(USA) Quality Assurance/Systems Manager (Import, Regional, Returns, Wm.Com) - job 17 of 35

Randstad Life Sciences has several pharmaceutical contract openings onsite in Norwood, MA. • **The fastest way to get considered is to apply here on LI and email me your resume and what your 2 shift preferences are to my work email: michael.anderson@randstadusa.com MUST work onsite, this is mandatory b/c you’re doing QC Lab work. The pay rates are also locked in with no flexibility so please know that if you decide to apply.There are 4 shifts available below…Contract Duration: 6 Months (potential for extensions)Also when you email me your resume, please tell me which shifts you are interested or available for, PLEASE try and pick 2 different shifts to have a backup one.Title: Associate I, Quality Control Chemistry (4 Onsite Contract Openings)Shift: WED-SAT, 2nd shift: 2:00pm-12:00am ($38.71 - 15% shift differential included)Shift: WED-SAT, 2nd shift: 2:00pm-12:00am ($38.71 - 15% shift differential included)Shift: WED-SAT, 3rd shift: 10:00pm-8:00am ($40.65 - 20% shift differential included)Shift: SUN-WED, 3rd shift: 10:00pm-8:00am ($40.65 - 20% shift differential included)Job SummaryIn 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.Job Responsibilities• 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 needed• Supports 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 LIMS• Stability program support• Managing/stocking of QC lab supplies• Complete 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 timeEducation & Qualifications• Education: BA/BS in relevant scientific discipline• Experience: 0-2 years of Laboratory experience.• Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations.