Specialist Manufacturing, Documentation
4 months ago
The Biologics Manufacturing Center (BMC) inc. is a new bio-manufacturing facility whose construction was completed in June 2021. As a not-for-profit organization having a public interest mandate, BMC is a key player in Canada's ability to respond rapidly to future national and global health emergencies. In addition, BMC supports projects of public interest, actively contributes to the overall growth and resilience of the Canadian life sciences industry and fosters industry development and innovation through Canadian production. Designed to manufacture biopharmaceuticals such as viral vector, protein subunit and virus-like particle vaccines, as well as other biologics, BMC is helping to increase domestic biomanufacturing capacity, ensuring that vaccines and other biologics can be made safely in Canada, for Canadians. With its committed and innovative employees, BMC fosters a culture of agility and transparency with a collaborative, results-oriented approach. Join us in supporting the public health of CanadiansThe BMC is looking for a **Specialist Manufacturing, Documentation** who will use his advanced knowledge in production and Good Manufacturing Practices (GMP) to support the quality activities of the Manufacturing team and projects related to the production.Under the supervision of the Director of manufacturing, the **Specialist Manufacturing, Documentation** **will have the following responsibilities:
- Create, draft, review and update production documentation: batch production record (BPR), work instruction (WI), standard operating procedure (SOP) based on corrective and preventive actions (CAPA), change control requests (CCR), and coordinate with other units the programming of training related to changes;
- Follow up on the resulting CAPAs that are defined as part of an investigation or continuous improvement, facilitating the completion of the necessary activities by stakeholders to ensure that actions are closed on time;
- Initiate, investigate, perform root cause analysis, and determine corrective actions for production related deviations;
- Manage CCR from end to end - write, present to the evaluation committee, follow up of evaluations, create of require actions, follow-up and closure of actions - which are defined following a CAPA or a continuous improvement project or for the modification of SOPs, BPR, logbooks and work instructions;
- Proactive contribute to quality control activities and their documentation from a GMP perspective;
- Play a key role in the initial, ongoing and strengthening training of GMP with Technologists Manufacturing;
- Support on key projects for production - introduction of a new equipment (CR, validation support), data integrity, etc.;
- Support for the review of production documents - i.e. logbook, BPR, etc;
- Support the implementation and maintenance of the data integrity management program in manufacturing.
**You are the person you are looking for if**:
- You hold at least a college diploma in life science/biotechnology or other appropriate discipline;
- You have three (3) years of experience in the pharmaceutical industry, in production and in a GMP role. Experience with vaccines is strongly preferred;
- You have knowledge of data integration management and IT system validation programs and an experience would be an interesting asset;
- You have a talent for writing procedures, batch records, detailed and clear protocols;
- You are customer-oriented, have good communication skills, a good spirit of collaboration and a great sense of organization and priority management.
**What we offer**:
- A respectful and friendly work environment in a new facility with state-of-the-art equipment;
- A competitive salary aligned with your skills;
- Attractive vacations allowances;
- A full range of benefits: group insurance, telemedicine, group RRSP and EAP;
- Teleworking;
- On-site parking.
-
Supervisor Manufacturing, Documentation
5 months ago
Montréal, Canada Centre de production de produits biologiques Inc Full time**Supervisor Manufacturing, Documentation** The Biologics Manufacturing Center (BMC) inc. is a new bio-manufacturing facility whose construction was completed in June 2021. As a not-for-profit organization having a public interest mandate, BMC is a key player in Canada's ability to respond rapidly to future national and global health emergencies. In...
-
Technical Documentation Specialist
4 months ago
Montréal, Canada WeighPack Systems Inc Full time**Who we are**: - WeighPack has become a leader in developing and manufacturing Packaging Machinery solutions worldwide alongside our partner companies in the US, Italy, and China. Our diverse and multi-disciplined team of professionals are fun and exciting to work with as our general population are skilled labor committed to growth. We are a transparent...
-
R&d Documentation Specialist
5 months ago
Montréal, Canada Boston Scientific Corporation Full time**Work mode**:Hybrid**Onsite Location(s)**:Montreal, QC, CA**Additional Location(s)**: Canada-QC-Montreal**Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance** - At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees,...
-
Document Specialist
4 months ago
Montréal, Canada Davies Ward Phillips & Vineberg LLP Full timeAbout Davies Davies is a top-tier Canadian law firm focused on high-stakes matters. With offices in Montreal, Toronto and New York, we are consistently at the centre of the most challenging deals and cases in Canada and abroad. A position at Davies is more than just a job. When you join the firm, you will be welcomed by a team that places as much emphasis...
-
Director, Manufacturing
3 months ago
Montréal, QC, Canada Centre de production de produits biologiques Inc Full timeThe Biologics Manufacturing Center ( BMC ) Inc. is a new biomanufacturing facility created in response to the pandemic. A not-for-profit organization, the BMC aims to better meet the biopharmaceutical needs of Canadians. The BMC helps support projects of public interest, actively contributes to the overall growth and resilience of the Canadian life sciences...
-
Specialist, Quality System
5 months ago
Montréal, Canada Centre de production de produits biologiques (CPPB) Inc. Biologics Manufacturing Centre (BMC) Inc. Full timeThe Biologics Manufacturing Centre (BMC) Inc. is a new 54,900 square foot biomanufacturing facility whose construction was completed in June 2021. The BMC, a not-for-profit organization, supports the expansion of Canada’s biologics manufacturing capacity, ensuring that vaccines and other related products can be safely manufactured at home. BMC is designed...
-
Qms and Documentation Specialist
2 weeks ago
Montréal, QC, Canada Medisca Pharmaceutique Inc Full time**Medisca** is a global corporation with locations throughout North America, Australia, and Europe, that contributes to healthcare by leveraging strong partnerships that deliver customized solutions with an unwavering commitment to quality and innovation. Backed by 30+ years and a strong foundation in pharmaceutical compounding, **Medisca** is a...
-
Document Management Specialist
2 months ago
Montréal, QC, Canada Via HFR Full timeAt VIA HFR, we are re-imagining passenger rail service on behalf of the Government of Canada! Our goal is to create a new sustainable train network that that will run faster, more often and will be more reliable between Toronto and Québec City. The HFR project is Canada's largest infrastructure project in generations. Are you ready to take on a stimulating...
-
Manufacturing Operations Administrator
5 months ago
Montréal, Canada Bixlers Full time**MANUFACTURING OPERATIONS ADMINISTRATOR** **SUMMARY** The Manufacturing Operations Administrator will work with both the manufacturing and purchasing team to launch jobs into production, update existing work orders, run manufacturing reports for the operations team, and assist in maintaining accurate data collection. This position will report to the...
-
Engineer, Manufacturing Engineering
3 weeks ago
Montréal, QC, Canada Boston Scientific Gruppe Full timeSenior Prototype Manufacturing Engineer - Electrophysiology Onsite Location(s): Montreal, QC, CA Canada-QC-Montreal Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing...
-
Manufacturing Technician
4 months ago
Montréal, Canada G Canada Therapeutics Full timeDo you want to join an international team working to improve the future of healthcare? Do you want to improve the lives of millions of people? Grifols is a global healthcare company which, since its foundation in Barcelona in 1909, has been working to improve the health and well-being of people all over the world. Our four divisions - Bioscience, Diagnostic,...
-
Training and Documentation Specialist
4 months ago
Montréal, Canada Manulife Full timeWe are a leading financial services provider committed to making decisions easier and lives better for our customers and colleagues around the world. From our environmental initiatives to our community investments, we lead with values throughout our business. To help us stand out, we help you step up, because when colleagues are healthy, respected and...
-
Legal Document Production Specialist
1 month ago
Montréal, QC, Canada INNER CIRCLE AGENCY Full time**Job Opportunity**: Legal Document Production Specialist (Litigation) - 100% Remote - Montreal, QC **Position Details**: - Location: 100% Remote, based in Montreal, QC - Salary: $50,000 to $80,000 annually depending on experience plus benefits **About the Role**: Start a new chapter in your professional journey with our esteemed law firm. Enjoy the...
-
Document Specialist, Residential Mortgages
5 months ago
Montréal, Canada CMLS Financial Full time**Document Specialist, Residential Mortgages** **Montreal, QC** **About the role**: - Establish and maintain positive relationships with broker partners - Interact with mortgage brokers for the collection of all required documents to satisfy all broker conditions - Review and verify accuracy of required documentation, including, but not limited to;...
-
Document Specialist, Residential Mortgages
4 months ago
Montréal, Canada CMLS Financial Full time**Document Specialist, Residential Mortgages** **Montreal, QC** **Salary Range**:$50,000 - $65,000/yr **About the role**: - Establish and maintain positive relationships with broker partners - Interact with mortgage brokers for the collection of all required documents to satisfy all broker conditions - Review and verify accuracy of required...
-
Document Control Officer
4 months ago
Montréal, Canada BBA Full time**Type of position**: Regular **With us, you’ll get the opportunity to...** - Monitor document quality and ensure engineering documents are processed and saved properly. - Save client and vendor documents in the computer system. - Ensure document control procedures are applied. - Validate transmission slip consistency. - Advise and support project team...
-
Manufacturing Technician
5 months ago
Montréal, Canada G Canada Therapeutics Full timeDo you want to join an international team working to improve the future of healthcare? Do you want to improve the lives of millions of people? Grifols is a global healthcare company which, since its foundation in Barcelona in 1909, has been working to improve the health and well-being of people all over the world. Our four divisions - Bioscience, Diagnostic,...
-
Manufacturing Technician
4 weeks ago
montréal (saint laurent), Canada Thorlabs Canada ULC Full timeAbout the RoleWe are seeking a skilled Manufacturing Technician to join our team at Thorlabs Canada ULC. As a key member of our production team, you will be responsible for manufacturing high-quality optical structures and components.Key ResponsibilitiesManufacture fused optical structures with precision and accuracy.Record and track manufacturing data in...
-
Manufacturing Technician
4 weeks ago
montréal (saint laurent), Canada Thorlabs Canada ULC Full timeAbout the RoleWe are seeking a skilled Manufacturing Technician to join our team at Thorlabs Canada ULC. As a key member of our production team, you will be responsible for manufacturing high-quality optical structures and components.Key ResponsibilitiesManufacture fused optical structures with precision and accuracy.Record and track manufacturing data in...
-
Specialist, Documentation
5 months ago
Montréal, Canada Jubilant Pharma Holdings Inc. Full timeEnglish description below. Êtes-vous prêt à vous lancer dans une aventure passionnante où votre expertise en matière de documentation et d'enquête sur les dispositifs médicaux peut briller de tous ses feux ? Rejoignez-nous chez JDI, où votre rôle en tant que **spécialiste de la documentation et de l'investigation des dispositifs médicaux** n'est...