What are the responsibilities and job description for the Program Manager, Quality Control position at Varite?
Job Description :
Work Schedule - Standard (Mon-Fri) 8am to 5pm
Environmental Conditions - Office
How will you make an impact?
The role supports manufacturing by collaborating with various functional teams to enhance operations and optimize processes.
Key Responsibilities :
Documentation Review & Updates -
Ensure batch manufacturing records and SOPs are accurate and meet ISO standards.
Identify discrepancies in the manufacturing process system versus records and update accordingly.
Evaluate and update documentation to ensure compliance with cGMPs and alignment with regulations.
Employee Support - Assist employees with documentation corrections and batch management processes through daily interactions.
Education / Experience
Bachelor's degree or 3-5 years of experience with previous experience in operations / Manufacturing or quality assurance in a medical device or pharmaceutical facility.
Project Management is a plus
Knowledge, Skill, and Requirements
bility to understand and analyze process manufacturing systems
Highly autonomous and able to identify and resolve opportunities through multiple functional groups.
Working Knowledge of BSI and ISO standards and regulations - ISO 17034
Excellent organizational skills and analytical and problem-solving abilities,
Possesses exceptional time management and multi-tasking abilities to meet commitments and deadlines.
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