Requires 5 to 6 years of cGMP cell therapy manufacturing experience. Should have prior document writing experience. Leadership Experience is a big plus. Serves as the floor SME authors and reviews batch records and procedures the same day drives right first time execution supports technical projects and tech transfer completes an accelerated onboarding.
First Shift: Sunday - Thursday 7am - 3:30PM
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 and reporting deviations
Demonstrates and assists others with aseptic technique
May participate in technology transfer and final process development from the Development to the Manufacturing group - Occasionally supports the development of Standard Operating Procedures (SOPs) or other documentation for manufacturing in collaboration with Development and Quality groups.
Ensures raw materials are identified and available in time for manufacturing activities - Transfer raw material inside cleanroom suite using sanitizing reagents
Supports Operations group to ensure proper coordination of resources
Ensures cGMP compliance through consistent execution
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
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
Pay Range
$48-$53/HR
Requisition Disclaimer
This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (Vertex). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation medical benefits fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors including skills competencies experience location and/or being pursued and other job-related factors permitted by addition this role will be eligible for overtime pay in accordance with federal and state requirements
By applying for this position you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials which may include your CV/Resume email address or phone number with Vertex. For more information on how Vertex handles your personal data related to your job application please see Vertexs Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings profiles articles news and other employment-related information as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners
(collectively Atrium Alerts). Atrium Alerts may be sent by email phone or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time please contact Atrium at .
Job DescriptionManufacturing SpecialistRequires 5 to 6 years of cGMP cell therapy manufacturing experience. Should have prior document writing experience. Leadership Experience is a big plus. Serves as the floor SME authors and reviews batch records and procedures the same day drives right first tim...
Job Description
Manufacturing Specialist
Requires 5 to 6 years of cGMP cell therapy manufacturing experience. Should have prior document writing experience. Leadership Experience is a big plus. Serves as the floor SME authors and reviews batch records and procedures the same day drives right first time execution supports technical projects and tech transfer completes an accelerated onboarding.
First Shift: Sunday - Thursday 7am - 3:30PM
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 and reporting deviations
Demonstrates and assists others with aseptic technique
May participate in technology transfer and final process development from the Development to the Manufacturing group - Occasionally supports the development of Standard Operating Procedures (SOPs) or other documentation for manufacturing in collaboration with Development and Quality groups.
Ensures raw materials are identified and available in time for manufacturing activities - Transfer raw material inside cleanroom suite using sanitizing reagents
Supports Operations group to ensure proper coordination of resources
Ensures cGMP compliance through consistent execution
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
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
Pay Range
$48-$53/HR
Requisition Disclaimer
This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (Vertex). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation medical benefits fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors including skills competencies experience location and/or being pursued and other job-related factors permitted by addition this role will be eligible for overtime pay in accordance with federal and state requirements
By applying for this position you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials which may include your CV/Resume email address or phone number with Vertex. For more information on how Vertex handles your personal data related to your job application please see Vertexs Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings profiles articles news and other employment-related information as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners
(collectively Atrium Alerts). Atrium Alerts may be sent by email phone or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time please contact Atrium at .