Integrated Resources Inc.
IRI believes in commitment, integrity, and strategic workforce solutions.
Integrated Resources, Inc., is led by a seasoned team with decades of industry experience. We deliver strategic workforce solutions that help manage talent and business more efficiently and effectively. Since 1996, IRI has attracted and retained key professionals, expanding into new sectors and experiencing steady growth.
We focus on finding qualified professionals in our specialty areas. Our partner-employers trust us to match the right candidates with their needs. By exceeding expectations, we build long-term partnerships based on performance and integrity.
Our team provides tailored solutions for each client, aligning skills and cultures for mutual success. At IRI, our success is linked to our clients' success.
Job Description
Participate in developing and maintaining quality systems, processes, and procedures to ensure product quality and safety. Assist the quality assurance site manager in preparing for audits and implementing corrective actions for non-conformities. Support risk management throughout the product lifecycle and provide senior management with key data to inform decisions. Support the development and maintenance of product approval, clearance, and licensing documentation as required by global regulatory agencies. Ensure 100% quality and regulatory compliance according to documented procedures. Communicate and implement strategies to ensure compliance. Review batch records supporting the disposition of bulk drug substances. Review equipment validation protocols and reports. Support compliance in raw material and solution release, including review of specifications and documentation. Manage the release of single-use disposable products, including label reconciliation. Review temperature charts and related documentation for excursions. Update label issuance and reconciliation processes. QA Documentation Support: Issue batch records and track logs, lab notebooks, and SOP binders. Scan and file excursion documents and batch-related documents for release support. Develop process improvement plans using tools like Six Sigma, Lean Manufacturing, SPC, DOE, etc. Qualifications
Bachelor's degree or minimum 5 years of work experience. At least 3 years of experience in a regulated industry. Understanding of drug or Pharma QMS and regulatory requirements, including FDA CFR 21 210 and 211. Proficiency with MS Office, including Word, Excel, PowerPoint, and databases. Additional Information Regards,
To be considered for an interview, please make sure your application is full in line with the job specs as found below. Monil Patel Technical Recruiter Integrated Resources, Inc (732) 844-8747 Ext. 338 monil@irionline.com
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Participate in developing and maintaining quality systems, processes, and procedures to ensure product quality and safety. Assist the quality assurance site manager in preparing for audits and implementing corrective actions for non-conformities. Support risk management throughout the product lifecycle and provide senior management with key data to inform decisions. Support the development and maintenance of product approval, clearance, and licensing documentation as required by global regulatory agencies. Ensure 100% quality and regulatory compliance according to documented procedures. Communicate and implement strategies to ensure compliance. Review batch records supporting the disposition of bulk drug substances. Review equipment validation protocols and reports. Support compliance in raw material and solution release, including review of specifications and documentation. Manage the release of single-use disposable products, including label reconciliation. Review temperature charts and related documentation for excursions. Update label issuance and reconciliation processes. QA Documentation Support: Issue batch records and track logs, lab notebooks, and SOP binders. Scan and file excursion documents and batch-related documents for release support. Develop process improvement plans using tools like Six Sigma, Lean Manufacturing, SPC, DOE, etc. Qualifications
Bachelor's degree or minimum 5 years of work experience. At least 3 years of experience in a regulated industry. Understanding of drug or Pharma QMS and regulatory requirements, including FDA CFR 21 210 and 211. Proficiency with MS Office, including Word, Excel, PowerPoint, and databases. Additional Information Regards,
To be considered for an interview, please make sure your application is full in line with the job specs as found below. Monil Patel Technical Recruiter Integrated Resources, Inc (732) 844-8747 Ext. 338 monil@irionline.com
#J-18808-Ljbffr