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StarpaxMedical: Biopharmaceutical Production Technician In A Cgmp Environment


This is a Full-time position in Montreal, QC posted September 20, 2020.

ABOUT STARPAXStarpax medical acquired a revolutionary technology for cancer treatment.

This technology is the work of 180 professionals in engineering, biochemistry, bacteriology and oncology over a period of 18 years from various laboratories and hospitals.

Starpax technology has the potential to treat 90% of cancer (solid tumor) without the side effect related to the chemotherapy and radiotherapy.

Starpax Medical is a private society from Quebec where our mission is to rapidly increase the accessibility of its technology to million of patients.LOCATION: St-Laurent, Montreal.

SUMMARYThe candidate will be responsible to produce various components (e.G.

bacteria, liposome) of the Starpax Medical Technology.

The candidate will execute various tasks pertaining to the production processes by operating specialised equipment, preparation of solutions and sterilisation of equipment using aseptic technics.

The candidate can also be asked to revise documentation and support the daily operation by performing related tasks.This position required a great understanding of aseptic technics within cGMP environment.

Experience related to the production of bacteria using fermentor or production of liposomes is an asset.

RESPONSIBILITYPerform various production tasks in accordance with the established procedures; Disinfect equipment or sterilize solutions that will be brought and uses inside a control environment; Inspect and verify equipment to confirm that they are within specification and perform accordingly (cleaning, sterilisation and decontamination); Clean and disinfect: walls, doors, windows, floors and equipment if necessary, by following procedures in place; Ensure the traceability and inventory of material used during production; Perform and calibrate the equipment used during production by following procedure in place; Collect samplesfor validation and verification of the cleaning; Maintain good level of documentation.

Ensure the integrity and traceability of all the data generated; Support the technology transfer between the development and production phase by following GLP and GMP guideline; Participate in the redaction and revision of various reports, technical reports and batch records; Provide assistance to other departments if neededThe candidate might have to move, lift and carry heavy objects; QUALIFICATIONSBachelor’s degree in biochemistry, microbiology or biotechnology or a technical degree in pharmaceutical production; At least 3 years of experience in pharmaceutical production with 3 years of experience in cGMP environment; Working proficiency in English and French required; Excellent knowledge of the cGMP guidelines, including aseptic techniques; Excellent knowledge of the requirement and expectation to develop and produce biopharmaceutical products; Skilled in fermentation (and associate system), liposomes production and chromatography; Proficient in Microsoft suites; SKILLS AND PERSONAL ATTRIBUTESAttention to details with high level of autonomy; Conscientious and methodical; Ability to plan, organise and manage various activity in a multitasking environment; Maintain harmonious relationship between coworkers and collaborators; Ability to workunder pressure and complete tasks within the deadlines; Excellent writing and verbal communication skills; Comfortable working in a small team and within a startup environment; CONDITIONSAvailability: Septembre 2020; Full time position; Conditions: Employees are called to perform physical and psychophysiological exams on a regular basis; Beneftis: Competitive salary, group insurance and other; Location: St-Laurent, Montreal.

Parking available.