Junior Executive - Quality Assurance -IPQA

Pelltech Healthcare; Nagpur District; Presencial; INR 250.000 - 350.000; Jornada completa

Descripción de la vacante

Pelltech Healthcare is hiring a Junior Executive for Quality Assurance (IPQA) to ensure GMP compliance and robust QA practices on the manufacturing floor. The role involves batch documentation, process monitoring, and cross-functional collaboration with QC and Regulatory teams.

The candidate should have a B.Pharm or M.Pharm with 1-3 years in IPQA, and be adept at handling deviations, change controls, and documentation across IPQA activities.

Formación

• Must have IPQA experience (1-3 years) in pharmaceutical manufacturing.
• Experience in reviewing batch records (BMR/BPR) and ensuring compliance.
• Familiar with calibration, validation, and procedures as per GMP.
• Knowledge of deviation handling, CAPA, and change control processes.

Responsabilidades

• Conduct in-process quality checks across manufacturing stages.
• Review and release batch records prior to product release.
• Ensure calibration and validation of instruments are timely performed.
• Monitor critical process parameters (temp, pressure, pH, mixing) within specs.
• Collaborate with QC, regulatory, and QA to resolve quality issues.

Conocimientos

Quality Assurance

GMP/Regulatory

Deviation Investigation

Change Control

Documentation

Educación

B.Pharm

M.Pharm

Descripción del empleo

Junior Executive - Quality Assurance -IPQA

1-3 Years

Factory

Job Responsibilities

• Conduct in-process quality checks at various stages of manufacturing, including sampling, inspections, and testing, to ensure compliance with SOPs and regulatory requirements.
• Review and compile complete batch records (BMR and BPR) prior to release.
• Monitor steps followed in manufacturing and packing are as per standard operating procedure.
• Ensure all instruments are calibrated and validations are carried out in timely manner.
• Issue Validation Protocol, Method Validation Protocol, URS & Qualification as per the schedule.
• Monitor critical process parameters, such as temperature, pressure, pH, and mixing times, to ensure they are within specified ranges.
• Review and approve batch records, manufacturing instructions, and other relevant documents to verify compliance with established procedures and specifications.
• Perform line clearance activities to ensure proper segregation and cleanliness of manufacturing areas, equipment, and materials.
• Collect and analyze samples during production runs for physical, chemical, and microbiological testing as per defined sampling plans.
• Withdraw stability sample & control samples for analysis at intermediate and finished product stage.
• Issue, Review & Maintain Change Control of Site, Corporate & their respective logs.
• Issue controlled copies and retrieval of old RMS, FPS, SPS, PMS, RM & PM Item Code List.
• Coordinate with the quality control (QC) department for timely testing and release of in-process samples.
• Investigate and document deviations, non-conformances, and out-of-specification results, and collaborate with the appropriate teams to identify root causes and implement corrective actions.
• Assist in the implementation and maintenance of quality systems, including change control, risk assessment, and document control.
• Support internal and external audits by providing necessary documentation and participating in audit activities.
• Collaborate with cross-functional teams, including manufacturing, quality assurance, and regulatory affairs, to resolve quality-related issues and drive continuous improvement initiatives.
• Maintain accurate and up-to-date records of all IPQA activities and documentation, ensuring compliance with GMP (Good Manufacturing Practices) and other regulatory guidelines.
• Identify and report the non-compliances observed in individual departments.
• Issue controlled copies & retrieval of old SOPs and QAPs.
• Handling of Deviations & CAPA.
• Handling / investigation of product complaints, incident reports, batch failures and product recalls.
• Preparation, Updation, issuance, retrieval of Price list.
• Document submission as per Regulatory requirement.
• Any other assignments allocated by Unit QA from time to time responsibilities
• Stay informed about current industry practices, regulatory requirements, and quality trends to enhance IPQA processes.

B.Pharm/ M.Pharm with minimum 1-3 Years of experience in IPQA