Vacancies for Stores Department, interested candidates can refer below and reply back to this mail: ------------ ---------- ---------- ---------- ---------- ---------- ---------- ---------- Job Description: ------ ------------ ------------ ------------ ------------ ------------ ------------ Supervision of raw and packing material receipt and checking of materials as per purchase order (PO). Preparation of GRN. Cross Verification of material with invoice/Delivery Challan (DC). Supervision of material arrangements. Miscellaneous material receiving and issued to concerned department. After approval GRN and invoice submit to accounts department. Contribute to team effort by accomplishing related results as needed. If any shortage and excess of raw and packing material intimate to HOD. If any goods damaged while transferring from supplier immediately intimate to HOD and purchase. Co-ordinate with QC, stores for smooth function. Preparation of shift schedule. ------------ ------------ ------------ ----------- ---------- ---------- ---------- Regards, Divya S (9945544952)

Job description Position Offers: Designation : QA Officer/Executive Reports to : Head Location : Precise Analytics Laboratory - Thane Wagle Estate Qual. : (MSC Chemistry/Nutraceuticals/Food Science/M Pharm Quality Assurance) Exp. : 2-3 years experience in Food Analysis . Industry : Only pharma company Open position : 1 Roles and Responsibilities 1) Knowledge of analytical methods and Instruments with software 2) Verification of reports of analysis and reports of method validation 3) Verify the implementation of laboratory management system and GLP 4) Maintenance of lab records. 5) Knowledge of ISO 17025:2017 standard. 6) Control of records and documents 7) Knowledge of IQC, ILC, PT testing

Designation :QC Officer - Microbiology / QC Officer Chemical Reports to : Head Location : Precise Analytics Laboratory - Thane Education - MSC Microbiology Exp. : (MSC Microbiology) -2-5 years experience in Pharmaceutical Microbiological testing Industry : Only pharma company Open position : 2 Job Description 1. Conduct microbiological analysis of Samples- MLT, Microbial Assays 2. To maintain all records as per cGLP and ISO 17025. 3. To monitor the quality of air & water. 4. Perform periodic calibration of Instruments/Equipments in Microbiology. 5. To Maintain the Microbial cultures. 6. Perform Swab Test MSC Chemistry/B. Pharm/M. Pharm) -2-3 years experience in Pharmaceutical Chemical Testing/Instrumentation Job Description. Conduct Chemical analysis of Pharmaceutical Samples Perform analysis of samples as per MOA on various instruments such as HPLC, AAS, UV Spectrophotometer To perform Validation of analytical methods To maintain all records as per cGLP and ISO 17025. Perform periodic calibration of Instruments/Equipments in Lab Preparation and Maintenance of standards

1. Lead and Responsible for formulation development of stable and robust formulations across various dosage forms including Oral Solids, Liquids, Semi-Solids, etc. 2. Conducting the trouble-shooting of formulations/products in terms of Quality improvement and cost improvement. 3. Knowledge of both Drug and Nutraceutical formulation development. 4. Supervising the daily work of assigned associates and also monitoring and resolving technical issues. 5. Visiting various Domestic and International production site for scale up-technology transfer and also to extend technical expertise. 6. Responsible for raw material screening, evaluation and regulatory compliance 7. Responsible for the documentation of formulation development (PDRs) and the generation of technical reports. 8. Preparation of formulation development protocols, and technology transfer dossier (TTD). 9. In dept knowledge of product development and current regulatory guidelines.

Role & responsibilities 1. For Understanding machine maintenance activities (Electrical & Mechanical), handling tools, understanding CGMP maintenance procedures and work conducts. 2. For up keeping dept. documentation and improvising whenever necessary. 3. For assisting HOD in planning maintenance activities, shift schedules. 4. Carrying out preventive maintenance activities in coordination with dept. technical team. 5. For checking and verifying spare stock, spares consumption & maintaining stock of necessary spares. 6. Technical guidance to technicians in trouble shooting machine issues. 7. For assisting in project related activities. 8. Preparing indents follow ups with purchase department for spares and tracking. 9. Coordination with vendors for technical requirements. 10.Day to Day work allocations to dept. technical team and handling dept. manpower. 11.Responsible to conduct on time maintenance and safety checks. 12. Participate in ongoing training to improve skills and knowledge and train the subordinates. 13.Any other jobs & responsibility as and when entrusted by HOD. 14. Conduct routine maintenance & safety checks. 15. Good coordination in dept. internal and external for smooth flow of works. 16. Maintaining Documents pertaining to International GMP Audits. Preferred candidate profile Education- B.E/B. Tech (Mechanical) Experience- 08-13 Years (Pharmaceutical Industry) Perks and benefits Regards, Divya S (Mob. 9945544952) Emai ID : divya@meyer.co.in

ERP Management: Create and update Bill of Process (BOP) entries for in-house and loan license (LL) manufacturing sites. Generate and revise Item Master Codes for packaging materials and finished goods. Maintain ERP item master update records as per Format No. QAD-FR-89. Raw Material Specification (RMS): Prepare and revise RMS documents in line with regulatory and internal requirements. Draft RMS for product registration, including compliance with UK market norms. Finalize and issue authorized RMS for submission to regulatory bodies. Sample Coordination & Analysis: Coordinate dispatch of AVD raw material and NPD samples for lab testing. Maintain records of sent samples in Format No. QAD/FR-42 and ensure timely follow-up for results. Working Standards Management: Arrange and distribute working standards for LL sites in coordination with concerned departments. Artwork Review: Review packaging artwork for: Domestic (Drugs and Foods) Export (Drugs and Foods) Products requiring artwork for regulatory registration Export Documentation: Review Certificates of Analysis (COAs) for export-bound raw materials. Coordinate with external labs (e.g., Precise Lab) to rectify discrepancies and ensure final approval. Destruction Certificates: Share approved destruction certificates with applicable manufacturing sites. Quality Management System (QMS) Documentation: Circulate QMS-related documents such as: Commercial deviations Change control authorizations Document Revisions: Revise Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) for domestic products. Safety & Analytical Documentation: Prepare Material Safety Data Sheets (MSDS) for relevant materials/products. Revise Method of Analysis (MOA) for finished products in coordination with stakeholders.