Grifols
Overview
Quality Assurance Inspector (1st shift) at
Grifols . On-site role at the Clayton, NC Facility. Hours: 1st shift Monday - Friday 5:00am - 1:30pm. This position supports manufacturing operations during the production process by approving raw materials and associated documentation for incoming plasma shipments and in-process production batches at the Plasma Logistics Center (PLC). QA Inspectors identify and document deviations and ensure corrections to help ensure a high-quality finished product for customers. Responsibilities
Approves incoming plasma shipment documentation and raw materials by confirming specifications, rejects and returns unacceptable materials as directed by QA Supervisor. Generates and documents non-conformance of plasma units or procedures associated with plasma shipments, PUs or final plasma lots. Approves PUs by confirming customer and regulatory specifications and communicating required adjustments to the QA Supervisor. Inspects final outgoing plasma lot shipments to ensure all pallets are properly packaged and loaded for sales and distribution. Investigates and reports in-process/final product and processes that do not meet quality specifications and documents in a deviation report. Participates in the writing or revision of policies and standard operating procedures related to Source Plasma and quality systems at GPLC. Executes repetitive functions with strict adherence to procedures and maintains record accountability. Documents approval activities in the organization's computer system. Knowledge, Skills, And Abilities
Good communication skills with the ability to express ideas with clarity and thoroughness in both verbal and written communications. Proactive, results oriented with strong attention to detail. Strong interpersonal skills to interface with manufacturing operators and various levels of management as well as with support and service departments. Ability to work in a team-oriented environment and follow safety guidelines. Must be computer literate with experience in the use of Microsoft applications. Able to perform basic arithmetic functions including addition, subtraction, multiplication, division and using decimals. Education And Experience
High School diploma or GED. Typically requires a minimum of 1 year of Quality Assurance related experience and 2 years working in pharmaceuticals. Experience in the pharmaceutical, plasma/blood banking or medical device industry is ideal and working knowledge of cGMP helpful. Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level typically requires an Associate’s degree plus 2 years of experience, an equivalent could include 4 years of experience or a Bachelor’s degree. This position is eligible to participate in up to 5% of the company bonus pool. We offer benefits including Medical, Dental, Vision, PTO, up to 5% 401(K) match and tuition reimbursement. Final compensation depends on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. Grifols is a global healthcare organization with employees in 30 countries and a family-like culture. Grifols has grown significantly over the last decade and offers opportunities for professional growth. Employment Details
Seniority level: Entry level Employment type: Full-time Job function: Quality Assurance Industries: Pharmaceutical Manufacturing and Medical Equipment Manufacturing Location: NORTH AMERICA : USA : NC-Clayton
#J-18808-Ljbffr
Quality Assurance Inspector (1st shift) at
Grifols . On-site role at the Clayton, NC Facility. Hours: 1st shift Monday - Friday 5:00am - 1:30pm. This position supports manufacturing operations during the production process by approving raw materials and associated documentation for incoming plasma shipments and in-process production batches at the Plasma Logistics Center (PLC). QA Inspectors identify and document deviations and ensure corrections to help ensure a high-quality finished product for customers. Responsibilities
Approves incoming plasma shipment documentation and raw materials by confirming specifications, rejects and returns unacceptable materials as directed by QA Supervisor. Generates and documents non-conformance of plasma units or procedures associated with plasma shipments, PUs or final plasma lots. Approves PUs by confirming customer and regulatory specifications and communicating required adjustments to the QA Supervisor. Inspects final outgoing plasma lot shipments to ensure all pallets are properly packaged and loaded for sales and distribution. Investigates and reports in-process/final product and processes that do not meet quality specifications and documents in a deviation report. Participates in the writing or revision of policies and standard operating procedures related to Source Plasma and quality systems at GPLC. Executes repetitive functions with strict adherence to procedures and maintains record accountability. Documents approval activities in the organization's computer system. Knowledge, Skills, And Abilities
Good communication skills with the ability to express ideas with clarity and thoroughness in both verbal and written communications. Proactive, results oriented with strong attention to detail. Strong interpersonal skills to interface with manufacturing operators and various levels of management as well as with support and service departments. Ability to work in a team-oriented environment and follow safety guidelines. Must be computer literate with experience in the use of Microsoft applications. Able to perform basic arithmetic functions including addition, subtraction, multiplication, division and using decimals. Education And Experience
High School diploma or GED. Typically requires a minimum of 1 year of Quality Assurance related experience and 2 years working in pharmaceuticals. Experience in the pharmaceutical, plasma/blood banking or medical device industry is ideal and working knowledge of cGMP helpful. Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level typically requires an Associate’s degree plus 2 years of experience, an equivalent could include 4 years of experience or a Bachelor’s degree. This position is eligible to participate in up to 5% of the company bonus pool. We offer benefits including Medical, Dental, Vision, PTO, up to 5% 401(K) match and tuition reimbursement. Final compensation depends on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. Grifols is a global healthcare organization with employees in 30 countries and a family-like culture. Grifols has grown significantly over the last decade and offers opportunities for professional growth. Employment Details
Seniority level: Entry level Employment type: Full-time Job function: Quality Assurance Industries: Pharmaceutical Manufacturing and Medical Equipment Manufacturing Location: NORTH AMERICA : USA : NC-Clayton
#J-18808-Ljbffr