Quality Inspector

Grifols

Los Angeles, CA

JOB DETAILS
SALARY
$21.35–$25 Per Hour
SKILLS
Biochemistry, Biotech and Pharmaceutical, Calibration, Chemistry, Communication Skills, Computer Skills, Current Good Manufacturing Practice (cGMP), Detail Oriented, Electricity, English Language, FDA (Food and Drug Administration), FDA Requirements, Forklift, GMP (Good Manufacturing Practices), Healthcare, High School Diploma, Insurance, International Health, Interpersonal Skills, Inventory Levels, Inventory Management, Laboratory Equipment, Lift/Move 35 Pounds, Manufacturing, Material Moving, Materials Analysis, Materials Testing, Medical Conditions, Medical Products, Medicine, Microsoft Excel, Microsoft Outlook, Microsoft Product Family, Microsoft Word, Multitasking, Office Equipment, Plasma, Presentation/Verbal Skills, Project/Program Management, Quality Assurance Methodology, Quality Control, Regulations, SAP Administration, Sampling Inspection, Testing, Time Management, Warehousing, Writing Skills
LOCATION
Los Angeles, CA
POSTED
Today
Quality Inspector

Location: CA-Los Angeles, US Contract Type: Regular Full-Time Area: OPERATIONAL TECHNICAL AREA

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.

Job Summary: Responsible for inspecting and sampling all raw materials that are used in production and packaging according to the Raw Material Specification (RMS) and associated approved procedures.

Primary Job Responsibilities:

  • 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.
  • 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 fill out.
  • Ensure all equipments used in the inspection and testing processes are calibrated.
  • Maintain Instrument Usage and Calibration Logs based on instrument usage during the preparation and testing of samples.
  • Monitor and maintain the inventory level of supplies used in the inspection process.
  • Maintain work area and equipment in a clean, safe, and orderly condition.
  • Exercise and Monitor GMP (logs, documentation practices, etc.) and safety compliance requirements in the work environment.

Knowledge, Skill and Abilities:

  • Understanding of cGMPs, FDA regulations, and industry guidelines, as well as international regulatory guidelines.
  • Ability to operate a forklift is preferred.
  • Ability to keep neat, accurate and complete records and logs.
  • Must be proactive, results oriented, with a strong attention to detail.
  • Self-starter with good work ethic and ability to work independently with minimum supervision or as a contributing member of a team.
  • Ability to manage multiple projects simultaneously, meet deadlines, and handle an ever changing, fast paced critical work environment.
  • Excellent verbal and written communication.
  • Must be able to read, write, and speak English.
  • Must be able to perform basic calculation such as addition, subtraction, multiplication, and division.
  • Strong interpersonal skills with ability to interact with all levels of personnel in a professional manner.
  • Good computer skills with basic knowledge of Microsoft programs, particularly Outlook, Word, Excel, etc.
  • Knowledge of SAP (Inventory Management System) is a plus.

Education and Experience:

  • Minimum of High School diploma.
  • Associates Degree in Chemistry, Biochemistry, or closely related scientific discipline is preferred.
  • Minimum of 0 -2 years of related experience.
  • Pharmaceutical industry experience or experience in a GMP or FDA regulated environment is preferred.

Occupational Demands:

  • 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* in production areas.
  • Exposure to electrical office and laboratory equipment.
  • Personal protective equipment 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 35lbs.
  • 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.
  • Able 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.

The estimated pay scale for Quality Inspector role based in California, is $21.35 to $25.00 per hour. Additionally, the position is eligible to participate in up to 5% of the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, life insurance, PTO, paid holidays and up to 5% 401(K) match and tuition reimbursement.

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, including but not limited to, the California Fair Chance Act, the Los Angeles County Fair Chance Ordinance for Employers, and the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

About the Company

G

Grifols

At Grifols, what we do matters

Are you passionate about making a difference in the world? At Grifols, we are pioneers in the development of therapies derived from blood and plasma. We contribute to building the future of healthcare to improve people's well-being. Since 1909, we have been defined by passion, innovation, teamwork and a sense of responsibility. Our people change lives while growing and developing into a forward-looking international company.

Your future at Grifols

At Grifols, you will be part of a growing international team of more than 23,000 people in more than 30 countries and regions with a common goal: to improve people's lives. You will contribute to developing scientific advances and providing innovative solutions for healthcare professionals and essential medicines for patients. We want to count on determined professionals who, by cultivating their talent, contribute to creating a positive impact on society.

COMPANY SIZE
10,000 employees or more
INDUSTRY
Healthcare Services
FOUNDED
1909
WEBSITE
https://www.grifols.com/