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
Eligible for weekend compensation differential
Saturday-Tuesday:
Saturday & Sunday 10:00am-10:00pm
Monday & Tuesday 10:00am-6:00pm
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 & escalate 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), escalate 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 5KEUR)
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
Your profile :
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
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