What are the responsibilities and job description for the MFG Associate-Filling & Visual Inspection position at Aequor?
MFG Associate-Filling & Visual Inspection
Location: Fremont, CA
Duration: Contract till Oct 2026 with possibility to extend
3rd Shift: Sun-Thurs-10PM-6:30AM
Duties:
Ability to independently and accurately prepare all assigned records, calculations, and documentation.
Demonstrated ability to independently and properly handle and dispose of hazardous waste.
Ability to read and follow schedules, procedures, and documents.
Demonstrated knowledge of safety precautions and procedures.
Will be required to assist in training other employees in an area of responsibility as assigned.
Assist staff in developing new procedures and methods or improving old ones.
Ability to practice aseptic techniques independently.
Ability to perform media fills with (process simulation testing) with passing results per applicable SOP.
Ability to perform clean room gowning and pass clean room garment validation consecutively.
Ability to independently prepare disinfectants and sanitizing solutions.
Ability to independently clean and sanitize production equipment, rooms and areas.
Demonstrated knowledge of an aseptic operation and the relationship of laminar flow systems and environmental monitoring.
Ability to assist in performing environmental monitoring, such as but not limited to, independently placing settling plates and air sampling.
Ability to use basic hand tools.
Ability to independently set-up, operate, maintain and troubleshoot steam sterilizers, capping machines, stoppering machines, bottle washers, sterilizing tunnels, equipment washing machines, sterile filtration equipment, L bar sealers/Bundler, vision systems, inkjets, vacuum check equipment as needed.
Ability to wear a respirator if required of the job, no pulmonary restrictions.
Ability to independently use and understand computer assisted data entry.
Ability to independently perform sterile filtration.
Ability to aseptically gather and transfer samples for QC testing.
Ability to independently perform filter integrity and prepare accurate documentation
Skills:
Experience with GMP production
Direct & relevant experience with Aseptic processing/filling.
Experience with:
Document Revision
Deviation Management
Production coordination/scheduling
Demonstrated knowledge of:
Federal, State, and international regulations, such as cGMP, USDA, DOT, EPA, OSHA
Corporate guidelines and Policies related to the employee’s work.
Standard Operating Procedures (SOPs)
Material Safety Data Sheets (MSDSs), safety procedures, and hazardous materials procedures.
Aseptic processing procedures related to the employee’s work.
Team process and leadership principles.
Appropriate processes and theory related to the employee’s work.
Documentation related to the employee’s work.
Equipment as defined in Duties Additional education and/or equivalent experience.
Successful completion of National Career Readiness Work Keys assessment.
Traffic Patterns.
Working with BPE Methods.
Understanding of Basic GMP/Documentation practices.
Ability and understanding of safe working habits.
Ability to work in a team environment.
Education:
High School diploma or GE
Years of experience: 2