Analyst I, Quality Control, Microbiology at Randstad USA

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 - 38.48 per hour
work hours: 9 to 5
education: Bachelors
 
responsibilities:

In this role, you will support cGMP microbiology methods for QC raw material, plasmid, drug substance, Stability and finished product testing for mRNA products produced at the company's manufacturing facility. This individual will contribute to non-testing projects and activities as needed example document certification, monthly biosafety cabinet cleaning etc.

• Execute compendial microbiological testing, and other methodologies as needed.
• Receive Environmental Monitoring Plates into MODA, Incubate, Microbial identification,
• Support testing for in-process samples, drug substance and drug product, including generation of testing data to support clinical studies.
• Assist in enumeration of test plates, review EM data, etc.
• Perform general laboratory support activities including reagent preparation, equipment maintenance, weekly and monthly cleaning of the BSCs, Document Certification, archival etc.
• Stock and perform inventory of lab supplies.
• Establish and maintain a safe laboratory working environment.
• Additional duties as may be assigned from time to time

 
qualifications:

• BS in a relevant scientific discipline with a minimum of 0 - 2 years (or MS in a relevant scientific discipline with 1 year) Quality Control experience in a cGMP organization
• Excellent troubleshooting and ability to communicate issues in a scientifically sound and understandable way.
• Familiarity with electronic databases (e.g. LIMS, SAP, LMS, or equivalent software)
• Strong written and oral communication skills as well as organizational skills
• Ability to prioritize, manage and complete multiple projects and tasks in a fast-paced environment efficiently and independently.
• Working knowledge of relevant and current 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.

 
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.