Aseptic Manufacturing & Filling Specialist

Aseptic Manufacturing & Filling Specialist Contract-to-Hire | Albany, NY (100% On-site) | Mid-August 2026 Start Engagement Type: 3-Month Contract with permanent conversion opportunity

Location:

Albany, NY — 100% On-site

Start Date:

Mid-August 2026 Pay Rate: $40 – $50/hr (W2) | Based on experience Experience Level: 1‑3 Years

Planet Pharma is partnering with a 503B outsourcing facility in Albany, NY to identify an Aseptic Manufacturing & Filling Specialist. This is a contract-to-hire opportunity for a motivated, detail-oriented professional looking to grow within a fast-paced, highly regulated sterile manufacturing environment. The right candidate will bring hands‑on aseptic compounding and filling experience, strong cleanroom discipline, and a genuine commitment to patient safety and product quality.

• Perform aseptic compounding, formulation preparation, sterile filtration, and filling operations according to approved batch records and SOPs

• Prepare and verify raw materials, components, and equipment prior to manufacturing activities

• Execute manufacturing operations within ISO-classified cleanroom environments while maintaining strict aseptic technique

• Perform line setup, equipment assembly, pre-use inspections, and batch reconciliation activities

• Monitor and document critical process parameters accurately and contemporaneously

• Operate semi‑automatic 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 are met during production

• Conduct line clearance and product changeover activities per approved procedures

• Perform labeling, packaging, and final product handling activities as required

• Adhere to cleanroom gowning procedures, personnel qualification requirements, and aseptic behavior standards

• Maintain strict compliance with contamination control strategies and sterility assurance practices

• Support environmental monitoring activities including viable and non‑viable monitoring during production

• Identify and report potential contamination risks, cleanroom excursions, or process abnormalities

• Complete Batch Production Records (BPRs) accurately and in accordance with ALCOA+ data integrity principles

• Document all manufacturing steps, process checks, equipment usage, and material reconciliation activities

• Review production documentation for completeness and accuracy before submission to Quality Assurance

• Ensure deviations, discrepancies, and non-conformances are documented promptly and completely

• Bachelor’s degree in Life Sciences, Chemistry, Biology, Engineering, Pharmaceutical Sciences, or related field preferred

• 1‑3 years of hands‑on experience in aseptic pharmaceutical manufacturing — 503B, 503A compounding, or sterile injectable production accepted

• Direct experience working in ISO‑classified cleanroom environments and aseptic processing

• Knowledge of cGMP regulations, FDA 503B requirements, USP , USP , USP , and Annex 1 guidance

• Experience with sterile filtration, semi‑automatic filling equipment, and manufacturing documentation

• Strong understanding of contamination control principles and sterility assurance practices

• High attention to detail, strong aseptic technique, and a commitment to quality and patient safety

This engagement begins as a 3‑month contract with the opportunity for permanent conversion based on performance and mutual fit. Permanent compensation will be discussed directly between the candidate and the client at the time of conversion.