Due to client requirement, applicants must be willing and able to work on a w2 basis. For our w2 consultants, we offer a great benefits package that includes Medical, Dental, and Vision benefits, 401k with company matching, and life insurance.
About the Role:
We are seeking a skilled CQV (Commissioning, Qualification, and Validation) Engineer to join our team for the commissioning of our second expansion project, focusing on bioreactors. This is a critical role that will support our efforts to ensure that all systems and processes are fully operational and compliant with industry standards.
Key Responsibilities:
Lead and execute commissioning, qualification, and validation activities for new pieces of equipment
Develop and implement CQV protocols and reports.
Collaborate with cross-functional teams to ensure project timelines and objectives are met.
Troubleshoot and resolve any issues that arise during the CQV process.
Ensure compliance with all regulatory requirements and industry standards.
Provide technical expertise and guidance to the project team.
Qualifications:
Proven experience in CQV activities, particularly with bioreactors, autoclaves, refrigerators and incubators
Experience with APS (Advanced Process Solutions) for filling processes is highly desirable.
Previous experience with companies like Novo Nordisk or Eli Lilly is a plus.
Strong understanding of regulatory requirements and industry standards.
Excellent problem-solving and communication skills.