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Alcami

Pharmaceutical and biologics CDMO services

Manufacturing Technician 2 - Sterile Injection

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeMorrisville, NC, USANo salary listed

About the Job

Requirements

  • A high school diploma or GED is required; an associate or bachelor's degree is preferred.
  • One to two years of work experience and prior cGMP pharmaceutical manufacturing experience are required.
  • Candidates with life sciences or engineering degrees will be considered without manufacturing experience.
  • The ability to operate, troubleshoot, and maintain complex manufacturing equipment is required.
  • Strong attention to detail, organizational skills, problem-solving ability, and basic troubleshooting ability are required.
  • The ability to perform basic math calculations and read, comprehend, and apply detailed written instructions is required.
  • The ability to move materials throughout the facility using appropriate methods and equipment is required.
  • The ability to use appropriate personal protective equipment based on product handling requirements, including PAPR or supplied-air respirators, is required.
  • Knowledge of general compounding equipment, including pH meters, mixers, stir plates, and rigid or soft vessels, is required.
  • Knowledge of single-use solution pathway parts, including aseptic connectors and filtration assemblies, is required.
  • Knowledge of drug product fillers, including isolators, is required.
  • The ability to detect minute defects or discrepancies in product appearance is required.
  • The ability to train and certify employees is required.
  • The ability to adapt to changing priorities and variable batch-to-batch operations is required.
  • The employee must have 20/20 vision, with or without corrective lenses, and pass a color-blind test.
  • The employee must be able to meet the physical demands, including standing, walking, climbing or balancing, kneeling or crouching, and lifting or moving materials as specified.
  • The employee must be able to work in environments with moving mechanical parts, airborne particles, toxic or caustic chemicals, and other stated workplace exposures, and wear required protective equipment.
  • The employee must be able to comply with facial-hair limitations when tight-fitting respirators are required.

Responsibilities

  • Learn and execute manufacturing operations, including setup, operation, and maintenance of equipment used in dispensing, compounding, filling with isolators, and visual inspection.
  • Become a subject matter expert on compounding and filling processes and equipment.
  • Perform production processes in accordance with standard operating procedures, batch records, and quality standards, and contribute to deviation reduction to maintain product quality.
  • Conduct in-process and end-of-process sampling and quality checks to ensure products meet standards.
  • Identify inefficiencies and promptly escalate them to area supervision to support continuous process improvement.
  • Maintain accurate, legible production documentation, minimize errors, and escalate recommendations for document revisions.
  • Complete required cGMP and other company training on time.
  • Use general manufacturing technologies in accordance with standard operating procedures and cGMPs.
  • Perform in-process sampling, weight checks, component counting, and basic mathematical calculations.
  • Perform in-process and finished-product visual inspections.
  • Clean rooms, tools, and equipment before and after use.
  • Assist in other manufacturing areas as needed and perform material handling, dispensing, compounding, and filling activities correctly the first time.
  • Follow general instructions for routine work and detailed instructions for new projects or assignments.
  • Follow safety requirements and model a safety-first culture.
  • Work occasional hours outside the scheduled shift, including weekends, based on business needs.
  • Prepare and sterilize equipment and components, including filter integrity testing, autoclaving, and parts wrapping.
  • Perform compounding, vial washing and depyrogenation, aseptic filling, stoppering and capping, lyophilization, visual inspection, facility cleaning and sanitation, and batch record and logbook review.
  • Perform other duties as assigned.

Desired Qualifications

  • Two to five years of work experience is preferred.
  • Experience in dispensing, compounding, aseptic filling, or visual inspection is highly desirable.
  • Basic computer skills, including Microsoft Office, and familiarity with electronic documentation systems are preferred.

About the Company

Alcami

Pharmaceutical and biologics CDMO services

Alcami is a contract development and manufacturing organization supporting pharmaceutical and biologics companies from early development through commercial production. Services span drug product manufacturing (sterile fill-finish and oral solid dose), analytical and microbiology lab testing, and cGMP storage with validation and environmental monitoring. What sets Alcami apart is its integrated, end-to-end capabilities across the development lifecycle. The goal is to help pharma and biotech partners deliver safe, high-quality therapies to patients.

Company size
51-200
Company stage
Not listed
Total funding
Not listed
Headquarters
Pepperell, MA
Founded
1984

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