Manufacturing Visual Inspection

Manufacturing Visual InspectionVARITE is looking for qualified Manufacturing Visual Inspection in Fremont, CA (Onsite). The client is a global, research-driven pharmaceutical company that focuses on developing innovative medicines in areas such as human pharmaceuticals, animal health, and biopharmaceutical contract manufacturing. Established in the Year 2000, VARITE is an award-winning minority business enterprise providing global consulting & staffing services to Fortune 1000 companies and government agencies. With 850+ global consultants, VARITE is committed to delivering excellence to its customers by leveraging its global experience and expertise in providing comprehensive scientific, engineering, technical, and non-technical staff augmentation and talent acquisition services.Job Title: Manufacturing Visual InspectionLocation: Fremont, CA 94555 (Onsite)Contract Duration: 6-month contract with possible extension.Pay Rate Range: $27.59 - $29.56/hr. on W2Shift: 2nd Shift: Mon-Fri, 2PM-10:30PMNote: Worker required to clear VISION TESTING (acuity & color blindness) before starting assignment.DutiesExecutes routine unit operations in Visual Inspection as assigned related to the manufacturing of drug product in a multi-product facility.Performs duties under limited supervision and according to standard operating and manufacturing procedures.Executes independently with adequate training, complex fundamental operations as visual inspection, advance visual inspection, palletizing, cleaning, inspection hood prep for operations, BioMES Operations and Exceptions.Performs internal support duties including assisting drug product filling and packaging.Executes independently with adequate training fundamental operations:Logistics CoordinationBatch record executionsEquipment use logsWork order initiation and trackingSupport ProjectsSupport Creation/Maintain Training KitsDocuments work according to cGMP and cGDP.Adheres to established regulations and follows cGMP established by site.Reports abnormalities and deviations in a timely and accurate manner.Adheres to safety standards and identifies unsafe situations / habits and escalates appropriately.Maintains production areas according to predefined standards (5s).Maintains own training within compliance and trains other technicians and associates on operations upon completion of trainer qualification.Contributes to Quality activities such as supporting investigations, corrective actions and area walk throughs.Skills1 or more years of experience in cGMP regulated industry.Ability to concentrate on detail-oriented work in a complex technical setup with a Quality and "Right the first-time" mindset.Strong written and verbal communication skills.Ability to work with computer-based systems and manufacturing execution systems (MES).Ability to read and understand SOPs and instructions and document work in a written format applying cGMP standards.Ability to work as part of a high performing team and collaborate effectively with staff.Must be able to read and see clearly.Physical DemandsDuties of this position may require the incumbent to exert some physical effort.Lifting requirements may vary dependent on the drug product manufacturing visual inspection area activity. Weight is typically no more than 25 pounds.EducationHigh school degree + minimum 1 year work experience in GMP regulated industryAssociates/Bachelor's degree or biotechnology vocational training preferredBenefitsHealth Insurance: Medical, dental, and vision coverageRetirement Plans: Participation in a company-sponsored retirement savings plan.Legal Service Plans: Offering access to attorneys for legal advice and representation.VARITE is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.