BIOVECTRA

Pharmaceutical

Manager,ManufacturingScienceandTechnology

$108–168k Canada FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Manager candidates.

The Brief

“Manager, Manufacturing Science and Technology at BIOVECTRA. Skills: Process design, Technology transfer, Cross-functional collaboration. Lead process design from bench to scale up. Determine appropriate process equipment”

Industry & Context.

Pharmaceutical
Problems you'll solve

Process engineering analysis

Eligibility Requirements

10% travel

What They're Looking For.

Must Have

Bachelor of Science, Two years leadership experience, Experience with drug substance projects, Six years pharmaceutical manufacturing experience

Nice to Have

Project management experience, Experience with facility start-up, Experience with process equipment commissioning, Experience with instrumentation commissioning, Possesses financial acumen, Understands business metrics, Basic understanding of codes, Basic understanding of quality standards, Basic understanding of regulatory standards

What You'll Do.

Lead process design from bench to scale up

Determine appropriate process equipment

Determine process flows

Ensure product life cycle

Lead best practices for technology transfer

Enforce best practices for technology transfer

Perform process engineering analysis

Determine equipment fit

Determine required technologies

Determine scale up risk

Ensure detailed review of process science

Ensure detailed review of CMC

Coordinate with Process Science

Coordinate with process transfer team

Develop technology transfer plan

Ensure robust systems are used

Technically evaluate manufacturing plans

Model alternative manufacturing plans

Showcase technical expertise

Participate in evaluation team

Collaborate with cross-functional teams

Identify Critical Process Parameters

Scale Critical Process Parameters

Qualify Critical Process Parameters

Identify Critical Quality Attributes

Scale Critical Quality Attributes

Qualify Critical Quality Attributes

Identify Critical Aspects

Scale Critical Aspects

Qualify Critical Aspects

Identify Control strategies

Scale Control strategies

Qualify Control strategies

Ensure robust commercial processes

Partner with cross-functional teams

Ensure technical feasibility

Prioritize project deliverables

Execute project deliverables

Manage procurement of pharmaceutical applications

Assist with procurement of pharmaceutical applications

Manage delivery of pharmaceutical applications

Assist with delivery of pharmaceutical applications

Manage procurement of new technologies

Assist with procurement of new technologies

Manage delivery of new technologies

Assist with delivery of new technologies

Select department personnel

Hire department personnel

Evaluate department personnel

Motivate department personnel

Provide guidance to employees

Provide training to employees

Ensure adherence to SOPs

Develop performance objectives

Monitor performance objectives

How You'll Work.

Team & Collaboration

Cross-functional teams

Process & Methodology

Project management

Full Job Description

## **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,

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