JT989 - TECHNICIAN III

Quality Consulting Group•Jayuya, PR

18d•Onsite

About The Position

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.

Requirements

Associate's Degree required; Bachelor's Degree preferred.
Computer proficiency, including Microsoft Windows and Microsoft Excel.
Knowledge of Good Documentation Practices (GDP) and the ability to identify documentation errors.
Strong mathematical skills for weighing, measuring, and calculating materials accurately.
Ability to read, interpret, and follow SOPs, safety rules, operating instructions, maintenance instructions, and procedure manuals.
Ability to prepare routine reports and production documentation.
Strong verbal and written communication skills in English and Spanish.
Ability to work effectively with supervisors, peers, and cross-functional teams.
Ability to lift and handle 100 lbs bags manually.
Willingness to work Sunday through Thursday or Sunday through Friday with one weekday off, depending on business needs.
Flexibility to work overtime, weekends, and different shifts as required.
Ability to work in a fast-paced manufacturing environment while maintaining quality, safety, and compliance standards.
Strong attention to detail, organizational skills, and commitment to maintaining a clean and safe work environment.

Responsibilities

Perform weighing and mixing of raw materials (drugs) such as Amino Acids, Metronidazole, Heparin, Milrinone, and others according to established procedures.
Perform the hydrolysis process of lactic acid.
Operate, start, and adjust mixing machines and valves to achieve required mixing specifications.
Operate auxiliary equipment to prepare mixtures for final processing.
Monitor and maintain automatic mixing equipment.
Ensure all weighing and mixing activities comply with SOPs, cGMPs, cGDPs, CFR requirements, and Good Documentation Practices (GDP).
Complete, review, and maintain production records and reports (daily, weekly, monthly, and annual) accurately.
Identify documentation errors and ensure compliance with documentation standards.
Perform manual weighing of raw materials and lift bags weighing up to 100 lbs.
Apply mathematical skills to accurately weigh and measure materials.
Coordinate, monitor, and perform sampling activities, referring samples to the Plant Pharmacist as required.
Conduct routine area audits to ensure compliance with company policies and regulatory requirements.
Troubleshoot daily quality and material issues to support safe and efficient product release.
Participate in new product protocols and validation activities.
Perform drug inventory head counts according to established procedures.
Support Manufacturing operations in the mixing area as needed.
Maintain work areas clean, organized, and inspection-ready.
Work collaboratively in a team environment.
Perform special projects and additional duties as assigned.
Work independently with minimal supervision.