6 Good Coordination Jobs

As a Forklift Driver, you should have experience working in manufacturing industries and possess the necessary qualifications such as a 10th/+12 degree. Immediate joining is preferred, and we are looking for male candidates who excel in teamwork and demonstrate good coordination with supervisors. It is essential to have an LMV vehicle license and be capable of comprehending assigned tasks promptly. The role requires you to be ready to undertake specific tasks to meet the job requirements efficiently. This is a full-time, temporary position with benefits including provided food and life insurance. The work schedule is during the day shift, and a yearly bonus is offered based on performance. The ideal candidate must have a minimum of 2 years of experience as a forklift driver and hold the necessary LMV vehicle license. A secondary education level of at least 10th pass is required to qualify for this role.,

As a Production Manager at Sanofi India Limited, your main responsibility is to plan and execute all production activities to ensure the delivery of high-quality products while meeting quantity targets. You will be in charge of managing resources efficiently to achieve total customer satisfaction while adhering to GMP/HSE standards. Resource And Time Management You will be responsible for allocating scheduled activities to operators in the shift according to the production plan. Additionally, you will allocate manpower and necessary accessories to operators when needed. Maintaining discipline among the manpower resources is crucial, and you must ensure that all activities are completed within the standard time to provide a continuous feed to the next process. Shift Handover and Vital Communication Effective communication with shift supervisors and subordinates is essential to share vital information about product criticalities during shift handovers. Line Compliance and Adherence to Quality Standards You must ensure that all activities adhere to SOPs and specified parameters in Batch Manufacturing Records (BMR). Conducting in-process tests as per standard frequency and acceptance criteria is crucial. Identifying and reporting quality defects/failures and adhering to stringent checks are part of your responsibilities. Compliance with quality standards, storage requirements, and implementation of the quality system are fundamental aspects of the role. SAP Management Managing SAP system tasks such as creating Purchase Orders, determining materials, issuing goods slips, and posting completed batches in SAP is important. Consuming tertiary packaging materials and carrying out Technically Complete (TECO) for finished process orders are also part of your duties. Production Planning and Scheduling You will receive production plans, interact with cross-functional departments, and monitor daily activities to maximize efficiency. Maintaining adequate Work-In-Progress (WIP) levels and implementing process improvements to enhance cost-effectiveness are key responsibilities. Training and Development Ensuring that you and your team are trained on relevant SOPs, implementing GMP/HSE systems, and developing people are crucial aspects of the role. Training new joiners and assisting in their onboarding process is also part of your responsibilities. Validation and Change Control Coordinating in product re-validations, process validations, and preparing validation protocols and reports are part of your duties. Adherence to site HSE systems, implementing compliance activities, and handling regulatory audits are crucial aspects of the role. Qualification & Change Control Assisting in the qualification of new equipment/modifications and ensuring compliance with GMP standards and user requirements are essential responsibilities. Knowledge, Skills & Competencies You should have at least 1+ years of experience in manufacturing line management, excellent communication skills, proficiency in documentation, experience in handling manpower, knowledge of SAP system, coordination skills, and the ability to improve multi-skills within operators. Training management for direct reports and subordinates is also required. In summary, as a Production Manager at Sanofi India Limited, you will play a vital role in ensuring the efficient production of high-quality products while maintaining compliance with industry standards and regulations. Your responsibilities will encompass resource management, quality control, communication, SAP management, production planning, training and development, validation, adherence to HSE systems, compliance activities, and change control. Your expertise and coordination skills will be essential in achieving production targets and ensuring a safe working environment.,

As a Back Office Executive, you will play a crucial role in the smooth functioning of office operations. Your responsibilities will include utilizing your computer knowledge efficiently to carry out tasks, ensuring good coordination within the team, and maintaining a high level of professionalism. The ideal candidate for this position should be below 35 years of age and possess excellent organizational skills. Your ability to work effectively within the office timing of 10 am to 8 pm will be essential in meeting the demands of the role. The office address where you will be based is 493/C/A, forshore road, Howrah Juit Mill, D.D house 2nd floor, Howrah West Bengal - 711102. This is a full-time and permanent position suitable for freshers who have completed their Higher Secondary (12th Pass) education. In addition to a competitive salary, you will also be entitled to benefits such as Provident Fund. Fluency in English is preferred for effective communication within the work environment. The work location for this role is in person, requiring your presence during the day shift. If you are looking to kickstart your career as a Back Office Executive and possess the required skills and qualifications, we welcome your application to join our dynamic team.,

The primary objective of the role is to facilitate timely approvals from FDA (Loan License units) by effectively collaborating with internal stakeholders and FDA teams to submit various applications. It also involves establishing strong relationships with external stakeholders and engaging in advocacy efforts to support licensing approvals for Cipla LL products. Responsibilities include: - Ensuring timely Regulatory Approvals from State FDA and CDSCO offices for loan license units by following up and obtaining approvals for various applications such as fresh loan licenses, Additional product permissions, Test Licenses, India Business Tender Certificates, WHO-GMP, COPP, State FDA NOC for new drugs, CDSCO applications, etc. - Strategizing and coordinating with internal stakeholders to ensure timely application submissions and resolution of queries and approvals. - Maintaining a master tracker list of all permissions/approvals of FDA (LL) team. - Coordinating with internal cross-functional teams for necessary documentation required for application filing. - Overseeing and checking the work done by LL team members. - Building and maintaining relationships with external stakeholders (FDA/CDSCO). - Monitoring and tracking timely release of CMCL for local and export markets. - Ensuring compliance with regulatory requirements and pharmacopeial changes. - Addressing major challenges such as obtaining India Business Tender Certificates, Test Licenses, and timely FDA permissions and label artwork approvals to support Tech transfer activities at loan license units. Key Interactions: - QA Departments - R&D Department - FDA coordination team - Regulatory Affairs - Deputy Drug Controller CDSCO - Assistant Drug Controller - Assistant Drug Inspectors - Drugs Inspectors The role requires a candidate with a B.Sc. / B.Pharm qualification, 5-10 years of experience in the pharmaceutical industry, good coordination, and communication skills, as well as regulatory experience with FDA and CDSCO online applications. Key decisions include strategizing for key license approvals in consultation with the Reporting manager, decisions related to various FDA/CDSCO applications and submissions at state FDA/CDSCO offices, and artwork approvals of new products. The role also involves monitoring and implementing regulatory and pharmacopeial upgradations to ensure compliance and avoid non-compliance issues. Overall, the position plays a crucial role in ensuring the smooth and timely approval process for loan license units and maintaining positive relationships with both internal and external stakeholders.,

As a Regulatory Affairs Coordinator at Cipla, your primary responsibility is to ensure timely approvals from the FDA (Loan License units) by effectively coordinating with internal stakeholders and FDA teams for the submission of various applications. Your role also involves developing strong relationships with external stakeholders and advocating for licensing approvals for Cipla LL products. Your key accountabilities include: - Securing timely regulatory approvals from State FDA and CDSCO offices for loan license units, which includes obtaining approvals for various applications such as fresh loan licenses, additional product permissions, test licenses, India Business Tender Certificates, WHO-GMP, COPP, etc. - Coordinating with internal stakeholders to ensure timely applications and resolution of queries for approvals. - Maintaining a master tracker list of all permissions/approvals for the FDA (LL) team. - Building and maintaining relationships with external stakeholders in FDA and CDSCO offices. - Monitoring the timely release of CMCL for local and export markets, ensuring compliance with regulatory requirements and pharmacopeial changes. - Addressing major challenges such as obtaining India Business Tender Certificates, test licenses, and timely FDA permissions and label artwork approvals to support the Tech transfer team. In this role, you will interact with various departments including QA, R&D, FDA coordination team, and Regulatory Affairs. Additionally, you will engage with Deputy Drug Controller CDSCO, Assistant Drug Controller, Assistant Drug Inspectors, and Drugs Inspectors. Your key decisions will involve various FDA/CDSCO applications and submissions at state FDA/CDSCO offices, as well as strategizing for key license approvals in consultation with your Reporting Manager. To excel in this role, you should possess a B.Sc./B.Pharm degree, have good coordination and communication skills, regulatory experience, and 5-10 years of experience in the pharmaceutical industry. Join us at Cipla and contribute to ensuring smooth regulatory approvals for our loan license units and fostering positive relationships with external stakeholders.,

Coordinate with sales & dispatch teams for order processing. Prepare & verify dispatch documents (invoice, challan) Track shipments & update delivery status Communicate with clients for dispatch schedules. Good coordination & communication skills