Descripción de la oferta
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company provides services for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.Manufacturing Scheduler / Planner IEstablish priorities across Manufacturing operations to optimize equipment turnaround, coordinating process orders with the Planning department and maintenance activities. Ensure the manufacturing process is not disrupted and solutions are completed on schedule.Responsibilities- Support creation and updating of master solution and process orders schedules to establish the sequence for daily activities coordinated by Biologic Coordinators.- Draw up master equipment schedules and monitor equipment turnarounds and processes using computerized systems (e.G., Delta V, POMS, SAP).- Document and monitor production process status and equipment maintenance.- Strictly adhere to current Good Manufacturing Practices (cGMP’s), Standard Operating Procedures (SOP) and accurately complete process‑associated documentation.- Assist operations with environmental management, occupational health and safety (EHS) systems and promote continuous improvement.- Comply with all EHS procedures and policies, including incident reporting, use of PPE, and other applicable programs.- Act as main point of contact for coordination of process orders with the Planning department and scheduling of maintenance activity windows.- Develop detailed production plans for manufacturing operations to meet customer demand and inventory targets.- Monitor daily production progress and update schedules to address delays, machine breakdowns, or material shortages.- Request and track work orders using the Maximo system.- Evaluate production performance, track KPIs, and develop "what‑if" scenarios to improve future planning.Qualifications- Associate Degree in Sciences (e.G., biology, micro‑biology, chemistry, etc.), Mechanics, Electricity, Instrumentation, or a related field- Five (5) years of experience in manufacturing operations in the biotechnology or pharmaceutical industry with an Associate Degree.- Bachelor’s Degree in Sciences (e.G., biology, micro‑biology, chemistry, etc.), Mechanics, Electricity, Instrumentation, or a related field- Two (2) years of experience in manufacturing operations in the biotechnology or pharmaceutical industry with a BS Degree.- Proficiency in computerized systems such as Power BI, Excel, Delta V, MES, and SAP.- Strong verbal and written communication skills in English and Spanish.- Strong interpersonal and communication skills.- Ability to manage multiple priorities with minimal supervision.- Proficiency using MS Windows and Microsoft Office applications.- Strong knowledge of cGxP and regulatory guidance and understanding of their application to regulatory compliance.- Available to work extended hours, including weekends and holidays.Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.#J-18808-Ljbffr
