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Packaging Specialist- 2nd Shift

Job in Fall River, Bristol County, Massachusetts, 02720, USA
Listing for: Cipla
Full Time position
Listed on 2026-01-01
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 72800 - 93600 USD Yearly USD 72800.00 93600.00 YEAR
Job Description & How to Apply Below

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Second Shift: 03:00 PM – 11:30 PM (may vary based on business needs)

Salary Range (Base/ Hourly)

$72,800 – $93,600

In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and 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, employee discounts, and other benefits.

Responsibilities/ Accountabilities

Assist in the coordination of daily packaging activities to meet production schedules of projects.

  • Monitor packaging processes for adherence to cGMP, FDA, and Cipla's quality standards.
  • Identify and resolve operational inefficiencies, escalating complex issues when necessary.
  • Ensure proper documentation of batch records, logs, and deviations.
  • Monitor production schedules to ensure timely execution and minimize delays to support ongoing projects.
  • Assist in investigating deviations, non-conformances, and CAPAs (Corrective and Preventive Actions).
  • Work closely with Quality Assurance (QA) to ensure adherence to standard operating procedures (SOPs).
  • Assist in coordinating materials, equipment, and workforce allocation for optimal resource utilization.
  • Identify areas for operational improvements, focusing on reducing waste and enhancing efficiency.
  • Assist in implementing new technologies and automation in production workflows.
  • Collaborate with Team, Quality, Supply Chain, Project Management, Engineering, and R&D teams to resolve operational bottlenecks.
  • Support training efforts by ensuring clear communication of standard operating procedures (SOPs).
  • Monitor operational metrics such as efficiency, compliance rates, and resource utilization.
  • Identify areas for improvement in packaging activities and contribute to process enhancements.
  • Support initiatives aimed at improving overall productivity through data analysis and performance reviews.
  • Develop and maintain strong professional relationships with suppliers/vendors to ensure compliance with quality standards and timely delivery of goods and services.
  • Create and manage purchase requisition (PR) using SAP for services, contracts, equipment, consumables, and miscellaneous items,
    ensuring accuracy & alignment with end-user requirements.
  • Maintain clear and effective communication with internal and external stakeholders to address issues, facilitate smooth operations, and ensure alignment with project strategies.
  • Follow strict internal protocols and Standard Operating Procedures (SOPs) as well as following current Good Packaging Practices (cGMP).
  • Participate in safety related programs and or safety teams as needed.
  • Enforce and follow safety regulations and ensure that their working area is clean.
  • Adhere to CIPLA’s Safety, Health, and Environmental policies.
  • Other duties assigned as required by Reporting management / Dept. Head.
Education Qualifications

Bachelor’s degree in pharmaceutical sciences/ electrical/ mechanical / production or related fields of study.

Experience

5-11 years of experience in packaging, operations, team management. Preference will be given to candidates with experience in pharmaceutical MDI packaging.

  • Understanding of cGMP, FDA regulations, and pharmaceutical packaging processes.
  • Experience in SAP system and packaging data analysis tools.
  • Strong problem-solving abilities, attention to detail, and ability to work in a fast-paced, regulated environment.
  • Excellent communication skills, drive, and sense of urgency.
  • Excellent computer skills, specifically Microsoft Office Suited.
  • Follow strict internal protocols and Standard Operating Procedures (SOPs) as well as following current Good Packaging Practices (cGMP), complying with legal regulations, monitoring the environment.
  • Knowledge of pharmaceutical packaging and related documents.
  • Knowledge and experience writing, revising, and creating cGMP records and SOP’s.
  • Experience with quality system compliance.
  • Ability to work effectively both independently and as part of a team.
  • Capable of handling and…
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