Scientist I - Fill Finish Operations

DescriptionHomeSearch JobsJob DescriptionScientist I - Fill Finish OperationsContract: Irvine, California, USSalary Range: 30.00 - 39.00 | Per HourJob Code: 368548End Date: 2026-05-24Days Left: 26 days, 3 hours leftApplyPosition Details:Industry: Pharmaceutical/BiotechnologyJob Title: Scientist I : Fill Finish OperationsDuration: 6 Months Contract (Possible Extension Based on Performance and Business Needs)Location: Irvine, CA 92606Shift: Monday-Friday | 8 Hours per Day | Standard Business HoursNumber of Positions Needed: 2Salary Range: $30.00 - $39.00 Per HourJob Summary:The candidate will support manufacturing and laboratory operations in a regulated environment. This role is responsible for assisting with the setup, operation, and documentation of moderately complex automated fill/finish equipment used in the production of prefilled syringes, as well as performing routine laboratory and manufacturing processes under minimal supervision.Top 3-5 Skills, Experience or Education Required:Ability to understand, set up, and operate moderately complex automated fill/finish equipment for production of prefilled syringes.With minimal supervision, familiarity with setting up and performing laboratory processes. Use of equipment including mixing vessels, filters, tanks, and associated utilities and connections.Ability to document information using good laboratory/manufacturing processes (GLP/GMP) in electronic systems, with excellent writing proficiency.Excellent communication skills, ability to work within a team setting, and follow strict adherence to quality requirements.Basic understanding of MS office tools, and ability to independently draft technical documents.Responsibilities:Understand, set up, and operate moderately complex automated fill/finish equipment for prefilled syringe production.Set up and perform routine laboratory and manufacturing processes with minimal supervision.Work with equipment and systems including mixing vessels, filters, tanks, and associated utilities and connections.Accurately document activities and results in electronic systems in accordance with GLP/GMP requirements.Independently draft clear and accurate technical documents as needed.Excellent communication skills, ability to work within a team setting, and follow strict adherence to quality requirements.Use Ms Office tools to support documentation and reporting tasks.Basic Qualifications:Bachelor's Degree in engineering, pharmaceutical sciences, chemistry, pharmaceutics, or related disciplines.Laboratory skills and experience with automated equipment.Scientific problem solving, experimental design, and trouble shooting skills.Preferred Qualifications:Experience in a regulated manufacturing or laboratory environment.Familiarity with sterile processing or fill/finish operationsBenefits:The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually - These all are subject to applicable eligibility).Job RequirementFill-FinishGMPGLPManufacturingLaboratoryAutomationSterileProcess DevelopmentDocumentationTroubleshootingValidationComplianceBiotechSyringesEquipment Operations Reach Out to a RecruiterRecruiterEmailPhoneSiddhi Kadakiasiddhi.kadakia@collabera.com