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Publié il y a 19 jours

Quality control analyst

@ Groupe Parima Inc.

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Saint-Laurent, Québec

Temps plein
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SIGNAUX

En bref

Groupe PARIMA, a contract development and manufacturing organization for non-sterile liquids, suspensions and semi-solid drug products, is hiring two Quality Control Analysts: one on weekday days (40 hours a week) and one on weekend shifts (Friday to Sunday, 12-hour days). The work is hands-on laboratory testing under GMP, including HPLC, titration, spectrophotometry and physical tests, with LIMS data entry and training of junior analysts.

Responsabilités :

  • Perform chemical and physical analyses to GMP and company specifications
  • Run HPLC, titration, spectrophotometry and physical tests
  • Enter and review analytical results in the LIMS
  • Maintain laboratory instruments, reagents and inventories
  • Train junior analysts and take part in investigations

Résumé des exigences :

  • Knowledge of USP and EP/BP pharmacopoeias
  • Ability to work independently on analytical testing
  • Understanding of GMP and laboratory health and safety rules
  • Experience with HPLC and titration methods

Outils et compétences

HPLCUV-Visible spectrophotometerLIMS
Source et dates

Flux d’un site d’emploi · jobillico

Date publiée par l’employeur
2026-10-19
Première détection par notre source
2026-10-20
Mise à jour du dossier source
2026-11-07

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

Détails du poste

NiveauDébutant
DomaineAssurance qualité
Heures par semaine40
Horairejour, fins de semaine
Déplacementsavion : aucun · route : aucun
Milieu de travailLaboratoire
PositionAssis et debout
Exigences physiquesphysique faible · ordinateur modéré

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

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Groupe Parima Inc.

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ChampValeur
Offres sur Jobsy1
Description

Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO), established in 1994. For over 30 years, we have developed an expertise in the development and manufacturing of non-sterile liquids, suspensions and semi-solid drug products. https://www.groupeparima.com/fr/

Quality Control Analyst

Two positions to fill:

  • Day: Monday to Friday (40 hours per week)
  • Weekend: Friday, Saturday and Sunday (12 hours per day)

The Quality Control Analyst...

Responsibilities:

  • Independently perform chemical and physical analyses according to the established schedule, following Groupe Parima's specifications, methods, procedures and Good Manufacturing Practices (GMP).
  • Participate in laboratory and instrument maintenance, reagent and inventory management, and the training of junior analysts.Work in compliance with health and safety rules and report health and safety risks to supervisors.
  • Good knowledge of the USP and EP/BP Pharmacopoeias.
  • Independently perform the following physical tests: pH, density, specific gravity, viscosity, deliverable volume, particle size, particle size distribution (PSD) and loss on drying.
  • Independently perform assay tests by volumetric and automatic titration
  • Independently perform UV-Visible spectrophotometer tests.
  • Prepare mobile phases, diluents and dissolution media.
  • Independently perform dissolution, assay and related substances tests by HPLC.
  • Analyze results critically and with concern for compliance with the standards set by current procedures.
  • Enter analytical results in the LIMS using sound judgment by comparing them with trend analyses.
  • Ensure data integrity and quality in the QC laboratory.
  • Assist and participate in the training of junior analysts.
  • Perform maintenance or calibration of laboratory instruments used in physical tests.
  • Help maintain inventories of reagents, solvents and consumables required for analyses or for the proper operation of the laboratory.
  • Actively participate in laboratory investigations.
  • Participate in laboratory problem solving and continuous improvement.
  • Follow health and safety rules and report health and safety risks to supervisors.
  • Occasionally cover certain senior analyst tasks based on operational needs.
  • Any other tasks required for the proper operation of the laboratory.

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