Role & responsibilities Responsible for carrying out all the production activities pertaining to his section in the shift following the standard operating procedures and safety norms Experience in Equipment Handling like Reactors, ANFS, Centrifuges, FBD, Miller, Sifter,. Experience in Cleanrooms. Adherence to CGMP and GMP processes. Preferred candidate profile

Roles and Responsibilities Experience in Electrical or Mechanical or Instrumentation or Fitter or Boiler Operator or Engineering Documentation or Civil Perform breakdown maintenance, preventative maintenance, and predictive maintenance tasks to ensure optimal equipment performance. Conduct routine checks on chillers, HVAC systems, boilers, electrical systems, instrumentation, and civil infrastructure to identify potential issues before they become major problems. Troubleshoot and resolve technical issues related to utility operations and plant maintenance. Collaborate with other teams to implement effective solutions for improving overall efficiency and reducing downtime. Ensure compliance with safety protocols and regulations during all aspects of work. Desired Candidate Profile 5-10 years of experience in a similar role within the pharmaceutical industry or manufacturing sector. Diploma in Any Specialization (Mechanical/Electrical/Instrumentation). Strong understanding of breakdown maintenance principles; ability to perform repairs independently. Proficiency in performing predictive maintenance activities using techniques such as condition monitoring.

Job description Sri Krishna Pharma invites both experienced professionals and fresh diploma holders, as well as graduates and self-driven individuals, to join its Specialty API and OSD Business located in Hyderabad. The available positions are listed below:. We are hiring for Freshers 2023 to 25 Pass outs API QUALITY ASSURANCE : Designation : Trainee Qualification : B. Pharm / M. Pharm / M.Sc. Experience : 0-2 Years Role : IPQA (In process QA API) PRODUCTION PHARMA: Designation : Trainee Qualification : B. Pharm / M. Pharm / M.Sc./B.SC Experience : 0-2 Years Role : Production Chemist (API) PRODUCTION PHARMA:(OSD) Designation : Trainee Qualification : B. Pharm / M. Pharm / M.Sc./B.SC Experience : 0-2 Years Role : Production Chemist (OSD) Quality Control:(API) & (OSD) Designation : Trainee Qualification : B. Pharm / M. Pharm / M.Sc./B.SC Experience : 0-2 Years Role : Production Chemist (OSD) Microbiology: Designation : Trainee Qualification : B. Pharm / M. Pharm / M.Sc. (Microbiology) Experience : 0-2 Years Role : Production Chemist (OSD) Interested Candidates can share their resumes to jayakishore.gollapalli@srikrishnapharma.com or vani.thiramdas@srikrishnapharma.com

We are looking for a Packaging and Development Specialist to join our team at Sri Krishna Pharma The ideal candidate will have experience in the pharmaceutical industry and will be responsible for ensuring that all products meet the highest quality standards. The QC, Regulatory Affairs, Packaging and Development Specialist will be responsible for: Developing and implementing quality control processes and procedures Ensuring that all products meet the required regulatory standards Working with the packaging team to ensure that all products are properly packaged and labelled Working with the development team to ensure that all products are developed to the highest standards Conducting regular quality checks and inspections Investigating and resolving any quality issues Maintaining accurate records and documentation The ideal candidate will have: A degree in a relevant field such as pharmaceuticals, chemistry, or engineering At least 3 years of experience in the pharmaceutical industry Knowledge of quality control processes and procedures Knowledge of regulatory standards and requirements Excellent problem-solving and communication skills Attention to detail and accuracy . If interested please share your resume to jayakishore.gollapalli@srirkishnapharma.com

Roles and Responsibilities Conduct quality audits, BMR reviews, CAPAs, deviation investigations, change controls, equipment qualifications, process validations, and vendor qualifications. Ensure compliance with USFDA regulations through IPQA activities Engineering Documentation ,Qualifications &Validations. Warehouse Documentation ,Qualifications &Validations. Cleaning Validation Perform analytical QA tasks such as OOS management and sterility testing. Participate in MHRA / USFDA inspections by providing necessary documentation and supporting audit findings. Collaborate with cross-functional teams to resolve quality issues. Regulatory Audit Exposer LIKE FDA, MHRA, TGA Audit Reponses and Audit Reediness if interested please share your resumes to jayakishore.gollapalli@srikrishnapharma.com

Role & responsibilities Analytical Research & Development (ARD) [API & FORMULATIONS] Experience in method validation, Method development and method transfer of new analytical methods by HPLC. Develop, optimize and validate new analytical methods for key starting materials, Intermediates and Active Pharmaceutical Ingredient products. Preparation of analytical method validation protocol, raw data and analytical method validation report as per ICH requirements. Manage and execute transfer of analytical methods from AR&D to internal QC. Analytical regular support for Process development team. Analytical regular support for Alternative vendor development projects. Perform hands on Residual solvents Unknown peak identification and quantification by GC troubleshooting. Maintenance of lab compliance such as calibration schedules etc. Performing a Qualitative and Quantitative tests which include analysis of raw materials, APIs and in process samples. Adequate Knowledge in Wet Lab Analysis. Formulations Research & Development [FRD] Entrusted with the task of conducting research and support activity In Formulation Department and handling various projects like Oral Solid Dosage forms (Tablets, Capsules), Liquid Dosage forms etc. Proactively involved in formulation of Robust, Stable. Cost effective, Time effective various enzyme preparations s/a Solid Oral Dosage Forms like Tablets (Dispersible, Film coated, and IR) & Capsules. Preparation of Product Development Report, Master Formula Card, various SOPs etc. Actively involved in planning, review of analysis related activities, Installation and calibration of various analytical instruments. Scale-up and technology transfer of Softgel capsules, Spray drying and Beadlets technology. Product improvement and cost reduction of existing products. Coordination with marketing and analytical team or successful completion of projects Trouble shooting and quality improvement of existing products Preparation and review of Master manufacturing document (MMD), NPD documents, batch manufacturing record (BMR), product development report (PDR) , HACCP plan and Technology Transfer documents. Process Research & Development (PRD) [API] Monitoring and planning of experiments with team. Recording the daily lab experiments as per cGMP and preparing weekly planning report. Preparation, identification, characterization and control of process related impurities and GTIs. Ability to complete the project with in stipulated time lines. Developing chemical processes for APIs and intermediates. Optimizing and validating the process at the lab,pilot and plant scale. Adequate response to the queries raised by competent regulatory bodies. Preparation of process development report(PDR) and technical packages. Co-ordinating with cross functional teams, collecting the data and supporting in the preparation of product development report. Identify & solve the plant related queries such as OOS OOT, CAPA. Obey & follow the safety norms. If interested, please share your resumes to jayakishore.gollapalli@srikrishnapharma.com

Role Description This is a full-time on-site role for a deputy manager / manager finance at Sri krishna pharmaceuticals ltd in Hyderabad. He will be responsible for overseeing finance activities which analysing financial data, preparing financial reports, managing budgets, conducting financial forecasting, and providing financial strategies and recommendations to the management team. Roles and Responsibilities preparing cash flow and CMA data for working capital processing. Communication with bankers, one spec for bankers, and borrowing. preparing the book debts and stock. explanation for the fund-based facility's drawing power. Apply for PCFC and packing credit in both rupees and foreign currencies. Follow up with banks and the marketing department regarding export receivables. Managing all EDPMS, IDPM, and E-BRC issues and setting them up for export bill realization. Getting the FFRs (FFR-1, FFR-2) ready The monthly closing actions for financial account closure Monthly average interest rates are calculated for all forms of borrowing. Working with export LCs and documentation (examining LCs and documents under LC and negotiating with banks) . Establishing Letter of credit both Inland and Import and Bank Guarantees. Remitting foreign currency for import advance and other expenses like travelling, Commission on export sale, consultancy and advertising Handling export bill discounting SAP Experience is advantage Revaluation of foreign currency accounts. If interested please share your updated resumes to jayakishore.gollapalli@srikrishnapharma.com

Job description We are Hiring Operators ,Chemists, Officers ,Executive for our Formulation (OSD) unit. Operators Designation : Technician / Senior Technician / Associate / Senior Associate Education Qualification : SSC / ITI / Inter / B.SC Responsibilities Able to handle pharmaceuticals manufacturing machines. Experience in machine handling in the area of granulation, compression , Capsule Filling coating, packing Experience is Operation and Cleaning of Machines Expertise is FMG, Sejong , FBD, BQS, Hi Cart , AWC ,Auto Coater Good Communication(Should be able to Read, Write ,Speak in English) is must. Need to work in shifts adherence to CGMP and GMP processes Preferable Male Candidates 2. Staff Designation :Chemist/Senior Chemist /Officer / Executive Education Qualification : M.SC / B. Pharmacy /M. Pharmacy Responsibilities Able to handle pharmaceuticals manufacturing machines. Experience in machine handling in the area of granulation, compression , Capsule Filling coating, packing Experience is Handling Manpower, Planning ,Shift Handling ,Report Generation . Expertise is RMG, Sejong , FBD, BQS, Hi Cart , AWC ,Auto Coater BMR Handling and Documentation Audit Exposer Must Good Communication(Should be able to Read, Write ,Speak in English) is must. adherence to CGMP and GMP processes Need to work in shifts Male Candidates 3. Production Documentation Designation :Chemist/Senior Chemist /Officer / Executive Education Qualification : M.SC / B. Pharmacy /M. Pharmacy Responsibilities Able to Take care Of production Documentation (Formulation) Incident ,Deviation ,Change Control, Equipment Validation Experience in area of granulation, compression , Capsule Filling coating, packing Experience is Handling Audit Reponses SOP Preparation and able to provide Trainings on SOP Expertise is RMG, Sejong , FBD, BQS, Hi Cart , AWC ,Auto Coater BMR Handling and Documentation Audit Exposer Must Good Communication(Should be able to Read, Write ,Speak in English) is must. adherence to CGMP and GMP processes 4.PPIC Designation :Executive /Senior Executive /Assistant Manager Education Qualification : M.SC / B. Pharmacy /M. Pharmacy Responsibilities production Planning as per the targets optimum utilization of available Man, Machine & Materials Raw and Packing material indenting as per order received . Material follow - up with purchase Must have experience in Contract manufacturing and Third party manufacturing Co - ordination with internal departments SCM, R&D, TSD ,QA, QC, Warehouse for day to day activities and other for new batch execution Maintain and update data for batch tracking , production tracking. Able to Enhance production Capacities and follow-up with both Internal & external Clients for the achieving Target Regular update of charts Update of MIS inventory Management in premises. Adherence to the batch Schedules as per the timelines If interested please share your profiles to jayakishore.gollapalli@srikrishnapharma.com

Greetings from Sri Krishna Pharma We are hiring Quality Control for our API , Formulation (OSD ) and Nutra .Biotech Units Roles and Responsibilities Conduct quality control tests on OSD (Oral Solid Dose) and API (Active Pharmaceutical Ingredient) products using various instruments such as HPLC, GC, UV-Vis Spectrophotometer, Polarimeter, Karl Fischer Titrator, pH Meter, Finished Products Analyzer, Melting Point apparatus, Auto titrator, IR Spectrometer, Potentiometer. Ensure compliance with cGMP guidelines during testing procedures. Maintain accurate records of test results and reports. Collaborate with cross-functional teams to resolve any issues related to product quality or manufacturing processes. Participate in continuous improvement initiatives to enhance laboratory operations. if interested please share your resumes to jayakishore.gollapalli@srikrishnapharma.com

Dear Aspirant , Roles and Responsibilities Manage warehouse operations, ensuring efficient storage and handling of raw materials (RM), packaging materials (PM), finished goods (FG) of API S or OSD products. Oversee inventory management, including receiving, storing, issuing, and tracking stock levels using FIFO method. Ensure compliance with SAP systems for accurate recording of transactions related to warehousing activities. Coordinate with cross-functional teams to resolve issues related to supply chain disruptions or product availability. Maintain a clean and organized warehouse environment adhering to company standard if interested please share resumes to jayakishore.gollapalli@srikrishnapharma.com or WhatsApp on 6300118513.

1.Production [API- Documentation] Designation :Officer /Executive Role & responsibilities Online BPCR Verification & Preparation Equipment usage for book review SAP entries Through knowledge Deviations & change control. Indent F ollow the validations as per protocols (Process /Cleaning) Ensuring the raw materials and intermediates storage handling as per defined procedure/ Instruction. Adherence to CGMP and GMP processes 2.Production [API] Designation : Chemist / Senior Chemist / Officer Role & responsibilities Responsible for carrying out all the production activities pertaining to his section in the shift following the standard operating procedures and safety norms Experience in Equipment Handling like Reactors ,ANFS ,Centrifuges, FBD, Miller, Sifter,. Experience in Cleanrooms Adherence to CGMP and GMP processes If interested please share your updated resume to vani.thiramdas@srikrishnapharma / jayakishore.gollapalli@srikrishnapharma.com can send me in whatsapp 6300118513