Head QA – Sterile | Immacule Lifesciences | Nalagarh

Apply Now

Job Overview

  • Date Posted
  • Location (State / UT)
  • Expiration date
  • Experience
    15 Years, 22 Years
  • Gender
  • Desired Qualification
    Bachelor Degree, Master’s Degree
  • Salary in (₹)

Job Description

  • To establish a quality management system and In Process Quality monitoring in the plant.
  • Responsible to ensure proper documentation.
  • Adherence to Safety and Quality policies and providing necessary support at all times.
  • Ensure adherence to cGMP and regulatory guidelines by the plant personnel and the same is part of the SOPs.
  • To conduct the Quality review meeting and monitor the QMS activities for timely closure.
  • Review and approval of core technical documents leading the Audit Compliance, QMS Documentation, and Validation.
  • To monitor & conduct Internal/external / Vendor & contract manufacturing audits as per the schedules.
  • Review and management of technology transfer documents.
  • Overall Monitoring of new product introduction through the technology transfer process.
  • Review & Approval of product quality-related documents (Product Quality Review, Annual Product Review, Stability data, BMR/BPR, and artwork (Domestic / Export). Coordinate document submissions for
  • regulatory approvals.
  • To approve all batch records & release the finished product.
  • To monitor the Stability study of dosage forms.
  • Responsible for Batch release.
  • Approval of protocols and reports related to validation and qualification activities.
  • Approval of calibration and preventive maintenance planner and ensuring its compliance.
  • To identify the resources for QA function and ensure optimum utilization.
  • To form the investigation team and monitor the effective implementation of CAPA associated with incidents, OOS, complaints, and recalls.
  • Responsible for recruiting technical competent persons in the department in handling the quality management systems.
  • Approve the master documents maintained in the department.
  • To approve the trend analysis reports.
  • To ensure compliance of the Corrective and Preventive Actions (CAPA) necessitated through various activities such as Regulatory Audits, Market Complaints, APR, and Product Recall.
  • Communicate the major product quality-related issues to Management and Regulatory Agencies.
  • Planning, Implementation, and compliance of Quality management system.
  • Host the Regulatory & Customer audits and preparation, review, and timely submission of audit compliance reports.
  • Hold administrative rights to all software systems.
  • Identification, evaluation, and Approval of outside testing laboratory.
  • To ensure compliance with safety requirements, cleanliness, hygiene, and environment in the working area.
  • Coordinate the vendor qualification activities and review the technical agreements.

Qualification: B.Pharma, M.Pharma, MS/M.Sc