Grifols
Fractionation Technician NFB (Nights)
Location: North America : USA : NC‑Clayton
Schedule: 12‑hour shift (nights)
Grifols is a global healthcare company that has been improving the future of healthcare since 1909. We are leaders in plasma‑derived medicines and transfusion medicine, developing, producing and marketing innovative medicines, solutions and services in more than 110 countries and regions.
Overview The Fractionation Technician is responsible for performing duties to manufacture products derived from human blood plasma. The role requires knowledge in science (biology or chemistry), engineering, mechanical aptitude, computers and various process equipment that interface with process controls automation.
Duties
Follow company safety guidelines and programs.
Demonstrate care of facility, equipment, systems and product.
Follow Standard Operating Procedures (SOPs) and complete Batch Production Records (BPRs).
Operate manufacturing process control system and equipment.
Operate Clean In Place (CIP) equipment and perform in‑process analytical analysis.
Monitor status of manufacturing processes and assist in sampling operations.
Assist in the harvest of intermediate products and the preparation, set‑up and transfer of buffer and process solutions.
Transfer intermediate product, raw materials and waste, and stage plasma, intermediate paste and raw materials.
Clean and 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.
Execute commissioning and validation activities associated with a new building.
Additional Responsibilities
Complete assignments in functional areas supporting departmental objectives.
Communicate effectively and promptly with other operators, technicians and supervisors.
Knowledge, Skills & 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.
Ability to work a 24/7 rotating shift schedule.
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 Requirements
High school education and completion of the "Bioworks Certification Program" through a community college,
High school education and 1 year pharmaceutical, chemical, and/or production manufacturing experience in a regulated industry (FDA, USDA, NRC) obtained within the last 5 years (completion of the "Bioworks Certification Program" through a community college a plus) or
Graduation from an accredited college/university with an Associate’s or Bachelor’s degree in Biology, Chemistry, Biochemistry, Engineering, Pharmaceutical Technology, Business, Teaching or a related curriculum (completion of the Bioworks Certificate program through a community college a plus).
Additional Experience
Ability to diagnose and troubleshoot process equipment used in manufacturing environment (preferred).
Work experience with distributed control systems and PLC operated equipment (preferred).
Experience in protein separation (preferred).
Start‑up or validation experience (preferred).
Occupational Demands
Work is performed in a laboratory/manufacturing environment.
Exposure to biological fluids with potential infectious organisms.
Exposure to electrical, pneumatic and other production equipment.
Potential exposure to high levels of noise on the production floor.
Personal protective equipment required (eyewear, garments, gloves).
Requires kneeling, climbing, squatting and frequent repetitive hand movements.
Frequently sits 4–6 hours per day and stands at times.
Frequently bends and twists neck and waist.
Light to moderate lifting up to 50 lbs.
Rotating shifts, including commissioning and validation periods.
Works at heights on platforms or ladders.
Benefits We offer a comprehensive package of benefits including medical, paid time off (PTO), pharmacy, dental, vision, disability insurance, life & AD+D insurance, 5% 401(k) match, and tuition reimbursement. We are committed to offering employees opportunities for professional growth and career progression.
Equal Employment Opportunity 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 in a manner consistent with the requirements of applicable state and local laws.
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Schedule: 12‑hour shift (nights)
Grifols is a global healthcare company that has been improving the future of healthcare since 1909. We are leaders in plasma‑derived medicines and transfusion medicine, developing, producing and marketing innovative medicines, solutions and services in more than 110 countries and regions.
Overview The Fractionation Technician is responsible for performing duties to manufacture products derived from human blood plasma. The role requires knowledge in science (biology or chemistry), engineering, mechanical aptitude, computers and various process equipment that interface with process controls automation.
Duties
Follow company safety guidelines and programs.
Demonstrate care of facility, equipment, systems and product.
Follow Standard Operating Procedures (SOPs) and complete Batch Production Records (BPRs).
Operate manufacturing process control system and equipment.
Operate Clean In Place (CIP) equipment and perform in‑process analytical analysis.
Monitor status of manufacturing processes and assist in sampling operations.
Assist in the harvest of intermediate products and the preparation, set‑up and transfer of buffer and process solutions.
Transfer intermediate product, raw materials and waste, and stage plasma, intermediate paste and raw materials.
Clean and 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.
Execute commissioning and validation activities associated with a new building.
Additional Responsibilities
Complete assignments in functional areas supporting departmental objectives.
Communicate effectively and promptly with other operators, technicians and supervisors.
Knowledge, Skills & 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.
Ability to work a 24/7 rotating shift schedule.
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 Requirements
High school education and completion of the "Bioworks Certification Program" through a community college,
High school education and 1 year pharmaceutical, chemical, and/or production manufacturing experience in a regulated industry (FDA, USDA, NRC) obtained within the last 5 years (completion of the "Bioworks Certification Program" through a community college a plus) or
Graduation from an accredited college/university with an Associate’s or Bachelor’s degree in Biology, Chemistry, Biochemistry, Engineering, Pharmaceutical Technology, Business, Teaching or a related curriculum (completion of the Bioworks Certificate program through a community college a plus).
Additional Experience
Ability to diagnose and troubleshoot process equipment used in manufacturing environment (preferred).
Work experience with distributed control systems and PLC operated equipment (preferred).
Experience in protein separation (preferred).
Start‑up or validation experience (preferred).
Occupational Demands
Work is performed in a laboratory/manufacturing environment.
Exposure to biological fluids with potential infectious organisms.
Exposure to electrical, pneumatic and other production equipment.
Potential exposure to high levels of noise on the production floor.
Personal protective equipment required (eyewear, garments, gloves).
Requires kneeling, climbing, squatting and frequent repetitive hand movements.
Frequently sits 4–6 hours per day and stands at times.
Frequently bends and twists neck and waist.
Light to moderate lifting up to 50 lbs.
Rotating shifts, including commissioning and validation periods.
Works at heights on platforms or ladders.
Benefits We offer a comprehensive package of benefits including medical, paid time off (PTO), pharmacy, dental, vision, disability insurance, life & AD+D insurance, 5% 401(k) match, and tuition reimbursement. We are committed to offering employees opportunities for professional growth and career progression.
Equal Employment Opportunity 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 in a manner consistent with the requirements of applicable state and local laws.
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