As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on oncology, cardiology, and bone health. With a strong legacy of scientific excellence and a mission to improve patient outcomes worldwide, they offer a dynamic environment where your contributions will drive real change. If you're seeking a rewarding career that makes a difference, let us help you take the next step!
location: West Greenwich, Rhode Island
job type: Contract
salary: $25.00 - 30.15 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Responsible for the maintenance of all required documentation for the Rhode Island site under the direction of Quality Management with coaching from the Document Management Subject Matter Expert.
- Provide comprehensive services in accordance with Good Manufacturing Practices (GMP) within Document Management with ability to flex support as needed within the Quality System space.
- Maintain an active presence in the Document Management work room to manage internal and external processes for record filing / archival / retrieval / destruction and Equipment Use Record ordering / issuance / reconciliation.
- Archive documentation organization, data entry, lifting and moving of boxes in preparation for offsite storage; must be able to lift up to 50 lbs.
- Follow step-by-step instructions and perform repetitive functions consistently and accurately.
- May answer general questions, troubleshoot problems, and complaint resolution as appropriate.
- Work both independently and in a team environment.
- Follow Current Good Manufacturing Practices (cGMP) regulations and Company policies and procedures.
- Work in a rapidly changing and demanding environment.
- Strong attention to detail.
- Additional projects, as assigned.
qualifications:
Required:
- Associates degree at a minimum
- Basic GMP experience
- Document management experience
- Familiar with working within a regulated industry
skills: SOP, Quality Assurance, 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).
This posting is open for thirty (30) days.
