Manufacturing Associate

Job Title: Downstream Manufacturing Associate Location: Insert Location Department: Manufacturing â Downstream Operations Employment Type: Full-Time Position Summary We are seeking a motivated Downstream Manufacturing Associate to join our biopharmaceutical manufacturing team. This entry-level position supports the purification and processing of biologic drug substances using downstream manufacturing operations in a cGMP-regulated environment. This role is ideal for recent graduates looking to launch a career in biopharmaceutical manufacturing. Comprehensive on-the-job training will be provided. Key Responsibilities Perform downstream manufacturing activities including filtration, chromatography, ultrafiltration/diafiltration (UF/DF), and bulk drug substance processing. Execute manufacturing processes according to batch records, standard operating procedures (SOPs), and current Good Manufacturing Practices (cGMP). Operate, assemble, clean, and maintain downstream processing equipment and single-use systems. Prepare buffers and process solutions required for manufacturing operations. Accurately complete batch records and manufacturing documentation following Good Documentation Practices (GDP). Monitor process parameters and report deviations, equipment issues, or process abnormalities. Maintain a clean and organized manufacturing environment while following safety and contamination control procedures. Collaborate with Manufacturing, Quality Assurance, Quality Control, and Engineering teams to support production schedules and quality objectives. Participate in training programs and continuously develop technical knowledge of downstream bioprocessing. Minimum Qualifications Bachelor's degree required in Biology, Chemistry, Biochemistry, or a closely related Life Science discipline. No prior industry experience required. Recent graduates are encouraged to apply. Basic understanding of biochemistry, protein purification, chemistry, microbiology, or laboratory techniques obtained through academic coursework or laboratory experience. Strong attention to detail and ability to follow written procedures. Excellent organizational, communication, and teamwork skills. Basic computer proficiency, including Microsoft Office. Preferred Qualifications Academic laboratory experience with protein purification, chromatography, filtration, biochemistry, or analytical laboratory techniques. Exposure to cGMP principles, aseptic practices, or biopharmaceutical manufacturing through coursework, research, or internships. Familiarity with laboratory equipment such as balances, pH meters, pumps, filtration systems, or chromatography instruments. KPG123