Compliance & Validation Manager

Reckitt; Nottingham; On-site; GBP 40,000 - 60,000; Full time

Job summary

Reckitt is seeking a Compliance & Validation Manager in Nottingham to oversee batch certification and ensure compliance with quality standards. This role involves close collaboration with project engineers and third-party sites, focusing on validation activities and proactive risk management, with a commitment to continuous improvement.

Benefits

Inclusive culture

Wellbeing benefits

Career development opportunities

Qualifications

• Proven track record in manufacturing environments.
• Validation, training, and auditing experience.

Responsibilities

• Batch release and certification of finished products.
• Maintain GMP compliance for all factory activities.
• Support regulatory audits to maintain manufacturing authorizations.

Skills

Pharmaceutical

Manufacturing Operations

Quality Management Systems

Education

Eligible to act as a Qualified Person in the UK

Knowledge of pharmaceutical manufacturing regulations in Europe

Job description

Social network you want to login/join with:

Compliance & Validation Manager, Nottingham

col-narrow-left

Client:

Reckitt

Location:

Nottingham, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Reference:

71cf7c92acf8

Job Views:

6

Posted:

17.06.2025

Expiry Date:

01.08.2025

col-wide

Job Description:

Compliance & Validation Manager

City: Nottingham

About Reckitt

Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose is to protect, heal, and nurture for a cleaner, healthier world. Join us in our mission to make access to quality hygiene, wellness, and nourishment a right, not a privilege.

Role Overview

As a Qualified Person supporting batch certification and release activities, you'll work closely with Project Engineers and the Technical team to oversee validation activities, ensuring new equipment and process changes meet quality standards. You'll collaborate with Third Party and Reckitt manufacturing sites to resolve quality issues and support product supply to Nottingham. The role involves proactive risk management and continuous improvement.

Your Responsibilities

• Batch release and certification of finished products at Nottingham.
• Maintain GMP compliance for all factory activities.
• Provide quality input and sign-off on validation activities, including facilities, equipment, NPD/EPD, and product transfers.
• Implement NPD/EPD with clear risk management.
• Coordinate with third-party and Reckitt manufacturing sites on quality issues and changes.
• Identify and communicate non-compliance and risks to supply management.
• Support regulatory audits to maintain manufacturing authorizations and export agreements.
• Display performance indicators and risks to management.
• Provide technical support for investigations and quality issues.

Qualifications & Experience

• Eligible to act as a Qualified Person in the UK.
• Understanding of manufacturing operations and quality management systems.
• Knowledge of pharmaceutical manufacturing regulations in Europe.
• Proven track record in manufacturing environments.
• Experience in pharmaceutical manufacturing of solid dosage forms.
• Validation, training, and auditing experience.

Skills for Success

Qualified Person, Pharmaceutical, Manufacturing Operations, Quality Management Systems.

What We Offer

Inclusive culture, wellbeing benefits, share plans, incentives, and career development opportunities.

Equality Statement

We hire for potential and value diversity. All qualified applicants will receive consideration without discrimination based on age, disability, ethnicity, gender, and other protected characteristics.