Lab Operations Manager
We are Reckitt
Research & Development
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.
About the role
We're in search of a proactive Quality Associate to join the Reckitt team, to drive QC processes & ensure their effective implementation. Work with HME, M&E & other supply functions & commercial for effective implementation of NPD/EPD/Projects. Quality Control processes and ensure compliance to DRAP, and RB GLP requirements through effective implementation.
Scope of this role includes but is not limited to;
- Overseeing quality compliance in Labs and related work in F-14 & F-18 Mauripur factory
- NPD/ EPD/ X-trim/ Squeeze/ Tech transfer/ Projects/ Cost saving initiative of HC & HyHo
- Lab resource management update system and documents as per requirement
- Management and maintenance of GMP certification – ISO 17025, ISO 22716 & ISO 9001
Your responsibilities
- Communication with the management on achievement of KPI’s related to Laboratories/ Global Quality Standards & other Quality related targets set for the year and ensure implementation
- Develop QC objectives consistent with site and regional/ global objectives
- Ensuring that QC procedures are in place and implemented for effectively
- Maintain QC staffing to necessary levels to fulfil site quality responsibilities
- Supervise subordinates to the extent of performance appraisal, selection, definition of responsibility, delegation of authority and setting of objectives
- Ensure that QC processes are in compliance with all regulatory requirements and RB Quality Management system defined in RB Manual
- Lead as technical Manager for ISO 17025 & support other GMP certifications to fulfil the requirements and continuation of standards and it its certifications
- Ensure that all incoming RM/PM/Bulk/FG and WIP materials are tested against specs or respective pharmacopoeia monograph, RB standards and released timely for manufacturing
- Manage assay validation of all active materials & related products for correctness of results
- Lead in bulk hold time study of products
- Ensure self-inspection of lab is quarterly conducted
- Highlight the gaps for continuous improvement ensure to implement it
- Ensure that all analytical testing is done on calibrated equipment’s and using approved test methods, standards, standardized solution or reagents, against standard specification and released on time with no production stoppage
- Arrange testing of all new source/ supplier materials timely, comply with vendor approval protocol and update Approved Vendor List accordingly
The experience we're looking for
- M.Sc. Chemistry/ B. Pharm or M. Pharm from a recognized university
- At least 7 years in a management position in Quality Control/ Quality Assurance in a Pharmaceutical company or any other company having similar setup
The skills for success
What we offer
Equality
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