Posted 18 August, 2026
Job Id: 629441
Aseptic Manufacturing & Filling Specialist
Job Description
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
ABOUT THE OPPORTUNITY
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.
WHAT YOU’LL BE DOING
Aseptic Manufacturing Operations
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Perform aseptic compounding, formulation preparation, sterile filtration, and filling operations according to approved batch records and SOPs
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Prepare and verify raw materials, components, and equipment prior to manufacturing activities
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Execute manufacturing operations within ISO-classified cleanroom environments while maintaining strict aseptic technique
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Perform line setup, equipment assembly, pre-use inspections, and batch reconciliation activities
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Monitor and document critical process parameters accurately and contemporaneously
Filling, Inspection & Packaging
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Operate semi-automatic filling equipment, pumps, filtration systems, and related production equipment
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Perform vial, syringe, or IV bag filling operations in compliance with validated manufacturing processes
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Ensure proper container closure integrity and visual inspection requirements are met during production
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Conduct line clearance and product changeover activities per approved procedures
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Perform labeling, packaging, and final product handling activities as required
Cleanroom & Contamination Control
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Adhere to cleanroom gowning procedures, personnel qualification requirements, and aseptic behavior standards
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Maintain strict compliance with contamination control strategies and sterility assurance practices
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Support environmental monitoring activities including viable and non-viable monitoring during production
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Identify and report potential contamination risks, cleanroom excursions, or process abnormalities
Documentation & Batch Record Compliance
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Complete Batch Production Records (BPRs) accurately and in accordance with ALCOA+ data integrity principles
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Document all manufacturing steps, process checks, equipment usage, and material reconciliation activities
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Review production documentation for completeness and accuracy before submission to Quality Assurance
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Ensure deviations, discrepancies, and non-conformances are documented promptly and completely
WHAT WE’RE LOOKING FOR
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Bachelor’s degree in Life Sciences, Chemistry, Biology, Engineering, Pharmaceutical Sciences, or related field preferred
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1-3 years of hands-on experience in aseptic pharmaceutical manufacturing — 503B, 503A compounding, or sterile injectable production accepted
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Direct experience working in ISO-classified cleanroom environments and aseptic processing
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Knowledge of cGMP regulations, FDA 503B requirements, USP <797>, USP <800>, USP <825>, and Annex 1 guidance
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Experience with sterile filtration, semi-automatic filling equipment, and manufacturing documentation
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Strong understanding of contamination control principles and sterility assurance practices
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High attention to detail, strong aseptic technique, and a commitment to quality and patient safety
CONVERSION OPPORTUNITY
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.
Equal Opportunity Employer
We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert
Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.