Quality Assurance Manager

We are Reckitt

Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.

About the role

• To ensure all the finished products released from site are fully in compliance with RB requirement and national standards.

• Proactively work on the issues & gaps in manufacturing area and ensure the compliance to reduce product quality risks.

• Lead site validation master plan and manage all kinds of validation activities, including 3Q（HVAC, water system, production equipment etc.), PV and CV. And ensure all validation activities are complied with Reckitt policy and GMP requirement. Lead deviation investigations and CAPA in all validation activities.

• To make sure site validation master plan implemented in time and guarantee all type of projects validated properly by following Reckitt validation policies, SOPs, Reckitt global product development manual, global product quality manual, risk management manual, and technical transfer manual etc.

Your responsibilities

• Comply with regulations pertaining to disinfectant products, cosmetics, medical devices, as well as the company's quality management system documents. 

• Ensure the technology transfer process are well followed for NPD, EPD and Sourcing change projects.

• Responsible for all quality issues investigation and robust CAPA in production area to prevent quality issue recurrence by coordinating cross functional team resource, share the trend to key stakeholders regularly.

• To ensure AQL team daily onsite checking and report about production area activities are in compliance with SOPs/WI/compliance requirement. Escalate medium/high severity issues to line manager immediately.

• Lead the quality agreement based on project’s needs, approve the packaging specification ensure the packaging specification are in consistent with quality agreement.

• To issue the GFS for NPD/EPD/Sourcing change projects and update the global GFS tracker.

• Responsible for timely release of finished goods in SAP system and make release/rejection decision when there is deviation or gap.

• CPBOM approval and review the BOM, MOM, Spec accuracy for quality manager’s approval. 

The experience we're looking for

• Bachelor’s degree or above in Chemistry Engineering, Applied Chemistry, Food or Pharma related.

• Familiar with relevant laws and regulations of disinfectants, cosmetics and medical device, JJF 1070, AQL classification, GB2828.

• At least 5 years’ experience in management field of quality.

• Entrepreneurial decision-making skills and communication skills.

• Strong target orientation and highly motivated.

• People management- Proven experience in leading and developing teams, able to effectively influence people of all levels to drive change and improvement.

• Flexibility in thinking and pragmatic problem-solving skills.

•Have ISO22716/ISO13485/GEP/ISPE/FDA/WHO professional knowledge.

• GMP

• Fluent English

Equality

We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.