Pharmaceutical Production Lead - 2nd/3rd Shift

Job Summary Responsible for performing advanced pharmaceutical drug manufacturing activities while providing day‑to‑day technical guidance and workflow coordination within regulated GMP environments. This role serves as a technical and operational resource on the production floor, supporting production flow, compliance, and continuous improvement without formal supervisory authority. Available Shifts 2nd Shift : Mon‑Fri 2 pm‑10:30 pm 3rd Shift : Mon‑Fri 10 pm‑6:30 am Major Responsibilities Acts as a technical and workflow lead by coordinating daily manufacturing tasks, prioritizing activities, and supporting efficient production flow without formal people management responsibility. Provides on‑the‑job guidance, mentoring, and training to manufacturing technicians and lower‑level operators to ensure adherence to procedures, safety standards, and GMP requirements. Performs advanced, hands‑on biopharmaceutical manufacturing activities, including media and buffer preparation, aseptic processing, equipment cleaning and sterilization, and any responsibilities to support production and schedule adherence. Sets up, operates, monitors, and adjusts bioprocessing equipment such as autoclaves, washer‑sterilizers, filtration systems, fermenters, and fill‑finish equipment. Prepares, cleans, assembles, and stages tanks, glassware, components, and systems for batch manufacturing operations in accordance with approved procedures. Monitors critical process parameters, production data, and outputs to ensure compliance with batch records, specifications, and quality standards. Identifies, documents, and escalates deviations, abnormal events, and process issues in accordance with quality systems and regulatory expectations. Maintains accurate and complete batch documentation, equipment logs, inventory records, and other GMP compliance documentation. Follows and reinforces standard operating procedures (SOPs), manufacturing instructions, and all applicable safety, quality, and regulatory guidelines. Collaborates with engineering, quality, and maintenance teams on troubleshooting, investigations, testing, and process optimization activities. Supports continuous improvement initiatives by providing technical input, identifying opportunities for efficiency or quality improvements, and assisting with implementation of approved changes. Minimum Job Requirements Education High school diploma or GED required Work Experience 2‑3 years of manufacturing experience. Experience in aseptic manufacturing in GMP and ISO‑cleanroom environments. Knowledge / Skills / Abilities Proven ability to operate, monitor, troubleshoot, and maintain biopharmaceutical manufacturing equipment. Demonstrated attention to detail with the ability to accurately complete GMP documentation and support investigations and escalations. Effective communication and interpersonal skills, including the ability to guide and collaborate with others. Comfortable working in cleanroom and controlled environments while adhering to gowning, safety, and quality requirements. Flexibility to work mandatory overtime based on business needs. Ability to speak, read, and write English with proficiency. Preferred Job Requirements Education Bachelor’s degree in a STEM field. Work Experience 2 years of hands‑on experience in GMP‑regulated pharmaceutical or biopharmaceutical manufacturing. Demonstrated experience performing advanced manufacturing operations such as aseptic processing, media/buffer preparation, and equipment operation. Knowledge / Skills / Abilities Advanced knowledge of upstream and/or downstream bioprocessing operations. Experience supporting audits, inspections, and regulatory interactions. Familiarity with continuous improvement methodologies and operational excellence initiatives. Strong problem‑solving skills with the ability to work cross‑functionally. Compensation The anticipated salary range for this position is $28.75 – $41.75 per hour. Actual salary will vary based on location, education, experience, skills, and abilities. Medline will not pay less than the applicable minimum wage or salary threshold. Benefits Our benefit package includes health insurance, life and disability coverage, 401(k) contributions, paid time off, and additional benefits for employees working 30 or more hours per week on average. For part‑time employees (less than 30 hours), benefits include 401(k) contributions, paid time off, access to the Employee Assistance Program, Employee Resource Groups, and the Employee Service Corp. For a more comprehensive list of benefits, please click here. Equal Employment Opportunity Medline Industries, LP is an equal‑opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws. #J-18808-Ljbffr JobRx, Inc.