Grifols
Grifols
Grifols is a global healthcare, biotechnology, and manufacturing company focused on plasma-derived medicines and other solutions for patients with rare diseases and chronic conditions. Its work spans research and development, pharmaceutical production, and worldwide distribution, making Grifols a relevant employer for professionals interested in biotechnology, biopharmaceutical manufacturing, and healthcare innovation.

Grifols Operations Supervisor, On-Site in Edinburg

Lead plasma center operations at Grifols in Edinburg, coordinating donor flow, plasma collection, production records, compliance, equipment, and staff training. The role supports safe, accurate operations and donor satisfaction in a regulated environment.

Description

  • Remain qualified to perform all tasks within the plasma center
  • Carry out production duties while supervising donor flow
  • Oversee donor selection, plasma collection, and manufacturing records
  • Maintain production standards under applicable regulations, SOPs, OSHA, CLIA, and cGMP requirements
  • Participate in required training sessions and staff meetings
  • Complete documentation accurately and thoroughly
  • Help keep the facility clean and equipment in proper working condition
  • Provide timely, accurate reports to the Center Manager or Assistant Manager
  • Assist with managing center donor funds
  • Train new employees and provide refresher training for current staff
  • Coordinate with other service areas to support accurate documentation and quality
  • Build positive donor relationships and support continued donations and customer satisfaction
  • Report unsafe conditions or situations
  • Complete training to repair plasma center equipment when assigned
  • Support the Center Manager or Assistant Manager with tasks aligned with company objectives

Requirements

  • High school diploma or GED
  • Certification as a Phlebotomist, Donor Processor, Plasma Processor, and Designated Trainer
  • Typically four years of related experience in phlebotomy, donor processing, and plasma processing
  • Proven ability to manage difficult situations effectively
  • Strong knowledge of and compliance with state and federal regulations
  • Familiarity with the FDA-approved Standard Operating Procedure Manual, OSHA, CLIA, cGMP, and internal company procedures
  • Ability to work in a plasma center with exposure to biological fluids, infectious organisms, electrical equipment, and very cold conditions
  • Ability to use required personal protective equipment
  • Ability to stand for four to six hours daily and sit for one to two hours daily
  • Ability to bend, twist, squat, crouch, make frequent hand and foot movements, and perform precise coordinated movements
  • Ability to routinely lift 15 pounds and lift up to 50 pounds maximum
  • Essential hearing acuity
  • Correctable near- and far-vision capability
  • Ability to communicate and understand spoken and written information
  • Ability to work independently and follow oral or written instructions
  • Ability to manage a broad range of tasks under variable demands and changing conditions
  • Ability to communicate sensitive information to diverse groups

Benefits

  • Regular full-time employment
  • Equal employment opportunity protections

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