2 to 4 Year Degree (science background preferred) and/or 0-3 years of relevant experience
Knowledge of cGMP/GLP requirements
Experience with Microsoft Office software (Word, Excel, and PowerPoint)
Strong attention to detail
Ability to work well independently and as a part of a team, and to work effectively with people at all levels within the organization
Ability to follow detailed instructions with coaching
Willingness to positively embrace change and flexibility in adjusting to changing priorities
Gain proficiency in 50% of the testing in a specified area
Preferred: Experience with cell culture and/or egg-based propagation of viruses
Preferred: Experience using aseptic technique
Preferred: Work experience in a cGMP/GLP environment
Physical: Must be able to walk, sit, or stand for long periods of time
Physical: Must be able to reach above shoulder level, bend/stoop, kneel, push/pull, and handle/grip frequently
Physical: Must be able to work scheduled 40 hours with the ability to work overtime as needed
Physical: Frequent lifting and carrying of 5 to 25 lbs
Physical: Regular reaching, bending, stooping, and twisting
Physical: Repetitive motion and substantial movement of the wrists, hands, and/or fingers
Physical: Ability to grasp and manipulate objects like pipettors, flasks, and bottles
Physical: Flexibility to cover rotating weekend duties
Responsibilities
Testing of blended vaccines and antigen stocks for potency, extraneous agents, inactivation, and identity using egg based and tissue culture-based methodology
Maintain testing schedules and prioritization of testing to ensure timely completion of assays to meet the established release dates
Following GMP documentation guidelines. Completion of test records and system data entry
Basic problem-solving skills and demonstrate trouble shooting ability and writing Laboratory Investigations when necessary, utilizing Method 1 and the DMAIC process
Contribute to the team’s productivity goals
Cleaning and maintaining lab equipment, instrumentation, and facility
Testing of samples from manufacturing to ensure Quality and compliance according to all applicable assays utilizing good aseptic practices
Maintaining testing schedules and reagent supply
Completion of documentation following cGMP guidelines
Following all Zoetis Quality Standards, Policies and Procedures
Providing minimum input for laboratory investigations (LIR), minimal project support
Understanding of the QC software packages used during routine work
Pipette work and analytical techniques
Preparation of media and reagents
Equipment monitoring
Properly utilize computer software used during routine work
Understand and execute excellent aseptic technique
Perform egg drilling, candling, and other egg manipulations
Perform culture of primary and continuous cell lines
Participate in Media Fill inspections
Participate in all required training activities
Work in a safe manner and follow safety policies and procedures
Demonstrate basic problem-solving skills and troubleshooting ability
Perform basic laboratory math accurately (dilutions, titrations, cell counts, etc.)
Record procedures and results using proper cGMP documentation
Effectively work in a team environment and communicate with multiple departments