On behalf of our client specializing in biotechnology, we are looking for a QC Microbiology Technician for a minimum period of 5 months. ...
Your role:
Execute testing such as Bioburden, Bacterial Endotoxin Test and identification according to established procedures in both GRP and GxP environments, delivering results within expected timelines, and performing various tasks assigned by the manager.
Perform result review and utilize GLIMS for data entry,
Perform Growth promotion testing for media verification.
Manage sample/material reception and testing, applying appropriate quality and EHS procedures, guidelines, and standards.
Initiate any deviation, OOS or event when found, perform lab investigation and define/implement CAPA as needed.
Update microbiology lab procedures and participate continuous improvement.
Cooperate as technical referent during the external/internal audits.
Work collaboratively with colleagues and other departments while adhering to established standards, including good documentation practices, and escalating any events that may impact operations.
Participate in scheduled piquet rotations (on?call / in site) to ensure operational support outside regular working hours.
Temporary task: involvement in GLIMS (LabVantage) system-related tasks (e.g.: Support QC master data maintenance and routine user activities )
Your profile:
At least 3 years’ experience in the role
Minimum CFC or equivalent diploma; Bachelor’s or Master’s degree in Microbiology, or related fields
Proven experience in GMP-regulated pharmaceutical environments
Strong knowledge of microbiological and analytical techniques
Result oriented and proactive / Sense of urgency
Strong collaboration skills and a team-oriented mindset
Excellent communication skills in English/French
Knowledge of LIMS (LabVantage) will be consider a plus
show more
On behalf of our client specializing in biotechnology, we are looking for a QC Microbiology Technician for a minimum period of 5 months.
Your role:
Execute testing such as Bioburden, Bacterial Endotoxin Test and identification according to established procedures in both GRP and GxP environments, delivering results within expected timelines, and performing various tasks assigned by the manager.
Perform result review and utilize GLIMS for data entry,
Perform Growth promotion testing for media verification.
Manage sample/material reception and testing, applying appropriate quality and EHS procedures, guidelines, and standards.
Initiate any deviation, OOS or event when found, perform lab investigation and define/implement CAPA as needed.
Update microbiology lab procedures and participate continuous improvement.
Cooperate as technical referent during the external/internal audits.
Work collaboratively with colleagues and other departments while adhering to established standards, including good documentation practices, and escalating any events that may impact operations.
Participate in scheduled piquet rotations (on?call / in site) to ensure operational support outside regular working hours.
Temporary task: involvement in GLIMS (LabVantage) system-related tasks (e.g.: Support QC master data maintenance and routine user activities )
Your profile:
...
At least 3 years’ experience in the role
Minimum CFC or equivalent diploma; Bachelor’s or Master’s degree in Microbiology, or related fields
Proven experience in GMP-regulated pharmaceutical environments
Strong knowledge of microbiological and analytical techniques
Result oriented and proactive / Sense of urgency
Strong collaboration skills and a team-oriented mindset
Excellent communication skills in English/French
Knowledge of LIMS (LabVantage) will be consider a plus
show more
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