Sterile Parenteral Manufacturing Technician — Flexible Shifts

Inteldot; Manatí (PR); On-site; USD 52,000 - 76,000; Full time

Job summary

Inteldot seeks an experienced Parenteral Manufacturing Technician to support sterile pharmaceutical operations in Puerto Rico. You will perform formulation, filling, and lyophilization tasks in a regulated environment, ensuring proper equipment setup, cleaning, autoclave use, and aseptic processing.

Strong cGMP, GDP, and documentation practices are essential. Responsibilities include in-process monitoring, CIP/SIP, batch record maintenance, and collaboration with QA, Validation, and Engineering

Qualifications

• High school diploma or equivalent required.
• 2+ years in parenteral or aseptic manufacturing, or 3+ years in pharmaceutical manufacturing.
• Experience in GMP environment with formulation, filling, and sterilization processes.
• Knowledge of cGMP, GDP, aseptic techniques, and contamination control.
• Able to read/execute procedures and batch records in English and/or Spanish.
• Strong communication, teamwork, and problem-solving skills.

Responsibilities

• Execute formulation, preparation, filling, and lyophilization steps where applicable.
• Set up, clean, sterilize, and changeover equipment per procedures.
• Operate autoclaves, isolators, and related processing equipment.
• Perform CIP/SIP operations and monitor filter integrity.
• Handle excipients and API materials; perform in-process sampling.
• Maintain Data Integrity and complete batch records accurately.
• Support environmental monitoring, QA, validation, and investigations.

Skills

Aseptic manufacturing

cGMP compliance

Data integrity

Attention to detail

Batch records documentation

English/Spanish reading

Education

High school diploma or equivalent

Tools

Autoclaves

Isolators

HMI systems

Electronic batch records

PLC-controlled equipment

Job description

Inteldot seeks an experienced Parenteral Manufacturing Technician to support sterile pharmaceutical operations in Puerto Rico. You will perform formulation, filling, and lyophilization tasks in a regulated environment, ensuring proper equipment setup, cleaning, autoclave use, and aseptic processing.

Strong cGMP, GDP, and documentation practices are essential. Responsibilities include in-process monitoring, CIP/SIP, batch record maintenance, and collaboration with QA, Validation, and Engineering