Job Description: As part of technical operations, you will be developing and applying your knowledge of procedures, techniques, tools, materials and equipment. Your receptiveness to new ideas will enhance the team’s ability to achieve goals and targets. You will follow standard procedures to complete tasks and identify process issues or problems that involve direct application of your skills/knowledge. Job Responsibilities: Manage the preparation, cleaning, and/or operation of various components, materials and equipment. Monitor, troubleshoot, perform quality level checks, and document processing steps for various manufacturing / packaging / inspection equipment. Maintain files and databases to ensure all documentation is current and complete. Participate in Response Development to Regulatory Inspection Observations and execute corrective actions recommended as a part of cGMP/Regulatory compliance. Manage own time, professional development, and be accountable for own results. Communicating with peers, supervisors, and interdepartmental groups to provide for an efficient drug production process. Perform the cleaning and sanitization of the area as per the procedure. Suggest innovative ideas for the process simplification. Be part of an ownership culture that values diversity and where all colleagues are energized and engaged. Be part of a team and work collaboratively with the broader Manufacturing Operations group. Job Requirements: Bachelor's Degree Pharmaceutical production experience Qualification & Experience: High School Diploma or GED Job Details: Company: Pfizer Vacancy Type: Full Time Job Location: Wichita, KS, US Application Deadline: N/A Apply Here careersvite.com
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