Lead Biopharma Manufacturing Technician

Grifols, S.A

Los Angeles (CA)

On-site

USD 47,000 - 48,000

Full time

9 days ago

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Benefits offered by this job

Medical benefits
Dental benefits
Vision benefits
PTO
401(k) match
Tuition reimbursement

Job summary

Grifols is seeking a Manufacturing Lead Technician for our Los Angeles, CA facility to oversee production scheduling, shift operations, and personnel coordination in a GMP-biotech environment.

You will operate equipment such as UF units, chromatography columns, CIP/SIP systems, and maintain strict adherence to FDA regulations while driving documentation and safety standards. This role requires leadership, a proactive mindset, and the ability to manage multiple tasks in a 24/7 plant.

Qualifications

  • Minimum 3 years of related pharmaceutical/GMP/FDA experience.
  • Demonstrated leadership ability to guide and develop department personnel.
  • Solid knowledge of cGMPs, FDA regulations, and industry guidelines.
  • Ability to work independently with minimal supervision; strong attention to detail.
  • Read, write, and speak English; proficient in MS Office.

Responsibilities

  • Oversee production schedule, shift, and personnel coordination.
  • Operate and set up equipment in a biologics manufacturing environment.
  • Ensure compliance with FDA procedures and documentation.
  • Maintain clean room and conduct basic process measurements (pH, turbidity, etc.).
  • Lead in management absence and assist scheduling daily operations.
  • Other duties as assigned.

Skills

Leadership skills
cGMPs
FDA regulations
English proficiency
MS Office

Education

High school diploma or GED
Associate's degree or certification

Tools

MS Office Suite

Job description

Grifols is seeking a Manufacturing Lead Technician for our Los Angeles, CA facility to oversee production scheduling, shift operations, and personnel coordination in a GMP-biotech environment.

You will operate equipment such as UF units, chromatography columns, CIP/SIP systems, and maintain strict adherence to FDA regulations while driving documentation and safety standards. This role requires leadership, a proactive mindset, and the ability to manage multiple tasks in a 24/7 plant.

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