functional teams to identify, scale, and qualify Critical Process Parameters, Critical Quality Attributes, Critical Aspects and Control strategies so that robust commercial processes are achieved. (Contributor to the validation protocols)
  • Partnering with cross-functional teams to ensure technical feasibility
  • Prioritizing and executing assigned project deliverables
  • Managing and/or assisting with the procurement and delivery of new pharmaceutical applications and technologies
  • Selecting, hiring, evaluating, and motivating department personnel.
  • Providing guidance and training to employees and ensuring adherence to SOPs
  • Developing and monitoring performance objectives for direct reports.
Qualifications Required:
  • Bachelor of Science
  • Two years of leadership experience
  • Experience with drug substance projects (Biologics)
  • Six years’ experience in a pharmaceutical manufacturing or similar regulated environment
Desired:
  • Project management experience
  • Demonstrated experience with the start-up and commissioning of facilities, process equipment and instrumentation
  • Possesses financial acumen, understands business metrics, and how to impact results
  • Basic understanding of applicable codes and quality/regulatory standards
  • Additional Details

This job has a full time weekly schedule. The full-time equivalent pay range for this position is $107,731.00 - $168,330.00/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 Graduate and Student Career Site 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.

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