Pay Rate Low: 26 | Pay Rate High: 32

Opportunity to join a global biopharmaceutical company developing innovative, proprietary medicines to address unmet needs in neuroscience.

Hours: M-F 8-5
12 month contract

The Process Development Technician contributes to the execution of experimental and clinical studies aimed at developing reliable and well-characterized oral solid dosage (OSD) manufacturing processes. This role involves conducting experiments, collecting and documenting data, and supporting overall process development activities.

Key Responsibilities

• Support the design of experimental programs and assist in compiling and analyzing study data.

• Perform experiments to improve process understanding and manufacture GMP clinical batches across multiple scales.

• Accurately complete all required documentation in compliance with regulatory standards, and assist in updating batch records and standard operating procedures (SOPs).

• Maintain a strong working knowledge of Manufacturing, Quality, and Development systems; provide support during regulatory inspections and audits as needed.

• Ensure adherence to all applicable cGMP requirements, safety guidelines, environmental regulations, and company policies.

Qualifications

• Associate’s or Bachelor’s degree in an engineering or scientific discipline (or equivalent experience) with 1–3+ years of experience in pharmaceutical solid oral dosage processing.

• Solid understanding of mechanical and chemical engineering principles.