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.
Night Shift (rotating)
7pm-7am
Summary:
The Fractionation Technician is responsible for performing duties to manufacture products derived from human blood plasma, which require comprehension in the following areas:
Science (i.e. biology or chemistry)
Engineering
Mechanical aptitude
Computers
Various process equipment (i.e. Centrifuge, Automatic Bottle Opener, CIP skids) that interface with process controls automation.
Primary responsibilities for role:
Follow company safety guidelines and programs
Demonstrate care of facility, equipment, systems, and product
Demonstrate appropriate personal hygiene and proper gowning
Follow Standard Operating Procedures (SOPs) and complete Batch Production Records (BPRs)
Complete record keeping in accordance with current Good Manufacturing Practices
Operate manufacturing process control system and equipment
Operate Clean In Place (CIP) equipment
Perform in process analytical analysis
Monitor status of manufacturing processes
Assist in sampling operations
Assist in the harvest of intermediate products
Assist in the preparation, set up and transfer of Buffer and Process solutions.
Transfer intermediate product, raw materials, and waste
Stage plasma, intermediate paste and raw materials
Clean and/or Sanitize designated manufacturing areas
Utilize SAP and / or ACSIS transactions
Support the supply chain requirements for production
Assist team members, including supervision, to perform additional tasks
Work in an ethical and compliant manner to manufacture a drug product that is safe for human use.
Additional Responsibilities
Completes assignments in functional areas supporting departmental objectives.
Communicates effectively and promptly with other operators, technicians and supervisors.
Knowledge, Skills and Abilities
Knowledge of safety guidelines and SOPs established by the company.
Strong knowledge of current Good Manufacturing Practices (cGMP), and State and Federal Health, Environment and Safety regulations.
Excellent oral and written communication skills.
Comfortable with using different computer systems to perform data entry.
Willingness to work with and learn from other members of the manufacturing team.
Desire to enhance one's skills and knowledge.
Education/Experience
High School Diploma. Bioworks Certification preferred.
Equivalency
Depending on the area of assignment, directly related experience or a combination of education and directly related experience and/or competencies may be considered in place of the stated requirements.
Occupational Demands
Work is performed in a laboratory/manufacturing environment.
Exposure to biological fluids with potential exposure to infectious organisms.
Exposure to electrical and pneumatic powered equipment.
Exposure to miscellaneous production chemicals, moving machinery and production equipment.
Potential exposure to high levels of noise on production floor.
Personal protective equipment required such as protective eyewear, garments and gloves.
Requires kneeling, climbing and squatting.
Frequently sits for 4-6 hours per day.
Frequent repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
Often performs duties standing.
Frequently bends and twists neck and waist.
Light to moderate lifting and carrying objects with a maximum lift of 50 lbs.
Able to communicate 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.
Frequently interacts with others.
Rotating shifts.
Works at heights on platforms and/or on ladders.
Third Party Agency and Recruiter Notice:
Agencies that present a candidate to Grifols must have an active, nonexpired, 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.
Grifols provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other characteristic or status protected by law. 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: NORTH AMERICA : USA : NC-Clayton:[[cust_building]]
Learn more about Grifols
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.
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.