JT959 - ENGINEERING TECHNICIAN III

Jayuya, Puerto Rico
Temporary
Medical Device
Experienced

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

  • Operates weighting and analytical scales and mixing machine to blend drugs into solutions for processing, assure that Company complies with all internal and external standards and procedures
  • Performs weighting and mixing process of raw material -drugs- (such as: Amino Acids, Metronidazole Heparin, Milrinoner etc) based on available resources and activities. This includes hydrolysis process of lactic acid.
  • Starts machine and adjusts valves for mixing process.
  • Operates machine until mixture reaches desired consistency as per mixing specifications.
  • Operates auxiliary equipment to prepare mixture for final processing.
  • Takes care of automatic mixing machine.
  • Assure that all drug mixing complies with all standards (SOPs), especially Good Documentation Practices.
  • Follow and comply with established SOPS, specifications and practices. Comply with CFR requirements.
  • Ability to solve daily quality and material issues to assure the most efficient, effective and safety product release.
  • Participate in the new products protocols.
  • Fill out, review and maintain all reports as required (daily, weekly, monthly, annually) in compliance with cGMPs, cGDP's and other internal and external standards.
  • Coordinate, monitor and perform sampling handling process, and refers them to Plant Pharmacist as required.
  • Perform routine area audit to ensure compliance with established company and regulatory requirements.
  • Performs drug head count as required by procedures.
  • Willing to work extra hours, any shift and during weekends when required.
  • Support and back up the manufacturing department (mixing area) as required.
  • Must be able to keep the work area in the cleanest and organize conditions.

Qualifications:

  • Associate's degree (A. D.) - Bachelor's degree preferred.
  • Computer knowledge is required (Windows: Excel).
  • Ability to read and interpret documents such as safety rules operating and maintenance instructions, and procedure manuals.
  • Ability to write routine reports and correspondence.
  • Ability to communicate, read, write and understand English/Spanish languages.
  • Must have knowledge of Good Documentation Practices (GDP), the ability to identify errors in documentation as part of their core competencies, and strong mathematical skills, as the position involves weighing raw materials.
  • Available for 3rd shift (Sunday through Thursday, or Sunday through Friday with one day off during the week, depending on business needs)

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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