Manufacturing Lead Technician

GRIFOLS, S.A.CA-Los Angeles, CA
$34 - $35Onsite

About The Position

In general, the Manufacturing Lead Technician is responsible for overseeing the coordination and operations of the production schedule, shift, and personnel. Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

Requirements

  • High school diploma or GED required.
  • Minimum of 3 years of related experience in a pharmaceutical, GMP, or FDA regulated environment is required.
  • Demonstrated leadership skills with the ability to motivate, guide, train, coach and develop department personnel.
  • Comprehensive knowledge and understanding of cGMPs, FDA regulations, and industry guidelines.
  • Ability to work independently with minimum supervision.
  • Must be proactive, results oriented, and have strong attention to detail.
  • Self-starter with strong work ethic and the ability to exercise good judgment.
  • Ability to effectively prioritize and manage multiple tasks to meet targeted deadlines.
  • Strong interpersonal skills with the ability to interact with personnel at all levels in a team environment.
  • Must be able to read, write, and speak English.
  • Computer literacy with proficiency in MS Office (Outlook, Word, Excel, PowerPoint).
  • Must be flexible with working hours / shifts in order to accommodate the 24-hour, 7 day plant operation.

Nice To Haves

  • Associate’s degree, applicable certification, and/or military veterans preferred.

Responsibilities

  • Responsible for equipment setup and operation in a biologics processing environment for plasma derived pharmaceuticals.
  • Strict adherence to procedures and practices according to FDA regulations.
  • Strong emphasis on documentation according to FDA regulations.
  • Adhere to departmental corporate safety policies.
  • Responsible for facility and equipment cleaning.
  • All work is performed in a clean room (sanitized) manufacturing environment.
  • Responsible for basic process analysis such as pH, refractive index, turbidity, and conductivity measurements.
  • Operates manufacturing equipment such as ultrafiltration (UF) units, chromatography columns, Clean In Place (CIP) systems, Steam In Place (SIP) systems and centrifuges.
  • Utilizes touch screen Operator Interface Terminals (OIT).
  • Trains entry level personnel.
  • Performs more complex and advanced job tasks.
  • Assist management in coordinating and scheduling the department's day to day operations.
  • Serves in a leadership role in the absence of direct supervision.
  • Other duties may be assigned.

Benefits

  • Medical
  • Dental
  • Vision
  • PTO
  • up to 5% 401(K) match
  • tuition reimbursement
  • company bonus pool
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