Experience- 15+ years in Pharma FDA Approval License must Age Group- 45 to 50yrs Job Types: Full-time, Permanent Benefits: Health insurance Schedule: Day shift Night shift Rotational shift Weekend only Work Location: In person
having experience in Pharma industry Job Type: Permanent Work Location: In person
having experience in Pharma industry Job Type: Permanent Work Location: In person
Job Description – Regulatory Affairs- Executive No.of vacancy: 01 Role Summary: The Regulatory Affairs professional will be responsible for preparing, reviewing, submitting, and maintaining regulatory documents to ensure compliance with national and international regulatory authorities. The role ensures smooth product registration, license renewals, and compliance with all statutory requirements. Key Responsibilities: 1. Dossier Preparation & Submission 2. Product Registration & Approvals 3. Regulatory Compliance 4. Documentation Control 5. Communication with Authorities 6. Artwork & Label Review 7. Cross-Functional Coordination Required Qualifications: * B.Pharm / M.Pharm (preferred) with 4-5 years of experience in Regulatory Affairs .* Strong understanding of regulatory guidelines (CDSCO, WHO, ASEAN, Africa, LATAM etc.). * Knowledge of dossier formats (CTD/eCTD/ACTD). * Experience in product registration and regulatory submissions. Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹35,000.00 per month Benefits: Paid sick time Paid time off Provident Fund Work Location: In person
Job Description: Quality Control Chemist ( HPLC) No. Of Vacancy: 04 Job Summary: The candidate will operate, calibrate, and maintain HPLC systems to analyze raw materials, in-process samples, and finished pharmaceutical products. They will ensure all tests comply with GMP, regulatory guidelines, and company SOPs, while accurately documenting results, troubleshooting instrument issues, and supporting quality control and product release activities. Keys and Responsibilities: Operate, calibrate, and maintain HPLC instruments. Perform analysis of raw materials, in-process, and finished products as per SOPs. Prepare samples, standards, and reagents accurately. Ensure all testing complies with GMP and regulatory guidelines. Record and review analytical data with accuracy and integrity. Troubleshoot routine HPLC issues and ensure instrument readiness. Maintain documentation, logbooks, and reports in accordance with ALCOA+ principles. Support OOS/OOT investigations and method validations when required. Requirements: 3-5 Years of Experience in Quality Control Department Specialised in HPLC Section Salary weill be properly discuss at the time of interview. need Good and perfect candidate for handling. Qualifications: MSC, BSc in Analytical Chemistry. Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Paid sick time Paid time off Provident Fund Work Location: In person
FDA approval license in TABLET manufacturing, 5-7 years experience in Pharma Inductry. Enagage in Manufacturing activities. will supervisor in Production planning and day to day activities. Job Types: Full-time, Permanent Pay: ₹40,000.00 - ₹50,000.00 per month Benefits: Flexible schedule Leave encashment Paid sick time Paid time off Provident Fund Work Location: In person
Job Description – Regulatory Affairs- Executive No.of vacancy: 01 Role Summary: The Regulatory Affairs professional will be responsible for preparing, reviewing, submitting, and maintaining regulatory documents to ensure compliance with national and international regulatory authorities. The role ensures smooth product registration, license renewals, and compliance with all statutory requirements. Key Responsibilities: 1. Dossier Preparation & Submission 2. Product Registration & Approvals 3. Regulatory Compliance 4. Documentation Control 5. Communication with Authorities 6. Artwork & Label Review 7. Cross-Functional Coordination Required Qualifications: * B.Pharm / M.Pharm (preferred) with 4-5 years of experience in Regulatory Affairs .* Strong understanding of regulatory guidelines (CDSCO, WHO, ASEAN, Africa, LATAM etc.). * Knowledge of dossier formats (CTD/eCTD/ACTD). * Experience in product registration and regulatory submissions. Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹35,000.00 per month Benefits: Paid sick time Paid time off Provident Fund Work Location: In person
FDA approval license in TABLET manufacturing, 5-7 years experience in Pharma Inductry. Enagage in Manufacturing activities. will supervisor in Production planning and day to day activities. Job Types: Full-time, Permanent Pay: ₹40,000.00 - ₹50,000.00 per month Benefits: Flexible schedule Leave encashment Paid sick time Paid time off Provident Fund Work Location: In person
Job Description: Head Quality No. of Vacany: 01 Role Summary: The Head Quality will be responsible for establishing, implementing and overseeing all Quality Control and Assurance systems to ensure compliance with regulatory standards, GMP requirements and company policies. This role requires leadership, strong documentation skills, and the ability to drive a robust quality culture across the organization independently. Key Responsibilities; Full management of; 1) Quality Control department. 2) Quality Assurance Department Required Qualifications & Skills: M.Pharm with 15-20 Years of experience in Quality (Control & Assurance) Strong understanding of cGMP, regulatory guidelines and documentation practices. Leadership, Decision Making and audit- handling skills. Good Communication skills and team management skills Experience in facing National And International Regulatory audits Since this is a very senior position candidates with long term association should only apply. Mandatory: CTC Offered: 18-20 Lacs Min Age: 40-45 yrs. Job Types: Full-time, Permanent Pay: ₹1,800,000.00 - ₹2,000,000.00 per year Benefits: Flexible schedule Internet reimbursement Leave encashment Paid sick time Paid time off Provident Fund Work Location: In person
Job Description – Executive Assistant to Director No. of Vacancy: 01 Required: * Qualifications: BBA/ MBA * 7-8 Years Experience in Orgabnizational Experience in a) Secretarial- Business meetings co-ordinating b) Business Planning c) Event organizor d) Statutory Compliances *Good communication skills (written & verbal). * Proficient in MS Excel, Word, and email communication. Role Summary: The Business Development Assistant/Executive will support the BD team in expanding business opportunities, managing client relationships, coordinating with internal departments, and ensuring timely execution of business activities. The role requires strong communication, analytical ability, and coordination skills. *Key Responsibilities: 1. Market Research & Lead Generation 2. Client Communication & Coordination 3. Sales Support Activities 4. Coordination with Internal Departments 5. Documentation & Reporting 6. Marketing & Promotion Package for the above post will be: Rs. 5- Rs. 5.50 Lacs per annum with good experience to between 30-35 years. Job Types: Full-time, Permanent Pay: ₹500,000.00 - ₹550,000.00 per year Benefits: Paid sick time Paid time off Provident Fund Work Location: In person
Job Description – Jr. Project Engineer No. of Vacancy: 01 Required: 1. Qualifications: Degree/Diploma in Machanical/Electrical Engineering. 2. 6-8 Years Experience in handling of projects in pharmaceutical company. Role Summary: Provide overall administrative & Technical support for Project Management, Engineering and other critical business functions. Effectively manage multiple priorities with clarity and focus. The project expeditor role must establish strong relationships with internal customers, external customers & suppliers to help facilitate successful project execution. *Key Responsibilities: 1. Drafting & Finalizing project URS with user consultation. 2. Entry & Tracking of customer requests & contact deliverables 3. Assist Project engineering with customer follow up for technical & commercial clarification, as necessary. 4. Review & Process customer drawing comments. 5. Review & Process vendor component drawings. 6. Assist project management with the change order process when deviation from scope are identified. 7. Assist with project data organization. 8. Assist with supply chain management & engineered material procurement including creation of inquiries to sub-suppliers for the purpose of component selection and/or costing. 9. Shipping coordination. 10. Participate in process improvement activities. 11. Work independently and within a team. 12. Collaboration with project team members. 13. Timely escalation of issues, as situation required. 14. Administrative and/or clerical duties, as required. 15. Exceptional customer facing communication skills and ability to communicate clearly and professionally with clients, suppliers, and internal team on a regular basis, both verbally and in writing. 16. Organized with strong attention to detail and ability to multi-task effectively. 17. Driven and self-motivated with excellent follow – through. 18. Excellent time management skills. 19. Proficiency in Microsoft office suite software including highly develop excel skills. 20. Ability to operate with minimal direct supervision. Package: Salary is no bar for the right/deserving candidate. Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹30,000.00 per month Benefits: Flexible schedule Leave encashment Paid sick time Paid time off Provident Fund Work Location: In person
Job Description: Quality Control Chemist ( HPLC) No. Of Vacancy: 04 Job Summary: The candidate will operate, calibrate, and maintain HPLC systems to analyze raw materials, in-process samples, and finished pharmaceutical products. They will ensure all tests comply with GMP, regulatory guidelines, and company SOPs, while accurately documenting results, troubleshooting instrument issues, and supporting quality control and product release activities. Keys and Responsibilities: Operate, calibrate, and maintain HPLC instruments. Perform analysis of raw materials, in-process, and finished products as per SOPs. Prepare samples, standards, and reagents accurately. Ensure all testing complies with GMP and regulatory guidelines. Record and review analytical data with accuracy and integrity. Troubleshoot routine HPLC issues and ensure instrument readiness. Maintain documentation, logbooks, and reports in accordance with ALCOA+ principles. Support OOS/OOT investigations and method validations when required. Requirements: 3-5 Years of Experience in Quality Control Department Specialised in HPLC Section Salary weill be properly discuss at the time of interview. need Good and perfect candidate for handling. Qualifications: MSC, BSc in Analytical Chemistry. Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Paid sick time Paid time off Provident Fund Work Location: In person