Closed listing
Senior Technical Services Scientist
- Moncton, NB, Canada
Full-time
This opening has closed.
The original listing is kept below for reference.
Job details
- Job type
- Full-time
- Closing date
- Experience
- A minimum of 5 years of experience in technical services.
- Posting language
- English · French
- Posted
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Search current openingsOriginal job description
Archived listing. The details below describe a past opening.
English section of this bilingual listing.
Based in Montreal
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
Based in Montreal
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
Compétences Et Qualifications
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.
- 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!
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.
- 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 !
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 knowledge, experience leading process validation, understanding of QbD, scale-up and GMP requirements, and proficiency in root cause analysis, risk assessment, Microsoft Office, and MS Project.
Skills
- Technical Transfer
- Scale-Up
- Process Validation
- GMP Manufacturing
- Scientific and Technical Documentation
- Pharmaceutical Manufacturing Processes
- Manufacturing Equipment
- Quality by Design
- GMP Regulations
- Root Cause Analysis
- Risk Assessment
- Analytical Problem-Solving
- Continuous Improvement
- Microsoft Office
- MS Project
- Confidential Information Management
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
Categories
- Manufacturing
- Science & Research
- Engineering
- Management & Leadership
Keywords
- Technical Services
- 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
- Risk Mitigation
- Continuous Improvement
- Product Quality
- GMP Regulations
- Validation Requirements
- Root Cause Analysis
- Risk Assessment
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
- Microsoft Outlook
- MS Project