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Agilent Technologies

Master Scheduler

Charlottetown, PE, Canada
Canada-Prince Edward Island-Charlottetown, Canada

Full-time

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Job details

Job type: Full-time
Posting language: English
Posted: Nov 6, 2026

Original job description

Job Description

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.

As Master Scheduler, you will own the Master Schedule for the Complex Chemistry business unit, ensuring ATD Canada meets revenue targets and client delivery milestones. You will use plant scheduling tools to avoid capacity conflicts, reduce schedule disruptions and delays, and give other departments (QC/QA, Maintenance, etc.) formal look-ahead information.

Key Responsibilities

Build and manage the Master Schedule for Complex Chemistry facilities, synchronizing labor, materials, equipment and timelines

Incorporate budgeted work center capacity and cycle times in line with SLAs, with a manufacturing job creation window of at least 12 weeks

Partner with Procurement, Supply Chain and Warehouse, using the 12–18 month S&OP view, to stage and secure the material, consumable and packaging inventory needed to meet customer commitments

Collaborate with PM, Manufacturing, QC, QA, SC, Facilities, Engineering and Maintenance to ensure resources are available and equipment calibration and maintenance are coordinated

Identify capacity constraints and disruption risks early, and work with management to eliminate or mitigate lost time

Lead schedule recovery after shutdowns, unplanned outages and quality disruptions, and contribute to root cause analysis, corrective action and continuous improvement

Update and publish the Master Schedule daily, tracking actual vs. planned execution, and report monthly on KPIs (schedule execution to plan, productivity, capacity utilization, output, variance to budget and projected revenue forecast) via the Master Schedule dashboard
Experience managing aggressive timelines and deliver results on time
Participate in recurring management meetings (daily huddle, operations review, JPT) and continuously improve scheduling processes, tools and methodologies

Comply with QMS requirements (current training, MOC participation) and the BIOVECTRA / ATD Canada Health and Safety Policy

Perform other duties as assigned to support business needs and customer expectations

Qualifications

Required:

Bachelor's degree or equivalent; post-graduate study, certification and/or license may be required

Four years of relevant experience

Pharma manufacturing
Knowledge of ICH Q7A and cGMP guidelines
Strong familiarity with scheduling software and reading/analyzing production schedules
Excellent written and verbal communication, organizational, interpersonal, and collaboration skills
Strong analytical and problem-solving skills
Attention to detail and a commitment to accuracy in maintaining and updating schedules
Proficiency with Syspro or higher-level ERP, MS Project, Excel, Word, and PowerPoint

Desired:

Experience in small molecule API or peptide manufacturing

Certification in project management

Additional Details

This job has a full time weekly schedule.The full-time equivalent pay range for this position is $73,061.00 - $114,158.00/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/locationsAgilent 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

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More about this job

Responsibilities

The Master Scheduler will own and manage the production schedule for the Complex Chemistry business unit to ensure revenue targets and delivery milestones are met. They will coordinate resources, materials, and equipment across multiple departments to optimize capacity and mitigate production risks.

Requirements

Candidates must hold a bachelor's degree and possess at least four years of relevant experience in pharmaceutical manufacturing. Proficiency in scheduling software, ERP systems, and knowledge of cGMP and ICH Q7A guidelines are required.

Skills

Master scheduling
Production scheduling
Capacity planning
Supply chain management
ERP systems
Syspro
MS Project
Pharma manufacturing
cGMP
ICH Q7A
Analytical skills
Problem-solving
Communication
Project management
Data analysis

Benefits

Bonus
Stock
Health Insurance

Visa sponsorship

Not detected in the job text

Keywords

Master Scheduler
Complex Chemistry
Manufacturing
Supply Chain
Procurement
S&OP
Capacity Planning
ERP
Syspro
MS Project
Pharma
cGMP
ICH Q7A
API
Peptide manufacturing
Project Management
KPIs
Root cause analysis
Continuous improvement
QMS
Production scheduling
Inventory management
Scheduling software
Operations review
Agilent

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