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Publié il y a 3 mois

Sr. Continuous Improvement Specialist

@ Pillar 5 Pharma inc.

Arnprior, Ontario

100k–125k $/an5+ ans d’expérience
Postuler
SIGNAUX

En bref

Pillar5 Pharma Inc. is hiring a Senior Continuous Improvement Specialist to lead Operational Excellence initiatives across pharmaceutical manufacturing in Arnprior, Ontario. The role applies Lean and structured problem-solving to improve productivity, quality, compliance and cost while staying within GMP requirements. Salary is $100,000 to $125,000 per year.

Salaire :

100 000 $–125 000 $ par année

Responsabilités :

  • Lead continuous improvement projects across manufacturing and support functions
  • Apply Lean, Kaizen, Value Stream Mapping and root cause analysis
  • Develop KPIs, dashboards and reports to measure results
  • Coach and train employees on improvement tools and practices
  • Ensure improvements align with GMP and regulatory requirements

Résumé des exigences :

  • Bachelor's degree in engineering, operations or manufacturing
  • 5+ years in continuous improvement or a regulated manufacturing environment
  • Lean Black Belt certification
  • Knowledge of CAPA, deviations, change control, validation, OEE, SPC and FMEA
  • Experience leading cross-functional projects
  • TPM experience is an asset

Outils et compétences

Source et dates

Site carrière / système de candidatures · adp

Date publiée par l’employeur
2026-08-25
Première détection par notre source
2026-10-08
Mise à jour du dossier source
2026-11-09

Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.

Détails du poste

NiveauSenior
DomaineAssurance qualité
Expérience5 an(s) et plus
Heures par semaine40 (estimé)
Déplacementsavion : aucun · route : aucun
Milieu de travailBureau, Usine
PositionAssis et debout
Exigences physiquesphysique faible · ordinateur élevé
LanguesEnglish
Permis et certificationsLean Black Belt
FormationBaccalauréat (exigé)
Domaines d’étudesEngineering, Operations Management, Manufacturing

Résumé et détails rédigés par l’IA à partir de l’offre; l’offre de l’employeur fait foi.

Pillar 5 Pharma inc.

Profil d’entreprise sauvegardé

Renseignements historiques provenant d’un profil The Jobs API sauvegardé (champs LinkedIn/Crunchbase). Ils ne sont pas vérifiés en temps réel; les chiffres peuvent avoir changé. Les valeurs manquantes restent inconnues.

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Description complète de l’entreprise

Founded in 2009, Pillar5 Pharma Inc. has grown to become an industry leading Canadian Contract Development and Manufacturing Organization (CDMO) across the North American Market. Pillar5 provides access to safe medications, through various partners, in solid dose tablets/capsules and Ophthalmics. The team at Pillar5 has proven experience in formulation and process development in the laboratory, the manufacturing environment, and on the plant floor. Pillar5 is currently the only CDMO with the ability to manufacture multi-dose preservative free solutions. Built by Pfizer in 1956, Pillar5 has an award-winning manufacturing facility that has been instrumental to the company's continued growth and success, located in the small town of Arnprior, ON. This facility has been successfully inspected by Health Canada in 2013 and the FDA in 2013 (no 483’s). Pillar5 runs on the foundation of these 5 pillars: Speed, Flexibility, Quality, Customer Service, and Reliability, and we work to achieve these every day. Visit: http://www.pillar5pharma.com or contact us at 1-613-623-4221

Abonnés LinkedIn
7 179
Personnes associées sur LinkedIn
149
Bureaux déclarés
  • 365 Madawaska Blvd., Arnprior, Ontario K7S 0C9, CA
Autres noms enregistrés
  • Pillar 5 Pharma inc.
  • Pillar5 Pharma Inc.
Spécialités
  • Sterile Filling Opthalmic/Otic/Nasal
  • FDA and Health Canada Successful Audits
  • Packaging
  • Tablets
  • Capsules
  • and Coating
Le profil indique une agence de recrutement
Non

Founded in 2009, Pillar5 Pharma Inc. has grown to become an industry leading Canadian Contract Development and Manufacturing Organization (CDMO) across the North American Market. Pillar5 provides access to safe medications, through various partners, in solid dose tablets/capsules and Ophthalmics. The team at Pillar5 has proven experience in formulation and process development in the laboratory, the manufacturing…

ChampValeur
SecteurPharmaceutical Manufacturing
Taille201-500 employees
Siège socialArnprior, Ontario
Type d’organisationPrivately Held
SpécialitésSterile Filling Opthalmic/Otic/NasalFDA and Health Canada Successful AuditsPackagingTabletsCapsulesand Coating
Offres sur Jobsy13
LinkedInVoir la page
Description

Pillar5 Pharma is a specialized aseptic manufacturer located in the Ottawa Valley Town of Arnprior, Ontario. At Pillar5, we are Building Our Future as North America's ophthalmic Centre of Excellence through best-in-class compliance, operational excellence and industry leadership. Our quality and safety trained team members work together in support of our Mission to produce reliable, high-quality eye-care products that improve and enrich the lives of our customers.

Pillar5 Pharma Inc. is seeking a Senior Continuous Improvement Specialist to lead Operational Excellence initiatives across pharmaceutical manufacturing operations to improve productivity, quality, compliance, reliability, and cost performance. Using Lean, and structured problem-solving methodologies, this role drives process improvements, reduces waste, and delivers sustainable business results while ensuring compliance with GMP and regulatory requirements. The Senior Continuous Improvement Specialist partners with Manufacturing, Quality, Engineering, Validation, Supply Chain, and Maintenance teams to identify opportunities, lead cross-functional improvement projects, and foster a culture of continuous improvement and operational excellence.

Key Responsibilities:

  • Lead continuous improvement projects across manufacturing and support functions.
  • Apply Lean, Kaizen, Value Stream Mapping, and Root Cause Analysis methodologies to improve operational performance.
  • Identify opportunities to improve throughput, yield, cycle time, quality, equipment reliability, and cost efficiency.
  • Facilitate investigations and corrective actions related to process performance, deviations, and recurring issues.
  • Lead cross-functional teams to implement and sustain process improvements.
  • Develop KPIs, dashboards, and reports to measure results and ensure long-term sustainability.
  • Coach and train employees on continuous improvement tools and best practices.
  • Ensure all improvement activities align with GMP, quality, validation, and regulatory requirements.
  • Partner with site leadership to prioritize improvement opportunities and align initiatives with business objectives.
  • Facilitate Kaizen events, workshops, and problem-solving sessions that drive employee engagement and operational excellence.
  • Monitor and report project outcomes, including productivity gains, quality improvements, cost savings, and risk reduction.
  • Support the development and standardization of processes, procedures, and performance management systems.
  • Promote a culture of continuous improvement by mentoring teams and encouraging data-driven decision making at all levels of the organization.
  • Collaborate with Manufacturing, Quality, Engineering, Supply Chain, and Maintenance teams to identify and implement sustainable solutions to operational challenges.
  • Support change management activities to ensure successful adoption and long-term sustainment of process improvements.
  • Benchmark industry best practices and identify opportunities to enhance operational excellence capabilities across the organization.

Qualifications and Requirements:

  • Bachelor's degree in Engineering, Operations Management, Manufacturing, or a related field.
  • 5+ years of experience in Continuous Improvement, Operational Excellence, Manufacturing Engineering, or a related role within a regulated manufacturing environment.
  • Lean Black Belt certification.
  • Strong knowledge of Lean Manufacturing, and structured problem-solving methodologies.
  • Experience leading cross-functional projects and delivering measurable results.
  • Strong analytical, project management, communication, and facilitation skills.
  • Experience in GMP pharmaceutical manufacturing.
  • Knowledge of CAPA, deviations, change control, validation, OEE, SPC, and FMEA.
  • TPM Experience and achievements is considered an asset.

COMPENSATION:

  • Salary range is $100,000 to $125,000 per year

This posting is for an existing vacancy. Pillar5 Pharma does not use AI at any stage of the recruitment or hiring process. Pillar5 Pharma is committed to diversity, inclusion, and equal opportunity in the workplace. Accommodations are available upon request throughout the recruitment and selection process.

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