Sam Taiym Email & Phone Number

Chicago, Il, Us

Middleboro-Lakeville, Massachusetts, Us

Los Angeles, California, Us

Plant shutdown

Los Angeles, California, Us

Chicago, Il, Us

-Audit external warehouses, co-manufacturers, and raw material suppliers in order to ensure compliance with governmental regulatory requirements, customer specifications, and company standards and guidelines. -Conduct internal assessments of all company locations to include compliance to company standards, regulatory requirements, and GFSI standards.-Maintain and update supplier documentation in accordance with regulatory and company requirements. -In partnership with local Quality teams, ensure timely responses to identified nonconformities and the implementation of effective corrective actions with internal and external partners. -Verify the effectiveness of corrective actions from audits conducted.-Ensure that second- and third-party partner’s management is knowledgeable on Blommer’s standards and requirements. Verify they can comply with quality expectations.-Aid in the creation and maintenance of internal specifications and guidelines for suppliers, services, and purchased materials.-Support efforts of Quality by cross-training on related projects and serving as a resource for supported activities.

Purchase, Ny, Us

-Manage all complaint-related activities, including investigation, issue resolution, severity assessment, and regulatory reporting.-Successful implementation of company-wide training matrix.-Successfully closed CAPA resulting in 50% increase of on-time regulatory reviews of incoming complaints.-Wrote several macros and scripts in Salesforce and ComplianceQuest to automate closure of priority complaints. -Developed process for hypertension monitor complaints, including investigation requirements, supplemental information, and talk tracks.-Key Member and Subject Matter Expert in Complaints Handling Task Force responsible for reducing complaint handing time, resulting in 40% reduced handling times, $60k in monthly cost savings, and $1million in annual cost avoidance.

Westchester, Illinois, Us

Lead on various CI/Lean projects designed to improve quality documentation processes and customer experience, including: •Implementation of Standard Work for the Quality Documentation Team to standardize processes across the group while providing transparence and insight via relevant metrics. •Consolidation of commonly requested quality documents into a single controlled document for 500+ SKU’s in order to reduce total number of requests. •Creation of manufacturing site assessments designed to empower quality specialists to provide efficient and accurate response in order to improve overall customer experience. •Results 2016-2019: Average TAT for customer requests: 15 Days ► 7 Days; On-time response rate: 63% ► 93%Worked with key accounts to align their document control systems with Ingredion’s document control systems.Fully integrated the document control systems of various company acquisitions with Ingredion’s systems.Owner and manager of the GMP and Pest Control audit program, overseeing various contractors and a 12-person cross-functional audit team.Provided support to the internal and external auditing teams by conducting internal ISO 9001 audits and external supplier audits.Worked cross-functionally with internal customers to ensure compliance with all applicable laws, regulations, and standard.

Houston, Texas, Us

Worked collaboratively with the quality department to design and implement various analytical methods in order to secure a key contract.

Led a temperature experiment that was used to successfully argue against a 483 during an FDA audit.Updated the sample retain program in order to reduce turnaround time for complaint and return investigations.

Bachelor'S Degree, Biology, General

Education record