Manufacturing Associate

Scope of Responsibilities:

• Support manufacturing operations to produce clinical supply products under cGMP conditions in a Lean Manufacturing environment
• Execute routine production activities following batch records standard operating procedures (SOPs) and work instructions
• Prepare operate and clean equipment and manufacturing areas in accordance with established procedures
• Accurately document manufacturing activities in compliance with GMP and company requirements
• Adhere to all safety guidelines environmental health standards and quality systems
• Assist with material handling activities including staging labeling and inventory tracking
• Identify document and communicate deviations non-conformances or safety concerns
• Collaborate with cross-functional teams including Quality Assurance and Manufacturing Sciences to support production goals
• Participate in training programs to build technical expertise and maintain compliance qualifications
• Contribute to continuous improvement initiatives and support a culture of operational excellence
• Support manufacturing area readiness for production activities and inspections

Qualifications:

• High school diploma or equivalent required; Associates or Bachelors degree in Science or Engineering preferred
• 02 years of experience in manufacturing biotechnology pharmaceutical operations or a related field (internships or academic lab experience acceptable)
• Basic understanding of GMP and regulated environments preferred
• Strong attention to detail and ability to follow written and verbal instructions
• Effective communication and interpersonal skills
• Ability to work collaboratively in a team environment
• Willingness to learn and grow in a fast-paced start-up environment

Additional Requirements:

• Ability to work in a cleanroom environment and wear appropriate personal protective equipment (PPE)
• Flexibility to support shift-based operations including evenings weekends or overtime as needed