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Associate II, Quality Control, Chemistry Data

4 months ago

Norwood, United States Randstad USA Full time
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 - 37.16 per hour
work hours: 9 to 5
education: Bachelors
 
responsibilities:
The company is seeking a Quality Control Chemistry Associate II. The individual in this role 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 including HPLC, UPLC, UV, Particle Analysis and Dynamic Light Scattering, etc.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.LIMS (LabVantage) sample result entry, execution of Electronic Assay Forms in LIMSPerform HPLC and NaOH plate reader based assays in support of manufacturing process stat testing as neededStability program supportManaging/stocking of QC lab suppliesWrite/revise SOPs, protocols and reports.Complete and maintain cGMP documentation for work performed.Participate in authoring quality systems records such as deviations, change controls, CAPAsEstablish 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. 
qualifications:
Education: BA/BS in relevant scientific disciplineExperience: 2 years of Laboratory experience.Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations. 
skills: Quality control, HPLC, SOP, Chemistry, 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.