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Analytical Techician

  • Laval, QC, Canada

Full-time

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Job details

Job type
Full-time
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Experience
3 years of prior work experience in a related field
Posting language
English
Posted

Original job description

Tasks And Responsibilities

  • Carrying out analyses relating to pharmaceutical product development work using various analytical techniques and equipment.
  • This may include, but is not limited to
  • HPLC
  • Sample preparation
  • Titration
  • Dissolution
  • Stability analyses
  • Physical characterisation of API, intermediates, and finished products
  • Conducting off-spec research
  • Respect the safety and hygiene rules of the laboratory;
  • Master the different analytical methods and techniques, and the operation of the equipment;
  • Respect deadlines and priorities;
  • Maintain all relevant documentation of their activities;
  • Respect the SOPs and GMPs relating to their work;
  • Actively participate in all required analytical investigations;
  • Monitor and carry out inventory of reagents, standards and chromatographic columns as required.
  • Ensure general maintenance of the laboratory.
  • Carry out analyses according to instructions, transcribe data into relevant reports, evaluate data against R & D / GMP criteria with guidance from supervisor.
  • Perform all related duties.

Qualifications

  • Diploma of Collegiate studies
  • 3 years of prior work experience in a related field
  • Bilingual (English, French)
  • Computer skills (MS Office 365)
More about this job

Responsibilities

Conduct analytical testing for pharmaceutical product development, including HPLC, sample preparation, titration, dissolution, stability, and physical characterization of APIs, intermediates, and finished products. Document and evaluate results, support analytical investigations, maintain laboratory supplies and equipment, and follow safety, hygiene, SOP, and GMP requirements.

Requirements

Requires a diploma of collegiate studies and three years of prior experience in a related field. Candidates must be bilingual in English and French and have computer skills, including Microsoft Office 365.

Skills

  • Sample Preparation
  • Titration
  • Dissolution Testing
  • Stability Analysis
  • Physical Characterization
  • Off-Specification Investigations
  • Analytical Methods
  • Laboratory Equipment Operation
  • Good Manufacturing Practices (GMP)
  • Standard Operating Procedures (SOPs)
  • Data Evaluation
  • Laboratory Documentation
  • Reagent and Standards Inventory
  • Laboratory Maintenance
  • Microsoft Office 365

Visa sponsorship

Not detected in the job text

Categories

  • Science & Research
  • Healthcare
  • Manufacturing

Keywords

  • Pharmaceutical Product Development
  • Pharmaceutical Manufacturing
  • Analytical Testing
  • Sample Preparation
  • Titration
  • Dissolution
  • Stability Analysis
  • Physical Characterization
  • Active Pharmaceutical Ingredients (APIs)
  • Intermediates
  • Finished Products
  • Off-Specification Research
  • Analytical Methods
  • Laboratory Equipment
  • Safety and Hygiene
  • Standard Operating Procedures (SOPs)
  • Good Manufacturing Practices (GMP)
  • Analytical Investigations
  • Reagents
  • Standards
  • Chromatographic Columns
  • Inventory Management
  • Laboratory Maintenance
  • Data Transcription
  • Data Evaluation
  • Research and Development (R&D)
  • Microsoft Office 365
  • English
  • French

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