Jobs in Akole, Ahilyanagar

Remote Data Entry Jobs in India (Part-Time & Full-Time)Company Name: M. Jobs EnterprisesJob Type: Part-Time / Full-TimeJob Location: Work From Home (Pan India)Experience: Fresher & ExperiencedEducation: 10th Pass, 12th Pass, ITI, Diploma & GraduateWork Mode: Remote / OnlineSalary: Performance-Based EarningsJob DescriptionM. Jobs Enterprises is inviting applications from motivated candidates across India for remote data entry and online back-office opportunities.Candidates can work from home using a smartphone, laptop, or desktop with a stable internet connection. Freshers are welcome.Roles & Responsibilities- Online Form Filling- Data Entry and Data Verification- Copy-Paste Operations- Data Processing and Updating- Basic MS Excel and Google Sheets- Online Documentation- Back-Office SupportEligibility Criteria- Minimum qualification: 10th Pass.- Freshers and experienced candidates can apply.- Basic typing and computer knowledge preferred.- Smartphone, laptop, or desktop with internet access.- Good attention to detail.- Candidates from all Indian states are welcome.Job Benefits- Work From Home opportunity.- Part-Time and Full-Time options.- Flexible working schedules, subject to project availability.- Online guidance and support.- Suitable for freshers.- Remote working opportunities across India.How to ApplyInterested candidates can contact our HR Department for further details and the application process.M. Jobs EnterprisesRecruitment Staffing Workforce Management

We are looking for enthusiastic individuals for the position of Fresher/Data Entry Operator. This is a part-time role that offers the flexibility of working from home. Ideal for freshers who have completed their 10th grade.Key Responsibilities:1. Data Entry: Accurately inputting information into databases and spreadsheets is essential. Attention to detail is crucial to ensure data integrity.2. Managing Records: Organizing and maintaining electronic records will be required. You should keep all files up to date and easily accessible.3. Quality Control: Regularly reviewing the data for errors or discrepancies is necessary to uphold the quality of work.4. Communication: You may need to interact with team members or supervisors to clarify requirements or report progress. Clear communication is important for teamwork.Required Skills and Expectations:Candidates should have a basic understanding of computer operations and be familiar with common software applications, including MS Office. Strong attention to detail and the ability to follow instructions are essential. As a fresher, you should demonstrate a willingness to learn and adapt to new tasks quickly. Good organizational skills will help you manage your workload efficiently. Reliability and punctuality are also important to ensure that work commitments are met consistently.

Urgent OpeningRegulatory Manager (Veterinary Pharmaceuticals)Veterinary Pharmaceutical Manufacturing CompanyVile Parle, Mumbai, MaharashtraQualification B.Pharm / M.Pharm / M.Sc. or an equivalent qualification. Additional certification in Regulatory Affairs will be an added advantage. Experience 4-8 years of experience in Regulatory Affairs within the veterinary or pharmaceutical industry. Experience in handling product registrations and regulatory approvals. Regulatory Affairs Manager to oversee all regulatory activities for veterinary pharmaceutical products. The candidate will be responsible for product registrations, dossier preparation, regulatory submissions, license management, and ensuring compliance with all applicable veterinary pharmaceutical regulations.Key Responsibilities Manage regulatory affairs activities for veterinary pharmaceutical products. Prepare, review, and submit product registration dossiers to regulatory authorities. Coordinate with the CDSCO, State FDA, and other regulatory authorities for approvals and licensing. Ensure compliance with the Drugs and Cosmetics Act & Rules, Schedule M, GMP, and other applicable regulations. Prepare and maintain regulatory documentation, technical files, and product dossiers. Handle applications for manufacturing licenses, product permissions, and renewals. Coordinate with QA, QC, Production, R&D, and Marketing departments for regulatory compliance. Review product labels, package inserts, and artwork to ensure regulatory compliance. Respond to regulatory queries and deficiency letters from authorities. Monitor changes in regulatory guidelines and implement necessary updates. Support internal, customer, and regulatory audits. Maintain regulatory records and ensure timely submission of required documents. Required Skills Strong knowledge of Veterinary Pharmaceutical Regulations. Experience in CDSCO, State FDA, and product registration processes. Knowledge of Drugs and Cosmetics Act & Rules, Schedule M, and GMP. Ability to coordinate effectively with cross-functional teams and regulatory authorities.