11 meilleures offres (software development manager, mirabel, qc) (à pourvoir)

IT validation spécialist
Neopharm Labs —Blainville, QC
- Informatique
- Ingénierie
- Anglais
- Programme d'Aide aux Employés
- Heures d'arrivée et de départ flexibles
Postuler rapidement
Engineering Manager (Software)
Parker Hannifin Corporation —Mirabel, QC
- Temps plein
- Ingénierie
- Anglais
- Baccalauréat
il y a 11 jours
IT Business Analyst
Sonepar —Laval, QC
- Systèmes PGI
- Conception de systèmes
- Anglais
- Assurance Invalidité
- Assurance Dentaire
Director IT Applications and Business Solutions
Sonepar —Laval, QC
- Informatique
- Compétences rédactionnelles
- Systèmes PGI
- Assurance Invalidité
- Assurance Dentaire
Project Engineer (Laval)
Trane Technologies —Laval, QC
- De 85 816,66 $ à 120 084,99 $ par an
- Temps plein
- Ingénierie
- Windows
- Microsoft Office
Spécialiste des logiciels/ Software Specialist
Bell Textron Inc. —Mirabel, QC
- Heures supplémentaires
- Informatique
- Ingénierie
- Anglais
- Jours fériés payés
- Bourses d'Études
Engineering Mgr (Hardware)
Parker Hannifin Corporation —Mirabel, QC
- Temps plein
- Schémas
- Ingénierie
- Anglais
il y a 11 jours
Directeur, Instrumentation et Centre de données, Essais en vol/Manager, Flight test Instrumentation & Data Center
Bell Textron Inc. —Mirabel, QC
- Temps plein
- Ingénierie
- Microsoft Office
- Baccalauréat
- Jours fériés payés
- Programme d'Aide aux Employés
Software Development Manager
BrightOrder Inc. —Canada
- De 115 000 $ à 125 000 $ par an
- Temps plein
- Télétravail
- Informatique
- Ingénierie
- Anglais
- Assurance Dentaire
- Assurance Vision
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IT Manager - Relocate to Port Hardy
k'awat'si Economic Development Corporation ( KEDC) —Canada
- De 66 000 $ à 75 000 $ par an
- Fins de semaine au besoin
- Contrôle de l'inventaire
- Informatique
- Windows
- Programmes de Bien-être
- Indemnité kilométrique
Postuler rapidement
il y a 3 jours
Project Manager & CAD Designer - Relocate to Port Hardy
k’awat’si Construction Company (KCC) —Canada
- De 80 000 $ à 90 000 $ par an
- Temps plein
- Microsoft Outlook
- CAD
- Service à la clientèle
- Programmes de Bien-être
- Indemnité de déménagement
Postuler rapidement
il y a 3 jours

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IT validation spécialist

Neopharm Labs -
Blainville, QC

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Détails du poste

Profil recherché

Français
Vérification et validation des systèmes
Informatique
Ingénierie
Systèmes de gestion des informations de laboratoire
Actions correctives et préventives (CAPA)
Anglais
Bonnes pratiques de fabrication (BPF)
Esprit d'analyse
Baccalauréat
Rédaction de rapports
Évaluation des risques

Description complète du poste

The use of the masculine gender has been adopted to facilitate reading and is not intended to be discriminatory.

WE ARE LOOKING FOR AN IT VALIDATION SPECIALIST...

For over 30 years, Neopharm Labs has played a vital role in the development of health products through its expertise in research and development, analytical testing, scientific analysis, and regulatory compliance. We are recognized for our commitment to industry best practices and compliance with national and international regulations.

Neopharm provides analytical services to manufacturers of pharmaceuticals, natural health products, and cosmetics. Our continuously updated quality systems ensure fast, reliable, and compliant results that meet the highest standards in both domestic and international markets.

The IT Validation Specialist, reporting to the Metrology supervisor, is responsible for validating laboratory systems by creating and implementing protocols, data integrity procedures, and master plans for validation projects.

Our Mission

To support life sciences companies — whether emerging or established — in their pursuit of medical innovation, with an approach based on:

Rigor
Transparency
Flexibility
Reliability

Key Responsibilities

Plan, execute, and maintain the validation of GxP-impacting computerized systems, including both hardware and software.
Develop and author validation plans and protocols (VMP, VP, IQ/OQ/PQ).
Review and approve validation deliverables, including URS, FRS, risk assessments, protocols, and validation reports.
Identify, document, and remediate validation deviations, including impact assessment and implementation of Corrective and Preventive Actions (CAPAs).
Prepare validation summary reports outlining results, conclusions, and recommendations.
Assess system changes using a risk-based approach and determine the appropriate level of revalidation required.
Ensure data integrity compliance in accordance with ALCOA+ principles, GMP, FDA regulations, and 21 CFR Part 11.
Maintain the validated state of systems throughout their lifecycle.
Draft, review, and maintain SOPs and policies related to computerized system validation.
Perform regulatory and industry guideline surveillance to remain current with evolving compliance requirements.
Participate in internal audits, client audits, and regulatory inspections.
Collaborate closely with IT, Quality Assurance, laboratory teams, and external vendors.
Perform other related duties as required

Profile Sought

More than 5 years of experience in the pharmaceutical and/or medical device industry, within regulated environments.
Minimum of 3 years of experience in Computer System Validation (CSV) for GxP-impacting systems.
Strong expertise in computerized system validation processes in accordance with ISPE GAMP 5, PIC/S, and ICH guidelines.
Solid knowledge and practical application of Good Manufacturing Practices (GMP).
Thorough understanding of Health Canada and FDA regulations.
Proven ability to apply a risk-based validation approach aligned with international regulatory standards.
University degree in Computer Science, Life Sciences, Engineering, or equivalent.
Experience with enterprise systems used in laboratory and quality environments, including:
- LIMS (LabWare – strong asset)
- Computerized systems supporting GxP activities
Strong knowledge of Data Integrity principles (ALCOA+).
Excellent analytical and technical documentation skills.
Ability to work independently with strong prioritization and time‑management skills.
Strong cross‑functional collaboration and communication abilities.
High level of attention to detail and rigor.
Ability to perform effectively under pressure.
Bilingual in English and French.

Why Join Neopharm?

A growing Canadian company in the life sciences sector
A stimulating environment focused on innovation and excellence
High-impact projects with globally recognized partners
A corporate culture built on quality, collaboration, and respect
Flexible work schedule
Dynamic and fast-paced environment that keeps you informed of the latest industry trends
Comprehensive benefits package, including group insurance, employer-contributed retirement plan, and other attractive perks
Employee Assistance Program and telemedicine services
Public transportation costs reimbursed by the company

Are you ready to contribute to the life sciences industry and help improve global health?

Join Neopharm Labs, a trusted partner of leading organizations in the sector.

Please note that your resume will be shared with the hiring manager. We thank you for your interest in Neopharm Labs Inc., but only selected candidates will be contacted.

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software development manager emplois - mirabel, qc

IT validation spécialist

Engineering Manager (Software)

IT Business Analyst

Director IT Applications and Business Solutions

Project Engineer (Laval)

Spécialiste des logiciels/ Software Specialist

Engineering Mgr (Hardware)

Directeur, Instrumentation et Centre de données, Essais en vol/Manager, Flight test Instrumentation & Data Center

Software Development Manager

IT Manager - Relocate to Port Hardy

Project Manager & CAD Designer - Relocate to Port Hardy

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