NCBiotech
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.
NFF‑Fractionation Technician I / II Day Shift – 7am‑7pm
Hiring Manager – Juan Quintanilla
Due to the growth at the GT site and ramping up multiple Manufacturing departments, it is vital that we focus on training newer employees and maintaining existing area expertise while we work through this growth phase, no GT Manufacturing production employees are eligible to bid for this position at this time. This is an internal NFF movement, only NFF night shift Tech I’s & Tech II’s are eligible to apply.
Summary The Fractionation Technician I / II 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
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 (SOP’s) and complete Batch Production Records (BPR’s)
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 SOP’s 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.
Communicates information and ideas so others will understand.
Frequently interacts with others.
Rotating shifts.
Works at heights on platforms and/or on ladders.
Recruiter – Angelina Acevedo
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 - Clayton
Learn more about Grifols https://www.grifols.com/en/what-we-do
Req ID:
537277
Type:
Regular Full-Time
Job Category:
MANUFACTURING
#J-18808-Ljbffr
NFF‑Fractionation Technician I / II Day Shift – 7am‑7pm
Hiring Manager – Juan Quintanilla
Due to the growth at the GT site and ramping up multiple Manufacturing departments, it is vital that we focus on training newer employees and maintaining existing area expertise while we work through this growth phase, no GT Manufacturing production employees are eligible to bid for this position at this time. This is an internal NFF movement, only NFF night shift Tech I’s & Tech II’s are eligible to apply.
Summary The Fractionation Technician I / II 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
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 (SOP’s) and complete Batch Production Records (BPR’s)
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 SOP’s 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.
Communicates information and ideas so others will understand.
Frequently interacts with others.
Rotating shifts.
Works at heights on platforms and/or on ladders.
Recruiter – Angelina Acevedo
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 - Clayton
Learn more about Grifols https://www.grifols.com/en/what-we-do
Req ID:
537277
Type:
Regular Full-Time
Job Category:
MANUFACTURING
#J-18808-Ljbffr