Description

The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, and perform basic laboratory tasks, including pH, conductivity, sampling, and routine sanitization tasks to maintain facility and equipment. A basic understanding of cGMP compliance is expected while training under close supervision, demonstrating aseptic techniques in handling products and materials.

Company Culture and Environment

The work environment emphasizes adherence to strict regulatory standards, cleanliness, and safety protocols. Team collaboration and effective communication are key, with associates attending shift exchanges and participating in project meetings.

Career Growth and Development Opportunities

Associates will have opportunities to attain qualifications for assigned tasks and maintain an individual training plan, promoting continuous learning and professional development within the manufacturing field.

Detailed Benefits and Perks

• Support for 6S programs to maintain organization and cleanliness in the workplace
• Opportunities for participation in various projects and team initiatives

Compensation and Benefits

• Competitive salary based on experience
• Health, dental, and vision insurance
• Retirement savings plan with company matching
• Generous vacation and paid time off policy
• Flexible working hours

Why you should apply for this position today

This role offers a unique opportunity to contribute to the production of life-changing therapeutics in a supportive and compliant environment. You will gain valuable experience in a critical industry while ensuring the highest quality standards in manufacturing processes.

Skills

• Understanding of cGMP compliance
• Aseptic technique handling products and materials
• Ability to execute process recipes and follow SOPs
• Strong attention to detail in monitoring production processes
• Effective communication skills for shift exchanges and documentation

Responsibilities

• Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations
• Report production in written and electronic documents in accordance with good manufacturing practices (GMPs) and good documentation procedures (GDPs)
• Perform material movements and transfer raw materials and chemicals across production areas
• Maintain facility and equipment through routine cleaning and sanitization
• Attend shift exchanges, meetings, and participate in projects as required
• Perform other duties as assigned

Qualifications

• Must be a US authorized citizen or Green Card holder
• Basic understanding of manufacturing processes and regulatory compliance

Education Requirements

• High school diploma or equivalent

Education Requirements Credential Category

• High School Diploma

Experience Requirements

• Experience in a manufacturing or laboratory environment preferred, but not required
• Knowledge of basic laboratory techniques and equipment operation

Why work in Portsmouth, NH

Portsmouth offers a vibrant coastal lifestyle with rich historical significance and a strong community spirit. The city features a blend of cultural attractions, outdoor recreational opportunities, and a thriving local economy, making it an ideal place to live and work.