Associate Quality Engineer
Participate with risk assessments for new systems and changes to existing systems. Write simple validation plans, protocols and reports. Create, own, and manage life cycle of minor deviations, corrective actions and change controls for GMP equipment, facilities and automation systems. Working closely with Engineering, Quality, Process Development, Validation, and Manufacturing to investigate and resolve deviations. Preparing material for internal and external regulatory and customer auditors. Participate in generating quality system metrics for the E&T department.
Working knowledge of GMP guidelines, ICH Q7, Q8, Q9, Q10 and other international regulatory requirements
Good knowledge and skills in biopharmaceutical and process engineering
Understanding of validation concepts for biopharmaceutical manufacturing process, instrumentation and utility equipment.
Customer Relationship Management
Time Management
MS Excel
MS Word
Process Improvement
Verbal communication
written communication
Self-Driven
Adaptability
According to JobzMall, the average salary range for a Associate Quality Engineer in 900 Ridgebury Rd, Ridgefield, CT 06877, USA is between $58,000 and $76,000 per year. This range may vary depending on the employer, experience, and qualifications.
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C.H. Boehringer Sohn AG & Ko. KG is the parent company of the Boehringer Ingelheim group, which was founded in 1885 by Albert Boehringer in Ingelheim am Rhein, Germany. As of 2018, Boehringer Ingelheim is one of the world's largest pharmaceutical companies, and the largest private one.
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