Description

The Manufacturing Associate I is a hands-on role responsible for executing buffers and media for both upstream and downstream manufacturing processes in a cGMP environment. This position requires technical expertise with equipment such as pH/conductivity meters, osmometers, weighing scales, and filter integrity operations. The candidate will work as part of a team to execute batches while also being capable of working independently with minimal supervision.

Company Culture and Environment

The work environment emphasizes teamwork and collaboration, with a focus on adherence to cGMP standards and safety policies. The culture values good communication skills and attention to detail, which are essential for successful execution of manufacturing processes.

Career Growth and Development Opportunities

This position offers opportunities for professional development through hands-on experience in a biopharmaceutical manufacturing environment. Team members are encouraged to expand their skills in buffer preparation and documentation.

Detailed Benefits and Perks

While specific benefits are not detailed, the position is expected to provide a supportive environment fostering career advancement and skill development.

Compensation and Benefits

• Competitive salary based on experience
• Opportunities for flexible working hours
• Supportive team environment

Why you should apply for this position today

This role offers a unique chance to contribute to the biopharmaceutical industry while developing critical skills in manufacturing processes. The dynamic environment and focus on teamwork make it an exciting opportunity for growth.

Skills

• Ability to work collaboratively with team members as well as independently
• Strong verbal and written communication skills
• Good computer skills, including knowledge of Word, Excel, and spreadsheets
• Detail-oriented with knowledge of GMP batch manufacturing documentation

Responsibilities

• Prepare buffers and media for downstream and upstream manufacturing processes
• Fill out all inventory cards post-preparation activities
• Participate in monitoring activities for manufacturing processes
• Ensure proper calibration and verification of pH/conductivity meters, osmometers, and scales
• Complete and review GMP batch records in a timely manner
• Follow GMP instructions and lead adherence to environmental health and safety policies
• Coordinate investigations and corrections for issues during batch execution
• Comply with all company policies and standards

Qualifications

• Bachelor’s or Master’s degree in chemical, biological, or biochemical sciences
• 1-2 years of related experience in the biopharmaceutical industry
• Previous experience in GMP and aseptic manufacturing environments
• Knowledge of buffer preparation for engineering and clinical batches

Education Requirements

• Bachelor’s degree in chemical, biological, or biochemical sciences
• Master’s degree preferred but not required

Education Requirements Credential Category

• Degree in scientific field relevant to the biopharmaceutical industry

Experience Requirements

• Minimum of 1-2 years in the biopharmaceutical industry with a focus on GMP environments
• Experience in buffer preparation and documentation processes

Why work in Piscataway, NJ

Piscataway, NJ is strategically located with access to a vibrant community and a robust network of biopharmaceutical companies. The area offers a blend of suburban tranquility and proximity to major urban centers, making it an ideal place for professionals to thrive both personally and professionally.