Panel manager jobs in Diu

Job Description:   Job Description: Regulatory & Compliance Manager     1. Position Description   Job title Regulatory & Compliance Manager    Department QA Reports to Vice President-R&D Direct Reports - Location Daman       2. Job Purpose   Job Statement... 

 ...Effectively manage the restaurant by ensuring the following: Oversee the Implementation of standards as detailed in the departmental standards and procedures manual Adhere to opening and closing procedures Adhere to bill paying procedures Conduct effective shift... 

 ...Transportation & Logistics Vendor & Stakeholder Engagement Admin Vendor bill checking and processing Telephone / mobile management Housekeeping & Hygiene HR /Admin related QMS Security day to day management Travel Estimate NA Job Requirements... 

 ...Job Title: Assistant Quality Manager Job Function: Supply Chain Location: Amli Factory Req ID: R-1172046 Job Responsibilities To implement Quality Management System, procedures & standards which enable the plant to achieve regulatory compliance, sustain external... 

✨ We're Hiring! Senior HR Executive/Manager - Daman ✨ Are you an experienced HR professional looking to make a significant impact in a manufacturing environment We are seeking a Senior HR Executive/Manager to join our team in Daman . If you have a passion for driving... 

 ...administer day-to-day transport arrangement, site security & Hospitality management To administer housekeeping of Admin block & Entire factory....  ...which we work, by using inclusive language, diverse interview panels, and diversified sourcing strategies. Selection is based on... 

 ...plans, sampling techniques, and daily checklists. Maintain detailed records of all test results and inspection reports. Team Management: Supervise the QC team across all shifts and ensure optimal resource allocation. Train team members and assign responsibilities... 

 ...weeks) Collaborate with internal stakeholders (Regional Planner, Warehouse/Logistics teams, Customer Service and Plant Operations Management) to mitigate any supply related risks – S&OE Collaborate with planner roles when issues arise that affect the S&OP horizon Track... 

 ...laboratory Standard Operating Procedures (SOPs) equipment calibration/qualification records and training documentation. Quality System Management: Participate in the CAPA process by reviewing root cause analyses and verifying the effectiveness of corrective actions; assist in... 

 ...QMS Oversight: Manage deviations change controls CAPA and incident investigations related to OSD manufacturing operations. Root Cause Analysis: Conduct detailed investigations and impact assessments for deviations and process discrepancies. Documentation... 

 ...Job Purpose To oversee and manage day-to-day production activities in the Oral Solid Dosage (OSD) manufacturing area, ensuring compliance with cGMP, USFDA, and other regulatory requirements while meeting production targets. Key Responsibilities Supervise and execute... 

 ...Job Purpose To ensure compliance with cGMP, USFDA, and other regulatory requirements by implementing and maintaining Quality Management System (QMS) practices within the Production department. Responsible for documentation, deviation handling, and continuous improvement... 

Position: Engineering Executive Location: Amli Factory, Unilever Requisition ID : R-1171665 Job Summary The ASRS Engineering Executive will be responsible for the maintenance, troubleshooting, and optimization of Automated Storage and Retrieval Systems (ASRS) within...

 ...Stability Testing: Monitor product samples over time to ensure they maintain quality under various environmental conditions. SOP Management: Assist in drafting and updating Standard Operating Procedures (SOPs) to reflect current best practices and safety protocols.... 

Job Purpose This position is open with Bajaj Finance ltd. Duties and Responsibilities Х To achieve given Sales nos through customer walk in Х Work closely with the branch Service executives to drive Gold loan customers for fulfillment Х Ensuring policy adherence and...

Supervise and monitor vial ampoule and PFS packing lines as per BPR and SOPs. Ensure proper functioning of labeling sealing inspection and serialization machines . Review and maintain Batch Packing Records (BPRs) logbooks and line clearance documentation . Coordinate...

The QC Micro Environmental Monitoring Officer will be responsible for performing environmental monitoring and microbiological testing to ensure that all production and laboratory areas comply with GMP and regulatory standards. This role ensures the safety and quality of pharmaceutical...

 ...Job Title Sr. Manager – Global Quality Lead Business Unit Global Quality & Compliance Job Grade G9B Location : Mumbai At Sun Pharma, we commit to helping you 'Create your own sunshine'— by fostering an environment where you grow at every step, take... 

 ...Position -: Manager Production Planning & Scheduling Job Accountabilities - Review production and consumption variance & identify improvement opportunities / actions Ensure model updation in APO based on the deviation between predicted vs. actual performance. Finalise... 

 ...Packaging development (PDD), Production, Engineering, Quality control, Quality Assurance, Supply chain, Business development, Project management and any other department for timely execution of New projects. To plan, monitor and support for execution of the trial batch,... 

 ...Job Responsibilities of the Microbiology Section head: 1. Laboratory Operations: Planning and Execution: Plan manage and oversee all day-to-day analytical activities within the Microbiology Laboratory. This includes scheduling resource allocation (personnel and equipment... 

 ...action item closing. Online Data update, Timely revisin and tracking of SOP. Coordination with cross functional for the full filling the management system requirements, Including ISO/IATF/IKEA/EHS. Responsibilities 职责 Major Roles & Responsibilities Maintain the... 

 ... Coordination with Production and Sales Team  PF Working.  Dispatch follow up and Coordination with Factory  Petty Cash Management  Basic Office Administration. Benefits  Cell Phone Reimbursement  PF & ESIC  Reimbursement of Travelling Timings:... 

Role & Responsibilities: Handle dispensing of Raw Materials (RM) and Packing Materials (PM) accurately as per batch requirements. Perform in-process quality checks to ensure compliance with defined standards. Review Batch Manufacturing Records (BMR), Batch Packing ...

Role & Responsibilities: Supervise Formulation & Development (F&D) activities and monitor operators/assistant operators within designated premises at the site. Conduct literature and patent searches and review findings as per product development requirements. Perform...

 ...receiving, issuance, and related inventory transactions. Ensuring proper documentation and compliance with internal audit and material management requirements. Supporting smooth warehouse and material flow operations across departments. Preferred Candidate Profile:... 

 ...Manufacturing Practices (GMP) in all packing activities. Have knowledge of Packing Material (PM) dispensing activities and PM store management. Perform reconciliation of packing materials to ensure accuracy and avoid discrepancies. Maintain all packing-related... 

 ...of GMP, GLP, and FDA/EMA regulatory requirements. Excellent documentation, problem-solving, and communication skills. Ability to manage multiple validation projects and work effectively under pressure. Certifications: Certification in Analytical Chemistry or related... 

Roles & Responsibilities: Ensure proper operation and cleaning of equipment and manufacturing areas related to Granulation, Compression, Coating, and Capsule Filling processes. Handle Change Control, Deviation, Incident, and Market Complaint activities in compliance with...

 ...Role & Responsibilities: Manage and maintain all documentation related to Quality Management Systems (QMS), including validation, qualification, deviation, and change control activities. Prepare and review MFRs, SOPs, and AMV (Analytical Method Validation) documents in...