Manufacturing Operator I - 1st Shift

Cipla; Fall River (MA); On-site; USD 35,000 - 55,000; Full time

Job summary

An established industry player is seeking a dedicated Manufacturing Operator to join their team in Fall River. This role involves ensuring the production of high-quality Metered Dose Inhaler products while adhering to strict safety and compliance guidelines. You will be responsible for operating machinery, managing inventory, and documenting manufacturing processes accurately. The ideal candidate will have a strong background in pharmaceutical manufacturing, excellent attention to detail, and the ability to work both independently and collaboratively. Join a company that values its employees and is committed to making healthcare accessible worldwide.

Qualifications

• Minimum one year of experience in pharmaceutical manufacturing, preferably with MDI.
• Proficiency in English required for communication and documentation.

Responsibilities

• Dispense raw materials and ensure quality according to work orders.
• Monitor production performance and document activities accurately.
• Coordinate with teams for cross-functional activities.

Skills

Manufacturing Experience

cGMP Knowledge

Mechanical Skills

Organizational Skills

English Proficiency

Education

High School Diploma

College Certificate/Degree

Tools

Manufacturing Equipment

Computer Systems

Job description

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Job Title: Manufacturing Operator 1
FLSA Classification: Full-Time, Non-Exempt/Hourly Professional
Work Location: Fall River, MA
Work Hours: First Shift: 7:00 AM – 3:30 PM (Flexibility requested based on business needs)

Reports To: Manufacturing Supervisor

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. Responsibilities include ensuring safe, efficient job execution and product compliance.

Essential Duties and Responsibilities

1. Dispense raw and primary packing materials according to work orders and verify their quality.
2. Plan and execute manufacturing batches effectively.
3. Perform cleaning and sanitation of production areas and machinery as per procedures.
4. Monitor daily production performance.
5. Document manufacturing activities accurately in batch records and logbooks.
6. Operate machinery with minimal rejections and maximum quality.
7. Maintain and perform necessary maintenance on equipment.
8. Coordinate with engineering for preventive maintenance and calibration.
9. Manage inventory of machine parts, tools, and accessories.
10. Work independently and collaboratively within a team.
11. Coordinate with packaging, maintenance, and quality teams for cross-functional activities.
12. Ensure proper labeling at all manufacturing stages.
13. Identify and assist in corrective actions.
14. Perform calibration/verification of instruments and equipment.
15. Conduct line clearance checks.
16. Wear PPE as per SOP before entering processing areas.
17. Follow safety procedures to complete tasks efficiently and safely.
18. Use equipment safely according to health and safety guidelines.
19. Perform additional related duties as assigned.
20. Operate computer systems proficiently.
21. Understand pharmaceutical manufacturing documentation.
22. Basic knowledge of deviation, CAPA, change control, FMECA, OOS, OOT, and OOAC processes.

Other Responsibilities

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

Training and Safety

All employees must complete initial and periodic training, including cross-training in manufacturing areas. Strict adherence to safety, health, and environmental guidelines is mandatory, especially when handling machinery.

Qualifications

1. High school diploma or equivalent required.
2. College certificate or degree preferred.
3. At least one year of manufacturing experience in pharma, preferably with MDI.
4. Proficiency in English (speaking, reading, writing).
5. Knowledge of cGMP and regulatory standards preferred.
6. Basic mechanical and control system knowledge.
7. Ability to follow instructions and work independently or in teams.
8. Understanding of Health & Safety procedures, including OSHA.
9. Strong math and organizational skills.

Physical Requirements

1. Ability to perform heavy lifting and frequent bending.
2. Ability to exert force up to 50 pounds using appropriate equipment.
3. Wearing PPE is required.
4. May need to wear respiratory protection, including various types of respirators.

About Cipla

Cipla is a global pharmaceutical leader committed to high-quality medicines. We value our employees as our greatest assets, striving to make healthcare accessible worldwide. Our focus remains on delivering affordable, quality medicines globally.

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