Puerto Life Sciences - Hiring for QA/QC/Production Departments
Designation: Assistant Manager/Manager
1) Department: Quality Assurance
Qualification: B. Pharma/M. Pharma
Skills Required for Sterile Manufacturing:
- Expertise in risk assessment, investigations, CAPA implementation, and effectiveness checks.
- Thorough knowledge of SOPs, change control processes, and compliance monitoring for sterile environments.
- Strong understanding of batch record reviews, protocol preparation, and regulatory compliance.
- Proficient in handling deviations, internal/external audits, and ensuring GMP adherence in sterile conditions.
- Experience in MQA operations and verification of global sterilization standards.
2) Department: Production
Qualification: B. Pharma/M. Pharma
Skills Required for Sterile Manufacturing:
- Expertise in sterile compounding processes, including CIP/SIP systems, component preparation, and sterilization.
- Hands-on experience in aseptic operations, media filling, sterilization processes, and area monitoring.
- Ability to troubleshoot and manage challenges in aseptic manufacturing environments.
- Strong leadership skills to oversee sterile production operations while ensuring adherence to GMP standards.
3) Department: Quality Control
Qualification: M.Sc. in Microbiology, Chemistry, or Biotechnology
Skills Required for Sterile Manufacturing:
- Strong understanding of both analytical and microbiological testing in sterile manufacturing.
- Proficiency in analytical testing techniques (HPLC, GC, UV, etc.) to ensure product quality and regulatory compliance.
- Expertise in environmental monitoring (viable/non-viable), bioburden analysis, and sterility testing.
- Knowledge of stability studies, release testing, and pharmacopoeial requirements for sterile products.
- Strong leadership to oversee both microbiological and analytical QC teams, ensuring adherence to GMP standards.
How to Apply:
Please share the following details via email:
- Updated Resume
- Current CTC
- Notice Period
Email: hr@puerto.in
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