Manufacturing Formulation Associate Biopharma

Job Description

Job Description

Manufacturing Formulation Associate (Entry Level)

A leading Contract Development and Manufacturing Organization (CDMO) dedicated to supporting the development and commercial manufacturing of innovative biopharmaceutical products. Committed to delivering high-quality manufacturing services while maintaining the highest standards of safety, quality, and regulatory compliance.

Position Summary

The Manufacturing Formulation Associate I is an entry-level role responsible for supporting the preparation, formulation, and manufacturing of biopharmaceutical products in a GMP-regulated environment. This position offers an excellent opportunity for recent graduates to begin a career in biopharmaceutical manufacturing and gain hands-on experience with industry-leading manufacturing processes.

Key Responsibilities

• Prepare buffers, media, and formulation solutions according to approved batch records and standard operating procedures (SOPs).
• Operate and monitor manufacturing equipment used in formulation and processing activities.
• Perform equipment setup, cleaning, sanitization, and routine maintenance.
• Accurately complete GMP documentation, batch records, and logbooks.
• Follow current Good Manufacturing Practices (cGMP), safety procedures, and company policies.
• Assist with material staging, inventory management, and manufacturing support activities.
• Participate in environmental monitoring and cleaning verification activities as required.
• Report process deviations, equipment issues, and quality concerns promptly.
• Collaborate with Manufacturing, Quality Assurance, Quality Control, Engineering, and Warehouse teams to ensure timely production.
• Participate in training and continuous improvement initiatives.

Minimum Qualifications

• Bachelor's degree in Biology, Chemistry, Biochemistry, Microbiology, Biotechnology, or another Life Science discipline is required.
• Recent graduates are encouraged to apply.
• Strong attention to detail and organizational skills.
• Effective written and verbal communication skills.
• Ability to work independently and as part of a team.
• Basic computer proficiency, including Microsoft Office applications.

Preferred Qualifications

• Previous laboratory, manufacturing, internship, or research experience is a plus.
• Familiarity with GMP or regulated laboratory environments is preferred but not required.
• Knowledge of aseptic techniques and pharmaceutical manufacturing processes is beneficial.