Sterile Batcher (Afternoon) Monday-Friday, 3:00pm

About the role

Bimeda is seeking a dedicated Sterile Batcher to join our team in Cambridge, Ontario. This full-time position offers an opportunity to work in a dynamic environment where you will play a crucial role in the production of high-quality veterinary pharmaceuticals. The Sterile Batcher will be responsible for ensuring that all batching processes are carried out in compliance with industry standards and company protocols. This role is integral to maintaining the integrity of our products and ensuring that they meet the stringent quality requirements expected by our clients.

Key facts

What you'll do

• Prepare and assemble materials and equipment necessary for sterile batching processes, ensuring all items meet quality standards.
• Operate and monitor batching equipment, making adjustments as needed to maintain optimal performance and product quality.
• Follow strict protocols for sterilization and sanitation to prevent contamination during the batching process.
• Document all batching activities accurately, including ingredient quantities, batch numbers, and any deviations from standard procedures.
• Collaborate with quality assurance teams to conduct regular inspections and audits of the batching area and processes.
• Troubleshoot and resolve any issues that arise during the batching process, ensuring minimal disruption to production timelines.
• Participate in training sessions to stay updated on best practices and new technologies related to sterile batching.
• Maintain a clean and organized work environment, adhering to safety protocols and company policies at all times.
• Assist in inventory management by tracking raw materials and supplies needed for batching operations.
• Contribute to continuous improvement initiatives by providing feedback on processes and suggesting enhancements.
• Work closely with other team members to ensure efficient workflow and communication throughout the production cycle.
• Ensure compliance with all regulatory requirements and company policies related to sterile manufacturing.

Requirements

• High school diploma or equivalent; a degree in a relevant field is preferred.
• Minimum of 2 years of experience in a manufacturing or production environment, preferably in the pharmaceutical or veterinary industry.
• Familiarity with Good Manufacturing Practices (GMP) and quality control processes.
• Strong attention to detail and the ability to follow detailed instructions accurately.
• Excellent problem-solving skills and the ability to work under pressure in a fast-paced environment.
• Effective communication skills, both verbal and written, to collaborate with team members and report findings.
• Ability to lift and move materials weighing up to 50 pounds as needed.
• Proficiency in using basic computer software for documentation and reporting purposes.
• Willingness to work flexible hours, including potential overtime as required by production demands.

Nice to have

• Experience with sterile compounding or aseptic processing in a pharmaceutical setting.
• Certification in a relevant field, such as a pharmacy technician or similar qualification.
• Knowledge of safety regulations and hazardous materials handling.
• Previous experience with inventory management systems or ERP software.
• Familiarity with laboratory equipment and sterile manufacturing processes.
• Bilingual abilities in English and French are an asset.

Skills & tools

• Strong organizational and time management skills to prioritize tasks effectively.
• Ability to work independently as well as part of a collaborative team.
• Proficient in using personal protective equipment (PPE) and following safety protocols.
• Familiarity with laboratory equipment and machinery used in sterile batching.
• Basic computer skills for data entry and documentation purposes.

Practical notes

• This position is based in Cambridge, Ontario, and candidates must have valid work authorization in Canada.
• The work schedule is Monday to Friday, starting at 3:00 PM, with potential for overtime based on production needs.
• Interested candidates can apply through the Bimeda career portal at the provided URL.
• Additional training and onboarding will be provided to ensure all new hires are equipped to succeed in their roles.
• Bimeda is committed to fostering a diverse and inclusive workplace and encourages applications from all qualified individuals.