Biopharma Manufacturing Technician — Impact & Growth

PCI TRGR Penn Pharmaceutical Services Ltd

Bedford (NH)

On-site

USD 42,000 - 65,000

Full time

4 days ago
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Job summary

PCI Pharma Services in Bedford, NH, is seeking a Manufacturing Technician I to support aseptic filling, formulation, and packaging under GMP/ISO guidelines. You will prepare solutions, operate filling and lyophilization equipment, and maintain accurate batch records in a cleanroom setting.

Ideal candidates have up to 2 years in pharma manufacturing, strong attention to detail, and the ability to follow SOPs. This is a hands-on role with shift flexibility and safety as a priority.

Qualifications

  • 0–2 years of manufacturing experience, preferably in pharma or medical devices.
  • High school diploma or equivalent required.
  • Able to weigh and measure raw materials and operate basic benchtop instruments.
  • Follow written instructions and SOPs; good verbal and written communication.
  • Detail oriented, mechanically inclined, honest and cooperative.

Responsibilities

  • Maintain safe work habits and follow PCI safety procedures.
  • Prepare solutions, aseptic filling, labeling of vials under sterile/non-sterile conditions.
  • Operate aseptic filling and lyophilization equipment in cleanrooms.
  • Assist in formulation, sanitizing, and equipment preparation for production.
  • Document batch records, logbooks, and production documentation accurately.
  • Escalate events deviating from normal operation; participate in investigations.

Skills

Aseptic techniques
Safety procedures
Documentation
Equipment operation
GMP/ISO awareness

Education

High school diploma/equivalency

Tools

Benchtop instruments
Autoclaves
Lyophilizer equipment
Vial filling equipment
Centrifuges

Job description

PCI Pharma Services in Bedford, NH, is seeking a Manufacturing Technician I to support aseptic filling, formulation, and packaging under GMP/ISO guidelines. You will prepare solutions, operate filling and lyophilization equipment, and maintain accurate batch records in a cleanroom setting.

Ideal candidates have up to 2 years in pharma manufacturing, strong attention to detail, and the ability to follow SOPs. This is a hands-on role with shift flexibility and safety as a priority.

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