Company Overview / Employee Value Proposition
Softenger offers a variety of managed services in the field of Information Technology. We are committed to provide the right services to maintain and enhance your IT infrastructure, so that you can focus on achieving your business vision. Ideas are the foundation of evolution. There must be a drive to act on those ideas. Our services start with precision, thinking, followed by focused approach and proficient execution. Softenger provides your business with a board array of enterprises system management services basedin Industry-Standard methodologies and practices. From system, database administration to security and continuity of business, we deliver services that will meet your business strategies and goals.
Responsibilities
Apply quality control and quality assurance techniques to ensure compliance with GMP-regulated pharmaceutical manufacturing standards
Perform qualification and validation of QC equipment to maintain operational accuracy and regulatory compliance
Support audit and inspection processes by preparing documentation and facilitating responses to regulatory inquiries
Collaborate in technology transfer projects to ensure seamless transition and compliance of manufacturing processes
Contribute to new product launches by validating quality systems and ensuring readiness for production
Preferred competencies and qualifications
Demonstrated experience supporting audits, inspections, technology transfers, or new product launches within pharmaceutical quality environments
3–5 years of relevant experience in pharmaceutical quality control, quality assurance, or manufacturing quality
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