Quality/Regulatory Manager - Canada-Nova Scotia-Windsor

The Manager of Quality & Regulatory oversees a dynamic team of microbiologists and environmental technicians to provide timely and accurate microbiological testing and environmental monitoring in support of the manufacturing of pharmaceuticals. · ...

BIOVECTRA is recognized as a leader in the contract development and manufacturing space of active pharmaceutical ingredients specializing in clinical-to-commercial scale production for microbial fermentation. · ...

The Manager of Quality Operations, Microbiology oversees a dynamic team of microbiologists and environmental technicians to provide timely and accurate microbiological testing and environmental monitoring in support of the manufacturing of pharmaceuticals. · Developing senior mem ...

BIOVECTRA is recognized as a leader in contract development and manufacturing space of active pharmaceutical ingredients. · Within Agilent's Advanced Manufacturing Partnerships Division (AMPD), you will have the opportunity to work with cutting-edge technologies and collaborate w ...

Biovectra joined Agilent in 2024 and is part of Agilents Advanced Manufacturing Partnerships Division (AMPD), which also contains Agilents Nucleic Acid Solutions Division. With BIOVECTRA, Agilent aims to align advanced manufacturing capabilities, expertise and resources to foster ...

BIOVECTRA is a leading contract development and manufacturing company of active pharmaceutical ingredients. · ...

The EHS Program Manager will be responsible for managing and implementing environmental health and safety programs across multiple locations. This includes developing and implementing policies, procedures, and training programs to ensure compliance with regulatory requirements. · ...

The Director of Engineering and Maintenance is responsible for the building equipment and system performance of a cGMP manufacturing facility. The Director leads manages and coaches engineering validation maintenance and capital project staff to ensure equipment systems are desig ...

BIOVECTRA is a leader in the contract development and manufacturing space of active pharmaceutical ingredients. · The Technical Investigations Lead leads the site investigation program for manufacturing events. · ...

BIOVECTRA supports over 100 clients in contract development and manufacturing space of active pharmaceutical ingredients. · ...

Biovectra is a leader in contract development and manufacturing of active pharmaceutical ingredients. As a Quality Assurance Associate, you will work with cutting-edge technologies and collaborate with a team of dedicated professionals committed to revolutionizing advanced manufa ...

BIOVECTRA, now a part of Agilent, is recognized as a leader in the contract development and manufacturing space of active pharmaceutical ingredients specializing in clinical-to-commercial scale production for microbial fermentation, synthetic small molecules including ADC, HPAPI. ...

BIOVECTRA joined Agilent in 2024 and is part of Agilent's Advanced Manufacturing Partnerships Division (AMPD), which also contains Agilent's Nucleic Acid Solutions Division. With BIOVECTRA, Agilent aims to align advanced manufacturing capabilities, expertise and resources to fost ...

BIOVECTRA is recognized as a leader in the contract development and manufacturing space of active pharmaceutical ingredients specializing in clinical-to-commercial scale production for microbial fermentation, synthetic small molecules including ADC, HPAPI, plasmid DNA, mRNA, LNP ...

The Director of Engineering and Maintenance is responsible for the building equipment system performance of a cGMP manufacturing facility.This role leads manages coaches engineering validation maintenance capital project staff ensuring equipment systems designed installed consist ...

BIOVECTRA is recognized as a leader in contract development and manufacturing space of active pharmaceutical ingredients. With over 650 employees at both Windsor and Charlottetown sites, BIOVECTRA supports over 100 clients. · The Production Technician will operate, monitor and ad ...

The Technical Investigations Lead leads the site investigation program for manufacturing environmental contamination and process-related events ensuring timely compliant scientifically sound investigations and drives the effectiveness of CAPAs that impact Windsor biologics operat ...

+ BIOVECTRA is recognized as a leader in the contract development and manufacturing space of active pharmaceutical ingredients. + Key Responsibilities include ensuring robust systems are used throughout the technology transfer exercise, performing process engineering analysis, pa ...

BIOVECTRA is recognized as a leader in the contract development and manufacturing space of active pharmaceutical ingredients. · The Technical Investigations Lead leads the site investigation program for manufacturing events. · ...

The Process Steward/Sanitation Technician will be responsible for executing routine production operations with the highest regard for safety, excellence and quality. Sanitizing and cleaning of an industrial clean room environment where pharmaceuticals are manufactured to include, ...