Officer - R&D Quality

Mcneil Ab; India; Remote; INR 900.000 - 1.500.000; Vollzeit

Zusammenfassung

Kenvue is seeking an Officer - R&D Quality to ensure QMS compliance across R&D labs and external providers. You will manage investigations, stability programs, training, documentation control, and supplier quality activities to support regulatory readiness and continuous improvement.

The role requires a degree in a scientific field and at least 4 years in QA/QC or regulated labs, with experience in GMP/GLP and validated systems. This is an onsite Mumbai-area position.

Qualifikationen

• Bachelor's or master's degree in Microbiology or related field; Biotechnology, Pharmacy, Chemistry, Life Sciences also considered.
• Minimum 4 years of experience in Quality Assurance, Quality Control, R&D Quality, or regulated labs.
• Working knowledge of GMP, GLP, QA processes, CAPA, change control, supplier quality, and computerized system validation.

Aufgaben

• Review Quality documents such as change controls, method validations, test methods, and technical justifications.
• Manage stability programs ensuring studies are executed and documented per quality requirements.
• Support laboratory investigations including review of OOS/OOT, root-cause analyses, corrective actions, retest evaluations.
• Oversee laboratory compliance activities and maintain audit/inspection readiness.
• Manage supplier qualification processes, supplier audits, approved supplier lists, and supplier CAPAs.
• Serve as site training coordinator, monitor training compliance and metrics.
• Support computerized system validation and periodic system assessments.
• Prepare and report quality metrics related to investigations, CAPAs, audits, training, and compliance.

Kenntnisse

GMP knowledge

GLP knowledge

Quality Assurance

Regulatory audits experience

Ausbildung

Bachelor's or master's degree in Microbiology or related field

Tools

Electronic QMS

Document management systems

Computerized system validation

Jobbeschreibung

Kenvue is currently recruiting for a:

Officer - R&D Quality

What we do

At Kenvue , we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

Who We Are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours. For more information , click here .

Role reports to:

Manager, R&D Q&C

Location:

Asia Pacific, India, Maharashtra, Greater Mumbai

Work Location:

Fully Onsite

What you will do

Officer - R&D Quality

Job Purpose

Responsible for ensuring Quality Management System (QMS) compliance across R&D laboratories and external service providers through management of laboratory investigations (OOS/OOT), stability programs, supplier quality activities, training compliance, documentation control, computer system validation, and quality metrics reporting. Supports regulatory compliance, inspection readiness, and continuous improvement initiatives within the R&D organization.

Key Responsibilities

• Reviewing Quality documents such as change controls, method validations, test methods, technical justifications, and periodic reviews.
• Managing stability programs to ensure studies are executed, monitored, and documented in compliance with quality requirements.
• Supporting laboratory investigations, including review of OOS/OOT events, root cause analyses, corrective actions, and retest evaluations.
• Overseeing laboratory compliance activities, conducting compliance assessments, supporting Gemba walks, and maintaining audit and inspection readiness.
• Managing supplier qualification processes, supplier audits, approved supplier lists, and supplier corrective action programs.
• Serving as the site training coordinator, monitoring training compliance, managing training systems, and reporting training metrics.
• Supporting computerized system validation activities, including review of validation documentation and periodic system assessments.
• Preparing and reporting quality metrics related to investigations, CAPAs, audits, training, and compliance performance.

Qualifications & Experience

• Bachelor's or master's degree preferably in Microbiology, other preferences are Biotechnology, Pharmacy, Chemistry, Life Sciences, or a related scientific discipline.
• Minimum 4 years of Experience in Quality Assurance, Quality Control, R&D Quality, or regulated laboratory environments.
• Working knowledge of GMP, GLP, laboratory investigations, CAPA, change control, supplier quality management, and computerized system validation.
• Experience with electronic quality management systems and document management platforms preferred.
• Exposure to regulatory audits like USFDA & EUGMP

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.