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Manufacturing Operator 2nd Shift

Job in North Great River, Suffolk County, New York, USA
Listing for: Cipla USA
Full Time position
Listed on 2026-01-01
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 18.25 - 20.75 USD Hourly USD 18.25 20.75 HOUR
Job Description & How to Apply Below
Position: Manufacturing Operator I 2nd Shift
Location: North Great River

Notice

Local applicants only – this posting is not for global assignment or employees working outside of Cipla's U.S. subsidiaries or affiliates.

Job Details
  • Title: Manufacturing Operator I (2nd Shift)
  • Organization: Inva Gen Pharmaceuticals, Inc.
  • Location: Central Islip, NY
  • Shift: 2nd Shift (3PM‑11:30PM)
  • Employment Type: Full Time
  • Salary Range: $18.25–$20.75 /hr (base)
Benefits

Comprehensive benefits package includes 401(k) savings plan and matching, health insurance (medical/dental/vision), health savings account, flexible spending account, paid time off (vacation/sick/flex time), paid holidays, short-term disability, long-term disability, parental leave, paid family leave, employee discounts, and other benefits.

Work Hours / Shift / Remote

Must be willing and able to work any assigned shift. Work schedule may be Monday to Friday, Tuesday to Saturday, or a combination based on business needs.

Responsibilities / Accountabilities
  • Must be willing to work in a pharmaceutical manufacturing setting.
  • Must be able to operate pharmaceutical production machinery independently.
  • Execute procedures for manufacturing processes in accordance with batch manufacturing record (BMR) and standard operating procedures (SOP).
  • Perform machine changeovers, cleaning and set up as per SOPs. Ensure the proper area & equipment cleanliness and setup in stipulated time.
  • Prepare a room and equipment for line clearance, replace room filters, ensure verification and calibration of balance/scale and check pressure differential for the rooms.
  • Ensure line clearance before initiating manufacturing activities in each area.
  • Receive/transfer material from/to dispensing/manufacturing storage and check dispensed materials/final mix blend/compressed tablets and labeling as per BMR.
  • Wear appropriate personal protective equipment (PPE) as stated in the SOP/BMR before initiating the process.
  • Able to operate applicable equipment independently as per area of operation.
  • Ensure adherence to quality standards during all stages of the manufacturing process.
  • Complete manufacturing documents on time, ensuring accuracy and completeness.
  • Responsible for training on all relevant SOPs and always maintain compliance with related SOPs and current Good Manufacturing Practices (cGMP) in the manufacturing process.
  • Perform duties through the proper, safe use of equipment, according to Health & Safety procedures and Equipment Manuals.
  • Flexible to work extended hours, to achieve manufacturing schedule when needed.
  • Maintain discipline and comply with company policies and procedures.
  • Perform entire duties as communicated time to time by department management/designee.
  • Participate in safety related programs and or safety teams as needed.
  • Enforce and follow safety regulations and ensure the working area is clean.
  • Adhere to CIPLA’s Safety, Health, and Environmental policies.
  • Must be able to work under general supervision and able to work independently and in a team environment.
  • Must be able to exercise appropriate professional judgment on matters of significance.
  • Other duties assigned as required by Manufacturing Management.
Education Qualifications
  • High School Diploma (or equivalent experience).
Experience
  • Zero to three years of direct work experience in pharmaceutical manufacturing. Preference will be given to candidates with experience in generic pharmaceutical manufacturing.
Skills / Competencies
  • Understanding of granulation, compression, coating, and encapsulation machines.
  • Capable of conducting troubleshooting, investigations and root cause identification and analysis.
  • Able to prioritize, plan and work under tight schedules and deadlines.
  • Must possess strong documentation and technical writing skills and be able to apply relevant scientific principles and practices.
  • Must communicate clearly and concisely across levels, both orally and in written.
  • Strong command over written and verbal English is required.
Physical Requirements
  • Should not have any restriction to work with powder containing active pharmaceutical ingredients.
  • This position requires the ability to do heavy lifting / bending frequently.
  • Long periods of standing up/walking during the working hours; ability to ascend/descend ladders; and…
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