Senior QA Specialist I
WuXi Biologics Group, Trenton, NJ, United States
Job Summary
We're seeking an experienced QA Specialist to join our Quality Assurance team. The successful candidate will be responsible for leading QA projects, ensuring quality and timely delivery, coordinating cross-functional teams, managing timelines, and ensuring GMP compliance. Drive project success through effective communication and risk management. Responsibilities
Oversee QA projects, ensuring timely completion and quality. Coordinate cross‑functional teams (QC, Regulatory and other relevant departments). Develop and execute project plans and timelines. Ensure compliance with GMP and regulatory requirements. Identify and mitigate project risks, track progress. Collaborate with stakeholders on project scope and changes. Support audits and other activities as required. Requirements
Bachelor's or Master’s in a relevant field (e.g., Life Sciences, Pharmacy). 3–5 years of QA/project management experience, preferably in pharma/biotech, with knowledge of GMP regulations and project management methodologies. Strong communication, problem‑solving, and organizational skills; proficiency with tools such as Project Management (Jira, Aspera, MS Project), Document control (SharePoint, Document Vault) is a plus. Salary range for this role is 72,800-116,500. Job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job‑related duties/responsibilities based on their expertise and company business needs. An Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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We're seeking an experienced QA Specialist to join our Quality Assurance team. The successful candidate will be responsible for leading QA projects, ensuring quality and timely delivery, coordinating cross-functional teams, managing timelines, and ensuring GMP compliance. Drive project success through effective communication and risk management. Responsibilities
Oversee QA projects, ensuring timely completion and quality. Coordinate cross‑functional teams (QC, Regulatory and other relevant departments). Develop and execute project plans and timelines. Ensure compliance with GMP and regulatory requirements. Identify and mitigate project risks, track progress. Collaborate with stakeholders on project scope and changes. Support audits and other activities as required. Requirements
Bachelor's or Master’s in a relevant field (e.g., Life Sciences, Pharmacy). 3–5 years of QA/project management experience, preferably in pharma/biotech, with knowledge of GMP regulations and project management methodologies. Strong communication, problem‑solving, and organizational skills; proficiency with tools such as Project Management (Jira, Aspera, MS Project), Document control (SharePoint, Document Vault) is a plus. Salary range for this role is 72,800-116,500. Job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job‑related duties/responsibilities based on their expertise and company business needs. An Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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