Sri Krishna Pharmaceuticals Limited Walk-in Interview.Sri Krishna Pharmaceuticals Limitedited Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.
Vacancy details:
- Department: Quality Control (OSD, API)/Research And Development/Production – API
- Education Qualification: B.SC/M.SC / B. Pharmacy /M. Pharmacy
- Experience: 2 to 7 years
- Salary: ₹Not Disclosed
- Openings: 100
Important Details :
Job Description: Greeting from Sri Krishna Pharmaceuticals Limited !!!
Greetings from Sri Krishna Pharma
We are hiring Quality Control for our API , Formulation (OSD ) and Nutra 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
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
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
- Follow 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.com / jayakishore.gollapalli@srikrishnapharma.com can send me in whatsapp 6300118513