associate i, quality control, raw materials
: Job Details :

associate i, quality control, raw materials.norwood , massachusettsposted september 11, 2024job detailssummary$25 - $34.67 per hourcontractbachelor degreecategory life, physical, and social science occupationsreference48877job detailsjob 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: Norwood, Massachusettsjob type: Contractsalary: $25.00 - 34.67 per hourwork hours: 9 to 5education: Bachelorsresponsibilities:Reporting to the Supervisor of Quality Control, Seeking a Quality Control Raw Materials Associate I, Sampler based at their Norwood, MA site. The individual in this role will perform QC Raw Material activities in support of GMP Manufacturing and further support special projects as assigned.Requesting, sampling, and shipping of raw materialsSample coordination including cross functional collaboration with internal and external labsSupporting domestic and international sample shipmentsSupporting testing for methods including pH, conductivity, TruScan RM spectroscopy, appearance, and dimensional verificationInspect product and raw material retain samples.LIMS (LabVantage) sample logging and result entryRaw material and consumable component inspection and releaseClean room gowning and aseptic techniques.Managing/stocking of QC lab supplies and routine lab cleaning.Complete and maintain cGMP documentation for work performed.Maintain a safe laboratory working environment.Foster a positive and inclusive work culture that promotes collaboration, innovation, and continuous improvement.Follow all relevant GxP regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements.Execute tasks precisely as defined in internal guiding documents including but not limited to standard operating procedures (SOPs) and work instructions.Follow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections.Complete training in assigned required learning plan according to the defined timing and the prescribed requalification cadence.qualifications:BA/BS in a relevant scientific discipline0-2 years or 3+ years in a GMP QC laboratory settingDemonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations.skills: Quality control, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management SystemEqual 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 ...@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).This posting is open for thirty (30) days.