• Technical      Expertise:     Proficiency in analytical techniques and methods such as HPLC/GC methods development      and validation.

• Create and optimize      analytical methods for testing the chemical composition, purity, and      stability of drug substances and formulations.

• Ensure that these methods      are accurate, reliable, and reproducible according to regulatory standards.

• Problem-Solving: Strong analytical and      troubleshooting skills.

• Communication: Excellent written and      verbal communication skills for documentation and collaboration with      cross-functional teams.

• To contribute maintaining      analytical laboratory as per the GLP and safety requirements.

• Proficiency in analytical      techniques and methods such as HPLC/GC methods development and validation.

• Create and optimize      analytical methods for testing the chemical composition, purity, and      stability of drug substances and formulations.

• Ensure that these methods      are accurate, reliable, and reproducible according to regulatory      standards.

· Preferred: - Only male candidate

Job Description:

1)  Carry out Experiments for process feasibility and optimization.  Impurity Synthesis and their Characterization using NMR and Mass  Techniques, following proposed ROS.

2) Writing LNB / ELNB and proper documentation.

3) Scale-up of Intermediates and products in Lab in the given timeline.

4) Learning and updating Job related knowledge, like process development, Quality and regulatory aspects.

5) Carryout Experiments to support Plant for trouble shooting in ongoing products to address OOS and OOT issues.

6) Adhering to SOPs / Guidelines, Safety Norms in Lab and maintain cleanliness of work area.

7) Providing assistance to senior colleagues in Development & Optimization activities.

8) Maintaining personal hygiene, safety and discipline in the workplace.

Preferred Skills -

1.Good knowledge of reaction mechanism and spectroscopy.

2. Individuals with strong experimentation skills to support the process development.

3.   Experience in transferring process from lab scale to pilot scale.

1. Responsible for follow-ups on pending consignments with associated suppliers & various internal departments.

2. Candidate must be self-confident with high ability learning skills & career objectives.

3. Strong communication skills mandatory with little proficiency in English can work.

4. Provide support in daily day to day tasks under the guidance of seniors.

5. Daily update of assigned work records along with detailed reporting’s to seniors.

6. Handle basic administrative tasks to support the daily routine activities of department.

7. MS office, Excel knowledge is must, Third party clear communications skills mandatory.

Preferred –     Male Only

Fixed Stipend – 12,000/- to 15,000/- per month

Note:  - This above position  is for 3 months internship or trainee role, We  can share full time opportunity depends on  your performance.

Responsible for monitoring of the ZLD (Zero Liquid Discharge) plant and handling all documentation preparation and implementation related to the EHS department.

Operating of pumps & flow reactors like peristaltic, piston, and diaphragm pumps,n-CSTR, Agitated Scalable baffled reactor, Thin film reactor, Fixed bed reactor and plug flow reactor… etc.

Project execution in pharmaceutical API manufacturing, including capital projects, process improvement, and technology implementation.

Operate Reactors as GLR,SSR, Centrifuge, filter, BPCR, Logbook etc

knowledge about UV, IR, instruments, chemical analysis, PH scale, etc.

Dispensing, loading, unloading, etc.

Motor Wiring, Panel wiring, electrical maintenance, Chiller maintenance, Electrical Meter Reading, etc.