Full-Time

Manufacturing Technician

Artech Information System

Artech Information System

1,001-5,000 employees

IT staffing and project-based workforce solutions

No salary listed

Sanford, NC, USA

In Person

Category
Biology & Biotech (2)
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Requirements
  • BA/BS in Technology/Business/Industry/Science with minimum 2 years direct regulated manufacturing pharmaceutical/biotech experience
  • AAS Science related with minimum 4 years direct regulated manufacturing pharma/biotech experience
  • HS or equivalent with minimum 8 years direct regulated manufacturing pharma/biotech experience
  • Or progression from Bio-processing Technician Level I that includes additional internal development curriculum
  • Must complete training in assigned area and comply with applicable safety, OSHA, and environmental safety requirements
  • Must complete training and comply with applicable cGMP requirements
  • GMP experience required
  • Be able to rationalize by suggesting solutions to unusual conditions and/or process concerns
  • Must possess mechanical ability to assemble and operate equipment
  • Must pay attention to detail by following procedures and noting unusual conditions
  • Must have written and oral communication to read procedures, write accurate observations and follow directions
  • Moderate repetitive standing, ladder climbing, repetitive bending, pushing, and lifting up to 40 pounds required on a daily basis
  • Basic understanding of the metric system
  • The incumbent will be required to attend quality-training programs and orientations on an annual or as needed basis
  • The incumbent will be required to become familiar with domestic and international regulatory requirements associated with manufacturing and biological processes
  • Annual performance goals and objectives will be evaluated against specific quality performance requirements as defined by the Manufacturing Supervisor
  • Mandatory commitment to report to management any potential or actual deviations from regulatory requirements
  • Ongoing input regarding quality process improvements
  • Master documentation procedures by following detailed written and verbal instructions in order to complete assigned tasks (follow area SOPs)
  • Demonstrate knowledge of procedures by performing tasks and duties and maintaining detailed records in a manner compliant with cGMPs
  • Perform routine job duties which may include vacuuming, mopping ceilings, walls and floors, emptying trashcans, etc.
  • Prepare production glassware and other equipment by operating industrial washers, autoclaves and depyrogenation ovens
  • Clean and sterilize process equipment (tanks, fermentors) as needed
  • Demonstrate and instruct proper gowning and aseptic processing procedures
  • Work with individuals as a team
  • Work various shifts and some weekends
  • Operate and troubleshoot production equipment in assigned area and report unusual conditions or concerns about the process or equipment to area Supervisor
  • Train new employees on production processes
  • Perform lab work such as: performing sample dilutions, pH, and conductivity readings
  • Minimum number of years of prior experience required to perform job duties. A minimum of four years pharmaceutical experience in biological manufacturing is preferred
Responsibilities
  • Operate all equipment in two assigned Manufacturing areas.
  • Clean equipment and facilities, and provide documentation of all duties in accordance with Good Manufacturing Practices.
  • Perform all duties in a manner consistent with site and corporate cGMP, safety, environmental and human resources policies and procedures.
  • Attend quality-training programs and orientations on an annual or as needed basis.
  • Become familiar with domestic and international regulatory requirements associated with manufacturing and biological processes.
  • Annual performance goals and objectives will be evaluated against specific quality performance requirements as defined by the Manufacturing Supervisor.
  • Report any potential or actual deviations from regulatory requirements.
  • Provide input regarding quality process improvements.
  • Master documentation procedures by following detailed written and verbal instructions in order to complete assigned tasks (follow area standard operating procedures).
  • Demonstrate knowledge of procedures by performing tasks and duties and maintaining detailed records in a manner compliant with cGMPs.
  • Perform routine job duties, which may include vacuuming, mopping ceilings, walls and floors, emptying trashcans, etc.
  • Prepare production glassware and other equipment by operating industrial washers, autoclaves and depyrogenation ovens.
  • Clean and sterilize process equipment (tanks, fermentors) as needed.
  • Demonstrate and instruct proper gowning and aseptic processing procedures.
  • Work with individuals as a team.
  • Work various shifts and some weekends.
  • Operate and troubleshoot production equipment in assigned area and report unusual conditions or concerns about the process or equipment to area Supervisor.
  • Train new employees on production processes.
  • Perform lab work, such as: performing sample dilutions, pH, and conductivity readings.
Desired Qualifications
  • Pharma experience highly preferred
  • Bioprocessing experience in a cGMP environment, knowledge of Clean and Steam in Place Systems, perform facility cleanings, collecting Water for Injection and Clean Steam samples
  • Experience with autoclave and industrial washers
Artech Information System

Artech Information System

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Artech Information System provides IT staffing and project-based services worldwide. It connects organizations with tech talent through staffing programs (contingent, direct hire, RPO, master vendor, payroll transition) and delivers end-to-end digital and technical projects (design, operations, development, and platforms). It stands out through its focus on applied human intelligence, diverse and inclusive culture, and a track record with Fortune 500 clients across multiple countries. Its goal is to be the ecosystem that connects people, technology, and opportunities, enabling global businesses and talent to grow together.

Company Size

1,001-5,000

Company Stage

N/A

Total Funding

N/A

Headquarters

Morristown, New Jersey

Founded

1992

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Simplify's Take

What believers are saying

  • Artech provides managed cloud and cybersecurity services to Fortune 500 firms.
  • Artech supports public-sector organizations amid AI and cloud shifts.
  • Artech generated over $775 million in global revenue as women-owned business.

What critics are saying

  • Trump's 2025 H-1B tightening cuts Artech's India staffing in 3-6 months.
  • Apex Group acquisitions erode Artech's position in 12-24 months.
  • 2026 recession freezes Fortune 500 IT budgets, hitting Artech revenue.

What makes Artech Information System unique

  • Artech is the largest women-owned IT workforce solutions firm in the U.S.
  • Artech holds Great Place to Work certification for its dynamic culture.
  • Artech expanded India offices in Bengaluru, Bhopal, Hyderabad, and Chennai.

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