Job Opportunity for experienced R&D Quality Executive at Sun Pharmaceutical Industries Limi[...]

Pharmaceuticalcarrier; Vadodara; On-site; INR 6,00,000 - 12,00,000; Full time

Job summary

A leading pharmaceutical company in Vadodara is seeking an Executive/Sr. Executive for R&D Quality. This vital role involves reviewing critical documents, ensuring compliance with regulations, and conducting quality assessments. Ideal candidates should possess an M.Pharmacy and 5 to 7 years of experience in quality roles. Join us to innovate and make a significant impact in the pharmaceutical sector!

Qualifications

• 5 to 7 years of experience in R&D or Quality roles.
• Certification in Six Sigma or equivalent is preferred.

Responsibilities

• Review formulation and packaging development documents.
• Evaluate Out of Specification (OOS) data and conduct risk assessments.
• Prepare internal reports for management decision-making.

Skills

Pharmaceutical formulations

Quality control

Regulatory compliance

Documentation standards

Oral communication

Written communication

Education

M.Pharmacy

Job description

About Sun Pharma

Sun Pharmaceutical Industries Limited, India’s No. 1 pharmaceutical company, is committed to delivering high-quality medications to the world. We are looking for passionate professionals to join our team and contribute to our continued success.

Position: Executive / Sr. Executive – R&D Quality

Location: Vadodara
Educational Qualification: M.Pharmacy
Certification: Six Sigma or equivalent (preferred)
Experience: 5 to 7 years

Job Responsibilities:

Document Review & Compliance:

• Review formulation and packaging development documents such as Master Formula, Product Development Reports, Stability Plans, Risk Assessments, Process Validation Protocols, and more.

• Ensure compliance with internal procedures and regulatory guidelines across various markets.

• Identify gaps in processes and bridge them through audits and document reviews.

Quality & Risk Assessment:

• Evaluate Out of Specification (OOS) and Out of Trend (OOT) data.

• Conduct Quality by Design (QbD) based risk assessments and Failure Mode Effect Analysis (FMEA).

Training & Coordination:

• Act as a Learning Management System (LMS) Training Coordinator.

• Assign job roles, manage learning activities, and oversee user training within the system.

• Collaborate with cross-functional teams (CFT) to address quality issues.

Electronic Document Management & Reporting:

• Function as an EDMS coordinator for documentation and records.

• Prepare internal reports for management information and decision-making.

Skills Required:

Strong technical understanding of pharmaceutical formulations and quality control
Excellent oral and written communication skills
Knowledge of regulatory compliance and documentation standards

If you are ready to take on a challenging and rewarding role in a leading pharmaceutical company, apply now and be a part of our growth story!

Join Sun Pharma – Innovate, Excel, and Make an Impact!

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