A premier international CDMO, making success more certain.
Taipei, Taiwan
Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in complex oral solid dose, liquids, semi-solids, opthalmics, biologics, and sterile injectable products. We provide early phase clinical through to commercial manufacturing with full packaging capabilities to biopharma companies worldwide. Bora owns and operates in ten state-of-the-art CGMP manufacturing facilities across Asia and North America – delivering to more than 100 markets around the world. Our sites have the highest international standards for manufacturing, packaging, R&D and analytical testing. As a future focused CDMO, we know better than most that our own success is shaped by our partners victories. That's why, when you choose Bora - we make success more certain by following Bora’s 5Ps – Promises, Partnerships, Pride, People, and Progress. These 5 principles are Bora’s Pledge to our customers. Follow us to find out more and keep up to date with Bora Pharmaceuticals.
On-site · Mississauga
The QC Stability Coordinator Assistant is responsible for maintaining the stability program, including managing sample inventory and monitoring stability chambers. They will also assist in data review, trending, and the preparation of stability reports for regulatory submissions.
On-site · Mississauga
Lead and manage the quality team to support significant projects, including new client onboarding and the manufacturing of development, clinical, and validation batches. Oversee quality documentation, deviation investigations, CAPAs, and represent the quality department during client and regulatory inspections.
On-site · Mississauga
Lead the quality team in managing the onboarding of new clients and the manufacturing of development, clinical, and validation batches. Oversee quality documentation, regulatory inspections, and the transition of projects into routine business operations.
On-site · Mississauga
The Controls Engineer will provide technical support for automation and control systems while leading cross-functional teams to implement equipment improvements. They are responsible for designing, specifying, and qualifying control systems while ensuring compliance with GMP and safety standards.
On-site · Mississauga
The Quality Manager is responsible for overseeing operational quality activities, including product release, deviation investigations, and ensuring compliance with GMP standards. They also lead, coach, and mentor the quality team while serving as a primary point of contact for customers and regulatory authorities.
On-site · Mississauga
The QA Compliance Specialist provides quality support for new project transfers and ensures GMP compliance across analytical, engineering, and production departments. Key duties include managing compliance requirements, leading investigations, and overseeing supplier management programs.
On-site · Mississauga
Responsible for the preventative, predictive, and routine maintenance of pharmaceutical manufacturing and packaging equipment to ensure maximum efficiency and reliability. This includes diagnosing malfunctions, performing complex repairs, and collaborating on equipment installation and validation projects.
On-site
About Bora Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing, and packaging of complex oral solid dose, liquid, semi-solid, biologics, and sterile injectable pharmaceutical products. From our world-class sites in North America and Asia, we deliver drug products with unparalleled quality to more than 100 markets around the world. Bora’s teams, technologies, and facilities work seamlessly together to enable our clients to deliver much-needed therapeutics to pat…
Hybrid · Mississauga
The HR Manager develops People & Culture strategies and oversees day-to-day HR activities for employees in Canada and the US. Key duties include managing performance reviews, leading workplace investigations, and advising leadership on employment legislation and talent development.
On-site · Mississauga
Responsible for the preventative, predictive, and routine maintenance of pilot plant equipment to support pharmaceutical formulation and scale-up. The role involves troubleshooting, repairing, and validating equipment while ensuring strict adherence to GMP standards.
