Quality Engineer
Pride Global
The Science Team at Pride Health is currently supporting a client in the pharmaceutical industry and is having the Quality Engineer in Phillipsburg, IL
Position Summary:Quality Engineer leads site quality assurance programs and continuous improvement initiatives. This role is responsible for ensuring compliance with cGMPs, ICH Q7, IPEC guidelines, ISO standards, and FDA regulations. The position supports key quality systems including CAPA, complaint investigations, audits, validation, and statistical process control.
Additional Details:
Pay range: $36 - $43/hour on W2 as per your experience
Contract Length: 12 Months with the possibility of extension Key Responsibilities
- Lead programs and improvement activities to maintain and enhance the Quality Management System in alignment with ISO and GMP requirements
- Manage customer complaint investigations, including direct interaction with customers and raw material suppliers
- Plan, lead, and execute audit activities (GMP, regulatory, customer, and internal audits); identify gaps and implement corrective actions
- Perform internal audits across multiple sites and support supplier audits as needed
- Own and manage CAPA (Corrective and Preventive Action) processes to ensure effective resolution of quality issues
- Ensure ongoing cGMP compliance and drive continuous improvement initiatives
- Provide GMP and GDP training to site personnel
- Monitor and improve global quality metrics, especially complaint resolution timelines and CAPA effectiveness
- Support Management of Change processes
- Conduct statistical analysis, process trending, and validation activities for new and existing products
- Collaborate with supplier quality teams to resolve quality-related issues
- Work cross-functionally with operations, R&D, procurement, and commercial teams to address product and process quality concerns
- Serve as a key point of contact for customers and host audits, including certification and surveillance audits
- Perform additional duties as assigned
Required Qualifications
- Bachelor's degree in chemistry or a related scientific field
- Minimum of 5 years of experience in quality engineering or a related role
- At least 3 years of experience in a GMP manufacturing environment
- 3-5 years of experience in Quality Assurance
- Experience in pharmaceutical, biotechnology, or chemical industries
- Strong understanding of cGMP and ISO 9000 standards
Skills & Competencies
- Excellent written and verbal communication skills
- Strong analytical and problem-solving abilities
- Knowledge of chemical nomenclature and quality control testing methods
- Ability to lead cross-functional teams and influence without authority
- Strong organizational and project management skills
- Ability to work effectively in a matrixed environment
- Detail-oriented with a high level of accuracy
APPLY NOW! About Us Russell Tobin is a leading minority-owned professional and technical recruitment and staffing advisory organization.
We are comprised of specialized practices focusing on a variety of skill sets and industries. Having a depth and breadth of industry expertise, our subject matter experts are able to provide tailored and swift sourcing solutions to fulfill client hiring needs. In other words, we connect top talent with companies.
We are the staffing arm of the Pride Global network, a minority-owned integrated human capital solutions firm, with additional offerings in vendor management, payroll programs, and business process optimization.
As a certified minority-owned business, Pride Global and its affiliates - including Russell Tobin, Pride Health, and Pride Now - are committed to creating a diverse environment and are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, pregnancy, disability, age, veteran status, or other characteristics.
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Vacancy posted 3 days ago
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