Manufacturing Operator II

Manufacturing Operator II

Organization: Inva Gen Pharmaceuticals, Inc.

Location: Central Islip, NY

Employment Type: Full Time

Salary Range: $21.00 - $24.00/hr

Benefits: In addition to a fulfilling career and competitive salary, the company offers a comprehensive benefits package including a 401(k) savings plan with matching, health insurance (medical, dental, vision), health savings account (HSA), flexible spending account (FSA), paid time off (PTO – vacation, sick, flex time), paid holidays, short‑term disability (STD), long‑term disability (LTD), parental leave, paid family leave, employee discounts, and other benefits.

Work Hours/Shift: 1st Shift 7:00 am – 3:30 pm

• Must be willing to work in a pharmaceutical setting.
• Must be able to operate pharmaceutical production machinery independently and complete required documentation accurately.
• Execute procedures for manufacturing processes in accordance with batch manufacturing records (BMR) and standard operating procedures (SOP).
• Perform machine changeovers, cleaning, and set‑up as per SOPs; ensure area and equipment cleanliness and setup within stipulated time.
• Prepare rooms and equipment for line clearance, replace room filters, verify and calibrate balances/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 maintain compliance with cGMP during 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 the manufacturing schedule when needed.
• Maintain discipline and comply with company policies and procedures.
• Perform duties as communicated from 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 independently and in a team environment.
• Must be able to exercise appropriate professional judgment on matters of significance.
• Other duties assigned by Manufacturing Management.

• High School Diploma (or educational equivalent, e.g. GED).
• Minimum three years of direct work experience in pharmaceutical manufacturing.
• Preference given to candidates with experience in generic pharmaceutical manufacturing.

• Legible handwriting and the ability to perform accurate documentation.
• Understanding of granulation, compression, coating, and encapsulation machines.
• Capability of conducting troubleshooting, investigations and root‑cause identification and analysis.
• Ability to prioritize, plan and work under tight schedules and deadlines.
• Technical writing skills and application of relevant scientific principles and practices (preferred).
• Clear and concise communication, both orally and in written form.
• English proficiency required.

• No restrictions to work with powders containing active pharmaceutical ingredients.
• Heavy lifting / bending frequently required.
• Long periods of standing, walking; ability to ascend/descend ladders; able to lift up to 35 pounds.
• Ability to move pallets/equipment weighing about 200–300 kgs using suitable moving equipment like pallet jacks.

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