Grifols
Quality Associate II-III, QC
at
Grifols
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well‑being of people around the world. We are leaders in plasma‑derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
Shift:
1st Shift (Monday through Friday 8:00AM to 4:30PM)
Primary Responsibilities
Collects, reviews, and analyzes data.
Makes decisions independently, but within a well‑defined area.
Addresses and resolves problems according to written procedures (i.e. SOP, etc.) or practice.
Coordinates work activities and scheduling.
Coordinates employee training.
Communicates effectively and promptly at all levels of the organization, supporting department objectives and management decisions.
Contributes cross‑functionally within the departmental hierarchy.
Demonstrates high levels of value and integrity.
Follows cGMP and department safety practices.
Additional Responsibilities
Apply expertise in testing to develop, validate and troubleshoot analytical methods.
Serve as SME for laboratory assays and act as a resource for laboratory staff.
Oversee the sterility aseptic gowning program.
Perform investigations and write reports.
Author SOPs and other laboratory documents.
Collaborate with production and Quality Assurance and Compliance on projects, incident investigations, and annual product reviews.
Evaluate data and perform statistical analysis for various projects.
Serve as system administrator and SME for various laboratory information systems and applications as required.
Requirements
BA/BS – preferably in a STEM (science, technology, engineering, or mathematics) curriculum and 2 years of relevant experience or an equivalent combination of education and experience.
Experience testing/gowning/operating in a classified environment.
Proficiency using SAP is strongly preferred.
Detail oriented and great organizational and communication skills are a must.
Excellent prioritization, multitasking and leadership skills are crucial.
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.
Work is performed in an office and a laboratory/manufacturing environment or warehouse. Exposure to biological fluids with potential exposure to infectious organisms.
Exposure to occasional extreme cold below 32°F in production areas, exposure to electrical office and laboratory equipment.
Personal protective equipment is required such as protective eyewear, garments and gloves.
Work is performed sitting or standing for 2‑4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple movements of the fingers, hands, and wrists.
Ability to make precise coordinated movements of the fingers to grasp and manipulate objects. Light to moderate lifting and carrying objects with a maximum lift of 35 lbs.
Occasionally walks, bends and twists neck and waist, may reach above or below shoulder height. Frequent foot movements.
Color perception/discrimination and near vision correctable in one eye to 20/30 and to 20/100 in the other eye.
Ability to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken and written words and sentences.
Performs tasks by following a set of written or oral instructions/procedures.
Quality Associate, III, QC (Sterility) This position is a technical and testing support position with the QC Sterility laboratory. Prior experience with instrumentation, software and the data entry system used to perform sterility testing and visual appearance assays is highly preferred. Hiring level will be dependent on experience level. A strong technical aptitude and experience with Microsoft Word, Excel and SAP as well as technical report writing is strongly desired.
Qualifications
BA/BS – preferably in a STEM curriculum and 3 years of relevant experience or an equivalent combination of education and experience.
The ideal candidate should be a fully qualified professional who requires minimal supervision and makes independent decisions within designated assignments.
Demonstrates high levels of integrity and value as well as consistent application of technical knowledge and expertise.
Addresses and resolves problems according to SOP or best practices and develops solutions to defined problems within area of assignments.
Communicates effectively and promptly with all levels of the organization, supporting department objectives and management decisions.
Preferred skills involve intermediate knowledge of Microsoft Excel and Word and experience with SAP.
Third Party Agency and Recruiter Notice Agencies that present a candidate to Grifols must have an active, non‑expired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
EEO Statement Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.
Location NORTH AMERICA : USA : NC - Clayton (USNC0002)
#J-18808-Ljbffr
at
Grifols
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well‑being of people around the world. We are leaders in plasma‑derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
Shift:
1st Shift (Monday through Friday 8:00AM to 4:30PM)
Primary Responsibilities
Collects, reviews, and analyzes data.
Makes decisions independently, but within a well‑defined area.
Addresses and resolves problems according to written procedures (i.e. SOP, etc.) or practice.
Coordinates work activities and scheduling.
Coordinates employee training.
Communicates effectively and promptly at all levels of the organization, supporting department objectives and management decisions.
Contributes cross‑functionally within the departmental hierarchy.
Demonstrates high levels of value and integrity.
Follows cGMP and department safety practices.
Additional Responsibilities
Apply expertise in testing to develop, validate and troubleshoot analytical methods.
Serve as SME for laboratory assays and act as a resource for laboratory staff.
Oversee the sterility aseptic gowning program.
Perform investigations and write reports.
Author SOPs and other laboratory documents.
Collaborate with production and Quality Assurance and Compliance on projects, incident investigations, and annual product reviews.
Evaluate data and perform statistical analysis for various projects.
Serve as system administrator and SME for various laboratory information systems and applications as required.
Requirements
BA/BS – preferably in a STEM (science, technology, engineering, or mathematics) curriculum and 2 years of relevant experience or an equivalent combination of education and experience.
Experience testing/gowning/operating in a classified environment.
Proficiency using SAP is strongly preferred.
Detail oriented and great organizational and communication skills are a must.
Excellent prioritization, multitasking and leadership skills are crucial.
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.
Work is performed in an office and a laboratory/manufacturing environment or warehouse. Exposure to biological fluids with potential exposure to infectious organisms.
Exposure to occasional extreme cold below 32°F in production areas, exposure to electrical office and laboratory equipment.
Personal protective equipment is required such as protective eyewear, garments and gloves.
Work is performed sitting or standing for 2‑4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple movements of the fingers, hands, and wrists.
Ability to make precise coordinated movements of the fingers to grasp and manipulate objects. Light to moderate lifting and carrying objects with a maximum lift of 35 lbs.
Occasionally walks, bends and twists neck and waist, may reach above or below shoulder height. Frequent foot movements.
Color perception/discrimination and near vision correctable in one eye to 20/30 and to 20/100 in the other eye.
Ability to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken and written words and sentences.
Performs tasks by following a set of written or oral instructions/procedures.
Quality Associate, III, QC (Sterility) This position is a technical and testing support position with the QC Sterility laboratory. Prior experience with instrumentation, software and the data entry system used to perform sterility testing and visual appearance assays is highly preferred. Hiring level will be dependent on experience level. A strong technical aptitude and experience with Microsoft Word, Excel and SAP as well as technical report writing is strongly desired.
Qualifications
BA/BS – preferably in a STEM curriculum and 3 years of relevant experience or an equivalent combination of education and experience.
The ideal candidate should be a fully qualified professional who requires minimal supervision and makes independent decisions within designated assignments.
Demonstrates high levels of integrity and value as well as consistent application of technical knowledge and expertise.
Addresses and resolves problems according to SOP or best practices and develops solutions to defined problems within area of assignments.
Communicates effectively and promptly with all levels of the organization, supporting department objectives and management decisions.
Preferred skills involve intermediate knowledge of Microsoft Excel and Word and experience with SAP.
Third Party Agency and Recruiter Notice Agencies that present a candidate to Grifols must have an active, non‑expired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
EEO Statement Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.
Location NORTH AMERICA : USA : NC - Clayton (USNC0002)
#J-18808-Ljbffr