Senior Specialist GMP Operational Quality

Posted 6 Days Ago
Be an Early Applicant
Boston, MA
5-7 Years Experience
Biotech • Pharmaceutical
The Role
Provide QA support for manufacturing operations, analytical lab operations, and materials management. Review batch data, deviations, in-process data, and quality systems documentation for product disposition. Support batch release process, annual product quality reviews, audits, and inspections. Communicate with internal and external partners. Maintain documentation and assist with quality system data review metrics. Escalate findings to Quality management. Work on-site 5 days a week with some flexibility.
Summary Generated by Built In

Job Description

General Summary:

The Operational Area Senior Quality Specialist will provide QA support of manufacturing operations, analytical laboratory operations and materials management for the external manufacturing programs at VCGT. This role will review batch data, including batch records, deviations, in-process data, EM data, QC release testing and other quality systems documentation as needed in support of product disposition.

***This role is onsite 5 days per week onsite ***

Key Duties and Responsibilities:

• Reviews master batch records and provides customer approval for quality tasks for externally manufactured products

• Performs final review of executed batch and/or critical systems documentation and determines acceptability by using standard operating procedures

• Ensures presence and acceptability of all required documentation prior to the release of the product and/or system.

• Reviews and approves investigations, CAPA’s and change controls for external programs

• Support the day to day management of the batch release process.

• Support annual product quality reviews

• Assist the facility in preparation for quality audits and participate in corporate audits and external inspections as needed.

• Communicates proactively with internal and external partners and management.

• Maintains files such that documents are readily available and easily retrievable.

• Assists department with monthly/quarterly Quality System data review metrics and reporting

• Escalate critical and major finding to Quality management and monitor key performance indicators in collaboration with Quality Systems and other GXP Operational areas.

Education and Experience:

• Bachelor’s degree in a scientific or allied health field or the equivalent combination of education and experience

• Experience providing QA support and oversight of GMP manufacturing operation

• Experience successfully leading event investigations, Root Cause Analysis and CAPA

• Experience with network-based applications such as Oracle, Veeva

• Knowledge of current industry trends and ability to use the latest technologies

On-Site designated role, you will work five days per week on-site with ad hoc flexibility.

#LI-Onsite #ND-2

Flex Designation:

Hybrid-Eligible Or On-Site Eligible

Flex Eligibility Status:

In this Hybrid-Eligible role, you can choose to be designated as: 
1. Hybrid: work remotely up to two days per week; or select
2. On-Site: work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at [email protected]

Top Skills

Oracle
Veeva
The Company
HQ: Boston, MA
5,000 Employees
Hybrid Workplace
Year Founded: 1989

What We Do

Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious and life-threatening diseases.

We discovered and developed the first medicines to treat the underlying cause of cystic fibrosis (CF), a rare, life-threatening genetic disease. In addition to clinical development programs in CF, Vertex has more than a dozen ongoing research programs focused on the underlying mechanisms of other serious diseases.

Founded in 1989 in Cambridge, Massachusetts, our corporate headquarters is now located in Boston’s Innovation District, and our international headquarters is in London, United Kingdom. We currently employ approximately 3,500 people in the United States, Europe, Canada, Australia and Latin America with nearly two-thirds of our staff dedicated to research and development.

Vertex is consistently recognized as one of the industry’s top places to work by Science Magazine, The Boston Globe, Boston Business Journal and the San Diego Business Journal. Our research and medicines have also received esteemed recognitions, including the Robert J. Beall Therapeutics Development Award, the French Prix Galien and the British Pharmacological Society awards.

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