Integrated Resources

Quality Engineer

Franklin Lakes, NJ
SAP
Description

Quality Engineer

Location: Franklin Lakes, NJ, us

Company Description

IRI believes in commitment, integrity and strategic workforce solutions.

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

We’ve stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity.

Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients’ success.

Job Description

• The Quality Engineer will be responsible for Consistent application of Quality system standards to assigned Quality system area

• Developing solutions to routine assigned activities of moderate scope & complexity, following applicable Company’s Unit procedures, updating procedures and policies when required, working within and across functions for assigned Quality systems

• Quality project management, data summary, interpretation, administration and maintaining a working knowledge of Quality Systems Regulatory requirements and application to Company /Unit requirements.

Qualifications

• BS degree in Quality or Life Sciences, Engineering (Biology, Chemistry, Microbiology,) and a minimum of 5-6 years of experience in Pharmaceutical/Biotechnology Industry required

• Professional certification is preferred (i.e. CQA-Certified Quality Auditor, CQE-Certified Quality Engineer, SQE-Software Quality Engineer, CQM- Certified Quality Manager, etc.)

• Must have experience with ISO 13485 and 21CFR 820 Quality Systems

• SAP experience preferred. 

• Auditing experience preferred

Additional Information

Kind Regards

Ricky

732-429-1925

Integrated Resources
Integrated Resources

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