In this Quality Associate position, you will have an opportunity to work in a well-respected Biotechnology company AND have the support you need with a career coach guiding you towards success :)
Why work a contract position with Randstad?
- Opportunity - Opportunity - Opportunity
- Career Advisor to assist
- Benefits available (Medical/Dental/Eye)
- High conversion rate to a full-time employee (avg 2 per month)
- Robust on the job training and eLearning's
- 6-month contracts with possibility of extension dependent on availability and performance·
- 100% onsite at the client's facility in RTP, NC (cafeteria, Starbuck's, gym)
- Mon – Fri, standard work weeks and hours with occasional overtime
- Work within the internal QA group supporting documentation creation, update, reviews, provide meeting support, support design questions making recommendations on improvements, compliance where appropriate.
- Support batch record traceability mapping activities in addition to other assignments as required by group management.
- Collaborate with project teams, contractors, and site operations staff.
salary: $30 - $34 per hour
shift: First
work hours: 8 AM - 5 PM
education: Associate
Responsibilities
Main Responsibilities:
- Review and approval of batch related documentation (Solution Lot records, Reports, Logbooks and Release of Autoclaved Equipment).
- Transport batch related documentation across RTP buildings supporting chain of custody and life cycle management.
- Resolution of both technical and compliance issues/gaps of mild to moderate complexity.
- Assists Quality Assurance Management in additional responsibilities related to the day-to-day implementation of the Quality Management Systems required to maintain cGMP compliance, ensuring the safety, efficacy and purity of the products manufactured.
- Complete and maintain GMP training.
- Opportunity to contribute to projects.
Qualifications | Skills:
- Experienced QA associate within a large molecule, drug substance facility
- 5+ years of experience within the pharmaceutical, biotech industry
- Regulatory requirements in the pharmaceutical industry (FDA, EMA)
- Able to manage multiple tasks in a fast-paced environment
- Experience working within a matrix teams’ environment
Education:
- Bachelor’s degree in science, engineering, or other technical field of study
The essential functions of this role include:
Skills
Qualifications
Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.
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.
