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Manufacturing Technician I - Live Downstream
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 :
Location: Lenexa, KS
Job Summary and Purpose: |
The Live Downstream Lab Technician I will work directly with a range of equipment including batching vessels, filling machines, capping machines and lyophilizers.
The Live Downstream Lab Technician I will work directly with live antigen, batching solutions and semi-finished products following aseptic technique and cGMP procedures.
Responsibilities and Key Duties: |
* Set up and turnaround of all process equipment
* Work with chemicals, steam, and pressurized vessels
* Operation of batching vessels, filling machines and capping machines
* Perform environmental monitoring during aseptic procedures
* Use aseptic technique during processes
* Perform APHIS certified sampling procedures
* Operate general production equipment such as autoclaves, pumps, scales, particle monitors, etc.
* Prepare solutions
* Perform daily cleaning and sanitation laboratories and equipment
* Assemble batching and filling equipment for use in processes
* Follow standard operating procedures (SOPs)
* Document and maintain activity records according to cGMP regulations
* Maintain an effective working relationship with others
* Perform all other duties assigned
* Utilize acceptable PPE and follow safety procedures
Core Competencies: |
* Solutions out of complexity - Work and evolve with immediate environment
* Client focus - Make sure needs and requests are treated equally and in a positive way
* Collaborate with empathy - Fully take part in the working group to share information, listen to others and have a clear idea of the decisions taken
* Engage and develop - Open to share knowledge and to receive feedback from others
* Drive ambition and accountability - Ensure accuracy of work with the use of KPI's and a responsible commitment
* Influence others -Show structure, confidence, and an ability to synthesize while speaking
Technical / Functional Competencies: |
* Excellent writing and communication, interpersonal and organization skills
* Good self-discipline and attention to details
* Must follow proper documentation procedures
* Must be able to work both independently and in a fast pace team environment
* Good math and computer skills
* Must have flexible work hours, and be willing to work outside of normal, scheduled hours; as necessary
* Must be able to work alternative shift hours and weekends as required
* Must possess planning and time-management skills
* Excellent communication skills, both written and verbal
* Demonstrated basic mechanical aptitude and problem solving skills
Qualifications: |
Education - Associate/Bachelor's degree in Life Science preferred but not required
Work Experience - Experience in a cGMP environment is preferred
Other (consider certifications, specialized knowledge and/or training, etc.) -
* Knowledge of cGMP and CGLP procedures is desirable
* Experience with Lean Manufacturing is preferred
Physical Requirements: |
* Ability to read, write legibly and understand English
* Color vision, frequent fine motor movements of the hands and wrist, periods of short term balancing, bending, stooping, squatting, twisting and reaching below knees to above shoulders
* Ability to stand and walk >90% of work day
* Ability to push/pull 50 lbs, up to 120 lbs occasionally
* Ability to lift up to 35 lbs overhead, up to 50 lbs overhead occasionally
* Ability to carry up to 50 lbs
* Ability to get up from seated on the floor to standing without assistance
* Ability to dress and operate in clean room environments
Working Conditions: |
* Must be able to tolerate cold working areas
Travel Required: |
* N/A
This job description is intended to convey information essential to understanding the scope of the job and general nature and level of work performed by job holders within this job. This job description is not intended to be an exhaustive list of qualifications, skills, duties and responsibilities or working conditions associated with the job. This job description is not an employment contract. Ceva reserves the right to modify job duties and/or job descriptions at any time to meet the needs of the business.
*VEVRAA Federal Contractor
**Ceva is an equal opportunity employer and all qualified applicants will be considered for employment without regard to race, color, religion, sex, national origin, age, genetic information, actual or perceived sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. Ceva encourages men and women, members of all racial and ethnic groups, individuals with disabilities and veterans to apply.
669B
Your profile :
Education - Associate/Bachelor's degree in Life Science preferred but not required
Work Experience - Experience in a cGMP environment is preferred
Other
* Knowledge of cGMP and CGLP procedures is desirable
* Experience with Lean Manufacturing is preferred