Senior Quality Management Specialist
3 hours ago
Key Responsibilities:
- Developing and implementing comprehensive quality management systems, including track-wise and master control.
- Configuring and integrating systems using Studio Designer for seamless performance.
- Designing specifications for customization and validation documents to ensure compliance.
- Delivering classroom training sessions for end-clients to enhance their understanding of quality management systems.
- Buildding and promoting customized solutions to QA and PROD environments to improve efficiency.
Requirements:
- Minimum 3-7 years of experience in technical and configuration services.
- Hold valid GMP and FDA certifications to demonstrate expertise.
- Proficiency in Crystal reporting and Tibco Spotfire to analyze and present data effectively.
- Familiarity with ISO 9000, cGMP, and FDA Regulations to ensure compliance.
- Strong writing and communication skills to convey complex ideas clearly.
- Proven problem-solving ability to overcome challenges efficiently.
- Sound knowledge of manufacturing or business processes to drive quality management initiatives.
- Experience in programming concepts to develop innovative solutions.
Preferred Qualifications:
- Experience in MRP systems and manufacturing concepts to enhance operational efficiency.
We seek candidates who can work collaboratively in a team environment and possess excellent communication skills to drive quality management initiatives forward successfully.
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