Biopharma Manufacturing Technician I — Aseptic GMP

PCI TRGR Penn Pharmaceutical Services Ltd; Bedford, Northern (NH, KY); Hybrid; USD 42,000 - 56,000; Full time

Job summary

PCI TRGR Penn Pharmaceutical Services Ltd. seeks a Manufacturing Technician I at the Bedford, NH site to perform aseptic filling, formulation, and related manufacturing tasks under supervision in a GMP/ISO environment.

You will handle equipment prep, documentation, and sterile processing while adhering to safety guidelines. With 0–2 years of experience and a high school diploma, you will follow SOPs, assist in media fills, and contribute to a culture of quality and continuous improvement as part

Qualifications

• 0–2 years of working experience, preferably in a manufacturing environment.
• Minimum of a High school diploma/equivalency.
• Ability to weigh and measure raw materials and operate basic benchtop instruments.
• Able to follow written instructions.
• Good verbal and written skills.

Responsibilities

• Maintain safe work habits and PCI safety procedures.
• Perform aseptic filling, labeling, and related tasks in sterile and non-sterile conditions.
• Operate aseptic filling equipment and lyophilizer in cleanroom environments.
• Prepare equipment for sterilization and lyophilization; run autoclaves and depyrogenation steps.
• Complete documentation: logbooks, batch records, etc.
• Identify and escalate deviations; participate in investigations as needed.
• Perform COP, CIP, and SIP operations.
• Review and revise SOPs and batch records as required.

Skills

Verbal communication

Written communication

Measuring & weighing

Benchtop instruments

Attention to detail

Mechanical aptitude

Education

High school diploma

Tools

Benchtop instruments

Job description

PCI TRGR Penn Pharmaceutical Services Ltd. seeks a Manufacturing Technician I at the Bedford, NH site to perform aseptic filling, formulation, and related manufacturing tasks under supervision in a GMP/ISO environment.

You will handle equipment prep, documentation, and sterile processing while adhering to safety guidelines. With 0–2 years of experience and a high school diploma, you will follow SOPs, assist in media fills, and contribute to a culture of quality and continuous improvement as part