ABOUT US

At Dalton Pharma Services, we are a leading CDMO supporting global pharmaceutical and biotech clients in bringing life-saving therapies to patients. We pride ourselves on innovation, quality, and collaboration. As we expand our operations, we’re seeking a strategic and detail-oriented Production Master Planner to join our dynamic team in a purpose-driven work environment.

QUALIFICATIONS

• Bachelor’s degree in Supply Chain, Engineering, Life Sciences, or related field
• 5+ years of experience in production planning and scheduling within a pharmaceutical, biotech or CDMO environment
• Proficiency in ERP systems and advanced Excel skills
• Understanding of GMP, regulatory standards, and manufacturing workflows
• Excellent communication, problem-solving, and organizational abilities
  We offer a competitive salary and benefits, as well as an excellent opportunity to build your career with a well-established company.
  While we appreciate all applications received, only those selected for an interview will be contacted.
  We are committed to providing accommodations for applicants with disabilities. If you require accommodation during the recruitment process, please contact careers@dalton.com
  Job Types: Full-time, Permanent
  Pay: From $70,000.00 per year

Benefits:

• Casual dress
• Dental care
• Disability insurance
• Employee assistance program
• Extended health care
• Flexible schedule
• Life insurance
• On-site parking
• RRSP match
• Tuition reimbursement
• Vision care
• Wellness program

Application question(s):

• Do you have a Bachelor’s degree in Supply Chain, Engineering, Life Sciences, or related field?
• Are you proficient in ERP systems and advanced Excel skills?
• Do you have 5+ years of experience in production planning and scheduling within a pharmaceutical, biotech or CDMO environment?

Education:

• Bachelor’s Degree (preferred)

Experience:

• Canadian GMPs, FDA GMPs: 10 years (required)

Work Location: In perso

ROLE OVERVIEW

As the Production Master Planner, you will be the key driver of our Master Production Schedule (MPS)—ensuring that client projects are delivered on time, in full, and in compliance with GMP standards. You’ll collaborate cross-functionally with material management, manufacturing, quality, and project management teams to optimize capacity, minimize delays, and drive operational excellence.

KEY RESPONSIBILITIES

• Develop and manage the Master Production Schedule (MPS) to align with client commitments, project timelines, and internal capacity
• Collaborate with procurement, manufacturing, and quality teams to ensure readiness for manufacturing
• Lead weekly operation meetings, provide schedule updates, risk assessments, and solutions to internal teams
• Monitor and adjust schedules to accommodate changes in demand, supply disruptions, or project timelines
• Analyze production data and KPIs to identify bottlenecks and recommend process improvements