Specialist, Quality Assurance

Procter & Gamble; Mumbai City; Sur place; INR 800 000 - 1 200 000; Plein temps

Résumé du poste

Procter & Gamble in Mumbai seeks a Quality Assurance role to manage external manufacturing site activities ensuring GMP compliance and regulatory adherence. The role focuses on QA leadership, documentation, and process improvements within the manufacturing network.

The candidate will support contract manufacturing quality initiatives, manage change control, NCRs, investigations, and CAPA, and collaborate with cross-functional teams to ensure product quality and regulatory compliance across sites.

Qualifications

• 3–5 years of relevant experience in QA/Contract Manufacturing
• Degree in pharmaceutical sciences or equivalent required
• Experience in the pharmaceutical industry and GMP knowledge
• Strong written and verbal communication skills, MS Office proficiency

Responsabilités

• Quality system management at external manufacturing sites to ensure GMP compliance
• Support quality and compliance projects for Contract Manufacturing sites
• Manage technical specifications, change control, NCRs, investigations and CAPA
• Assist in stability planning, self-inspection readiness and CAPA reporting
• Review and approve validation and transfer documents

Connaissances

MS Office

Communication skills

Quality mindset

Formation

Degree in pharmaceutical sciences or equivalent

Outils

Electronic tools

Description du poste

Job Location

MUMBAI GENERAL OFFICE

Job Description

P&G was founded over 180 years ago as a simple soap and candle company. Today, we’re the world’s largest consumer goods company and home to iconic, trusted brands that make life a little bit easier in small but meaningful ways. We’ve spanned three centuries thanks to three simple ideas: leadership, innovation and citizenship. The insight, innovation and passion of hardworking teams have helped us grow into a global company that is governed responsibly and ethically, that is open and visible, and that supports good causes and protects the environment. This is a place where you can be proud to work and do something that matters.

Dedication from Us: You’ll be at the core of breakthrough innovations, be given exciting assignments, lead initiatives, and take ownership and responsibility, in creative workspaces where new insights thrive. All the while, you’ll receive outstanding training to help you become a leader in your field. It is not just about what you’ll do, but how you’ll feel: encouraged, valued, purposeful, challenged, heard, and inspired.

What we Offer: Continuous mentorship - you will collaborate with peers and receive both formal training as well as day-to-day mentoring from your manager dynamic and encouraging work environment- employees are at the centre, we value every individual and support initiative, promoting agility and work/life balance.

Overview of the job

To manage the day-to-day activity by ensuring quality and compliance at external manufacturing sites involved in manufacturing & supply of P&G Products, ensuring ongoing activity at external manufacturing sites following the Quality Management System as per Company Standards and Consumer Healthcare business meet customer expectations along with regulatory and legal requirements.

This role requires a degree in pharmaceutical sciences or equivalent, management, FDA understanding or a related field preferred. Previous experience as a technical departments like Operation, R&D, Quality supervisor or a similar management position. Strong working knowledge of Quality Assurance department, Experience in Pharmaceutical industry, and management. Proficiency in MS office, electronic tools, Professional written and verbal communication skills.

Your team

This role reports to Manager, Quality Assurance.

How success looks like
Quality Assurance: Good manufacturing practices (GMP) involvesecuring manufacturing & supplies from the external manufacturing sites in a way that ensures products are always available in good condition, making it easier to find and retrieve products, Meeting all regulatory compliance and GMP practices.

Quality system management at external manufacturing sites: Activities for Technology transfer at sites, approval of technical specifications, Change Control Management, NCR Management, Investigations - Complaints Management, CAPA management via any other tool as an when implemented.

Responsibilities of the role

Quality system management at external manufacturing sites:

• Support quality and compliance related projects for Contract Manufacturing sites.
• Supplier management related etc.
• Support in Quality technical agreement management as an when required.
• Activities for Change Control Management, NCR Management, Investigations - Complaints Management, CAPA management via any other tool as an when implemented.
• Data compilation, reporting of scorecard.
• Support for review & approval of technical specifications
• Review & approval of validation and transfer documents
• Support in planning, supervising, and reporting of stability
• Support for self-inspection audits, CAPA compliance reports, etc.
• Support in GxP training activities

Job Qualifications

• Desired exp. level: 3-5 years
• Desired minimum qualification level: Degree in pharmaceutical sciences or equivalent

About us

We produce globally recognized brands, and we grow the best business leaders in the industry. With a portfolio of trusted brands as diverse as ours, it is paramount our leaders are able to lead with courage the vast array of brands, categories and functions. We serve consumers around the world with one of the strongest portfolios of trusted, quality, leadership brands, including Always®, Ariel®, Gillette®, Head & Shoulders®, Herbal Essences®, Oral-B®, Pampers®, Pantene®, Tampax® and more. Our community includes operations in approximately 70 countries worldwide.

Visithttp://www.pg.comto know more.

We are an equal opportunity employer and value diversity at our company. We do not discriminate against individuals on the basis of race, color, gender, age, national origin, religion, sexual orientation, gender identity or expression, marital status, citizenship, disability, HIV/AIDS status, or any other legally protected factor.

Job Schedule

Full time

Job Number

R000160278

Job Segmentation

Experienced Professionals