Associé(e), Surveillance Environnementale (Soir) / Environmental Monitoring at Jubilant HollisterStier General Partnership
Montréal, QC, Canada -
Full Time


Start Date

Immediate

Expiry Date

30 Nov, 25

Salary

0.0

Posted On

31 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Ep, French, Computer Literacy, Microbiology, English, It, Sap, Working Experience, Microsoft Office, Operations

Industry

Pharmaceuticals

Description

ASSOCIÉ(E), SURVEILLANCE ENVIRONNEMENTALE (SOIR)

Jubilant HollisterStier, une filiale de Jubilant Pharma Holdings Inc., est actuellement à la recherche d’un(e) Associé(e), Surveillance Environnementale (Soir) pour se joindre à notre équipe !

QUALIFICATIONS REQUISES – FORMATION :

  • DEC ou Baccalauréat en microbiologie ou dans un domaine connexe.

EDUCATION QUALIFICATION:

  • DEC or BSc in Microbiology or closely related discipline.

EXPERIENCE REQUIRED:

  • Working experience in microbiology laboratory preferably within quality control or research & development environment.
  • Practical experience (microbiology) in effective testing of samples from classified clean rooms and aseptic operators and critical utilities.
  • Strong knowledge and application of compendia (USP, EP, BP) and cGMP as it applies to laboratory operations and to production environment.
  • Solid report writing ability.
  • Computer literacy (Microsoft Office, SAP, and Electronic Data Acquisition System).
    Bilingual (French & English). Proficiency in English is essential.

SKILLS REQUIRED:

  • Complete analysis by adhering to methods and/or SOPs as written.
  • Accountable for meeting timeline commitments.
  • Communicates promptly any deviations.
  • Work in a team environment.
    Job Overview

How To Apply:

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Responsibilities
  • Responsible of performing the environmental monitoring of classified areas and personnel monitoring of gowns and glove monitoring as well as overseeing filling operations to observe critical activities such as aseptic connections, set up, manufacturing and filling and to report on any deficiencies observed.
  • Responsible to perform the sampling of filled sterile products.
  • Maintains legible and complete records of all test results, instrument readings and observations. Ensures integrity and traceability of all data generated and reported and makes all necessary corrections in accordance with GMP requirements and Jubilant standards.
  • Notifies immediately Supervisor of any out of specification, out of trend, or incomplete testing result, and other irregularities.
  • Provides support for areas such as: trouble-shooting, training and help in investigation.
  • Performs other duties as delegated.
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