Manufacturing Superintendent (Pharmaceutical Manufacturing)

Location: Charlottetown, Prince Edward Island, Canada. Nights-only position from 7:00 p.m. to 7:00 a.m.; 12-hour rotating shifts, with after-hours and weekend work as required.

Salary: CAD 93,521–146,126 per year, plus eligibility for bonus, stock, and benefits.

Company

hirify.global’s BIOVECTRA business provides contract development and manufacturing services for active pharmaceutical ingredients and related products, supporting clinical-to-commercial production for pharmaceutical and biotechnology clients.

What you will do

• Supervise team leads and guide employees in GMP production, purification, isolation, and packaging activities.
• Review batch production records, quality-control documentation, deviations, cleaning records, labels, and QA actions for completeness and compliance.
• Update batch production records and work instructions to improve process efficiency.
• Support manufacturing schedules through documentation, staging requests, material and solvent counts, and equipment readiness checks.
• Identify and resolve equipment, process, and facility issues and contribute to process risk assessments.
• Participate in hiring, training, performance evaluations, regulatory inspections, audits, client meetings, and cross-functional coordination.

Requirements

• High school diploma.
• At least one year of demonstrated technical experience.
• Ability to communicate and work effectively in a dynamic, project-driven team environment.
• Experience with software programs, spreadsheets, and word-processing tools.
• Strong judgment, integrity, independence, self-motivation, and decision-making skills.
• Ability to work nights, 12-hour rotating shifts, after hours, and weekends when required; heavy lifting of up to 50 lbs. and respirator use are required.

Nice to have

• Post-secondary degree or diploma in a scientific field.
• Two years of leadership experience.
• Two years of GMP experience with protocols and FDA guidance.
• Five years of related technical experience.

Culture & Benefits

• Full-time employment with no specified end date.
• Eligibility for bonus, stock, and benefits.
• Work in a multi-product pharmaceutical manufacturing environment supporting more than 100 clients.
• Collaboration with manufacturing, quality, regulatory, and other multidisciplinary teams.