Puerto Life Sciences Hiring for QA, QC – Manager, AM Positions

Puerto Life Sciences, a renowned name in sterile pharmaceutical manufacturing, is inviting talented professionals to join its expanding team. The company is currently hiring for Manager and Assistant Manager positions in Quality Assurance (QA) and Quality Control (QC). If you have 5-8 years of relevant experience, a passion for excellence, and are seeking a dynamic work environment focused on innovation and compliance, Puerto Life Sciences offers the perfect platform for your career growth.

Located in India, Puerto Life Sciences operates with the mission of delivering world-class sterile pharmaceutical products, adhering to the highest global quality standards.

Job Openings at Puerto Life Sciences: QA and QC Manager/AM Positions

1. Quality Assurance (QA) – Manager / Assistant Manager

Key Responsibilities:

• Oversee daily QA operations to maintain quality integrity across all processes.
• Lead Corrective and Preventive Actions (CAPA) and manage deviation control activities.
• Support and lead regulatory audits and inspections ensuring compliance with international regulatory standards.
• Develop and implement QA strategies to enhance process efficiency and ensure regulatory readiness.
• Manage and mentor the QA team to drive performance excellence and foster a culture of continuous improvement.

Qualification & Experience:

• Bachelor’s/Master’s degree in Pharmacy, Chemistry, or related science disciplines.
• 5-8 years of experience in Quality Assurance within the pharmaceutical/sterile manufacturing sector.
• Strong knowledge of regulatory guidelines (USFDA, MHRA, WHO-GMP, etc.).

2. Quality Control (QC) – Manager / Assistant Manager

Key Responsibilities:

• Lead the QC team to ensure timely and accurate analysis of raw materials, in-process samples, and finished products.
• Manage internal and external audits ensuring seamless compliance with regulatory standards.
• Strategize and implement QC procedures to optimize lab performance and maintain regulatory compliance.
• Oversee laboratory supply management and ensure accurate documentation of results as per Good Laboratory Practices (GLP).
• Foster team development and performance management initiatives.

Qualification & Experience:

• Bachelor’s/Master’s degree in Pharmacy, Chemistry, Microbiology, or related fields.
• 5-8 years of hands-on experience in Quality Control within a sterile pharmaceutical environment.
• Proficiency in handling laboratory instruments and understanding of regulatory inspection requirements.

Application Process

Candidates interested in the QA and QC – Manager, AM roles are requested to share their updated resume, along with details of current CTC and notice period at:

Email: hr@puerto.in