Manufacturing Specialist (Contract)
About this role
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 law. In 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 Vertex’s 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
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If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at [email protected]. Please include the job title in the subject of your email.
No C2C or Third-Party Vendors
Company at a glance
Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases and has made significant advancements in cystic fibrosis, sickle cell disease, transfusion-dependent beta thalassemia, and acute pain — and continues to progress clinical and research programs in these diseases. We also have a robust clinical pipeline of investigational therapies across a range of modalities in other serious diseases where we have deep insight into causal human biology, including acute and neuropathic pain, APOL1-mediated kidney disease, IgA nephropathy, autosomal dominant polycystic kidney disease, type 1 diabetes and myotonic dystrophy type 1.
Our global headquarters is in Boston, and we have research and development (R&D) sites and commercial offices worldwide.
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. We have also earned a spot on TIME Most Influential Companies, TIME Best Inventions, and Fast Company Most Innovative Companies lists. Our research and medicines have received esteemed recognitions, including the Robert J. Beall Therapeutics Development Award, the Prix Galien, the Scrip Award and the Breakthrough Prize awards.
Read our community guidelines: https://www.vrtx.com/vertexs-community-guidelines/
Top Benefits
- Medical benefits
- Fringe benefits
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