QA Inspector II - 2nd shift

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates.

Job Title: QA Inspector a" Packaging (2nd Shift)

Location: Central Islip, NY (Onsite)

Hourly rate: $18.72 - $26.00

Department: Quality Assurance

Industry: Pharmaceutical Manufacturing / Packaging

Reports To: QA Supervisor

Position Overview:

We are seeking a detail-oriented and motivated Quality Assurance (QA) Inspector to join our 2nd shift packaging operations. This role plays a critical part in ensuring product quality, adherence to cGMP standards, and compliance with internal and regulatory requirements. The QA Inspector will work cross-functionally to conduct quality inspections, support documentation accuracy, and drive continuous improvement efforts on the production floor.

Key Responsibilities:

• Verify packaging components during dispensing and line clearance processes.
• Dispense printed packaging materials to packaging lines as needed.
• Conduct in-process quality checks during batch manufacturing and packaging per batch records.
• Collect finished product and validation samples as per SOPs and protocols.
• Perform IPQA testing on packaging lines in alignment with production requirements.
• Confirm proper cleaning of equipment and areas, and provide line clearance prior to production.
• Accurately post dispensed materials and sample information into SAP (ERP system) and perform related transactions.
• Participate in the investigation of deviations, OOS (Out of Specification), OOT (Out of Trend), and other quality events.
• Complete assigned training and ensure full compliance with company policies, SOPs, and safety standards.
• Review batch records, logbooks, and calibration/PMP records for accuracy and compliance.
• Isolate and document any rejected materials and ensure accountability within batch documentation.
• Review engineering records including temperature/humidity logs, calibration certificates, and maintenance records.
• Conduct daily quality rounds to verify that shop floor operations remain in a state of GMP compliance.
• Escalate any discrepancies or issues to QA management in a timely manner.
• Perform other quality-related duties as assigned by management.

Required Skills & Competencies:

• Solid knowledge of GMP (Good Manufacturing Practices) and 21 CFR Part 820 regulations.
• Strong verbal and written communication skills.
• Proficiency in basic computer applications (Microsoft Word, Excel, PowerPoint).
• Highly organized, with strong attention to detail and multitasking abilities.
• Strong mathematical skills and analytical thinking.
• Self-starter capable of working independently in a fast-paced environment.

Physical Requirements:

• Ability to stand or walk unassisted for at least 75% of an 8-hour shift.
• Must be able to lift up to 35 lbs. without assistance.
• Must be able to wear personal protective equipment (PPE) as required.

Qualifications:

• High School Diploma or equivalent (required); strong background in science preferred.
• 1a"2 years of pharmaceutical industry experience, particularly in manufacturing or packaging (preferred).
• Prior experience in generic pharmaceutical manufacturing/packaging is a plus.

GLOBAL COMPANY

Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in Indiaas pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.

Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Ciplaas focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.

CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.)

About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited.