Aseptic Technician

• Execute aseptic compounding, formulation preparation, sterile filtration, filling, and visual inspection activities following approved batch records and SOPs.
• Prepare and verify raw materials, components, and equipment before manufacturing activities.
• Operate and monitor aseptic filling equipment, pumps, filtration systems, and related production equipment.
• Perform vial, syringe, or IV bag filling operations in compliance with validated manufacturing processes.
• Ensure proper container closure integrity and visual inspection requirements during production.
• Adhere to cleanroom gowning procedures, personnel qualification requirements, and aseptic behavior standards.
• Maintain compliance with contamination control strategies and sterility assurance practices.
• Perform equipment setup, cleaning, sanitization, and basic troubleshooting activities.
• Complete Batch Production Records (BPRs) accurately and in accordance with ALCOA+ data integrity principles.
• Report manufacturing deviations and participate in investigations related to manufacturing events., Scheduling Operations Leadership Coordinating Construction Shop Drawing Change Orders Data Analysis Subcontracting Quality Control Microsoft Office Project Schedules Performance Review Project Management Project Engineering Contract Interpretation Submittals (Construction) Verbal Communication Skills Interpersonal Communications Building Information Modeling Request For Information (RFI) +0

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Albany, NY*On-Site

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Chemistry Visionary Operations Innovation Cleanrooms Filtration Outsourcing Cleanliness Sanitization Life Sciences Investigation Critical Care Data Integrity Detail Oriented Quality Control Batch Production Quality Assurance Aseptic Processing Visual Inspections Regulatory Oversight Contamination Control Facilities Engineering Artificial Intelligence Pharmaceutical Sciences Manufacturing Operations Environmental Monitoring Engineering Design Process Good Manufacturing Practices Pharmaceutical Manufacturing Compounded Sterile Preparations Troubleshooting (Problem Solving) Current Good Manufacturing Practices (cGMPS), Join a dynamic team involved in aseptic manufacturing operations, where you will perform critical tasks such as aseptic compounding, formulation preparation, sterile filtration, filling, and visual inspections according to approved batch records and SOPs. This role requires a keen attention to detail and a commitment to maintaining the highest standards of sterility and cleanliness within ISO classified cleanroom environments., * Bachelor’s degree in Life Sciences, Chemistry, Biology, Engineering, Pharmaceutical Sciences, or related field preferred.

• 1 to 3 years of experience in aseptic pharmaceutical manufacturing, sterile compounding, or sterile injectable production.
• Experience in ISO classified cleanrooms and aseptic processing environments.
• Knowledge of CGMP regulations, FDA 503B requirements, USP <797>, USP <800>, USP <825>, and Annex 1 guidance.
• Understanding of contamination control principles and sterile manufacturing processes.

Additional Skills & Qualifications

• Experience with aseptic filling operations, sterile filtration, and manufacturing documentation.
• Strong understanding of contamination control principles and sterile manufacturing processes., Planning Coaching Hoisting Patience Curiosity Mechanics Leadership Management Innovation Proactivity Self-Starter Problem Solving Lean Enterprise Lean Principles Microsoft Office Project Schedules Lifelong Learning Project Management Lean Manufacturing Influencing Skills Process Improvement Strategic Alignment Operations Management Contract Interpretation Verbal Communication Skills Interpersonal Communications Building Information Modeling Influencing Without Authority Continuous Improvement Process +0

Work in an FDA-registered 503B outsourcing facility in Albany, NY, specializing in sterile compounded medications for critical care settings. Operate under strict current Good Manufacturing Practices (cGMP) and regulatory oversight. Collaborate closely with Quality Assurance, Quality Control, Environmental Monitoring, Facilities, Engineering, Validation, and Compliance Teams. The schedule is Monday to Friday from 9 am to 5 pm in a clean room environment, where garbing and PPE are required. Job Type & Location

This is a Permanent position based out of Colonie, NY. Pay and Benefits

The pay range for this position is $30.00 - $50.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.