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Added 2 mins ago
Continuing Care Assistant
Shannex Incorporated
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Temporary
…healthcare sector, Shannex offers opportunities for growth, development and advancement. And at the end of every day, you will know you’ve made a measured difference in the lives of our…
Added 2 mins ago
Night Housekeeper
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Full-time
…healthcare sector, Shannex offers opportunities for growth, development and advancement. And at the end of every day, you will know you’ve made a measured difference in the lives of our…
Added 2 mins ago
Continuing Care Assistant
Shannex Incorporated
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…healthcare sector, Shannex offers opportunities for growth, development and advancement. And at the end of every day, you will know you’ve made a measured difference in the lives of our…
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Health Care Aide Bow Valley Sept 2026
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…Heritage, you will provide leadership of a :15 person team and senior level project management and project director expertise to support a variety of projects that range in type, size and…
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Group Manager, Heritage
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…Heritage, you will provide leadership of a :15 person team and senior level project management and project director expertise to support a variety of projects that range in type, size and…
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…healthcare sector, Shannex offers opportunities for growth, development and advancement. And at the end of every day, you will know you’ve made a measured difference in the lives of our…
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Group Manager, Heritage
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…Heritage, you will provide leadership of a :15 person team and senior level project management and project director expertise to support a variety of projects that range in type, size and…
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Group Manager, Heritage
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…Heritage, you will provide leadership of a :15 person team and senior level project management and project director expertise to support a variety of projects that range in type, size and…
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Group Manager, Heritage
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…Heritage, you will provide leadership of a :15 person team and senior level project management and project director expertise to support a variety of projects that range in type, size and…
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Group Manager, Heritage
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Added 17 mins ago
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Added 33 mins ago
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MacDonald Search Group

Senior Technical Services Scientist

Montreal, QC, Canada

Job type: Full-time
Apply by: Oct 25, 2026
Experience: A minimum of 5 years of experience in technical services.
Posting language: English · French
Posted: Sep 25, 2026

Apply About employer

Applications open in a new tab.

Original job description

English section of this bilingual listing.

The Senior Technical Services Scientist plays a key role in supporting technical transfer and scale-up activities from R&D to GMP manufacturing. This position is responsible for leading process validation activities, managing scientific and technical documentation while ensuring the efficient transfer of knowledge and processes across teams and stakeholders. Responsibilities include documentation related to development studies, such as protocols, manufacturing instructions, bills of materials (BOMs), master batch records, and summary reports. The ideal candidate will contribute to continuous improvement initiatives, support risk mitigation efforts, and enhance product quality through a strong technical understanding of pharmaceutical manufacturing processes.

Skills And Qualifications

Bachelor's degree (B.Eng. or B.Sc.) in Chemistry, Pharmaceutical Science, or a related field.
A minimum of 5 years of experience in technical services.
Strong knowledge of manufacturing processes and equipment - OSD and/ or Sterile
Excellent analytical and problem-solving skills.
Proven ability to lead process validation projects.
Solid understanding of Quality by Design (QbD) and scale-up principles.
Strong grasp of GMP regulations and validation requirements.
Skilled in root cause analysis and risk assessment.
Proficient with Microsoft Office (Word, Excel, PowerPoint and Outlook), and MS Project.
Ability to work independently and maintain confidential information.
Makes independent decisions within defined areas of responsibility.

What We Offer:

Competitive Salary $90,000-$110,000
Comprehensive Health Benefits
Group RRSP (with 4% match program)
Annual Vacation and additional Personal Time Off (PTO) program (we are a work/life balance culture)
Health and Wellness Support Programs (Homewood Health EAP & Telus Health Virtual Care)
Team building and fun corporate events
And you'll join a diverse and multi-disciplinary team!

Read the full bilingual original

Bachelor's degree (B.Eng. or B.Sc.) in Chemistry, Pharmaceutical Science, or a related field.
A minimum of 5 years of experience in technical services.
Strong knowledge of manufacturing processes and equipment - OSD and/ or Sterile
Excellent analytical and problem-solving skills.
Proven ability to lead process validation projects.
Solid understanding of Quality by Design (QbD) and scale-up principles.
Strong grasp of GMP regulations and validation requirements.
Skilled in root cause analysis and risk assessment.
Proficient with Microsoft Office (Word, Excel, PowerPoint and Outlook), and MS Project.
Ability to work independently and maintain confidential information.
Makes independent decisions within defined areas of responsibility.

What We Offer:

Competitive Salary $90,000-$110,000
Comprehensive Health Benefits
Group RRSP (with 4% match program)
Annual Vacation and additional Personal Time Off (PTO) program (we are a work/life balance culture)
Health and Wellness Support Programs (Homewood Health EAP & Telus Health Virtual Care)
Team building and fun corporate events
And you'll join a diverse and multi-disciplinary team!

Le/La Scientifique principal(e), Services techniques joue un rôle clé dans le soutien des activités de transfert technologique et de mise à l’échelle entre la R&D et la production GMP. Ce poste est responsable de diriger les activités de validation des procédés, de gérer la documentation scientifique et technique, et d’assurer un transfert efficace des connaissances et des procédés entre les équipes et les parties prenantes. Les responsabilités comprennent la préparation de la documentation liée aux études de développement, notamment les protocoles, instructions de fabrication, nomenclatures (BOM), dossiers maîtres de fabrication et rapports sommaires. Le/la candidat(e) idéal(e) contribuera aux initiatives d’amélioration continue, soutiendra les efforts de gestion des risques et optimisera la qualité des produits grâce à une solide compréhension technique des procédés de fabrication pharmaceutique.

Compétences Et Qualifications

Baccalauréat (B. Ing. ou B. Sc.) en chimie, en sciences pharmaceutiques ou dans un domaine connexe.
Solide connaissance des procédés de fabrication et des équipements.
Excellentes aptitudes en analyse et en résolution de problèmes.
Capacité démontrée à diriger des projets de validation de procédés.
Bonne compréhension des principes de la qualité dès la conception (QbD) et de la mise à l’échelle.
Maîtrise des règlements BPF et des exigences en matière de validation.
Compétence en analyse des causes fondamentales et en évaluation des risques.
Maîtrise de la suite Microsoft Office (Word, Excel, PowerPoint, Outlook) et de MS Project.
Capacité à travailler de façon autonome et à gérer des informations confidentielles.
Bon jugement et aptitude à prendre des décisions éclairées dans son champ de responsabilité.

Ce que nous offrons:

Salaire concurrentiel $90,000-$110,000
Avantages complets pour la santé
REER collectif (avec programme de contrepartie de 4 %)
Programme de vacances annuelles et de congés personnels supplémentaires (PTO) (nous sommes une culture d'équilibre travail / vie personnelle)
Programmes de soutien en santé et au mieux-être (PaE Homewood Health et Telus Health Virtual Care)
Possibilités de perfectionnement professionnel
Consolidation d'équipe et événements d'entreprise amusants
Et vous vous joindrez à une équipe diversifiée et multidisciplinaire !

Apply About employer

More about this job

Responsibilities

Lead process validation and support technical transfer and scale-up from R&D to GMP manufacturing. Manage development and manufacturing documentation, facilitate knowledge transfer across teams, and contribute to continuous improvement, risk mitigation, and product quality.

Requirements

Requires a bachelor's degree in chemistry, pharmaceutical science, or a related field, and at least five years of technical services experience. Candidates should have pharmaceutical manufacturing and equipment knowledge, experience leading process validation, and a strong understanding of QbD, scale-up, GMP, root cause analysis, and risk assessment.

Skills

Technical Transfer
Scale-Up
Process Validation
GMP Manufacturing
Scientific Documentation
Technical Documentation
Pharmaceutical Manufacturing
Manufacturing Processes and Equipment
Quality by Design
GMP Regulations
Root Cause Analysis
Risk Assessment
Analytical Problem-Solving
Continuous Improvement
Microsoft Office
MS Project

Benefits

Comprehensive Health Benefits
Group RRSP With 4% Match
Annual Vacation
Additional Personal Time Off
Health and Wellness Support Programs
Employee Assistance Program
Virtual Health Care
Professional Development Opportunities
Team-Building Activities
Corporate Events

Visa sponsorship

Not detected in the job text

Keywords

Technical Transfer
Scale-Up
R&D
GMP Manufacturing
Process Validation
Development Studies
Protocols
Manufacturing Instructions
Bills of Materials
Master Batch Records
Summary Reports
Pharmaceutical Manufacturing
Oral Solid Dosage
Sterile Manufacturing
Quality by Design
GMP Regulations
Validation Requirements
Root Cause Analysis
Risk Assessment
Continuous Improvement
Risk Mitigation
Product Quality
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Microsoft Outlook
MS Project
Chemistry
Pharmaceutical Science

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