Quality Engineer

Position: Quality Engineer

18 month c2h

M-F onsite

Bachelors degree in Chemistry or other science field

3 yrs in GMP manufacturing facility

3-5 exp working in quality assurance

Address: Phillipsburg, NJ, 08865

Remote: onsite M-F

Length: 18 months

Hours: 8-5p

Process/Interview Availability: 15min teams interview then 2 hr in person interview

Potential start date: asap

On boarding requirements:

Background: yes

Drug Screen: yes

Location: New JerseyJob Description:

Quality Engineer 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 Senior Quality Engineer 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.

Quality Engineer acts as the key contact working directly with customers to investigate and resolve complaints and inquiries to ensure expectations are met as well as hosting and managing customer audits, certification/surveillance audits as well as the internal audit program. He/she works collaboratively with other departments in both a leadership and participative manner to integrate the necessary systems.

Work Schedule: 1st Shift (Monday - Friday)

MAJOR JOB DUTIES AND RESPONSIBILITIES:

• 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

Skills/Experience:

KNOWLEDGE, SKILLS AND ABILITIES:

• 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

WORKING CONDITIONS:

The work environment is a manufacturing facility, and the appropriate PPE will be required in designated areas. Domestic travel is required on occasion.

Required Skills:

QUALIFICATIONS:

• 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