Manufacturing Support Associate Day Shift (6am 6pm)

Job Title: Manufacturing Support Associate – Day Shift (6am – 6pm)
Contract Duration: 12 Months
Location: East Syracuse, NY 13057
Pay Rate: $21.50 Hourly

Qualifications:

• The Manufacturing Support Associate provides operational support to biopharmaceutical manufacturing operations through the execution of cleaning, sanitization, reagent preparation, and other support activities within a GMP classified cleanroom environment.
• Work is performed in controlled biologics production areas requiring adherence to gowning procedures, cleanroom hygiene standards, and personal protective equipment (PPE).
• This is not a laboratory-based position.
• This is an entry-level, 100% onsite role. Comprehensive training in GMP practices, safety procedures, and job-specific functions will be provided.

Responsibilities:

• Perform cleaning and sanitization of classified manufacturing suites and controlled areas in accordance with approved Standard Operating Procedures (SOPs).
• Execute equipment cleaning activities, including manual cleaning and Clean-in-Place (CIP) processes, for production vessels, transfer lines, and ancillary manufacturing equipment as required.
• Replenish materials and supplies and perform a variety of operational support tasks to ensure successful execution of manufacturing activities.
• Sustain a clean and orderly work environment, always maintaining inspection-ready conditions.
• Safely handle hazardous materials including caustics, acids, disinfectants, and steam systems in accordance with Health, Safety & Environmental (HSE) guidelines.
• Prepare cleaning agents, disinfectants, buffers, and process-related reagents according to approved SOPs and manufacturing documentation.
• Perform required calculations, measurements, and dilutions to ensure accurate reagent preparation.
• Identify and escalate abnormal conditions, safety concerns, or deviations from procedures.
• Complete and maintain accurate, timely documentation in cleaning logs, batch records, and electronic systems.
• Adhere to cGMP requirements, site policies, and quality systems.
• Participate in training programs to achieve and maintain qualification for assigned tasks.

Responsibilities (Qualifications):

• High school diploma.
• Ability to follow written procedures, verify data, perform basic mathematical calculations, and accurately document results while executing work in a safe and compliant manner.
• Ability to work effectively within a team environment to execute scheduled activities.
• Strong communication skills.
• Basic proficiency with computer systems, Microsoft Office applications (Word, Excel, Outlook), and web-based applications.
• Possess a continuous improvement mindset, a desire to learn, and a drive to contribute to a culture of excellence and our mission of delivering benefits to patients worldwide.

Preferred:

• Mechanical aptitude.
• Background in Science related field.
• Prior manufacturing experience.
• Prior experience or familiarity with cGMP operations or aseptic technique.

Physical Demands & Work Environment:

• Work is performed in classified cleanroom environments requiring gowning and extended periods in PPE.
• Position includes physical demands such as bending, twisting, squatting, kneeling, climbing, reaching, and prolonged standing.
• Infrequent unassisted lifting up to 50 lbs may be required.
• Regular exposure to cleaning chemicals, disinfectants, and steam systems.