Site Quality Liaison Manager
We are Reckitt
Research & Development
This role requires ensuring compliance in Complaint Management and related work in Mauripur Factory in line with Reckitt Quality manual, global complaint management & any other applicable procedure in addition to;
- Supplier Audit & support in new supplier approval & maintenance of local / regional supplier in line with Reckitt Quality Manual, Global supplier management policy and procedure.
- NPD / EPD/ X-trim/ Squeeze / Tech transfer / Projects / cost saving initiative of HC & HyHo
- Reviewing & signing off MoH Queries as Qualified Person or warrantor.
- Attending show cause hearings, personal hearings or any other meetings with MoH or any other regulatory body e.g PQCB, CDI on behalf of Mauripur Factory as Qualified Person.
About the role
Reckitt is looking for a Site Quality Liason Manager to drive processes of complaint handling, MoH query handling supplier management and NPD / EPD & ensure effective implementation. Work with Legal, Regulatory, Production, Procurement & other supply functions & commercial for effective implementation assignment/Project.
Your responsibilities
- Perform GAP Analysis of local SOP’s Vs Global policies and procedures. Update local SOPs accordingly.
- Prepare risk based annual supplier audit plan and conduct Audits, prepare and publish timely report and obtain CAPA from supplier with effective follow-up till action closure. Escalate any Critical or Major issue on time to senior management.
- Prepare and update list of suppliers (AVL) applicable for Mauripur factory as and when required.
- Ensure that the factory related customers / consumers complaints received through email or CLARE Salesforce are handled and respond. A Quality One Complaint Assessment / Deviation is to raise specially related to factory issues except suspected counterfeited/ Inquiry and other related information with effective follow-up till action closure. Escalate any Critical or Adverse Event issue on time to senior management.
- Prepare and update Level 2 tracker along with timely closure of actions and supplier CAPA (where applicable) and conduct monthly governance meeting on Level 2 to update SLT.
- Lead in effective RCA, ensure proper implementation and closure of action plan.
- Fix supplier related production issues with supplier using CAPA and other communication ways
- Provide effective support in Internal & External Audits along with timely closure of Global & Internal audit findings with effective RCA and CAPA
- Responsible for arranging HALAL certificates from supplier for relevant materials.
- Engage in NPD/ EPD meeting and support site related to supplier development / issues.
- Update global KPI’s related to Complaint Management and Supplier Audit to management.
- Responsible for approval of TDS related to supplier management
- Any other job / task assigned by Site Quality Head or regional management
- Support Site Quality Head in all tasks as assigned.
- Prepare & Manage Approved Vendor List for the site.
- Prepare supplier audit plan and execute it accordingly.
- Prepare monthly summary sheet on complaint management activities and report it in management review.
- Duties and responsibilities within this role may change over the course of employment, which will require flexibility
The experience we're looking for
- M.Sc Chemistry/ B. Pharm or M. Pharm or Pharm-D with at least 10 years of experience in different functions of Quality in pharmaceutical company along with good experience in management position or any other having similar setup.
- Degree in Chemistry, Biology, Engineering, or a related science field.
The skills for success
Commercial Awareness, Business Partnership, Collaboration, Partnership building, Ability to challenge the status quo, Propose improvement, Accountability, Adaptability, Collaborator, R&D, Product Lifecycle Management.
What we offer
Equality
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