Job Summary Required Qualifications and Skills
This is a great opportunity for candidates with 1 to 2 years of experience, prior manufacturing exposure, or a science-related background who want to build hands-on experience in bioprocessing and pharmaceutical manufacturing operations. The work environment is team-oriented, structured, and focused on training, compliance, and continuous improvement. Successful candidates will contribute to meaningful work that supports the delivery of important products to patients worldwide.
Key Responsibilities
- Perform cleaning and sanitization of classified manufacturing suites and controlled areas in accordance with approved SOPs.
- Execute equipment cleaning activities, including manual cleaning and Clean-in-Place processes for production vessels, transfer lines, and related manufacturing equipment.
- Replenish materials and supplies while supporting operational tasks needed for successful manufacturing execution.
- Prepare cleaning agents, disinfectants, buffers, and process-related reagents following approved documentation and procedures.
- Complete required calculations, measurements, dilutions, cleaning logs, batch records, and electronic documentation accurately and on time.
- Identify and escalate abnormal conditions, safety concerns, or procedural deviations while maintaining a clean, orderly, inspection-ready work environment.
Compensation and Benefits
- Pay: $21.50 per hour.
- Job Type: Contract, temporary.
- Contract Length: 6 months.
- Schedule: Night shift, 6:00 p.m. to 6:00 a.m.
- Rotating schedule: 36 hours one week and 48 hours the following week, alternating.
- Must be willing to work scheduled holidays, weekends, and overtime.
- Work Location:Thompson Road, East Syracuse, NY 13057.
- Support bioprocess manufacturing operations by cleaning, sanitizing, and maintaining controlled production areas.
- Prepare reagents, cleaning solutions, disinfectants, and process-related materials according to approved procedures.
- Perform documentation, calculations, measurements, and data verification in a compliant manufacturing environment.
- Follow cGMP requirements, site policies, quality systems, and safety procedures while supporting scheduled production activities.
- High school diploma required.
- Ability to follow written procedures and execute work safely, accurately, and compliantly.
- Ability to verify data, perform basic mathematical calculations, and accurately document results.
- Basic proficiency with computer systems, Microsoft Office applications including Word, Excel, and Outlook, and web-based applications.
- Strong communication skills and the ability to work effectively in a team environment.
- Ability to safely handle hazardous materials including caustics, acids, disinfectants, and steam systems according to HSE guidelines.
- Continuous improvement mindset, willingness to learn, and motivation to contribute to a culture of quality and excellence.
- Ability to participate in training programs and maintain qualification for assigned tasks.
Preferred Qualifications
- Mechanical aptitude.
- Background in a science-related field.
- Prior manufacturing experience.
- Prior experience or familiarity with cGMP operations.
- Prior experience or familiarity with aseptic technique.
Equal Opportunity Employer / Disabled / Protected Veterans
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For temporary assignments lasting 13 weeks or longer, AppleOne is pleased to offer major medical, dental, vision, 401k and any statutory sick pay where required.
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