Job Description

We are seeking a detail-oriented Manufacturing Operations Senior Associate with experience in aseptic processing and cleanroom operations. The ideal candidate will have hands-on experience working in Grade B cleanroom environments, executing batch processes, and maintaining accurate documentation in compliance with regulated laboratory and manufacturing standards.

Current Shift: Wednesday-Saturday 12:30pm - 11:00pm (This maybe updated to Tuesday-Saturday 2:30pm - 11:00pm)

Key Responsibilities:

• Execute batch processing activities in a laboratory or manufacturing setting following established batch records and SOPs
• Following Batch Records, SOPs, policies and all other relevant work instructions to ensure the successful and compliant operation of thedrug product facility
• Perform aseptic techniques and aseptic processing in a Grade B cleanroom environment
• Prepare, process, and transfer media for cell culture operations, including filling, harvesting, filtering, and centrifugation
• Handle downstream processes such as waste removal and transfer of final product into drug product bags
• Operate and maintain equipment including peristaltic pumps, tube welders, and balances
• Accurately document all laboratory and manufacturing activities in compliance with GMP standards
• Utilize LIMS (Laboratory Information Management Systems) and MES (Manufacturing Execution Systems) for data entry, tracking, and reporting
• Ensure adherence to safety, quality, and regulatory requirements at all times

Qualifications:

• HSD +3 years experience
• Experience working in a laboratory or biopharmaceutical manufacturing environment
• Hands-on experience with aseptic techniques and cleanroom operations (Grade B preferred)
• Familiarity with batch record execution and GMP documentation practices
• Experience with LIMS and MES systems
• Proficiency in operating laboratory/manufacturing equipment such as peristaltic pumps, tube welders, and centrifuges
• Strong attention to detail and ability to follow precise instructions
• Good organizational and documentation skills

Preferred Qualifications:

• Experience in cell culture processing or bioprocessing
• Prior experience in regulated environments such as pharmaceutical or biotech manufacturing

Pay Range

$38-$42/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

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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 tempstaffing@vrtx.com. Please include the job title in the subject of your email.

No C2C or Third-Party Vendors