- $71,880.00 -102,050.00/year*
69 Rose St
Responsibilities: Maintain and continuously improve quality system processes and procedures. Review documentation supporting GMP activities for accuracy and completeness. Release Batch Records and labeling for manufacturing. Review executed Batch Records and associated test results. Coordinate or perform investigations of quality issues and product complaints and implement corrective/preventive actions. Review change controls and validation documentation. Assist with internal audits and supplier audits as needed. Monitor performance of quality systems and generate reports to communicate status to management.
Qualifications & Experience: Bachelor s Degree in Science or related technical field. 3+ years of experience in pharmaceutical, biotech or medical device industry. Excellent organiz6063.#######2ational skills and attention to detail. Good verbal and written communication skills. Strong interpersonal skills and ability to work efficiently on a team. Ability to make decisions and resolve issues with minimal guidance. Knowledge of FDA and international regulations and GxP guidelines.
Associated topics: armed, border patrol, fire marshal i, fire protection, guard, jail, law enforcement, prison, police department, public safety
* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.
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