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Grifols

Fractionation Technician – Nights

Grifols

Fractionation Technician responsible for manufacturing products derived from human blood plasma. Following SOPs and ensuring compliance in a laboratory/manufacturing environment.

Posted 7/31/2026full-timeClayton • North Carolina • 🇺🇸 United StatesJuniorWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates strong knowledge of Good Manufacturing Practices (cGMP) and safety guidelines while effectively operating manufacturing process control systems and equipment. Possesses the ability to work collaboratively in a team environment and maintain accurate record keeping in compliance with industry standards.

Highest-signal resume keywords
Good Manufacturing Practices (cGMP)Standard Operating Procedures (SOP's)Manufacturing Process Control SystemsData Entry SkillsBioworks 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
Basic Math SkillsMechanical AptitudeAnalytical AnalysisRecord KeepingClean In Place (CIP) OperationBuffer and Process Solutions PreparationIntermediate Product TransferSafety Guidelines KnowledgeBatch Production Records (BPR's)Supply Chain Support
Soft Skills
Detail OrientedTeamworkGood JudgmentCommunication SkillsWillingness to Learn
Tools & Technologies
SAPACSIS
Certifications & Qualifications
High School Diploma or EquivalentBioworks Certificate
Industry Keywords
Safety RegulationsHealth RegulationsEnvironment RegulationsEthical Manufacturing24/7 Rotating Shift

About the role

Key responsibilities & impact
  • 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.

Requirements

What you’ll need
  • Level I: Basic math skills, basic computer skills, mechanical aptitude, detail oriented, ability to work in a team environment and exercise good judgment. Candidate must possess a high school diploma or equivalent. Bioworks Certificate preferred.
  • Level II: Typically requires a minimum of 12 months as a Technician in his/her respective department before receiving consideration for advancement to Fractionation Tech II. Employee must receive a minimum of a meets expectations overall rating on his/her most recent performance review.
  • 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.
  • 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.

Benefits

Comp & perks
  • 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.
  • Executes commissioning and validation activities associated with a new building.