Position Details
Qa Contractor Gmp Quality Assurance Apply
For further inquiries about this opportunity, please contact our Talent Specialist, Hema, at (630) 847-0275
Title: QA Contractor, GMP Quality Assurance
Duration: 12 Months
Location: Research Triangle Park, NC
Duration: 12 Months
Location: Research Triangle Park, NC
Only W2 candidates are eligible for this position. Third-party or C2C candidates will not be considered.
Description:
The QA Contractor, GMP Quality Assurance, reporting to the Director, GMP Quality Assurance, or designee. This role will assure corporate compliance with applicable GMP national, international, and state regulations. This position will be based at our headquarters facility in RTP, NC with domestic travel (less than 10% of the time) expected.
Job Responsibilities
Manage assigned day-to-day QA responsibilities in support of the company's Product Quality systems.
Provide timely support for Third Party Deviations, Third Party Change Controls, and Vendor Management (qualification and oversight of vendors, contract manufacturers, contract laboratories, and service providers) activities. Liaison with applicable department record owners to ensure their complete and timely resolution.
Collaborate successfully with the other departments to ensure that direct and supportive tasks are completed within project timelines. Providing deliverables and resolving issues, as needed.
Communicate project status to stakeholders and escalate issues in a timely manner.
Perform daily customer-facing activities, as assigned by area management.
Perform and support other duties as assigned by area management.
About you
Bachelor's degree in a scientific field and 2+ years of experience in GMP based Quality Assurance, particularly in support/oversight of a company QMS, or 5+ years of GMP based Quality Assurance experience using a company QMS.
Experience working within a pharmaceutical/biotech Quality Management system, such as Trackwise, ZenQMS, Veeva, is a requirement.
Strong understanding of GMP guidelines and Quality Systems with the ability to apply GMPs in conformance to U.S. standards, and where appropriate, other regulatory authority standards.
Ability to identify and/or resolve quality issues/discrepancies with others in a proactive, diplomatic, flexible, and constructive manner.
Strong attention to detail, highly organized and the ability to multitask in a fast-paced, highly interactive environment.
Strong service-oriented mindset with excellent verbal and written communication skills, and the ability to effectively collaborate with peers including scientific/technical colleagues.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, etc.).
About us:
DivIHN, the 'IT Asset Performance Services' organization, provides Professional Consulting, Custom Projects, and Professional Resource Augmentation services to clients in the Mid-West and beyond. The strategic characteristics of the organization are Standardization, Specialization, and Collaboration.
DivIHN is an equal opportunity employer. DivIHN does not and shall not discriminate against any employee or qualified applicant on the basis of race, color, religion (creed), gender, gender expression, age, national origin (ancestry), disability, marital status, sexual orientation, or military status.
