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Assist QA Inspection Manager in all in-process and inspection checks of production operations and facilities (e.g., building / environmental / equipment / utilities / systems etc.) per Abbott Policies, AQ, EQDs, SOPs, GMP and Drug Act 1976. Perform GEMBA of respective areas to assure inspection readiness and verify that area logbooks and other documents are maintained with reference to Data integrity. Additionally, perform sampling of bulk, intermediate and finished products as per respective sampling plans.
**Major Responsibilities:**
+ To make sure that activity does not result in,
+ Delay or non-availability of product.
+ Delay in introduction of new products.
+ Any non-compliance of cGMP (current Good Manufacturing Practices), GSP (Good Storage Practices) and EHS (Environment, Health & Safety) requirement.
+ Line clearance and In process checks of production manufacturing and finishing operations, GEMBA Inspection of Warehouses, Utilities and facilities (e.g., building / environmental / equipment / utilities / systems etc.) per Abbott Policies / Procedures, and cGMP Guidelines.
+ To assure verification of all necessary checks and requirements for the dispensing activities before granting line clearances as per respective procedures.
+ Raw Materials issue verifications as per approved Manufacturing Shop Order.
+ Packaging Commodities Issue verifications as per approved Finishing Shop Order.
+ Perform sampling activities as and when required per the applicable procedures.
+ Maintain and improve existing quality processes to assure continuously appropriate and compliant operations in production and storage areas.
+ Responsible for SOP write up / Revision / Implementation as per AQ, EQDs, SOPs, Drug Act, cGMP etc.
+ To ensure that all necessary documentation is completed accurately in respective areas, in a timely manner, and in compliance with data integrity and regulatory requirements.
+ To ensure calibration / verification of equipment / instruments used for In-process checks.
+ To participate in Validation and Qualification activities related to Process, Equipment and Facilities, whenever required.
+ Audit follow-up for corrective action implementation in his/her area of activity.
+ To actively participate in handling of exception reports, internal quality investigations and customer complaints related to his / her area for root cause identification and CAPA implementation.
+ To ensure that workplace is compliant with all applicable health and safety regulations. Report any workplace safety / near miss incidents and follow-up till closure.
+ Handling of Regulatory samples for submitting to respective Drug Inspectors.
+ To assist QA Inspection Manager in data collection for PQR.
+ Any special project assigned by QA Inspection Manager.
+ Work closely with other departments to facilitate in maintaining compliance of the applicable systems for change controls, CAPA, ERs, complaints, internal GxP audit observation follow ups and CAPA effectiveness.
+ Proceed for Rejected material incineration activity when assigned.
**Education/Knowledge & Experience:**
+ Science Graduate/Master; preferably Chemist/Pharm D
+ 2-3 years' experience in the same capacity
+ Knowledge of QA documentation, technical problem resolution, and other all activities taking place in QA
+ Proficient in MS Office
+ Analytical Skills
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

**Job Description**
**Are You Ready to Make It Happen at Mondelēz International?**
**Join our Mission to Lead the Future of Snacking. Make It With Pride.**
You lead the plan-do-check-act (PDCA) process of the site quality management system and report results to the quality section manager.
**How you will contribute**
You will support elements of the site's quality system, including internal documentation and change management control including quality policies amendments and registration of internal and external documentation, internal audits, effective PDCA cycles and CAPA system management and management review. In addition, you will coordinate the eQCMS bi-annual review, handle consumer complaints from start to finish, and serve as a key contact for food regulatory agency inspection and contacts management.
**What you will bring**
A desire to drive your future and accelerate your career and the following experience and knowledge:
+ Relevant experience in a laboratory.
+ Working efficiently on a team
+ Flexibility and adaptability to meet customer/business requirements
+ Attending to detail and following written instructions
+ Communicating effectively, verbally and in writing
+ Project management and working on multiple activities at the same time
+ MS office applications
**More about this role**
**What you need to know about this position:**
To manage and lead management system activities including scheduling and execution of internal and external audits, Quality Policies, NCR & CAPA system within designated Confectionary & PB site and coordinate with cross functional teams to implement compliance.
To develop the quality culture within the factory and drive CIQ agenda through following:
+ Ensure document management on site - eQCMS benchmark. Train each new starter in using the tool, ensure the continuous updating of the document register and the proper use of the tool.
+ Ensure deployment and implementation of Enablon and conduct training session to the targeted audience to ensure Enablon is deployed on site level.
+ Implement product quality, & laboratory QPs within the factory sensory training, OOS etc.
+ Facilitate achievement of customer and consumer expectations.
+ Lead risk management and continuous product/process quality improvement activities.
+ Provide technical analysis and input for decision making.
+ Develop functional/technical skills of quality team and site employees.
+ Lead Food Safety and Compliance audits, including FSSC 22000, QCMS, QMS, HALAL.
+ Identify and lead efforts of product/process quality and cost management improvement opportunities and subsequent productivity gains.
**What extra ingredients you will bring:**
+ Effective communication with internal and external partners
+ Strong analytical skills
+ An ability to build strong relationship and influence team members
+ Time management, ability to multitask prioritization and ability to work under pressure.
**Education:**
BE or Bachelors in Food Sciences
**Job specific requirements:**
+ At least three year within Audits/Systems and Process preferably in the Food, Chemical or Pharmaceutical industry.
+ Demonstrated experience in championing an idea from start to finish
+ Ability in dealing with shop floor issues and concerns raised by employees or their representatives.
+ Working knowledge and effective understanding of the production process in a systems environment
**Work schedule:**
Full-time
No Relocation support available
**Business Unit Summary**
**Mondelēz International in the Middle East, North Africa and Pakistan serves the Middle East and Africa markets as well as Australia, New Zealand, the UK and Canada. Headquartered in Dubai, UAE, we have more than 2600 employees working across seven plants and six commercial offices; we make, bake, sell and deliver our products to customers. We are market leaders in key snacking categories with iconic global and local brands including Cadbury Dairy Milk chocolate, Milka, Oreo and belVita biscuits, Barni Cakes,Tang powdered beverage, Chiclets and Trident gum and Halls candy.**
Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.
**Job Type**
Regular
Supply Chain Quality Assurance
Product Quality, Safety and Compliance
At Mondelēz International, our purpose is to empower people to snack right through offering the right snack, for the right moment, made the right way. That means delivering a broader range of delicious, high-quality snacks that nourish life's moments, made with sustainable ingredients and packaging that consumers can feel good about.
We have a rich portfolio of strong brands - both global and local. Including many household names such as Oreo, belVita and LU biscuits; Cadbury Dairy Milk, Milka and Toblerone chocolate; Sour Patch Kids candy and Trident gum. We are proud to hold the number 1 position globally in biscuits, chocolate and candy as well as the No. 2 position in gum
Our 80,000 Makers and Bakers are located in our operations in more than 80 countries and are working to sell our products in over 150 countries around the world. They are energized for growth and critical to us living our purpose and values. We are a diverse community that can make things happen, and happen fast.
Join us and Make It An Opportunity!
Mondelez Global LLC is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran status, sexual orientation, gender identity, gender expression, genetic information, or any other characteristic protected by law. Applicants who require accommodation to participate in the job application process may contact for assistance.