Looking for a career opportunity in the pharmaceutical API and Bulk Drugs industry? Tooba Pharmaceuticals Private Limited, a WHO-GMP Certified API & Bulk Drugs Manufacturer, has announced a mega walk-in recruitment drive for multiple departments including Quality Control, Research & Development (R&D), and Production.

Fresh graduates and candidates with Chemistry and Pharmacy backgrounds are encouraged to participate in this recruitment drive and gain hands-on industrial exposure in a WHO-GMP certified manufacturing facility.

Job Overview

Available Departments

1. Quality Control (QC)

Tooba Pharmaceuticals is recruiting fresh candidates for its Quality Control Department with practical exposure to advanced analytical instruments and WHO-GMP laboratory practices.

QC Instrument Training

• HPLC (PDA Detector)
• HPLC (UV Detector)
• Agilent HPLC (MWD Detector)
• Agilent HPLC (VWD Detector)
• FTIR Spectrometer
• HS-GC
• UV/VIS Spectrometer
• Karl Fischer Auto Titrator
• Polarimeter
• pH Meter
• Melting Point Apparatus
• Potentiometer
• Stability Chambers
• Micro Balance
• Vacuum Oven
• Hot Air Oven

Quality Control Training Program

• Raw Material Analysis
• Intermediate Analysis
• Finished Product Analysis
• Purified Water Analysis
• Sampling Procedures
• Stability Studies
• Analytical Method Verification (AMV)
• Analytical Documentation Practices
• Instrument Handling & Maintenance
• WHO-GMP Guidelines
• Good Laboratory Practices (GLP)
• Data Integrity Practices
• OOS/OOT Investigation Awareness
• Laboratory Safety Practices
• Calibration Awareness
• SOP Understanding & Compliance

2. R&D – API Bulk Drugs

Candidates interested in research and pharmaceutical innovation can build their careers in the API Bulk Drugs R&D Department.

R&D Training Includes

• Personality Development
• Corporate Behavior Development
• GMP & GLP Training
• Literature Searching
• Carrying Out Reactions
• Reaction Monitoring by TLC, GC & HPLC
• Reaction Work-Up
• Sulfonation, Amination, Reduction & Oxidation Reactions
• IR, NMR & Mass Predictions
• Analytical Instrument Handling
• Plant Facility Exposure
• Handling Non-Hazardous & Hazardous Chemicals
• SOP Training
• MSDS Training
• Rotavapor, Overhead Stirrer & Autoclave Handling

3. Production Department

Candidates will receive practical training in API manufacturing operations and GMP equipment handling.

Equipment Exposure

• Stainless Steel Reactors
• Glass Lined Reactors
• Glass Assemblies
• Centrifuges
• Sparkler Filters
• Buckner Filters
• Rotary Cone Vacuum Dryer (RCVD)
• Tray Dryer (48 Trays)
• Vacuum Tray Dryers (VTD)
• Milling Machines
• Sifters

Process Training

• Reflux
• Distillation
• Work-Ups
• Filtration
• Drying

Roles & Responsibilities

Quality Control

• Perform analytical testing of raw materials and finished products
• Operate analytical instruments
• Maintain laboratory documentation
• Follow GLP and WHO-GMP guidelines
• Support quality investigations and compliance activities

R&D

• Assist in API process development
• Perform laboratory reactions and documentation
• Monitor reactions using analytical techniques
• Support research projects and innovation activities
• Follow SOPs and safety guidelines

Production

• Support API manufacturing operations
• Operate production equipment under supervision
• Follow GMP and safety procedures
• Maintain production records
• Participate in process improvement initiatives

Required Qualifications

Quality Control

• B.Pharm (Freshers)
• M.Pharm (Freshers)
• B.Sc (Chemistry)
• M.Sc (Chemistry)
• M.Sc (Analytical Chemistry)

R&D

• B.Sc (Chemistry)
• M.Sc (Chemistry)

Production

• B.Sc (Chemistry)
• M.Sc (Chemistry)
• B.E. Chemical Engineering

Freshers will be preferred.

Skills Preferred

• Basic pharmaceutical knowledge
• Good laboratory practices understanding
• Teamwork and collaboration
• Learning attitude
• Communication skills
• Documentation ability

Salary & Benefits

Expected Stipend / Salary

• Estimated Range: ₹2.2 LPA – ₹3.6 LPA (depending on qualification, performance and achievements)

Additional Benefits

• Hands-on training on QC instruments
• WHO-GMP guideline training
• GLP guideline training
• Weekly classroom sessions
• Practical exposure in WHO-GMP certified facility
• FDA approval exposure
• Career growth opportunities
• Training by experienced professionals
• API manufacturing exposure
• Cross-functional learning opportunities
• Positive working environment

Selection Process

• Walk-In Interview
• Document Verification
• Technical Discussion
• HR Interaction
• Final Selection

Interview Details

Interview Date: Sunday, 21 June 2026

Time: Sharp 11:00 AM

Interview Venue

Tooba Pharmaceuticals Private Limited

Plot No A-117, A-118 & A-119
MIDC Paithan,
Dist. Chh. Sambhajinagar – 431148
Maharashtra, India

Important Instructions

• Candidates should bring all original documents at the time of interview.
• No TA/DA will be paid for attending the interview.
• Candidates should be willing to work in shifts and rotation shift system.
• Male candidates shall be preferred as mentioned in the official notification.
• Stipend will depend upon qualification and achievements.

How to Apply

Interested candidates should send their updated CV to:

Email: info@toobapharma.in

Eligible candidates can also directly attend the walk-in interview at the above venue with all original educational documents and updated resume.