Investigation Lead

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website http://www. qrcgroup.com / to learn more about our services and solutions! We are seeking an Investigation Lead to provide operational and scientific expertise, together with compliance knowledge, in support of manufacturing sterile and non-sterile operations .

The resource will execute manufacturing investigations ( Quality Events , or QEs) and facilitate the collection and coordination of information required to support those investigations.

Responsibilities

Ensure that all QEs, NTRs, and NOEs are completed and closed within the established timeframe, using the appropriate tools to prevent recurrence. Review and provide input to regulatory submissions applicable to the area of responsibility. Lead QE and CAPA trend evaluations . Participate in regulatory inspections when necessary.

Support site initiatives and other assignments based on business needs. Bachelor's degree in Science, Pharmacy, and/or Engineering. Five (5) years of experience in a parenteral manufacturing facility . At least one (1) year of experience in the investigation process . Strong technical writing and presentation skills. Ability to interpret and analyze statistical data.

Knowledge of cGMPs, OSHA, EPA, and other regulatory standards. Proficiency with Microsoft Word, Excel, and PowerPoint. Excellent interpersonal skills and a teamwork-oriented approach. Excellent written and verbal communication skills in Spanish and English.

Benefits

What We Offer

Opportunities for learning, development, and professional growth. A collaborative and supportive work environment. The opportunity to work with industry-leading clients on impactful projects. Your information will be kept confidential according to EEO guidelines.