Production Laboratory Technician (M-F 2:00-10:00pm)

CEVA SANTE ANIMALE; Guelph; On-site; CAD 48,000 - 59,000; Full time

Job summary

Ceva Animal Health is seeking a Production Laboratory Technician for our Guelph, ON facility. The role includes vaccine production activities in a GMP environment, ensuring quality, safety, and accurate documentation, while driving continuous improvement on the line.

The position operates Monday–Friday from 2:00 pm to 10:00 pm and requires a technical college diploma with GMP experience; bioreactors knowledge is a plus. Located in Guelph, the role supports a diversified animal health portfolio.

Qualifications

• Bachelors or equivalent in chemical/biological fields is preferred.
• Experience in GMP laboratory environments is required or highly desired.
• Experience with bioreactors or vaccine production processes is a plus.

Responsibilities

• Carry out vaccine production operations in accordance with GMP, safety, and quality standards.
• Propose and implement productivity improvements and maintain organized workstations.
• Perform calibration, documentation, and batch record review.
• Ensure compliance with 5S and housekeeping standards and participate in audits.

Education

Technical College diploma in a related technical / biological field

Bachelor's degree in chemical, biological or Engineering Technology considered an asset

Tools

Bioreactors

Job description

The success of a company depends on the passionate people we partner with.

Together, let's share our talents.

As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing , producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet.

We are committed to ensuring the highest possible level of care and well-being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife.

Indeed, Our “Together, Beyond Animal Health” vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach.

As part of our “Diversity, Equity and Inclusion” policy, Ceva Animal Heath is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team.

Your Missions

Production Laboratory Technician

Monday-Friday, 2:00-10:00pm

The Vaccine production operator carries out manufacturing operations in accordance with appropriate procedures, in compliance with HSE standards, productivity targets and quality standards (GMP, hygiene). Propose ideas to improve productivity and they own their environment (workstations organization, quality and safety). The operator will propose ideas to improve productivity and take accountability for their workspace He/she is responsible for the daily activities of the laboratory and ensures they meet the appropriate specifications for the production of animal vaccines (harvesting, purification and aseptic filling activities). The Vaccine production operator will participate in the construction of the new documentation system and the validation of the equipment and processes (clean zone, autoclaves, centrifuge, tangential flow filtration system).

Responsibilities

• Suggest set-up of the team’s work in daily Tier 1 based on the given production schedule
• Execute production planning, reporting quality standards
• Inform & elevate in case of issue or in case can’t solve/deviation
• Monitor & improve his activity on continuous basis
• Close & control work orders
• Complete the processing, documentation and cleaning in an aseptic processing area
• Work independently, complete daily tasks accurately and efficiently
• Collect samples from various tanks, surfaces and environment
• Perform equipment and instrument calibrations according to established procedures
• Identify and report irregularities identified with any aspects of work
• Review production batch records
• Respect operating time yield standards
• Analyze some variances and propose implementation of action plans
• Set-up/write SOP’s
• Apply all standards (environment, quality, safety/ HSE, aseptic, cost)
• Perform In-Process Controls (IPC)
• Complete and check batch reports
• Raise alert in case of dangerous situations, near miss/miss, QA deviation etc
• Run internal audits
• Participate in writing new SOP and Batch Production Records
• Ensures 5S standards are met and maintained
• Follows all health and safety rules and regulations
• Participate in the validation process with guidance
• On the assigned workstations, ensure that CPS standards are applied
• Update & monitor performance indicators on his/her line/zone, analyse gaps, propose and perform resolution actions
• Propose and implement ideas for improvement (short/medium term)
• Carry out process confirmation as provided by the corresponding planning function
• Guarantee compliance with performance and workshop storage standards in the assigned workshops; raise alert if needed
• Ensure first level of maintenance and changeovers (=clean machines and keep them in good condition), elevate if any deviation/issue
• Act as a responder for incoming spill calls. Be part of the spill response team
• Suggest small CAPEX investments to improve performance (below 5K€)
• Actively participate in occasional site/department projects and in continuous improvement workshops
• Share good practices
• Train temporary workers and/or junior operators
• Own personal development: know skill matrix and suggest training to supervisor
• Perform other duties as assigned

Competencies

• Drive Ambition & Accountabilities
• Influence Others
• Collaborate with Empathy
• Engage & Develop
• Shape Solutions out of Complexity
• Client Focus

Qualifications

• Technical College diploma in a related technical / biological field.
• A bachelor's degree in chemical, biological or, Engineering Technology is considered an asset
• Experience in lab GMP environment.
• You have previous experience with Bioreactors

Disclosures

• This requisition is for a current opening at our Guelph, ON facility
• Standardized annual compensation is $53,833.82