Vertex Pharmaceuticals Incorporated
Senior Specialist, Manufacturing Operations (2nd Shift)
Vertex Pharmaceuticals Incorporated, Boston, Massachusetts, us, 02298
Job DescriptionThe Manufacturing Operations Senior Specialist serves in a project lead role within Cell Manufacturing. This position is responsible for driving projects to completion within the GMP cell processing operations team. The incumbent will have expertise in cell culture and GMP as well as exceptional project management skills.The work schedule for this position is Wednesday-Saturday, 2nd shift (12:30 pm - 11 pm) for a total of 40 hours/week.Key Duties and Responsibilities:
Perform clinical product manufacturing for cell therapy according to cGMP standards. Includes assembling raw materials, following specific standard operating procedures (SOP), aseptic technique, completing batch records, reporting deviations.Provides experience-related information to drive more efficient technology transfer and final process development from the Development to the Manufacturing group. Assists in the development of Standard Operating Procedures (SOPs) for manufacturing in collaboration with Research and Quality Systems groups.Ensures cGMP compliance through manufacturing oversight and tracking.Monitors scheduling and assists with coordinating resources such as materials, personnel, and equipment to ensure seamless operation of manufacturing activities.Manage individual projects, including managing timelines and leading small group meetings.Receive and manage equipment alarms.Serves as the main technical SME for the team, troubleshoots problems independently.Demonstrate the Vertex Phenotype behaviors: Lead by Example; Learn, Teach & Develop; Foster Exceptional Collaboration; Drive Breakthrough Results; and Promote Enterprise Thinking.Other duties and projects as assigned to meet departmental requirements.Knowledge and Skills:
Minimum of 3 years cell culture experience, ideally in both adherent and suspension cultures.Excellent computer skills including Word, Excel, Project, Outlook, equipment interfaces, and electronic quality systems.Extensive experience with technical writing.Minimum 6 years working experience in relevant field (may be reduced based on education level).Extensive GMP experience, including as a lead or trainer.Expertise in cell processing technologies for clinical production.Experience with bioreactors for cell culture.Working knowledge of federal requirements for GMP manufacturing (21CFR 210,211) and Quality Systems (21CFR 820).Environment:
Works in a cleanroom and office setting.Must be able to remain in a stationary position 50% during processing activities.Frequently move about inside the cleanroom to accomplish process tasks.Occasionally moves lab equipment and materials weighing up to 50 pounds.Compressed gasses and LN2 are used in this process.Flex Designation:
On-Site DesignatedFlex Eligibility Status:
In this On-Site designated role, you will 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 InformationVertex 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 ApplicationAssistance@vrtx.com.
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Perform clinical product manufacturing for cell therapy according to cGMP standards. Includes assembling raw materials, following specific standard operating procedures (SOP), aseptic technique, completing batch records, reporting deviations.Provides experience-related information to drive more efficient technology transfer and final process development from the Development to the Manufacturing group. Assists in the development of Standard Operating Procedures (SOPs) for manufacturing in collaboration with Research and Quality Systems groups.Ensures cGMP compliance through manufacturing oversight and tracking.Monitors scheduling and assists with coordinating resources such as materials, personnel, and equipment to ensure seamless operation of manufacturing activities.Manage individual projects, including managing timelines and leading small group meetings.Receive and manage equipment alarms.Serves as the main technical SME for the team, troubleshoots problems independently.Demonstrate the Vertex Phenotype behaviors: Lead by Example; Learn, Teach & Develop; Foster Exceptional Collaboration; Drive Breakthrough Results; and Promote Enterprise Thinking.Other duties and projects as assigned to meet departmental requirements.Knowledge and Skills:
Minimum of 3 years cell culture experience, ideally in both adherent and suspension cultures.Excellent computer skills including Word, Excel, Project, Outlook, equipment interfaces, and electronic quality systems.Extensive experience with technical writing.Minimum 6 years working experience in relevant field (may be reduced based on education level).Extensive GMP experience, including as a lead or trainer.Expertise in cell processing technologies for clinical production.Experience with bioreactors for cell culture.Working knowledge of federal requirements for GMP manufacturing (21CFR 210,211) and Quality Systems (21CFR 820).Environment:
Works in a cleanroom and office setting.Must be able to remain in a stationary position 50% during processing activities.Frequently move about inside the cleanroom to accomplish process tasks.Occasionally moves lab equipment and materials weighing up to 50 pounds.Compressed gasses and LN2 are used in this process.Flex Designation:
On-Site DesignatedFlex Eligibility Status:
In this On-Site designated role, you will 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 InformationVertex 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 ApplicationAssistance@vrtx.com.
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