GRIFOLS USA , LLC
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Quality Inspector 1 - (Raw Materials) 1
at GRIFOLS USA , LLC
Grifols is a global healthcare company whose mission is to improve the health and well-being of people. Our three divisions –Bioscience, Diagnostic and Hospital–develop, produce and market our innovative products and services to medical professionals in more than 100 countries.
We are committed to fostering an environment that creates continuous learning opportunities and encourages professional development and growth. As a company devoted to improving the health and well-being of people, we are looking for talented professionals worldwide. Make a difference and join us in this challenging and rewarding enterprise.
Responsible for inspecting and sampling all raw materials that are used in production according to the Raw Material Specification (RMS).
ESSENTIAL DUTIES & RESPONSIBILITIES include the following. Other duties may be assigned.
- Sample raw materials for QC testing and for the Reference Sample program.
- Perform identification test for all chemical containers.
- Perform visual inspections and dimensional analysis of incoming materials per RMS (Raw Materials Specification).
- Record deficiencies associated with each lot received under the supplier quality history trending program.
- Review all inspection records to ensure entries are correct and completely filled out.
- Stack/load pallets and transport material by operating various types of material handling equipment (e.g. forklift, electric pallet jack).
- Will share general responsibilities for equipment maintenance and calibration, housekeeping, and other support functions (e.g., inventory of consumables and reagents).
- Maintain sample logs on a daily basis to ensure timely testing and tracking of all samples.
- Maintain Instrument Usage and Calibration Logs based on instrument usage during the preparation and testing of samples.
- Strict adherence to procedures and practices according to FDA regulations.
- Strong emphasis on documentation according to FDA regulations.
- Adhere to departmental corporate safety policies.
REQUIRED EXPERIENCE/SKILLS & EDUCATIONAL QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.
- Associate’s degree in Chemistry, Biochemistry, Biology or closely related scientific discipline is required.
- Related experience in a pharmaceutical, GMP, or FDA regulated environment is preferred.
- Requires a basic understanding of quality inspection and verification / testing of incoming raw materials.
- Forklift experience (stand up or sit down) in a warehouse environment is preferred.
- Strong organizational, analytical, and problem-solving skills with the ability to make structured decisions on a routine basis.
- Must be proactive, results oriented, and have strong attention to detail.
- Self-starter with strong work ethic and the ability to exercise good judgment.
- Ability to effectively prioritize and manage multiple tasks to meet targeted deadlines.
- Strong interpersonal skills with the ability to interact with personnel at all levels in a team environment.
- Excellent verbal and written communication skills in the English language.
- Computer literacy with proficiency in MS Office (Outlook, Word, Excel, PowerPoint).
- Must be flexible with working hours / shifts in order to accommodate the 24 hour, 7 day plant operation.
- Ability to lift /move up to 50 pounds.
- Ability to stand for extended periods - up to four (4) hours at a time.
- Manual dexterity to perform all job functions.
- Exposure to toxic/caustic chemicals and biological hazards.
- Must have color perception/discrimination for inspection and/or testing.
- Must be able to work in cold environments.
*This job description is accurate at the date of publication and may change over time. It is not intended as an exhaustive description of the job. Other duties may be assigned and qualifications required may change.
Grifols is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and local laws that prohibit employment discrimination on the basis of race, color, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability or veteran's status or any other classification protected by applicable State/Federal laws. We will consider for employment all qualified Applicants, including those with Criminal Histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance.
Location: CA-Los Angeles
Across three major divisions – Bioscience, Diagnostic, and Hospital – Grifols is a leading healthcare company with a global reach that extends to more than 100 countries. Our innovative products and services focus on life-saving protein therapies for patients around the world. As our company continues to grow, we are searching for capable, compassionate individuals who are ready to thrive in an environment that challenges their skills and rewards their performance.
Here at Grifols, we believe that it takes more than a solid paycheck to recruit and retain a stellar staff. As a result, we’re committed to creating a culture that fosters diversity and supports the goals of each and every valued member of our team. As a Grifols associate, you’ll enjoy highly competitive compensation and a comprehensive total rewards package that offers medical, dental, life, and disability insurance, as well as a strong 401(k) retirement savings plan.
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