Quality Engineer II

The Opportunity:

Avantor is looking for a Quality Engineer II to support our chemical manufacturing facility in Phillipsburg, NJ! The Quality Engineer II leads efforts in site quality assurance programs and improvement activities. He/she is responsible for identifying and implementing programs to ensure regulatory compliance with cGMPs, ICHQ7, IPEC guidelines, ISO regulations as well as FDA requirements. 

The Quality Engineer II is accountable for direct support of several systems, including CAPA, cGMP, Complaint Investigation and Response, ISO System, Stability, SPC (supporting the microelectronic, pharmaceutical and reagent product lines as necessary) and Validation.

This is a full-time, onsite position in Phillipsburg, NJ (1st Shift, Monday – Friday).

What we’re looking for  

• Education: Bachelor’s Degree in chemistry or a related field required

• Experience:  Minimum of five (5) years of experience in quality engineering or a related role required

• Experience working within pharmaceutical, biotechnology and/or chemical environments required

• Experience working within cGMP/ISO 9000 regulated environments required

• Excellent writing and presentation skills

• Demonstrated ability to accomplish goals through others

• Demonstrated familiarity with chemical nomenclature and Quality Control testing and methods

• Ability to merge divergent resources into an effective and efficient cross-functional team

• Highly detail oriented with demonstrated strong analytical and problem-solving skills

• Ability to navigate in a matrixed environment and work collaboratively in a team environment

• Excellent organization and project management skills

• Ability to interface effectively with people at all levels of the organization, from executive to production line

How you will thrive and create an impact  

• Leads programs and improvement activities focused on ensuring ongoing effectiveness of the quality management system in accordance with the ISO and GMP requirements

• Leads customer complaint investigations requiring direct interaction with customers as well as raw material suppliers

• Manages and leads audit activities within the site including GMP, regulatory, customer and internal audits; recommends and implements activities to close gaps identified in audits to ensure compliance with applicable requirements

• Performs internal audits at other Avantor sites and may participate in supplier audits as required

• Responsible for maintaining Corrective and Preventive Action program activities within specific scope of responsibility to identify and implement effective corrective actions

• Ensures facility cGMP compliance is maintained and identifies/implements improvement programs as required

• Provides GMP and GDP training to site personnel

• Leads efforts to drive improvement efforts in global metrics with specific focus on complaints and complaint response time as well as CAPAs

• Works with and provides input to Management of Change process

• Performs statistical evaluations for processes and trending and leads validation activity associated with new products or changes to existing processes and products

• Works collaboratively with supplier quality personnel to identify and resolve quality related issues impacting site performance as well as customer complaint

• Partners collaboratively with external customers, operations leadership, and interacts with all levels of plant operations, R&D, procurement, commercial and quality teams

• Works with all departments to investigate and resolve process and product quality issues

• Performs other duties as assigned with or without accommodation

Disclaimer:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.

Why Avantor?

Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome ch