quality control tester salaries in boston, massachusetts

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: Norwood, Massachusetts job type: Contract salary: $25.00 - 33.55 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Quality Control is seeking a Quality Control Raw Materials Associate. The individual in this role will perform QC Raw Material activities in support of GMP Sampling and Component Inspection and further support special projects as assigned. This position will be 2nd shift working Monday through Friday. 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: BS Degree OR AS degree/HS degree with 2+ year experience in GMP QC laboratory setting.Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations.A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.  skills: Quality control, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System 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). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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: Norwood, Massachusetts job type: Contract salary: $30.00 - 38.06 per hour work hours: 11 to 7 education: Bachelors   responsibilities: In this role, you will perform routine environmental monitoring and critical utility (WFI and Gas) Sampling at the company's Norwood, MA manufacturing facilities in support of both Clinical and Commercial Manufacturing Operations. Conduct Environmental Monitoring (Routine, In-Process, and EMPQ's), WFI Sampling, and Compressed Gas Sampling.Maintain lab equipment and perform housekeeping tasks.Write, revise, and follow SOPs, protocols, and reports.Ensure data entry, review, and trending are performed using LIMS.Collaborate with internal and external labs for sample coordination and testing.Troubleshoot equipment and test methods.Support quality systems records such as deviations, change controls, and CAPAs.Participate in audits and continuous improvement initiatives.  qualifications: STEM degree with 0 years of experience in a GMP QC laboratory setting, focusing on microbiology.Hands-on experience with particle counters, viable air samplers, and gas equipment. Proficiency with Microsoft Office Programs and electronic databases (LIMS, SAP, eQMS).Excellent troubleshooting skills and the ability to communicate scientific issues clearly.Strong written and oral communication skills and organizational abilities.Knowledge of GMP, microbiology, aseptic techniques, and general laboratory instrumentation.Ability to work effectively in a fast-paced, cross-functional matrix environment.Familiarity with relevant FDA, EU, ICH guidelines, and regulations.A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.This position is site-based, requiring you to be onsite full-time. This position is not eligible for remote work.  skills: Quality control, SOP, FDA, MS-WORD, MS-EXCEL, Microbiology, ICH Regulations, GMP (Good Manufacturing Practice), Environmental Sampling, Health and Safety Monitoring, LIMS (Laboratory Information Management System 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). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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: Norwood, Massachusetts job type: Contract salary: $30.00 - 40.65 per hour work hours: 3 to 11 education: Bachelors   responsibilities: In this role, you will perform cGMP QC Chemistry testing for QC Chemistry, release, stability and in process samples. This role may support special projects as needed. Performs routine analytical chemistry testing such as Wet chemistry which includes APP, Osmolarity, Particle analysis, Dynamic Light Scattering, etc.Perform basic HPLC testing and NaOH plate reader-based assays in support of manufacturing process stat testing as neededSupports special projects as assigned.May assist with Troubleshoots assay methods and equipment. Performs data entry and supports trending.Performs general laboratory support activities including reagent preparation, sample management, equipment maintenance, lab housekeeping etc.Supports authoring of SOPs, protocols, and reports as needed.LIMS (LabVantage) sample result entry, execution of Electronic Assay Forms in LIMSStability program supportManaging/stocking of QC lab suppliesComplete and maintain cGMP documentation for work performed.Participate in authoring quality systems records such as lab events, deviations and CAPAs as needed.Establish and maintain a safe laboratory working environment.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.Additional duties as may be assigned from time to time  qualifications: Education: BA/BS in relevant scientific disciplineExperience: 0-2 years of Laboratory experience. Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations.A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.  skills: Quality control, HPLC, SOP, CAPA, 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). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.