Job Description : Caring for the world, one person at a time has inspired and united the people of Johnson &amp; Johnson for over 125 years. We embrace research and science bringing creative ideas, products and services to advance the health and well-being of people. Every day, our more than 130,000 employees across the world are blending heart, science and ingenuity to profoundly change the trajectory of health for humanity. At Johnson &amp; Johnson Medical Devices Companies, we are using our breadth, scale and experience to reimagine the way healthcare is delivered and help people live longer, healthier lives. In a radically changing environment, we are making connections across science and technology to combine our own expertise in surgery, orthopedics, vision and interventional solutions with the big ideas of others to design and deliver physician and patient-centric products and solutions. As pioneers in medical devices, we continually focus on elevating the standard of car working to expand patient access, improve outcomes, reduce health system costs and drive value. We create smart, people-centered healthcare to help the patients we serve recover faster and live longer and more vibrantly. DUTIES &amp; RESPONSIBILITIES : Updates supervisor of work status or problems with recommendations for improvement or correction. Implements approved corrective action. Modifies procedures to improve equipment operation or processes. Responds to basic system alarms and reset alarms as necessary. Records assignments and prepare documentation concerning materials, parts used, concepts, designs, drawings and processes. Compiles data to develop reports for management. Administers testing protocols and documents results. Coordinates manufacturing phase in of new products or product changes. Responds to safety issues by recommending and implementing a resolution. Completes specialized studies or experiments and prepares reports on results. 2.1. manufacturing Operations: 2.1.1 Responsible for log book, cleaning record, Leak rate test record and run sheets review of Sterilization process. 2.1.2 Co-ordinate Secondary Sealing and Packing operations to meet production objectives &amp; targets. 2.1.3 Get the daily plan from Production Supervisor of Suture Finishing Department/Needle &amp; Non-Abs. Start the work as per applicable SOPs and SPECs. 2.1.4 Visually inspect the batch material as per batch card &amp; reconcile the quantity received for production. 2.1.5 Ensure production machines are cleaned and activity documented in daily cleaning record and Batch Manufacturing records. 2.1.6 Ensure availability of input RM and PM as per production plan. 2.1.7. Allot required manpower to individual work stations. 2.1.8 Ensure effective verification of line clearance done by concerned associates and document the same in Batch Manufacturing record. 2.1.9 Ensure machine operating parameters are documented at respective workstations in Batch Manufacturing record. 2.1.10 Ensure environmental parameters and challenge test wherever applicable is documented in Batch Manufacturing record. 2.1.11. Ensure IPQA samples are withdrawn at each workstation and handed over to IPQA for testing. 2.1.12. Ensure output at each workstation is properly identified, segregated, labeled and quantity is reconciled. Qualifications ; REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS- Technical Skills / Behavioral Skills : - Detailed knowledge of Manufacturing processes, fabrication technology and process capability. - Ability to analyze plan &amp; map progress against decided manufacturing plan. - Ability to train, certify &amp; allocate manpower as per requirement at various stages of manufacturing. - Product knowledge with respect to product functionality, product requirements, product characteristics and field applications - Business Excellence - Knowledge of applicable laws and regulations in a manufacturing environment - Thorough understanding of process criteria and regulations and business impact of decisions and actions - Strong technical, planning and execution capabilities - Ability to analyze, balance and prioritize risks - Acquaintance with GMP, machines and equipment - Adequate understanding of process system improvement in terms of process control, process development and process optimization - Quality and Compliance - Thorough understanding and application of process specific knowledge - Ability to understand and apply the knowledge of financial aspects - Ability to understand and apply the system modeling techniques - EHS&amp;S - Ability to apply Process Analytics &amp; Problem solving techniques &amp; Process System Improvement - Technology &amp; Data Management Are you ready to impact the world? Johnson &amp; Johnson offers an unusual experience to professionals looking for an opportunity to work with hardworking people who share your real passion for caring in an environment that empowers you to drive your own career.We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. This description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job. The apply button will redirect you to an external URL, please apply there as well.

Aurangabad

Maharashtra

Johnson & Johnson - Executive - Manufacturing 

Johnson & Johnson - Executive - Manufacturing  ,Job Description for Johnson & Johnson - Executive - Manufacturing  in Johnson & Johnson in  Aurangabad Maharashtra for (4-8) years of experience. Apply Now!

Job Description for Johnson & Johnson - Executive - Manufacturing  in Johnson & Johnson in  Aurangabad Maharashtra for (4-8) years of experience. Apply Now!