Asst. Manager-IPQA Jobs in Zeiss Pharma Limited - Samba, Jammu and Kashmir

institute logo

Asst. Manager-IPQA Jobs in Zeiss Pharma Limited - Samba, Jammu and Kashmir

work outline icon8 - 14 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Zeiss Pharma Limited

time outline iconSamba, Jammu and Kashmir, India

Posted on 15-04-2026

1 Vacancy

Description

  • Job Title: Asst. Manager-IPQA
  • Qualification: BPharm/MPharm
  • Location: Zeiss Pharma Limited - Samba, Jammu and Kashmir
  • Work Experience: 8 to 14 Years

Job Description

  • Ensure implementation and maintenance of the Quality Management System (QMS) as per GMP and regulatory requirements.
  • Review and approve quality documents such as SOPs, BMR/BPR, protocols, reports, and specifications.
  • Monitor and investigate deviations, OOS, OOT results, and ensure appropriate CAPA implementation.
  • Oversee activities related to change control, document control, and risk assessment.
  • Participate in internal audits, vendor audits, and regulatory inspections and ensure audit readiness.
  • Coordinate with Production, QC, Engineering, and other departments to maintain product quality and compliance.

Take this opportunity to join Zeiss Pharma Limited - Samba, Jammu and Kashmir as a Asst. Manager-IPQA in Samba, Jammu and Kashmir and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.

Category

Pharmaceuticals

Functional Area

Pharma IPQA

Preferred Education

MPharm (Master Of Pharmacy)BPharm (Bachelor Of Pharmacy)

Key Skills

Team LeadershipDocumentationQuality Management skillTeam working Skills

About Organization

Zeiss Pharma Limited is a pharmaceutical manufacturing organization focused on producing high-quality medicines with a strong emphasis on regulatory compliance, product quality, and global standards. The role involves working in a manufacturing or operational environment to support production processes and ensure adherence to industry regulations. Responsibilities include assisting in production activities, monitoring process parameters, maintaining accurate batch records and documentation, and ensuring compliance with safety, hygiene, and environmental guidelines. The role also requires coordination with quality assurance and quality control teams, following Good Manufacturing Practices (GMP), and contributing to consistent product quality and efficient operations.

Aggregated job.

Learn more