Founded in Ireland in 1960, Bimeda is an international developer, manufacturer and marketer of veterinary pharmaceuticals and animal care products. In addition to distributing Bimeda branded products in over eighty countries world-wide, Bimeda also manufacture private label for distributors, agents and international companies. Bimeda has 9 manufacturing facilities based in Ireland, the UK, Canada, the US, Brazil, and China. The company employees over 1,000 employees worldwide and has its global headquarters in Carrickmines, Dublin, Ireland. Bimeda's North American headquarters are in Schaumburg, Illinois. To find out about career opportunities at Bimeda, visit bimedacareers.com
On-site · Cambridge
The specialist coordinates investigations into production incidents and deviations to ensure compliance with pharmaceutical regulations and cGMP. They are responsible for conducting root cause analyses, writing SMART investigation reports, and implementing corrective and preventive actions (CAPA).
On-site · Cambridge
Leads technology transfer, process validation, and lifecycle management of pharmaceutical products to bridge R&D and commercial manufacturing. Ensures robust manufacturing processes and drives continuous improvement across sterile and non-sterile platforms.
On-site
Job title: QC Analyst II Location: Cambridge, ON (In-office) Position Type: Full-time, regular Shift: Day Shift, Friday- Monday, 7:00am - 5:30pm Vacancy Status: This position is currently vacant AI Disclosure in Hiring: We do not use artificial intelligence to screen, assess, or select applicants Job Summary Reporting to the Quality Control Project Lead, the QC Analyst II is responsible for the analysis of raw materials, in-process, finished products and stability samples using various wet chemistry and instrumentation techniques to assure compliance to cGMP, SOPs and Bimeda quality standard…
On-site
Job Title: Validation Specialist Location: Cambridge, ON (In-Office) Position Type: Full-time regular Shift: Day Shift, Monday - Friday Vacancy Status: This role is currently vacant AI Disclosure in Hiring: We do not use artificial intelligence to screen, assess, or select applicants Job Summary Reporting to the Validation Manager, the Validation Specialist initiates and executes validation studies throughout the facility. Key Role Specific Requirements Interact with all levels of management and staff to manage and facilitate the validation process from inception to completion by enlisting…
On-site · Cambridge
Lead the rapid deployment of scalable automation solutions across North American manufacturing facilities to improve efficiency and reliability. Manage the end-to-end project lifecycle from concept and vendor sourcing to installation and post-go-live stabilization.
On-site
Job Title: QA Assurance Compliance Associate Location: Cambridge, ON Position Type: Full-time Regular Shift: Day Shift, Monday - Friday, 6:30am- 3:00pm Vacancy Status: This role will be vacant AI Disclosure in Hiring: We do not use artificial intelligence to screen, assess, or select applicants Job Summary Reporting to the QA Compliance Associate, this role will work within an established culture of quality assurance and continuous improvement in all GMP areas. This role will be directly involved in all areas of quality assurance, including change controls, Annual Product Reviews (APRs), rev…
On-site
Job Title: Non-Sterile Batcher Location: Cambridge, ON (On-Site) Position Type: Full-time regular Shift: Afternoon Shift, Monday - Friday (3:00PM - 11:30PM) Vacancy Status: This role is currently vacant AI Disclosure in Hiring: We do not use artificial intelligence to screen, assess, or select applicants Job Summary Reporting to the Production Supervisor, the Non-Sterile Batching Operator manufactures quality pharmaceutical products by following all relevant Standard Operating Procedures (SOP), Master Batch Records (MBR), and Health and Safety requirements in compliance with cGMP. We are cu…
On-site
Job title: Sterile Batcher Location: Cambridge, ON (In-office) Position Type: Full-time, regular Shift: Afternoon Shift , Monday-Friday, 3:00pm - 11:30pm Vacancy Status: This position will be vacant in May 2026 AI Disclosure in Hiring: We do not use artificial intelligence to screen, assess, or select applicants Job Summary Reporting to the Production Supervisor, the Sterile Batching Operator manufactures quality pharmaceutical products by following all relevant Standard Operating Procedures (SOP), Master Batch Records (MBR), and Health and Safety requirements in compliance with cGMP. Compe…
On-site · Cambridge
The Maintenance Millwright provides expert mechanical support for building services, manufacturing, and packaging operations. Responsibilities include troubleshooting, preventative maintenance, and repairing cGMP process equipment and utility systems.
