Associate, Engineer

Role: Entry-level engineer/analyst supporting biopharmaceutical manufacturing operations, ensuring compliance with GMP, cGMP, and safety standards. Responsibilities: assist in defining project scopes, plan and execute small projects related to equipment, processes, and facility systems; support qualification activities such as IQ/OQ/PQ; collaborate across teams including Quality, Validation, and Engineering; contribute to process improvements and cost efficiencies; document and communicate findings effectively. Requirements: Bachelor's in Mechanical, Chemical, Electrical, Process, Biomedical Engineering or related; 0-2 years' experience in pharma or GMP manufacturing; understanding of biopharma manufacturing processes, GMP regulations, and CQV principles; proficiency in engineering tools like AutoCAD, SAP, and project management software; strong problem-solving and communication skills. Preferred: familiarity with upstream/downstream bioprocessing, utilities, and validation protocols; experience with Lean/Six Sigma methodologies. High-Value: biopharmaceutical manufacturing, GMP compliance, CQV, process equipment, utility systems, and cross-functional collaboration. Work Setup: not specified; likely on-site based on GMP environment requirements.