Zentiva Hiring QA Executive in Ankleshwar | Pharma Professionals - PHARMA STUFF

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Oct 1, 2024

Zentiva Hiring QA Executive in Ankleshwar | Pharma Professionals

Zentiva Hiring Executive - Quality Assurance | M Pharm / B Pharma

Zentiva,, is hiring a QA Executive in Ankleshwar. This role is ideal for individuals with a background in Pharmacy or Chemistry, combined with experience in Quality Management Systems and Regulatory Compliance. Location: Ankleshwar, Gujarat Job Role: QA Executive Application Deadline: November 15, 2024 Experience Required: 3-8 years in Pharma Quality Management Key Responsibilities of the QA Executive Role As a QA Executive at Zentiva, your primary responsibilities will revolve around ensuring Quality Management and Continuous Improvement at the Ankleshwar manufacturing site. You will be integral to ensuring that Zentiva adheres to its stringent quality standards and meets regulatory requirements. Quality Management & Continuous Improvement
  • Conduct line clearance and ensure shop floor compliance.
  • Perform in-process checks and sampling activities to ensure product quality.
  • Implement Zentiva's corporate policies, manage Standard Operating Procedures (SOPs), and control essential documents.
  • Oversee the complaint investigation system and coordinate Annual Product Quality Review.
Compliance & Regulatory Adherence
  • Ensure adherence to local FDA and MHRA regulations by conducting gap analysis and preparing compliance plans.
  • Lead regulatory dossier reviews and participate in external regulatory audits.
  • Manage the implementation of Corrective Actions/Preventive Actions (CAPA) and ensure their effectiveness.
Validation & Qualification
  • Oversee the preparation and review of the Validation Master Plan.
  • Ensure the validated status of all equipment, processes, and cleaning procedures.
  • Lead the qualification and validation of facilities, instruments, and processes.
[caption id="attachment_58336" align="aligncenter" width="930"]Zentiva Recruitment Notification Zentiva Recruitment Notification[/caption] Documentation Control
  • Manage the controlled distribution and archival of documents and records.
  • Control master documents, issuance of batch records, and manage SOP compliance.
  • Investigate customer complaints and conduct batch reviews for manufacturing and packing.
cGMP Training & Development
  • Develop and execute training modules in GMP (Good Manufacturing Practices).
  • Organize training programs in coordination with various departments to ensure compliance.
Qualifications and Experience Required Zentiva seeks a QA Executive with the following qualifications and skills: Education: Graduate or Postgraduate degree in Pharmacy or Chemistry. Experience: 3-8 years in the Pharmaceutical Industry, particularly in Quality Management Systems, Process Validation, Qualification, and Regulatory Requirements. Skills: Strong knowledge of Good Manufacturing Practices (GMP) and regulatory standards, excellent communication skills, and the ability to manage teams and present complex technical issues in an easily understandable manner. How to Apply for Zentiva QA Executive Position Interested candidates can apply for the Zentiva QA Executive position at the Ankleshwar facility through the company’s official career page. Application Deadline: November 15, 2024 Location: Ankleshwar, Gujarat https://pharmastuff.org.in/job/zentiva-hiring-executive-qa

 

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