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Added 32 mins ago
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SOLVET

Production Supervsior

Calgary, AB, Canada

Job type: Full-time
Apply by: Mar 29, 2027
Experience: Minimum of 3–5 years of experience in pharmaceutical, biotechnology, or regulated manufacturing operations.
Working hours: 40 hours/week
Posting language: English
Posted: Sep 30, 2026

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Original job description

WE'RE HIRING

Let's help you launch your career with Alberta Veterinary Laboratories ("AVL/Solvet")! We are looking for an energetic and dedicated Production Supervisor to join our team on-site in our Calgary facility working 40 hours/week (Monday - Friday)

THE ROLE

The Production Supervisor is responsible for overseeing and coordinating all day-to-day manufacturing activities to ensure production schedules, quality standards, and safety requirements are consistently met. This position leads production teams, enforces compliance with cGMP, SOPs, and EHS standards, and ensures accurate documentation and efficient workflow. The Production Supervisor collaborates cross-functionally to optimize processes, support new product introductions, and drive continuous improvement initiatives that enhance efficiency, quality, and team performance.

DAY-TO-DAY

Supervise and coordinate daily manufacturing operations to meet production schedules, quality standards, and safety requirements.
Ensure compliance with GMP, SOPs, WIs, MBRs, and all safety and quality standards.
Lead, engage, and develop production teams, leveraging experience to make sound decisions on critical production issues.
Maintain and enforce cGMP standards, work instructions, and company procedures.
Ensure production timelines are met, and safety protocols are consistently followed.
Oversee accurate and timely completion of all production documentation, electronic records, and label requests.
Audit and verify production records for accuracy, completeness, and compliance.
Collaborate with the Operations Manager and Production Planner to identify and implement efficiency improvements.
Report, investigate, and support resolution of deviations, non-conformances, and CAPAs.
Serve as a liaison between management and production teams to promote safety and communication.
Drive continuous improvement initiatives and performance optimization within production teams.
Maintain and update training matrices; coordinate cross-training and skills development for Production Assistants.
Identify and implement process improvements to enhance efficiency, throughput, and product quality.
Ensure real-time documentation and ERP processing of production batches.
Participate in internal and external audits; implement corrective and preventive actions as required.
Oversee hiring, onboarding, and ongoing training of production staff.
Conduct performance reviews for Production Leads and Assistants; ensure team leaders complete evaluations effectively.
Approve time sheets and review attendance, sick leave, and vacation requests.
Request emergency repairs and coordinate preventive maintenance of production equipment.
Monitor compliance with safety and environmental regulations; enforce EHS policies and conduct regular inspections.
Assist in ordering materials and maintaining inventory of spare parts and production supplies.
Ensure proper sanitation of manufacturing equipment and train staff on sanitation procedures.
Support Production Leads in product manufacturing and train new staff on production processes.
Participate in cross-functional teams for new product introductions and process validations.
Utilize KPIs and data analysis to drive performance improvements and meet departmental goals.
Perform other duties as assigned.

IDEAL FIT

Education & Experience

Bachelor’s degree in Engineering, Life Sciences, or a related technical field preferred; equivalent experience considered.
Minimum of 3–5 years of experience in pharmaceutical, biotechnology, or regulated manufacturing operations.
Prior supervisory or team leadership experience in a GMP-regulated environment required.
Strong understanding of cGMP, GDP, and FDA, Health Canada, or EMA regulatory requirements.
Experience with electronic batch records (EBR), ERP systems, and production scheduling tools.

Skills and Attributes

Proven leadership and team management skills with the ability to motivate, coach, and develop staff.
Strong problem-solving, decision-making, and organizational abilities.
Excellent attention to detail and commitment to quality and complianc
Ability to interpret and enforce SOPs, batch records, and regulatory documentation.
Effective communication and interpersonal skills to collaborate with cross-functional teams.
Proficient in Microsoft Office Suite and familiarity with manufacturing data systems or MES software.
Demonstrated ability to identify and implement process improvements and efficiency initiatives.
Knowledge of EHS principles and experience promoting a safe work environment.

REQUIREMENTS

Physical ability to work in a manufacturing environment, including standing for extended periods and wearing appropriate PPE.
Successful Criminal Record Check completion
Medical Clearance required
Safety Certifications including but not limited to: WHMIS, TDG, First Aid.

WORKING CONDITIONS

On-site in SE Calgary
GMP compliant pharmaceutical facility
40 hours/week (Monday - Friday)
Daily interaction with chemicals and hazardous materials, PPE Provided.

WHAT’S IN IT FOR YOU

We are committed to keeping our team healthy and motivated, so they can do the best work of their lives. We’ve built a company where people love to come to work, and we think you will too! Team members benefits include:

Casual dress
Paid time off (including vacation, sick and personal days)
Life insurance and comprehensive healthcare benefits
Performance reviews and ongoing conversations plus annual compensation reviews
Opportunities for professional growth through learning & development initiatives
A dynamic, inclusive, and collaborative work environment

NEXT STEPS

If this opportunity sounds like a great fit apply now through our company website with a copy of your resume!

We appreciate the interest from all candidates in our career opportunities however, only those selected for an interview will be contacted.

Apply About employer

More about this job

Responsibilities

Oversee daily manufacturing operations, production schedules, quality, safety, documentation, and compliance with cGMP, SOPs, and regulatory requirements. Lead and develop production staff, resolve operational issues, support audits and new product introductions, and drive process improvements using performance data.

Requirements

A bachelor’s degree in engineering, life sciences, or a related technical field is preferred, or equivalent experience; 3–5 years of experience in pharmaceutical, biotechnology, or regulated manufacturing and prior GMP supervisory or team leadership experience are required. Candidates should understand cGMP, GDP, and relevant regulatory requirements, and have experience with electronic batch records, ERP systems, production scheduling, and workplace safety.

Skills

Production Supervision
Team Leadership
GMP Compliance
Regulatory Compliance
Production Scheduling
Electronic Batch Records
ERP Systems
Quality Assurance
Safety Management
Continuous Improvement
Process Optimization
Deviation Investigation
CAPA Management
Training And Development
Inventory Management
Performance Analysis

Benefits

Casual Dress
Paid Time Off
Life Insurance
Comprehensive Healthcare Benefits
Professional Growth Opportunities
Learning And Development Initiatives

Visa sponsorship

Not detected in the job text

Keywords

Pharmaceutical Manufacturing
cGMP
GMP
GDP
FDA
Health Canada
EMA
SOPs
Work Instructions
Master Batch Records
Electronic Batch Records
ERP Systems
MES Software
Production Scheduling
EHS
WHMIS
TDG
First Aid
CAPA
Deviation Management
Non-Conformance Management
Process Validation
New Product Introduction
Preventive Maintenance
Sanitation
Microsoft Office Suite
Performance Reviews
Inventory Management
Key Performance Indicators
Personal Protective Equipment

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