job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! location: Rocklin, California job type: Contract salary: $23 - 25 per hour work hours: 9 to 5 education: Associate responsibilities: Perform paperwork preparation, bioburden, and all basic laboratory tasksTrack inventory levels and order materials as requiredUse local ERP system to accurately document work where requiredStock area inventories on a daily, weekly, and monthly basisMaintain lab cleanliness in compliance with cGMP requirementsMaintain records and keep inventory updatedEscalate non-conforming products to management, and participate in investigation processMeet productivity standards and strive to increase productivity without sacrificing quality and safetyLook for ways to improve and promote qualityDemonstrate accuracy and thoroughnessManage time and priorities to meet deadlinesTroubleshoot equipment problemsMaintain knowledge of SOPs and GMP regulations and guidelinesMaintain cGMP complianceParticipate on various projects to improve efficiency or complianceMaintain and demonstrate a high level of personal and professional integrity and report any suspicious activity to laboratory managementRespond promptly to customer needs, solicit customer feedback to improve service, meet commitments.Approach others in a tactful manner, react well under pressure, treat others with respect and consideration, present a professional image in all business mattersMeet productivity standards, strive to increase productivity without sacrificing quality and safetyLook for ways to improve and promote quality; demonstrate accuracy and thoroughnessObserve safety procedures, report potentially unsafe conditions, use equipment and materials properlyMust be willing and able to work on weekends or extended hours as neededFollow regulatory and standard requirements as applicable to the site, i.e., MDSAP, ISO 13485, IVDR, and compliance with the site Quality Manual.Other duties as assigned or required by the business qualifications: Minimum AA/AS degree in a biological science or related field is requiredBA/BS degree in biological science or equivalent life science degree is preferredMinimum two (2) years of experience in an FDA/ISO or other regulated environment is preferredExperience with calendaring, word processing, and spreadsheet software required; experience with Microsoft 365 (Word, Excel, PowerPoint) preferredGeneral knowledge of FDA QSRs cGMP, and ISO 13485 or other related industry standards is requiredKnowledge of FDA QSRs cGMP, and ISO 13485 or other related industry standards is preferredKnowledge of SAP and/or SAP NEXT preferredGood oral and written communication skillsGood interpersonal skillsGood documentation skillsGood math skills: able to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals; able to compute rate, ratio, and percentageAbility to read, analyze, and interpret instructions, correspondence, policies, proceduresAbility to write reports, correspondence, and procedures skills: Quality control, SOP, FDA, GLP (Good Laboratory Practice), GCP (Good Clinical Practice), GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). Applications accepted on ongoing basis until filled. Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.