Packaging Specialist

Packaging Specialist- 2nd Shift Responsibilities/ Accountabilities ssist in the coordination of daily packaging activities to meet production schedules of projects. Monitor packaging processes for adherence to cGMP, FDA, and 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. ssist 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). ssist in coordinating materials, equipment, and workforce allocation for optimal resource utilization. Identify areas for operational improvements, focusing on reducing waste and enhancing efficiency. ssist 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. dhere 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. Skills/ Competencies 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. bility to work effectively both independently and as part of a team. Capable of handling and participating in compliance and regulatory audits at the local and federal levels. Experience in Inhalation products (Metered Dose Inhaler) is a plus. Must-Haves : Bachelor's degree in pharmaceutical sciences/ electrical/ mechanical / production or related fields of study. 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. 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. Experience in Inhalation products (Metered Dose Inhaler) is a plus.

Created: 2026-04-01