Machine Operator I - 3rd Shift

Cipla USA; 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 dynamic team in Fall River. This role involves producing high-quality MDI products while adhering to strict cGMP standards. As a key player in the manufacturing process, you will dispense materials, monitor production performance, and ensure compliance with safety protocols. The ideal candidate will have a strong background in manufacturing, excellent communication skills, and a commitment to maintaining high standards. If you're ready to contribute to a company that values quality healthcare, this opportunity is for you!

Qualifications

• 1+ year of manufacturing experience in the pharmaceutical industry.
• Knowledge of cGMP and regulatory requirements preferred.
• Ability to perform heavy lifting and work extended hours.

Responsibilities

• Dispensing raw materials and ensuring quality compliance.
• Monitoring production performance and documenting activities.
• Cleaning production areas and operating machinery safely.

Skills

Manufacturing Experience

Knowledge of cGMP

English Proficiency

Mathematical Skills

Health & Safety Procedures

Ability to Follow Instructions

Education

High School Diploma

Higher Education

Tools

Computer Systems

Job description

Job Title: Manufacturing Operator 1

Hourly rate: $19/hr

Work Location: Fall River, MA

Work Hours: Third Shift: 11:00 PM to 7:30 AM (Flexibility is requested based on business needs)

Job Description

The Manufacturing Operator performs functions related to the production of MDI (Metered Dose Inhaler) products, in accordance with established cGMP, customer requirements, and SOPs. Responsibilities include ensuring safe and efficient job execution and product compliance to standards.

Essential Duties and Responsibilities

1. Dispensing raw materials and primary packing materials as per work order and verifying their quality.
2. Planning and executing manufacturing batches.
3. Cleaning and sanitizing production areas and machinery per procedures.
4. Monitoring production performance daily.
5. Documenting manufacturing activities in batch records and logbooks.
6. Operating machinery with minimal rejections and maintaining quality standards.
7. Performing equipment operation and maintenance.
8. Coordinating with engineering for equipment upkeep, preventive maintenance, and calibration.
9. Maintaining inventory of machine parts, tools, and accessories.
10. Working individually and as part of a team, collaborating with packaging, maintenance, and quality teams.
11. Ensuring proper labelling at all manufacturing stages.
12. Identifying and assisting in corrective actions.
13. Calibrating and verifying instruments and equipment as scheduled.
14. Performing line clearance checks.
15. Wearing PPE as per SOP before entering processing areas.
16. Following safety procedures for tasks and equipment use.
17. Performing other duties as assigned.
18. Operating computer systems effectively.
19. Understanding pharmaceutical manufacturing documentation.
20. Basic knowledge of deviation, CAPA, change control, FMECA, OOS, OOT, and OOAC processes.

Other Responsibilities

1. Maintaining 100% cGMP, GDP, and SOP compliance during operations.
2. Adhering to company policies and reporting issues promptly.
3. Performing daily equipment maintenance.
4. Completing documentation accurately and timely.
5. Maintaining discipline within the department.
6. Assisting in training new employees as needed.
7. Working extended hours to meet manufacturing schedules when required.

Training and Safety

All employees undergo initial and periodic training. Cross-training may be required. Strict adherence to safety, health, and environmental guidelines is mandatory, including proper handling of machines and PPE usage.

Qualifications

1. High school diploma or equivalent required; higher education preferred.
2. At least 1 year of manufacturing experience in the pharmaceutical industry; MDI experience preferred.
3. Proficiency in English (speaking, reading, writing).
4. Knowledge of cGMP and regulatory requirements preferred.
5. Basic mechanical and control systems knowledge.
6. Ability to follow instructions and work independently or in teams.
7. Understanding of Health & Safety procedures, including OSHA.
8. Strong mathematical and organizational skills.

Physical Requirements

1. Ability to perform heavy lifting, bending, and standing for extended periods.
2. Force exertion up to 50 pounds with equipment assistance.
3. Wearing PPE and respiratory devices as required.

About Cipla

Cipla is a leading global pharmaceutical company committed to high-quality medicines. We value our employees as our greatest assets, driven by a vision to make affordable, quality healthcare accessible worldwide.

InvaGen Pharmaceuticals, a Cipla subsidiary

InvaGen develops, manufactures, and markets generic medicines across various therapeutic areas. Founded in 2003, based in New York, and part of Cipla since 2016.