Manufacturing Operator

Cipla

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profile Job Location:

Fall River, MA - USA

profile Monthly Salary: $ 20 - 24
Posted on: 18 hours ago
Vacancies: 1 Vacancy

Job Summary

Job Title: Manufacturing Operator

FLSA Classification:Full-Time Non-Exempt/Hourly Professional Over-time elgible

Work Location:Fall River MA

Work Hours:- 12hr shift 4 on 3 off (7am-7pm 7pm-7am)

Hourly Rate:$20 24/hr(DOE)

The Manufacturing Operator performs all functions relating to the production of Metered Dosage Inhaler (MDI) products; consistent with established Current Good Manufacturing Practices (cGMP) customer requirements and in conjunction with all Standard Operating Procedures (SOP). Operators are responsible for the safe and efficient execution of their job duties while ensuring product compliance to established standards.

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 partstoolsand accessories.

  • Working individually and in collaboration with others as part of a team.

  • Coordinating with other departments like packaging engineeringQAand 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.

  • Performcheckand ensure calibration/verification of instrumentsequipmentand 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 integrityaccuracyand 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 muststrictly 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 pharmaceutical or aerosol products.

  • 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 pharmaceuticalcompanydedicated to high-qualitybrandedand generic medicines. We are trusted by healthcare professionals and patientsacrossgeographies. Over the last eight decades we have strengthened our leadership in Indias 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 Ciplas 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 2016InvaGenPharmaceuticals 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.

Job Title: Manufacturing OperatorFLSA Classification:Full-Time Non-Exempt/Hourly Professional Over-time elgibleWork Location:Fall River MA Work Hours:- 12hr shift 4 on 3 off (7am-7pm 7pm-7am)Hourly Rate:$20 24/hr(DOE)The Manufacturing Operator performs all functions relating to the production of Me...
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Cipla is a market-leading medicine maker in India. The company has roughly 5,500 pharmaceutical products. Some are sold domestically, while the rest reach international markets in some 170 countries. It offers prescription drugs for all kinds of ailments -- arthritis, cancer, depressi ... View more

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