Quality Control is searching for an analyst (Associate QC) to support routine testing for the QC Night Shift Team D (Tuesday-Friday from 9:45pm - 8:15am) at Company Rhode Island.
This person will be responsible for working in the Quality analytical laboratory, using GMPs and GDPs to execute analytical testing.
The ideal candidate enjoys tackling challenges and excels at time management with attention to detail.
Weekday shift: - Tuesday - Friday
Weekend Shift - Saturday - Tuesday
location: West Greenwich, Rhode Island
job type: Contract
salary: $30.00 - 38.59 per hour
work hours: 9 to 5
education: High School
responsibilities:
- Performing analytical testing including time sensitive samples from Manufacturing (Titer/ MMV/ Mycoplasma/ Endotoxin/ Bioburden/ TOC/ Conductivity), Centralized Raw Material testing (compendial testing & microbiology), Environmental Monitoring and Critical Utilities, Sample Receipt and Aliquot.
- Ensures that facilities, equipment, materials, organization, processes, procedures and products comply with safety guidelines, cGMP (Good Manufacturing Practices) practices and other applicable regulations
- Generates complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks
- Operates laboratory equipment and instrumentation
- Performs review and approval of assays, documents and records
- Supports troubleshooting and problem solving
- Alerts management of quality, compliance, supply and safety risks
- Supports TRAs and deviations, as applicable
- Completes required assigned training to permit execution of required tasks
- Performs additional duties as specified by management
qualifications:
- Bachelors degree OR Associate's degree and 1-2 years of Quality or Analytical Laboratory experience OR High school diploma/GED and 3 years of Quality or Analytical Laboratory experience.
- 1-3 years of experience in GMP analytical laboratory
- Experience executing analytical /biological testing per Methods and/or Compendia
- Experience with QC analytical systems and/or Quality systems
- Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervision
- Strong communication skills (both written and verbal)
- Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories.
- Understanding of biopharmaceuticals process and related unit operations
- Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy
- Independent, self-motivated, organized, able to multi-task in time-sensitive environments.
- Demonstrated experience in investigations and QC processes
skills: Environmental Monitoring, Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), Quality Control (QC), Quality Control Testing
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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
