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PCI Pharma Services

Pharmaceutical packaging and contract services

Manufacturing Technician 1/2/3

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeBedford, NH, USANo salary listed

About the Job

Requirements

  • Minimum of a high school diploma or equivalent.
  • Zero to two or more years of work experience, preferably in manufacturing and ideally in the pharmaceutical or medical device industry.
  • Ability to weigh and measure raw materials and operate basic benchtop instruments.
  • Ability to follow written instructions and seek help with complex and non-routine tasks.
  • Attention to detail and mechanical aptitude.
  • Ability to wear personal protective equipment, gown and enter controlled manufacturing areas, lift, pull, or push equipment requiring up to 25–50 pounds of force, and stand for six hours in a production suite.
  • Ability to work any shift of up to 10 hours as business needs require; expected to be flexible with the process and adjust work hours accordingly.
  • Ability to adapt to daily process changes and work under client scrutiny.
  • Ability to conduct business according to legal and ethical standards and receive and implement feedback.

Responsibilities

  • Perform routine and critical manufacturing operations under supervision and in accordance with manufacturing instructions, current GMP/ISO requirements, and safety guidelines, including equipment preparation, formulation, aseptic compounding, and filling activities for biopharma and medical device products.
  • Maintain safe work habits and adhere to applicable safety procedures and guidelines.
  • Demonstrate knowledge of aseptic techniques.
  • Prepare solutions; perform aseptic filling and vial labeling under sterile and non-sterile conditions; and perform routine solution and filtration, vial and component preparation, and sterilization.
  • Assemble, disassemble, and operate aseptic filling and lyophilizer equipment in classified cleanrooms and controlled non-classified environments; operate vial cappers; and unload products from lyophilizers and liquid fill lines.
  • Prepare equipment and components for sterilization and lyophilization.
  • Operate processing equipment, including autoclaves, ovens, vial washers, depyrogenation equipment, centrifuges, and mills.
  • Assist with product formulation and dispensing in a cleanroom environment in accordance with standard operating procedures and master batch records.
  • Sanitize production areas and prepare equipment for production.
  • Complete and maintain work documentation, including logbooks and batch records, and accurately document production steps.
  • Follow verbal instructions and written procedures when operating production equipment and performing processing steps.
  • Identify, escalate, and document deviations from normal operation, and participate in investigations as needed.
  • Maintain compliance, cleanliness, and orderliness in operational areas according to applicable procedures.
  • Perform clean-out-of-place, clean-in-place, and sterilize-in-place operations to prepare equipment for manufacturing.
  • Review and revise relevant standard operating procedures and production batch records as required.
  • Successfully participate in media-fill and aseptic proficiency testing.
  • Interact with cross-functional support teams, including Operations, Quality Assurance, Quality Control, Engineering, Research and Development, and Validation.

Desired Qualifications

  • Manufacturing experience, preferably in the pharmaceutical or medical device industry.

About the Company

PCI Pharma Services

Pharmaceutical packaging and contract services

PCI Pharma Services provides end-to-end pharmaceutical packaging and related services, including folding cartons, labels, contract packaging, clinical services, and brand protection, acting as a one-stop source for healthcare product development and commercialization. It handles packaging operations from cartons and labels to contract packaging and labeling, plus clinical packaging and brand protection, with processes built on cGMP and ISO compliance, lean manufacturing, and ongoing R&D, supported by mandatory training and strict security, hygiene, and inspections. It differentiates itself with eight decades of experience and a broad, integrated service suite under one roof, reducing risk and handoffs for clients. Its goal is to be a trusted packaging partner that delivers reliable, compliant, and scalable solutions so healthcare brands stay protected and clients can focus on their core business.

Company size
1-10
Company stage
Debt Financing
Total funding
$4B
Headquarters
Burlington, Canada
Founded
1971

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