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: Marlborough, Massachusetts job type: Contract salary: $30.00 - 36.10 per hour work hours: 11 to 7 education: Bachelors responsibilities: In this role, you will perform routine environmental monitoring and critical utilities (water and process gasses) sampling of the GMP manufacturing facility. The Quality Control Associate l will also support microbiological testing for GMP QC raw materials, excipients, drug substance and finished product testing for mRNA products produced at the company's manufacturing facility. The Quality Control Associate may perform projects as assigned.
- Perform routine environmental monitoring and critical utility sampling activities.
- Conduct analysis of water samples to include TOC, Conductivity, Bioburden, and Endotoxin.
- Conduct process gasses testing for Total particulates, Viable Air, Hydrocarbons and Dewpoint.
- Perform routine testing in support of manufacturing processes to include bioburden, sterility, endotoxin, culture purity and cell stock identity.
- Prepare and ship contract laboratory testing samples including those intended for microbiological identification.
- Perform general laboratory support activities including equipment maintenance and housekeeping.
- May participate in equipment and method qualifications, validations, and method transfers.
- Perform data entry utilizing good documentation practices.
- Support initiation/closure of quality system records such as environmental monitoring excursion notifications and deviations.
- Write/revise standard operating procedures.
- Additional duties as may be assigned from time to time
qualifications:
- BS in a relevant scientific discipline or 5 years Quality Control experience in a cGMP organization with a focus in Microbiology
- 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 at Moderna's site 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 ...@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.