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.
In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance.
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
We're in search of a proactive Quality Associate to join the Reckitt team, where innovation and science converge to make a real-world impact. You'll contribute to the growth of our trusted product portfolio, ensuring the highest standards of quality. Your expertise will drive activities from concept to execution, fostering an environment of continuous improvement. If you thrive in a dynamic atmosphere and are looking for a role where your actions directly contribute to the company's success, we would love to see your application.
To monitor the site quality system compliance requirement of Schedule M, MHRA, SAHPRA, ISO 9001 and other regulatory authorities.
To Monitor planning and conduct of Self Inspection. Initiate and approve the corrective action plans. Compliance follow-ups for external audits.
Investigate, review Deviations, Quality incidents and ensure adequate CAPA plans, its implementation and close-out in Quality One software.
Ensure change controls are initiated, reviewed, & documented in Quality One software.
Investigate, review consumer complaints & ensure appropriate CAPA implementation.
Monitor the annual supplier audit schedule, Assessments and conduct audits for raw material and packing material suppliers as per schedule.
Lead and manage the local Quality Assurance team.
Ensure that finished products released as per the release procedure
Review and approval of Supplier based on document assessment and audit outcome
Prepare audit compliance reports and ensure CAPA in co-ordination with suppliers
Monitor the Out of Specification & Out of trend results investigations
Review audit trails for laboratory instruments.
Review and approval of batch records and release of FG.
Review, approve the Quality assurance SOP’s and SOP’s related to Mysore site.
To review the site policy and procedure’s like VMP, SMF, PVMP, Protocols, specifications, test methods, batch documents & other site documents.
Trend analysis of quality management system key performance indicators.
To ensure that appropriate qualification, requalification and validations are done for site equipment’s, area, and systems.
Ensure control, maintenance, and issue of documentation for manufacture, compliant with the marketing and manufacturing authorizations requirements (regulatory bodies) and effective/efficient delivery of operational activities.
To ensure the management review and annual product review program are maintained according to concerned GMP and QMS requirement.
Ensure store checks are performed as per procedure
Ensure the maintenance of department and premises.
To manage Quality Critical Event and ensure that event is escalated to the concerned party according to concerned global policy. To contribute as a member of quality critical event for reviewing of decision for the event such as continuing production and sales and level of recall etc.
To ensure and monitor key quality process during NPD/EPD roll out from site.
Ensure appropriate qualification and validations for site equipment’s, area and systems
Ensure required initial and continuing training of department personnel & adapted according to need. Provide GMP trainings.
To support all key initiative at the site as key member of the Site leadership team.
Site Management review meetings & ensure completion of follow up actions.
Other responsibilities assigned by the management time to time.
Motivate and drive the Quality team to continually improve the Quality Culture at site.
To perform, review of the site risk register and evaluation.
Ensure the monitoring and control of the manufacturing environment, plant hygiene, process validation, training.
Commercial Awareness, Business Partnership, Collaboration, Partnership building, Ability to challenge the status quo, Propose improvement, Accountability, Adaptability, Collaborator, R&D, Product Lifecycle Management.
With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy.
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.
