Sr. Engineer II, Quality Control, Equipment & Automation
at Moderna
Marlboro, Massachusetts, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 01 Jun, 2024 | Not Specified | 01 Mar, 2024 | N/A | Good communication skills | No | No |
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Description:
The Role
Moderna is seeking a Sr. Engineer II, Quality Control Equipment & Automation to support our Quality Control team specializing in Individualized Neoantigen Therapy (INT) commercial production. This position will be based in our cGMP Manufacturing site in Marlborough, MA. This role will develop, execute, and enhance the organization’s quality control procedures and methods aligning them with new equipment focusing on innovative automation and digital solutions.
The successful candidate will have an extensive background in automation, and equipment installation/release. Experience with quality control and laboratory technology is preferred. The Sr. Engineer II, Quality Control Equipment & Automation will be a key player in our organization, ensuring that our quality control processes are efficient, effective, and robust.
Here’s What You’ll Do
Partner to design and execute strategies to advance quality control processes via technology and automation.
Support daily functions related to quality control automation, including equipment selection, proof of concept, and implementation.
Establish and update department protocols and procedures related to laboratory automation or digital tools/capabilities.
Support department digital systems, including inventory, maintenance, access reviews, etc.
Develop and deploy innovative digital solutions that contribute to achieving Moderna’s sustainability goals.
Analyze and interpret equipment data, prepare reports, and present findings to management.
Collaborate with other departments to ensure that quality control automation aligns with overall business objectives.
Stay up to date with industry trends, new technologies, and regulatory changes.
Responsible for the regular maintenance, calibration, and troubleshooting of all QC equipment to ensure optimal performance.
Maintain accurate and up-to-date records of all equipment calibration and maintenance activities.
Work with cross functional teams to support the qualification and release of QC equipment and automation systems.
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Marlboro, MA, USA