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Analyste AQ (Assurance Qualité) pharmaceutique/Pharma QA Analyst

  • Longueuil, QC, Canada

On-site

Full-time

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Job details

Job type
Full-time
Workplace
On-site
Posting language
English · French
Posted

Original job description

English section of this bilingual listing.

Serving the world with your talent
Since 1997, KABS has offered a broad range of product development services to the bio-pharmaceutical industry, worldwide. We support pharmaceutical development programs from initial discovery to phase III. Our GMP compliant services include strategic planning, pre-clinical development, analytical testing, formulation development, manufacturing of prototypes and clinical supplies, and distribution of clinical supplies to clinical sites and CMC aspects of regulatory affairs.

Sommaire des tâches

Informations supplémentaires

The person entitled will be integrated in a continuous training program for performing the following activities: 

  • Execute audit programs;
  • Train production staff on procedures, protocols, regulatory issues ;
  • Review daily operations ;
  • Write SOPs and Protocols ;
  • Update SOPs when needed ;
  • Manage training programs related to the SOPs ;
  • Follow up with QA Director.

Qualifications
The technical, regulatory and ethical standards of the company but also of the pharmaceutical industry are very demanding. We are looking above all for an organized, rigorous, meticulous and ambitious person. 

  • Degree in Chemistry, Biochemistry, Pharmacology or any other related field;
  • Ability to analyze, write reports and protocols;
  •  Leadership and initiative.

Please note that the masculine includes the feminine; it is used to make reading easier.

Your career with KABS
We aspire to offer all team members a work environment filled with multiple challenges and opportunities. We also offer many social benefits.

  • Permanent position
  • Dynamic team
  • A good RRSP
  • Group insurances
  • Virtual Healthcare for employee and family
  • 5 flexible days

We thank all applicants but only those under consideration will be contacted

Read the full bilingual original

Description de l'entreprise

Servir le monde avec votre talent
KABS offre depuis 1997 un large éventail de services comprenant les analyses pharmacopées, le développement de nouvelles méthodes d'analyse, le développement de nouveaux médicaments et génériques, la fabrication de prototypes pour fin d'études cliniques. Nous travaillons avec des clients et partenaires des quatre continents. Nos services aux standards BPF comprennent la planification stratégique, le développement préclinique, la mise au point de méthodes analytiques, le développement de formulations, la fabrication de prototypes et de lots cliniques, la distribution de produits finis aux sites cliniques, et les affaires réglementaires.

Serving the world with your talent
Since 1997, KABS has offered a broad range of product development services to the bio-pharmaceutical industry, worldwide. We support pharmaceutical development programs from initial discovery to phase III. Our GMP compliant services include strategic planning, pre-clinical development, analytical testing, formulation development, manufacturing of prototypes and clinical supplies, and distribution of clinical supplies to clinical sites and CMC aspects of regulatory affairs.

Description du poste

Sommaire des tâches

Le (la) titulaire du poste sera intégré dans un programme de formation continue pour procéder aux activités suivantes:

  • Exécuter les programmes d'audits;
  • Former le personnel de l'usine sur les procédures, protocoles, problèmes réglementaires;
  • Réviser les opérations quotidiennes;
  • Rédiger des SOP et protocoles;
  • Mettre à jour les SOP lorsque nécessaire;
  • Gérer les programmes de formation reliées au SOP;
  • Assurer un suivi au directeur QA.

Qualifications

Votre profil
Les normes techniques, réglementaires et éthiques de l’entreprise mais aussi de l’industrie pharmaceutique sont très exigeantes. Nous recherchons avant tout une personne organisée, rigoureuse, minutieuse et ambitieuse.

  • Diplôme en Chimie, Biochimie, Pharmacologie ou tout autre domaine connexe;
  • Capacité d'analyse, rédaction de rapports et de protocoles;
  • Leadership et initiative.

Votre carrière avec nous
Nous aspirons à offrir à chaque membre de l'équipe un environnement de travail stimulant et rempli de défis, ainsi que des opportunités de développement de carrière. En plus de vous permettre de travailler dans un environnement professionnel de premier plan, nous vous proposons aussi toutes sortes d’avantages. 

  • Emploi permanent
  • Équipe dynamique
  • REER collectif avantageux
  • Des assurances collectives
  • Télémédecine pour l'employé et sa famille
  • 5 journées de maladies 

Nous contacterons uniquement les candidats retenus.

Veuillez noter que le masculin inclut le féminin; il est employé afin d'alléger la lecture.

Informations supplémentaires

Job summary

The person entitled will be integrated in a continuous training program for performing the following activities: 

  • Execute audit programs;
  • Train production staff on procedures, protocols, regulatory issues ;
  • Review daily operations ;
  • Write SOPs and Protocols ;
  • Update SOPs when needed ;
  • Manage training programs related to the SOPs ;
  • Follow up with QA Director.

Qualifications
The technical, regulatory and ethical standards of the company but also of the pharmaceutical industry are very demanding. We are looking above all for an organized, rigorous, meticulous and ambitious person. 

  • Degree in Chemistry, Biochemistry, Pharmacology or any other related field;
  • Ability to analyze, write reports and protocols;
  •  Leadership and initiative.

Please note that the masculine includes the feminine; it is used to make reading easier.

Your career with KABS
We aspire to offer all team members a work environment filled with multiple challenges and opportunities. We also offer many social benefits.

  • Permanent position
  • Dynamic team
  • A good RRSP
  • Group insurances
  • Virtual Healthcare for employee and family
  • 5 flexible days

We thank all applicants but only those under consideration will be contacted

More about this job

Responsibilities

The QA analyst at KABS will run audit programs and train plant staff on procedures and regulatory issues. They will also review daily operations, write and update SOPs and protocols, and report to the QA Director.

Requirements

Candidates need a degree in chemistry, biochemistry, pharmacology or a related field, plus strong analysis and report and protocol writing skills. Leadership, initiative and an organized, meticulous approach are expected.

Skills

  • GMP
  • SOP writing
  • Protocol writing
  • Audit execution
  • Regulatory compliance
  • Staff training
  • Analytical methods
  • Report writing
  • Data analysis
  • Quality assurance
  • Leadership
  • Process review

Benefits

  • Group insurance
  • Group RRSP
  • Virtual healthcare for employee and family
  • Permanent position

Categories

  • Healthcare
  • Science & Research
  • Manufacturing

Keywords

  • QA analyst
  • pharmaceutical quality assurance
  • GMP
  • SOP writing
  • protocol writing
  • audit
  • regulatory compliance
  • pharmacopoeia analysis
  • analytical method development
  • validation
  • training
  • chemistry
  • biochemistry
  • pharmacology
  • pharma QA
  • quality control
  • CMC
  • bio-pharmaceutical
  • clinical supplies

Seniority

Entry level

Perks

  • Retirement plan

Languages

  • English
  • French

Fields of study

  • Chemistry
  • Biochemistry
  • Pharmacology

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