specialist quality assurance Position Available In Wake, North Carolina
Tallo's Job Summary: As a Specialist Quality Assurance in Apex, North Carolina, you can earn $34 - $37.96 per hour on a contract basis. Responsibilities include overseeing GMP documents for site startup activities, communicating with stakeholders, and ensuring document adequacy. Qualifications include a Doctorate, Master's with 3 years of experience, Bachelor's with 5 years, or equivalent experience. Skills in quality assurance, regulatory briefing documents, and GMP are required.
Job Description
jobs
life, physical, and social science occupations
specialist quality assurance
specialist quality assurance.
apex, north carolina
posted 2 days ago job details summary $34 – $37.96 per hour
contract
bachelor degree
category
life, physical, and social science occupations
reference
50704
job summary:
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:
Apex, North Carolina
job type: Contract
salary: $34.00 – 37.96 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
Primary responsible for quality oversight of GMP documents related to site startup activities. Some of these activities include reviewing and approving GMP documents, communicating with site SMEs for document adequacy, communicating action progress to Sr Manager level.
qualifications:
Required:
Doctorate degree OR Master’s + 3 years experience OR Bachelor’s + 5 years experience OR Associate’s + 10 years experience OR High school/GED + 12 years experience.
Experience in GMP document review and approval.
General knowledge of cGMP and filing regulations for biopharma manufacturing, testing, and distribution.
Ability to prioritize and meet deadlines.
Excellent leadership, problem-solving, analytical, and customer service skills for a matrix GMP environment.
Document management experience.
#LI-HK1 skills: Quality Assurance, Regulatory Briefing Documents, 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.
