Candidates need a B.Sc. in life science or a related field, some regulatory affairs experience, and knowledge of the Canadian Food and Drug Regulations and submission processes. Strong communication, attention to detail and the ability to manage multiple projects on tight timelines are also required.
Candidates need a life sciences or related bachelor's degree and experience with clinical trial biospecimen management and laboratory systems. They also need vendor and budget oversight experience, knowledge of clinical development and GxP rules, and strong influence without direct authority.
Baccalauréat ou expérience équivalente, diplôme scientifique avancé un atout; Expérience en oncologie, médicaments spécialisés ou marché hospitalier; Succès démontré dans l'atteinte d'objectifs commerciaux
Microsoft Office, Outils numériques, Analytique de données
Candidates need a bachelor's degree or equivalent experience, plus oncology, specialty medicine or hospital market experience and a record of meeting commercial targets. A valid driver's licence and strong analytical, communication and scientific literacy skills are required.
Candidates need a bachelor's degree or equivalent experience, plus relevant oncology, specialty medicine or hospital-based market experience. They must show commercial results, strong scientific communication, a valid driver's licence and proficiency with Microsoft Office.
3+ ansCandidates need 3+ years of field sales or territory management experience in pharmaceutical or healthcare, a bachelor's degree in life sciences, business or healthcare, and a valid driver's licence. Strong communication, self-direction and CRM skills are required.
Candidates need an MD or equivalent with board certification or eligibility in oncology, haematology or a related specialty. Clinical trial experience, knowledge of GCP and ICH guidelines, and experience working in cross-functional matrix teams are required.
5+ ansDiplôme universitaire en sciences, technique ou ingénierie; Minimum de 5 ans d'expérience technique pertinente; Expérience en validation du nettoyage, validation de procédés ou contrôle de la contamination
Candidates need an MD or equivalent with board certification or eligibility in oncology, haematology or a related specialty. They also need clinical trial experience, including medical monitoring and safety review, and experience working in cross-functional matrix teams.
3+ ans3+ gestionCandidates need a scientific or quality-related bachelor's degree, demonstrated GCP and clinical trial quality expertise, and at least 3 years of supervisory experience leading a global team. Veeva QMS and CTMS experience and knowledge of oncology, immunology, respiratory and vaccines are also required.
Diplôme universitaire en sciences, ingénierie ou discipline technique connexe; Expérience significative en pharmaceutique, biopharmaceutique ou fabrication de vaccins; Expérience en gestion de personnel et de projets
Decision making, Provide technical expertise, Process improvement, Collaboration, Regulatory compliance, Pharmaceutical industry
3+ ans3+ gestionCandidates need a university or college degree in pharmaceuticals, food, or a similar field, plus about three years of staff management and two to three years in a highly regulated industry. Strong communication, problem-solving, and organizational skills are needed, along with openness to shifts and on-call duty.
Lead a team, Inspection, Lead process optimisation, Collaboration, Technical support, Quality assurance
Candidates need a DEC in analytical chemistry or a related field, a science DEC with at least 12 credits in microbiology, or a relevant science DEC for virology. They also need basic Office skills, knowledge of Good Manufacturing Practices and a passed visual exam.
Baccalauréat en sciences ou génie; maîtrise ou doctorat préféré; Expérience en fabrication requise; connaissance de la fabrication de vaccins contre la grippe un atout; Solide connaissance des BPF et des exigences réglem
Baccalauréat ou maîtrise en génie, sciences pharmaceutiques, biotechnologie ou informatique (IA/données); Diplôme obtenu d'ici août 2027; Maîtrise du français et de l'anglais, écrit et oral
5+ ans5+ gestionBaccalauréat en ingénierie, automatisation, mécanique, électrique, informatique ou chimique; 5-10 ans d'expérience de gestion en automatisation, contrôles industriels, TI ou ingénierie; Membre de l'Ordre des ingénieurs d
Good manufacturing practices, Risk management, Cybersecurity, Documentation, Inspection, Security regulations
5+ ansBaccalauréat en génie, SST, sciences de l'environnement ou domaine connexe; 5 à 7 ans d'expérience SSE en milieu manufacturier ou pharmaceutique; Connaissance des réglementations canadienne et québécoise en SST
5+ ansDiplôme universitaire scientifique, technique ou d'ingénierie; Minimum de 5 ans d'expérience en fabrication; Connaissance des exigences réglementaires applicables
Manufacturing processes, Provide technical expertise, Troubleshooting, Technical support, Process improvement, Problem solving
5+ ansBaccalauréat en administration, opérations, logistique ou chaîne d'approvisionnement; Minimum cinq ans d'expérience en approvisionnement ou planification de production; Expérience en environnement manufacturier complexe,
Candidates need an MD with board certification or eligibility in oncology, hematology or hematology oncology, including experience treating clonal myeloid disorders. They also need clinical trial experience covering medical monitoring and safety review, and familiarity with GCP, ICH guidelines and matrix team work.
Candidates need a life science B.Sc., extensive Canadian regulatory affairs experience leading multiple submissions, and a thorough knowledge of the Canadian Food and Drug Regulations and drug development. Strong communication, negotiation, influencing and project management skills are required.
Regulatory affairs, Patient care, CTAS, Regulatory compliance, Pharmacology, Process improvement
2+ ansBaccalauréat en génie de la production automatisée ou en génie électrique; 2 ans d'expérience en automation et programmation d'automates; Maîtrise de Rockwell, Allen-Bradley, Siemens ou GE iFIX