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Grifols

Fractionation Technician – Days

Grifols

. Manufacture products derived from human blood plasma .

Posted 11/11/2026full-timeClayton • North Carolina • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Good Manufacturing Practices (cGMP) and safety regulations while effectively operating manufacturing process control systems. Capable of performing detailed analytical analysis and maintaining accurate production records in a team-oriented environment.

Highest-signal resume keywords
Good Manufacturing Practices (cGMP)Batch Production RecordsClean In Place (CIP) Equipment OperationSAP and/or ACSIS TransactionsBioworks Certificate

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Analytical AnalysisManufacturing Process Control SystemsBuffer and Process Solutions PreparationData EntryMechanical Aptitude
Soft Skills
Detail OrientedTeam CollaborationExcellent Communication SkillsGood JudgmentWillingness to Learn
Tools & Technologies
SAPACSISManufacturing Equipment
Certifications & Qualifications
High School Diploma or EquivalentBioworks Certificate
Industry Keywords
Safety GuidelinesStandard Operating Procedures (SOPs)State and Federal Health RegulationsEnvironment and Safety RegulationsBiological Fluids Handling

About the role

Key responsibilities & impact
  • Manufacture products derived from human blood plasma
  • Follow company safety guidelines, programs, SOPs, and current Good Manufacturing Practices
  • Complete Batch Production Records and maintain required records
  • Operate manufacturing process control systems and process equipment
  • Operate Clean In Place (CIP) equipment
  • Perform in-process analytical analysis
  • Monitor manufacturing processes
  • Assist with sampling operations and harvesting intermediate products
  • Prepare, set up, and transfer buffer and process solutions
  • Transfer intermediate products, raw materials, and waste
  • Stage plasma, intermediate paste, and raw materials
  • Clean and sanitize designated manufacturing areas
  • Utilize SAP and/or ACSIS transactions
  • Support supply chain requirements for production
  • Assist team members and supervisors with additional tasks
  • Execute commissioning and validation activities associated with a new building
  • Communicate with operators, technicians, and supervisors
  • Work ethically and compliantly to manufacture safe drug products

Requirements

What you’ll need
  • Basic math skills
  • Basic computer skills
  • Mechanical aptitude
  • Detail oriented
  • Ability to work in a team environment and exercise good judgment
  • High school diploma or equivalent required
  • Bioworks Certificate preferred
  • Knowledge of company safety guidelines and SOPs
  • Strong knowledge of current Good Manufacturing Practices (cGMP)
  • Knowledge of State and Federal Health, Environment and Safety regulations
  • Excellent oral and written communication skills
  • Ability to work a 24/7 rotating shift schedule
  • Comfortable using different computer systems for data entry
  • Willingness to learn from other manufacturing team members
  • Ability to perform duties involving kneeling, climbing, squatting, standing, bending, twisting, repetitive hand movements, and working at heights
  • Ability to lift and carry up to 50 lbs
  • Ability to work around biological fluids, infectious organisms, chemicals, moving machinery, electrical and pneumatic equipment, and high noise levels
  • Ability to adapt to a fluid schedule during commissioning and validation
  • Level II advancement typically requires a minimum of 12 months as a Technician in the respective department and a minimum meets-expectations performance review

Benefits

Comp & perks
  • Regular full-time employment
  • 12-hour day shift
  • Equal employment opportunity protections