Machine Operator I - 3rd Shift

Cipla; Fall River (MA); On-site; USD 10,000 - 60,000; Full time

Job summary

An established industry player is seeking a dedicated Manufacturing Operator to join their team in Fall River. This role involves the production of Metered Dose Inhaler products while adhering to strict quality and safety standards. The successful candidate will be responsible for dispensing materials, operating machinery, and ensuring compliance with cGMP regulations. With a focus on teamwork and independent work, this position offers an opportunity to contribute to the production of high-quality medicines. If you have a passion for pharmaceutical manufacturing and a commitment to excellence, this role could be your next career step.

Qualifications

• Minimum one year of manufacturing experience in the pharmaceutical industry.
• Knowledge of cGMP and regulatory requirements preferred.

Responsibilities

• Dispense raw materials and pack materials as per work orders.
• Monitor daily production performance and document activities.
• Ensure compliance with cGMP, GDP, and SOPs during operations.

Skills

Pharmaceutical Manufacturing

Quality Control

Basic Mechanical Skills

Mathematical Skills

Organizational Skills

English Proficiency

Education

High School Diploma

College Degree

Tools

Computer Systems

Job description

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Job Title: Manufacturing Operator 1
Hourly rate: $19/hr
Work Location: Fall River, MA
Work Hours: Third Shift: 11:00 PM – 7:30 AM (Flexibility is requested based on business needs)

Job Overview

The Manufacturing Operator performs functions related to the production of MDI (Metered Dose Inhaler) products, adhering to established cGMP, customer requirements, and SOPs. The role ensures safe and efficient execution of duties while maintaining product compliance with quality standards.

Essential Duties and Responsibilities

1. Dispense raw materials and primary packing materials as per work orders and verify their quality.
2. Plan and execute production batches effectively.
3. Perform cleaning and sanitation of production areas and machinery following procedures.
4. Monitor daily production performance and document activities in batch records and logbooks.
5. Operate machinery with minimal rejections, maximizing output while maintaining quality standards.
6. Maintain and perform routine maintenance on equipment, coordinating with engineering for preventive maintenance and calibration.
7. Manage inventory of machine parts, tools, and accessories.
8. Work independently and collaboratively within a team, coordinating with packaging, maintenance, and quality teams.
9. Ensure proper labeling at all manufacturing stages and assist in corrective actions when necessary.
10. Perform calibration/verification of instruments and equipment as scheduled.
11. Conduct line clearance checks and wear appropriate PPE as per SOPs.
12. Follow safety procedures and operate equipment safely, adhering to health and safety guidelines.
13. Perform other related duties as assigned.
14. Operate computer systems proficiently.
15. Understand pharmaceutical manufacturing processes and documentation.
16. Basic knowledge of deviation, CAPA, change control, FMECA, OOS, OOT, and OOAC processes.

Additional Responsibilities

1. Maintain 100% compliance with cGMP, GDP, and SOPs during operations.
2. Follow all company policies and procedures.
3. Report issues promptly to supervisors.
4. Perform daily maintenance and complete documentation accurately and timely.
5. Maintain discipline within the department.
6. Assist in training new employees as needed.
7. Work extended hours when required to meet manufacturing schedules.

Training and Safety

All employees must complete initial and periodic training. Cross-training in manufacturing areas may be required. Strict adherence to safety, health, and environmental guidelines is mandatory, including proper machine handling and PPE use.

Qualifications

• High school diploma or equivalent required; college degree preferred.
• Minimum one year of manufacturing experience in the pharmaceutical industry; MDI experience is highly preferred.
• Proficient in English (speaking, reading, writing).
• Knowledge of cGMP and regulatory requirements preferred.
• Basic mechanical skills and understanding of control systems.
• Ability to follow instructions and work independently or in a team.
• Good understanding of OSHA safety procedures.
• Strong mathematical and organizational skills.

Physical Requirements

• Ability to perform heavy lifting, bending, and manual tasks frequently.
• Ability to exert force up to 50 pounds with equipment assistance.
• Must wear PPE and possibly respiratory devices as required.

About the Company

Cipla is a global pharmaceutical leader committed to high-quality medicines. With a presence in India, South Africa, the U.S., and emerging markets, Cipla values its employees as its greatest assets. We focus on making affordable, world-class medicines with uncompromising quality.

InvaGen Pharmaceuticals, a Cipla subsidiary, specializes in developing and manufacturing generic medicines across various therapeutic areas, based in New York since 2003.