Master Scheduler

BioVectra Inc.; Charlottetown; Vor Ort; CAD 73.000 - 114.000; Vollzeit

Zusammenfassung

BIOVECTRA joined Agilent in 2024 and operates within AMPD Canada. The Master Scheduler owns the Master Schedule for the Complex Chemistry unit, coordinating labor, materials and equipment to meet revenue targets and customer milestones.

This role uses scheduling tools, publishes daily updates, and reports KPIs to guide decision-making. Requirements include a Bachelor's degree (or equivalent), 4 years in pharma manufacturing, knowledge of ICH Q7A and cGMP, and proficiency with Syspro, MS Project,

Qualifikationen

• Bachelor's degree or equivalent; post-graduate study may be required.
• Pharma manufacturing experience is essential.
• Knowledge of ICH Q7A and cGMP guidelines.

Aufgaben

• Build and manage the Master Schedule for Complex Chemistry facilities.
• Coordinate capacity with Labour, materials, and equipment to meet SLAs.
• Publish daily schedule, report KPIs, and participate in management reviews.
• Identify risks, lead schedule recovery after outages, and drive improvements.

Kenntnisse

Strong communication

Organizational skills

Analytical thinking

Problem solving

Collaboration

Ausbildung

Bachelor's degree or equivalent

Tools

Syspro ERP

MS Project

Excel

Word

PowerPoint

Jobbeschreibung

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 ResponsibilitiesBuild and manage the Master Schedule for Complex Chemistry facilities, synchronizing labor, materials, equipment and timelinesIncorporate budgeted work center capacity and cycle times in line with SLAs, with a manufacturing job creation window of at least 12 weeksPartner 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 commitmentsCollaborate with PM, Manufacturing, QC, QA, SC, Facilities, Engineering and Maintenance to ensure resources are available and equipment calibration and maintenance are coordinatedIdentify capacity constraints and disruption risks early, and work with management to eliminate or mitigate lost timeLead schedule recovery after shutdowns, unplanned outages and quality disruptions, and contribute to root cause analysis, corrective action and continuous improvementUpdate 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 dashboardExperience managing aggressive timelines and deliver results on timeParticipate in recurring management meetings (daily huddle, operations review, JPT) and continuously improve scheduling processes, tools and methodologiesComply with QMS requirements (current training, MOC participation) and the BIOVECTRA / ATD Canada Health and Safety PolicyPerform other duties as assigned to support business needs and customer expectationsQualificationsRequired:Bachelor's degree or equivalent; post-graduate study, certification and/or license may be requiredFour years of relevant experiencePharma manufacturingKnowledge of ICH Q7A and cGMP guidelinesStrong familiarity with scheduling software and reading/analyzing production schedulesExcellent written and verbal communication, organizational, interpersonal, and collaboration skillsStrong analytical and problem-solving skillsAttention to detail and a commitment to accuracy in maintaining and updating schedulesProficiency with Syspro or higher-level ERP, MS Project, Excel, Word, and PowerPointDesired:Experience in small molecule API or peptide manufacturingCertification in project managementAdditional DetailsThis 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:OccasionalShift:DayDuration:No End DateJob Function:Manufacturing