Executive

Aurobindo Pharma; Visakhapatnam; On-site; INR 600,000 - 1,200,000; Full time

Job summary

Aurobindo Pharma in Visakhapatnam is seeking an experienced professional to drive equipment qualification, validation, and related documentation in alignment with cGMP guidelines. The role requires hands-on execution of IQ, OQ, PQ, URS, and other validation protocols while ensuring regulatory compliance.

The ideal candidate will have 5–10 years of experience in EQL roles within the pharmaceutical industry, with a strong understanding of CGMP and 21 CFR 820 standards, and proficiency in multiple

Qualifications

• Execute equipment qualification, validation, and documentation activities per OSD equipment requirements and cGMP guidelines.
• Conduct IQ, OQ, PQ, URS, and other validation protocols per SOPs.
• Ensure compliance with regulatory requirements by maintaining accurate records of validation activities.

Responsibilities

• Execute equipment qualification and validation activities.
• Perform IQ/OQ/PQ and related validation protocols.
• Maintain accurate documentation to meet cGMP standards.
• Collaborate with cross-functional teams to resolve equipment performance issues.
• Develop and implement quality control procedures for manufacturing processes.

Skills

Equipment Qualification

Validation

IQ/OQ/PQ

CGMP compliance

Regulatory knowledge

Education

B.Pharm (Bachelor of Pharmacy)

M.Pharm (Master of Pharmacy)

Tools

URS

SOPs

Validation protocols

Job description

Roles and Responsibilities

• Execute equipment & utility qualification, validation, and documentation activities according to OSD equipment requirements and cGMP guidelines.


• Conduct IQ, OQ, PQ, URS, and other validation protocols as per SOPs.


• Ensure compliance with regulatory requirements by maintaining accurate records of all validation activities.


• Collaborate with cross-functional teams to resolve issues related to equipment performance and maintenance.


• Develop and implement effective quality control procedures for pharmaceutical manufacturing processes.

Desired Candidate Profile

• 5-10 years of experience in Equipment Qualification & Validation (EQL) role in a pharmaceutical industry setting.


• Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma).


• Strong understanding of CGMP regulations and 21 CFR part 820 standards.


• Proficiency in executing various types of validations such as IQ, OQ, PQ, URS etc.