Career Opportunities: QA Specialist I (5351)
Job Title – QA Specialist
Work Location – Cranbury, NJ
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. Coordinate cross-functional teams, manage timelines, and ensure 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 etc.)
- Develop and execute project plans, timelines
- Ensure compliance with GMP, regulatory requirements
- Identify and mitigate project risks, track progress
- Collaborate with stakeholders on project scope, changes
Qualifications:
- Bachelor's/Master's in relevant field (e.g., Life Sciences, Pharmacy)
- 1-2 years in QA/project management, preferably in pharma/biotech
- GMP regulations, project management methodologies
- Strong communication, problem-solving, and organizational skills and Tools such as Project management: Jira, Aspera, MS Project, Document control: SharePoint, Document Vault ( any skill would be a plus)
Salary range for this position is 60,200-96.300
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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Job Title – QA Specialist
Work Location – Cranbury, NJ
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. Coordinate cross-functional teams, manage timelines, and ensure 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 etc.)
- Develop and execute project plans, timelines
- Ensure compliance with GMP, regulatory requirements
- Identify and mitigate project risks, track progress
- Collaborate with stakeholders on project scope, changes
Qualifications:
- Bachelor's/Master's in relevant field (e.g., Life Sciences, Pharmacy)
- 1-2 years in QA/project management, preferably in pharma/biotech
- GMP regulations, project management methodologies
- Strong communication, problem-solving, and organizational skills and Tools such as Project management: Jira, Aspera, MS Project, Document control: SharePoint, Document Vault ( any skill would be a plus)
Salary range for this position is 60,200-96.300
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
-
- The job has been sent to
Job Title – QA Specialist
Work Location – Cranbury, NJ
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. Coordinate cross-functional teams, manage timelines, and ensure 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 etc.)
- Develop and execute project plans, timelines
- Ensure compliance with GMP, regulatory requirements
- Identify and mitigate project risks, track progress
- Collaborate with stakeholders on project scope, changes
Qualifications:
- Bachelor's/Master's in relevant field (e.g., Life Sciences, Pharmacy)
- 1-2 years in QA/project management, preferably in pharma/biotech
- GMP regulations, project management methodologies
- Strong communication, problem-solving, and organizational skills and Tools such as Project management: Jira, Aspera, MS Project, Document control: SharePoint, Document Vault ( any skill would be a plus)
Salary range for this position is 60,200-96.300
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