Cipla

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title :Manufacturing Operator I - MDI - 1st Shift FLSA Classification :Full-Time, Non-Exempt/Hourly Professional Work Location :Fall River, MA Work Hours: First Shift: 7:00AM - 3:30PM / Flexibilityall Shifts: (weekends may be required based on business needs) Reports To :Production Supervisor Hourly Rate:$20 - 24/hr(DOE) Purpose : The purpose of this role is toassistin manufacturing metered dose inhalation (MDI) products in a pharmaceutical manufacturing company. Job Description : The Manufacturing Operator performs all functions relating to the production of MDI products; consistent with established Current Good Manufacturing Practices (cGMP), customer requirements and in conjunction with all Standard Operating Procedures(SOP). Incumbents in this positionare responsible forthe safe and efficient execution of their job duties, while ensuring product compliancetoestablishedstandards. Essential Duties and Responsibilities : Dispensing rawmaterialand primary packing materials as per work order. Ensure the proper planning and execution of batches. Monitoring cleaning and sanitation of production area and machinery as per respective SOP during batch to batchand product toproduct changeover. Daily monitoring and recording of production materials and production lines. Conducting process checks and recording in batch manufacturingrecord. Controlling machine operations with minimum rejections and maximum outputs whilemaintainingquality standards within the standard norms. Operating equipment and performing necessary maintenance on machinery. Safeguard equipment for smooth functioning with co-ordination of engineering for preventive maintenance and calibration. Manufacturing andfilling ofproducts as per Batch Manufacturing Records and SOP. Maintaining inventory of machine parts,toolsand accessories. Working individually and in collaboration with others as part of a team. Coordinating with other departments like packaging, engineering,QAand QC for better planning and execution. Sampling as per schedule and in coordination with QA and QC. Check and ensure status labels at all stages of manufacturing and filling. Identifyingandassistingin any corrective actions. Perform,checkand ensure calibration/verification of instruments,equipmentand weighing balances as per schedule. Ensuring line clearance during batch to batch and product to product change over. Online documentation andtimelyentries related to manufacturing and filling operations and activities. Wearingappropriate PPEasstatedin the SOP before entering any processing areas. Executing procedures to complete tasks in a safe and efficient manner. Performing duties through the proper safe use of equipment, according to Health & Safety procedures and Equipment Manuals. Performing other relatedduties asassigned. Other Responsibilities: Maintaining 100% cGMP and SOP Compliance during complete operation hours. Complyingwith all company policies and procedures. Reporting all issues that arise to the department head or reporting manager. Performing daily maintenance on equipment and machinery. Completing all documentationin a timely manner, ensuring their integrity,accuracyand completeness. Maintaining discipline indepartment. May berequiredtoassistin the training of other employees in the department. Flexibleto workextended hours, to achieve manufacturing schedule when needed. Training and Safety: All employees must undergo various training activities at the start of their employment. New training and re-training will occur periodically. Operators mayberequiredcross-trainin all areas of the manufacturing operations. Employees must strictly adhere to all safety, health, and environmental guidelinesat all timesand ensure that all safety precautions are being taken during handling of machines. Qualifications : High school diploma or equivalent isrequired. Accredited college certificate or university degree is preferred. Minimum one (1) year of manufacturing experience with MDI or aerosol productsrequired. Proficient in the English language (Speaking/Reading/Writing) to understand work instructions and document results. Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environmenthighlypreferred. Basic understanding of mechanical machinery and the operating principles of control systems. Ability to follow both verbal and written instructions. Demonstrated ability to work in both independent and team environments. Good knowledge of Health & Safety procedures, including OSHA. Strong mathematical and organizational skills. Physical Requirements : This position requires the ability to do heavy lifting / bendingfrequently. Exert an amount of force continuously and/or up to 5 pounds of forcefrequentlyand/or up to 25 pounds of force occasionally and/or up to 50 pounds of force rarely byutilizinga hand truck to lift, carry, push, pull or otherwise move objects. Abilityto wearappropriate PPEis required. Individualmay be required to wear respiratory devices that include but are not limited to: Air Purifying Respirators (APR) which include half-face and full-face negative pressure respirators, hooded powered air purifying respirators, or Supplied Air Respirators (SAR), which include hooded or full face supplied air respirators. GLOBAL COMPANY Cipla is a leading global pharmaceuticalcompany,dedicated to high-quality,brandedand generic medicines. We are trusted by healthcare professionals and patientsacrossgeographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus byconsolidatingand deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.) AboutInvaGenPharmaceuticals, a Cipla subsidiaryInvaGenPharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016,InvaGenPharmaceuticals, Inc.operatesas a subsidiary of Cipla (EU) Limited. EEO Statement: Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexualorientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status. Salary: . Date posted: 07/08/2026