Job Fair

The Clinical Applications Specialist is in charge of supporting and educating Hexoskin clients on how to best use Hexoskin products and solutions in different contexts. The chosen candidate will work closely with the Sales & Marketing team and interact with people throughout the company (biomedical, software, hardware, design). Our team is result-oriented and passionate about delivering leading innovative products to a large international community.

We are looking for a creative and passionate person to fill the position of Biomechanical Specialist at Shapeshift 3D. In this role, you will work in a multidisciplinary team to develop a new generation of 3D printed user-specific medical, sports and protective equipment to be customized on Shapeshift 3D proprietary platform. With projects ranging from insole to football helmets, you will combine skills in product design, biomechanics, and human factors to tackle challenges from various industries. You will be responsible for defining products requirements and designing advanced 3D models using CAD modeling tools such as Fusion 360 and generative design, planning and conducting testing and offering consulting services to clients new to digital and additive manufacturing.

We are looking for a resourceful and passionate person to fill the position of Algorithm Developer at Shapeshift 3D. In this role, you will test, develop, implement and improve algorithms used through our state-of-the-art cloud-based customization platform to improve its efficiency and range of application. You will be part of the software development team and will contribute to packaging and optimizing algorithms for clients’ projects and real-world applications. ​ You will work in close collaboration with people with background in mechanical, biomedical, software and physics engineering. You will also act as a consultant to guide the development of our Shapeshift 3D software to improve user experience and ease future application integrations and onboarding.

We are looking for an individual who is motivated by results and teamwork for the position of Sales Representative at Shapeshift 3D. In this role, you will sell state-of-the-art software to innovative manufacturers in the medical, sports and protection industries. As a Sales Representative, you will immerse yourself in the world of mass customization in order to develop effective, market-driven presentations and sales strategies to propel Shapeshift 3D’s growth. You will be responsible for generating and qualifying potential customers and partners, mastering products and services to make compelling presentations, and improving and adjusting sales processes based on the results. On a daily basis, you will collaborate with a multidisciplinary team, the R&D and integration departments, to ensure a smooth and efficient sales experience for customers.

We are looking for a resourceful and passionate person to fill the position of Application Specialist at Shapeshift 3D. In this role, you will be the bridge between our core software development team and our clients. As someone with both interpersonal and technical skills, you will be translating high-level client’s requirements into technical tasks, provide support for existing clients, implement application-specific software improvement and manage client onboarding. Shapeshift 3D is a highly performing toolbox for customization workflows, you will be using and improving these tools to develop workflow for new applications and use cases

We are looking for an organized and highly analytical individual who is motivated by results and teamwork for the position of Compliance Officer In this role, you will develop, monitor, and execute compliance programs for the financial, legal and information security departments. You will work on policies that will structure the company fast expansion in the healthcare, sports and protection industries.

We are seeking a passionate postdoctoral fellow with experience in radiochemistry to join our team developing targeted radiotheranostics for precision oncology. Ideal candidates for this position will have strong experience with the synthesis of metal chelators and bifunctional linkable compounds, as well as inorganic characterization and radiolabelling. Research activities will include investigating novel methods to couple metal ion carriers/chelators with proteins and antibodies, radiolabeling novel, protein-linked chelators with radiometals for pre-clinical diagnostic and therapeutic investigations, and executing in vitro and in vivo studies of novel radiopharmaceuticals. As well, the candidate will be expected to design and execute multi-step syntheses to prepare bifunctional linkable compounds for targeted radiopharmaceuticals.

We are working to advance innovative biologic programs to the clinic for cancer patients, using a variety of therapeutic modalities including, but not limited to, immune-cell engager bispecific antibodies, chimeric antigen receptor (CAR) cell therapy, and oncolytic virus driven disruption of immunosuppression and resistance in the tumour microenvironment. We are seeking a highly driven and passionate post-doctoral fellow with strong biologics and immunotherapy expertise to join the teams working on these programs. The ideal fellow will have expertise in engineering biologics, specifically those involving T-cell activation, and analysing their functional effects in immune cell assays, including multi-color flow cytometry. Experience in choosing in vivo models and designing studies, and in IHC, fluorescent imaging, and biodistribution analysis is an asset.

We are seeking an experienced Senior Director of Biologics Drug Product Development to lead the biologics drug discovery and development efforts and drive the development of novel therapeutics. Based at adMare’s Vancouver site, the successful candidate will have a track record of >15 years in biologics drug discovery in the biotechnology/pharmaceutical industry coupled with an exceptional grasp of state-of-the-art biologics and cell-based techniques including antibody based therapeutic development, gene and nucleic acid based therapies and emerging cellular therapy technologies. Strong awareness of industry expectations is required, along with the ability to design programs and manage key day-to-day activities for the biologics group. The candidate will play a central role in coordinating biologic and cell based therapeutic programs to scientifically and strategically lead scientists at adMare, from early discovery and development through life cycle management.

The Director, adMare Academy plays an essential role in executing on adMare Academy’s strategy aligned to adMare’s mission to train the next generation of highly qualified personnel to drive the development of innovation. This role serves as the subject matter expert and project manager for implementing processes and program lifecycle across all Academy offerings.

We are seeking a Senior Level Partnerships candidate to join a dynamic and results-driven team to lead and accelerate business analysis, sourcing, and deal flow activities. This position will report to the Vice President, Program Development & Partnerships and will be based in Montreal, QC.

We are seeking a passionate postdoctoral fellow with experience in radiochemistry to join our team developing targeted radiotheranostics for precision oncology. Ideal candidates for this position will have strong experience with the synthesis of metal chelators and bifunctional linkable compounds, as well as inorganic characterization and radiolabelling. Research activities will include investigating novel methods to couple metal ion carriers/chelators with proteins and antibodies, radiolabeling novel, protein-linked chelators with radiometals for pre-clinical diagnostic and therapeutic investigations, and executing in vitro and in vivo studies of novel radiopharmaceuticals. As well, the candidate will be expected to design and execute multi-step syntheses to prepare bifunctional linkable compounds for targeted radiopharmaceuticals.

This company is looking for a highly talented computer scientist to join a dynamic team building a world-class platform for life scientists integrating bioinformatics, systems biology and AI. In this role, you will work closely with systems biologists, bioinformaticians, data scientists, AI and software engineers to build solutions for the top BioPharma and Agritech companies in the world. This full-time position will focus on workflow design, development and implementation, data visualization, quality assessment and mentoring of junior bioinformaticians in software development

The mission of the Recruiter is simple : to enable the company’s accelerated growth, and to act as a trusted advisor to all hiring leaders including the company’s cofounders and executives. You will report directly to the COO and you will have the opportunity to build the function, the tools, shape the processes and shape the future.

This company is looking for a talented Senior Bioinformatician to join a dynamic team building a world class augmented intelligence R&D platform for life scientists working in BioPharma and agriculture companies.

The incumbent will work in close collaboration with the IRICoR team, external patent agents and the researchers assigned to the portfolio projects. The incumbent will provide support for intellectual property (IP) activities, will be called upon to maintain the IP portfolio and carry out important preliminary research for the development of projects. Her work will be coordinated and validated by the senior IP manager.

The coordinator will have the opportunity to work under the supervision of Dr Stella Daskalopoulou (Associate Professor at McGill, Department of Medicine) and Dr Ioannis Psaromiligkos (Associate Professor of McGill, Department of Electrical and Computer Engineering), as well as alongside members of PLAKK, a medtech start-up that focuses on the development of image analysis software platforms for clinical research and healthcare applications. The coordinator will be responsible for the acquisition, selection, and analysis of ultrasonic images of atherosclerotic plaques.

This company is seeking a detail-oriented and thorough Clinical Research Assistant to assist in the conduct of clinical research studies. The Clinical Research Assistant will primarily perform quality control, organize and reconcile large amounts of imaging and clinical data, and resolve queries for neuroimaging studies. In addition, responsibilities will include the development and maintenance of study-related material and the conduct of other study-related activities while ensuring compliance with Biospective procedures, quality assurance requirements, and Good Clinical Practices. Reporting to Project Leaders, the Clinical Research Assistant will be part of a multidisciplinary

We are currently looking for a Quality Assurance Associate, for one of our clients, a CRO dedicated to the development and analysis of biological tests specialized in infectiology, metabolism and oncology. In this key role for the company, you will be responsible for monitoring and maintaining quality assurance systems and ensuring that good practice requirements are met.

We are currently looking for a Scientific Assistant in Protein Sciences, for one of our clients, a CRO dedicated to the development and analysis of biological tests specialized in infectiology, metabolism and oncology. The ideal candidate is motivated, dynamic and wants to be part of a growing project.

We are looking for Motivated Scientists to evaluate the immunogenicity and efficacy of new vaccine candidates. This role requires an in-depth knowledge of immunological techniques such as flow cytometer and ELIspot cell assays.

Senior Scientist – Full time senior scientist Protein Crystallography Ph.D. minimum 5 years demonstrated experience in the field. Ph.D. and post-doc in the field

We are looking for candidates to fill Research Associate and Scientist positions in our Chemisty department. The candidates specialized in organic synthesis and medicinal chemistry will be working from our new facilities in Saint-Laurent, Montreal. Nuchem provides integrated services to early drug discovery projects for our clients spanning from Medicinal Chemistry, ADME/PK, Biochemistry, Cell Biology and In Vivo Pharmacology, in the area of small molecule drug discovery.

This full time position will focus on designing data integration and multi-omics modeling strategies and supporting their implementation in the organization’s solutions in terms of population stratification (clinical trials, personalized medicine), target discovery and biomarker signature/endotype research.

We are looking for a motivated Scientific Research Associate to evaluate the immunogenicity and efficacy of new vaccine candidates. This role requires an in-depth knowledge of immunological techniques such as flow cytometer and ELIspot cell assays.

Associate Scientist – full time associate scientist production and purification of recombinant proteins in mammalian cells M.Sc. proven experience in the field

The specialized analyst or IT analyst will have to work in a context of major change and great complexity following the merger and integration of several institutions with dissimilar S/he will be responsible for working with teams across ICSU to help develop a cohesive, user-oriented environment and modern data architecture to standardize data collection and use across the organization, providing all data users with rapid access to relevant and quality data, thereby improving the delivery and quality of care and services.

In this role, you will work closely with a biostatistician more oriented towards computational biology and systems biologists who drive needs through their expertise in molecular biology, genetics and biomodeling. This full time position will focus on the design and prototyping of bioinformatics solutions with the major challenges of providing the most efficient solutions in terms of population stratification (clinical trials, personalized medicine), target discovery and research of signature/endotype biomarkers.

This full time position will focus on the design and prototyping of bioinformatics solutions with the major challenges of providing the most efficient solutions in terms of population stratification (clinical trials, personalized medicine), target discovery and research of biomarker signature / endotypes

Are you passionate about science? Do you have a positive attitude and a sense of leadership? Are you interested in the pharmaceutical industry? This role is for you! The candidate will have as tasks:

• Clean laboratory equipment (glassware)
• Clerical work
• Assist our laboratory analysts (store equipment)
• Stability management
• Printing controlled documents
• Records management
• Manage orders

The Laboratory Analyst is responsible for performing physical and chemical analyzes by applying pharmacopoeial analysis methods or those developed and validated by the company. He contributes to research activities by ensuring to maintain the quality of the products by respecting the requirements and the health / safety regulations on a daily basis. This person has an approach to solving analytical and practical problems while improving analytical methods.

The specialist analyst or analyst specializing in IT will have to work in a context of major change and great complexity following the merger and integration of several institutions with different facilities, missions and professions. He / she will be responsible for working with teams across the CIUSSS to help develop a cohesive, user-oriented environment and modern data architecture to standardize data collection and use. across the organization, giving all data users quick access to relevant, quality data, thereby improving the delivery and quality of care and services.

Taking into account the goals and objectives of the department, collaborates with the chief managers of functional teams in the review of business processes, including change management and communication plans, and in the implementation of new processes . Acts as a change agent by reviewing processes to identify opportunities and eliminate redundant or unnecessary tasks. Suggest new ways of working in order to reduce overall costs and improve the health and safety of colleagues, product quality and supply (lead time and reliability).

As a senior advisor, you will manage or lead the various IT architecture mandates under your responsibility. Through these mandates, you will contribute to the development and continual updating of the IT master plan, to the definition of orientations, norms and standards, and technological perimeters of its programs and projects.

Reporting to the Director of the Product Qualification Laboratory, the Quality, Compliance and Operational Projects Coordinator coordinates projects as well as all laboratory activities related to good manufacturing practices.

The Validation Coordinator is responsible for validating equipment, facilities, utility systems, cleaning, and IT systems according to quality rules, following GMP regulations, corporate compliance standards and all other relevant regulatory requirements.

• Design, write, review and edit as necessary, study plans, amendments and study schedules that define and plan all activities for bioanalytical validations.
• Validation (GLP) of quantitative assays for the analysis of pharmaceutical products in biological matrices by LC-MS/MS.
• Principal Investigator for analysis of incurred study samples, requiring interaction and co-ordination with the Study Director.
• Oversee and co-ordinate all aspects of laboratory work, preparation of GLP driving documents and instructions for the technical group, and ensure that projects are performed according to SOP and GLP.
• Project management and Client interaction.
• Prepare as necessary draft or final reports that document all laboratory procedures and results.
• Method troubleshooting, as required.

We are looking for AI developers to join our multi-disciplinary neurotech team. We are open to various degrees of collaborations: –

• leadership roles including company equity,
• student-entrepreneurs projects or internships,
• tech-transfer research agreements.

The night production operator will perform all the tasks of preparation, packaging of pharmaceutical products, cleaning and assembly of equipment, cleaning of rooms and work areas, inspection and controls required for the packaging of products. pharmaceuticals.

You carry out the different stages of the transformation process of organic products; You perform the tasks relating to the distribution of products to hospitals; You carry out partial or complete inventories of products and their derivatives; You complete and verify various controlled documents

Reporting to the Head of Epidemiology, Monitoring and Biological Risk Management, you provide the Vice-Presidency for Medical Affairs and Innovation, as well as for certain business sectors of the company, with support for the drafting of reports and scientific articles. , analysis methods, study protocols as well as any relevant documentation for the transfer of knowledge and the enhancement of the organization.

Participate in the drafting and / or revision, if necessary, of study schedules, study plans, amendments and interim and final reports of independent scientists and contributors. The Scientist I / II may be required to communicate promptly, orally or in writing, with study directors and / or sponsors on issues related to the study, and to produce and distribute interaction reports with study leaders. customers (CIR) in a timely manner. Oversee and coordinate all aspects of laboratory science procedures related to the study, whether performed within the department or by service departments. Know the standard operating procedures (SOP), good laboratory practices (GLP) and regulations published by the FDA, EPA, JMHW and OECD. Review and approve raw data. Ensure that a safe working environment is maintained by staff through adherence to safety procedures, the use of protective clothing and equipment, and the dissemination of relevant safety information. Notify Director of Laboratory Sciences and / or Scientific Director / Laboratory Manager of technical issues or deviations from budgeted costs as soon as they arise. Perform any other related task as assigned.

These people design and / or implement scientific testing strategies and studies. They direct test development, validation or study conduct, or They are involved in the preparation of materials [eg, proteins, nucleic acid, cells, etc.]. They review and interpret study data, communicate results to clients, and write final reports. They fulfill the role of project scientist, principal investigator, contributing scientist, project manager and study director as appropriate. They ensure compliance with protocols and all applicable Standard Operating Procedures [SOPs]. They troubleshoot and resolve technical or laboratory testing problems when scientific expertise is required. They may be required to present new technologies or improvements to existing technologies. They provide guidance to clients designing a program or experiment, working on interpreting specific data sets, or responding to questions from regulatory authorities as necessary.

• Develop, optimize and use flow cytometry and immunoserological techniques (ELISA, ECLs, Luminex) as well as cell assays (ELIspot, bioassay, etc.).
• Write scientific documents, correct and revise the results.
• Analyze scientific problems, diagnose / correct analytical methods and technical problems and interpret raw data.
• Responsible for the management of the scientific project and the technical staff related to the conduct of the study.
• The position involves laboratory work (50%) and project management (50%)

Responsibilities:

• Develop, optimize, validate and use immunoserological and ligand binding techniques (ELISAs, ECLs using Meso Scale Discovery technology).
• Write scientific documents, correct and revise the results.
• Analyze scientific problems, diagnose / correct analytical methods and technical problems and interpret raw data.
• Responsible for the management of the scientific project and the technical staff related to the conduct of the study.

Responsible for the design, conduct and reporting of Laboratory Science studies in an efficient, cost-effective manner and with maximum scientific quality. Research Scientist I / II scientifically directs analysts and other technical personnel associated with the conduct, interpretation and presentation of studies. We are looking for a Research Scientist for our Genetic Toxicology Department located in Senneville, QC.

Responsibilities:

• Works as an independent Director of Studies.
• Must ensure that projects are executed in accordance with the PNOs and GLP
• Must communicate with clients, for everything related to studies.
• Must contribute as needed to cost estimate projects in collaboration with the Scientific Director and / or the Marketing department.
• Attend scientific meetings or workshops at the discretion of the Scientific Director and / or Director of Laboratory Sciences.
• Attend discussions with clients regarding upcoming projects

The main responsibilities associated with this position are as follows:

• Support and improve formulas and manufacturing processes for current products or new products (Liquids / Semi-Liquids / Solids) in order to meet quality and compliance requirements as well as meeting commercial needs.
• Validate manufacturing processes for new and existing products.
• Provide technical support and solve problems related to the manufacture of products.
• Develop, review and approve master manufacturing documents.
• Qualify new raw materials and establish their specifications.
• Participate in projects for product launches, technology transfers, continuous improvement, product reformulations, etc.

The I QA specialist is responsible for ensuring that all operations and analyzes relating to the manufacture of products are carried out in accordance with licenses, applicable regulations and the expectations of our customers. It guarantees that the products released for use, sale or distribution are of satisfactory quality.

We are looking for a Scientific Templates Specialist to work remotely as part of a 1 year mandate to support the Senneville site.

Support for protocol and report templates will transfer and systematically analyze all protocol and report templates during the year 2021. Support for protocol and report templates will also be transferred:

• Upload and identify differences between all report and protocol templates for assigned sites
• Use high technical skills in Word and a good understanding of the application of formatting with styles, links, fields, references and other requirements to templates and sections of templates
• Collaborate with the department team
• Perform quality checks for other team members

We are looking for a GMP-Chemistry specialist for our Sainte-Foy site in Quebec. The specialist supports his sector by playing an expert role in GMP regulations as well as the process or technical process of his sector by setting up and improving the systems and activities related to his group.

Reporting to the Head of Quality Assurance – Operations, the incumbent is responsible for ensuring that the development of analytical products, processes and services is carried out in accordance with applicable regulations (Health-Canada, AATB, BPF, ISO 15189, ASHI, FACT, WMDA, CSA and others) and the expectations of our customers. He is responsible for ensuring that biological products and analytical results released are of satisfactory quality.

The packaging supervisor will:

• Perform activities to support operations
• Manage employees (tours, coaching, discipline, evaluation, schedule management, tasks, payroll, etc.)
• Know and enforce Good Manufacturing Practices (GMP) and company standards in terms of quality, health and safety
• Analyze and monitor quality and OHS issues
• Ensure that employees have the tools, information and training necessary to carry out their jobs
• Participate in process improvement
• Follow up on documentation (logbook, etc.)
• Assist in the hiring process (interviews)

Reporting to the department head, you perform a variety of specialized analyses in a production environment where good laboratory practices are rigorously applied.

Reporting to the department head, you perform a variety of specialized analyses in a production environment where good laboratory practices are rigorously applied.

Responsibilities:

• Supervise and simultaneously manage various R&D projects in the field of artificial intelligence, more specifically in biomechanics
• Ensure adequate follow-up with the various employees in the field university and industrial partners
• Develop and design databases: collect, process, analyze and large volumes of data from many data sources large-scale structured and unstructured.
• Study and analyze biomechanical analyzes
• Participate in the creation of clinical decision trees
• Participate in correlation and prediction analyzes
• Transfer and integration of AI methods into Emovi software solutions
• Keep abreast of the latest AI research in the field of biomechanics
• Document the different stages of R&D projects according to ISO 13485 standards and product development
• All other related tasks

Responsibilities:

• Supervise and simultaneously manage various R&D projects in the field of biomechanics
• Participate in the development of new technologies in connection with the assessment function of patients with musculoskeletal disorders
• Collaborate in the development of new applications integrating biomechanical data to personalize and monitor patient progress
• Ensure adequate follow-up with the various collaborators in the field university and industrial partners
• Carry out technological watches to be aware of the latest technologies implemented for the study of movement
• Document the different stages of R&D projects according to ISO 13485 standards and product development
• All other related tasks

Ventus is seeking a highly motivated experienced medicinal chemist to join our Chemistry team. We are looking for a talented, collaborative and dynamic scientist to support our research efforts, and help us build out our pipeline of preclinical programs. This role is a unique opportunity to contribute to a well-funded start-up, using breakthrough science to drug previously challenging targets.

Responsibilities:

• Perform and document quality tests on:
  • Emovi Knee3D software suite
  • Customer portal and cloud administrator
  • Integration with third party software
• Develop and write in partnership with the scenario development team for functional tests
• Quality tests and documentation of KneeKG systems before delivery to customers
• Software installation and update
• Software technical support for customers (answering service calls, solve and document requests and problems)
• Ensure that user needs are met during the testing phases
• All other related tasks

Main responsibilities:

• Manage the process of screening, qualifying, and selecting, and contracting with investigators, sites and vendors required for conduct of clinical trial.
• Ensure studies are on track for site initiation, patient recruitment, and enrollment, and take corrective actions where necessary to address issues.
• Develop SOPs and work instructions to assure internal files and clinical study files conform to Good Clinical Practice regulations and standards.
• Maintain surveillance of published literature/clinical results and competitive products across all pertinent indications for strategic purposes and use in regulatory submissions.
• Develops budgets for all clinical projects and adheres to company financial goals.

Responsible for executing the Aifred product development vision through actionable long and short-term medical software development and medical product deployment plans. Manages the Aifred software development, from requirements, architecture design, UX/UI, AI capabilities, product security to verification and validation, using 3rd party developer teams as required. Drives the Aifred product deployment at customer sites through planning and overseeing electronic medical records (EMR) integrations on time and on budget, and through building effective strategic liaisons and enabling appropriate knowledge sharing across various stakeholders.

The quality and regulatory consultant is involved in mandates with clients who are mainly medical devices manufacturers. Her experience in the field allows her to be also involved at AVISIO in the improvement of internal tools and services to support and actively participate in the development of the company.

This company, a leading pharmaceutical company is looking for a Senior Director, Clinical Affairs to join their team. Reporting to the Senior Vice-President, Medical Affairs and Chief Medical Officer, the Director will be responsible for the design of clinical trials including protocol development, clinical trial discussions with regulatory authorities, and development of the timeline and budget.

Responsibilities:

• Receipt of parts and components
• Assembly
• Software installation
• Quality tests
• Shipping
• Technical customer support
• All other related tasks

We are looking to hire highly motivated scientists to lead and support our research and development program. The incumbents will ensure that the timeline and milestones are met and may be asked to participate in the development of novel scientific strategies. As Modulari-T grows the candidate will be presented with challenging and exciting opportunities for career advancement.

Reporting to the Manager – Servers and Storage, you will act as a resource person in the architecture of the infrastructure and you will be responsible for its evolution and maintenance. You will participate in work aimed at setting up technological orientations and architecture, and evaluate complex issues affecting the server and workstation fleet. Finally, you will ensure that the optimal availability of the server environment is maintained.