Quality Control L1-1

Sanofi; Verna; On-site; INR 4,50,000 - 6,75,000; Full time

Job summary

Join a forward-thinking company dedicated to advancing healthcare through quality control. This role in the Quality Control department involves testing raw materials and finished products, ensuring compliance with regulatory standards, and utilizing advanced analytical instruments. With a focus on progress and innovation, your contributions will help improve medication outcomes and scientific advancements. If you are passionate about quality assurance and eager to make a difference in the pharmaceutical industry, this opportunity is perfect for you.

Qualifications

• 1-2 years of experience in Quality Control or similar roles.
• Strong communication skills and technical knowledge in UV and dissolution testing.

Responsibilities

• Sampling and analysis of raw materials and finished products as per SOPs.
• Documentation and maintenance of analytical records in compliance with regulations.
• Calibration and validation of analytical methods and instruments.

Skills

Communication Skills

UV Analysis

Dissolution Testing

Instrumental Analysis

Education

MSC

Tools

HPLC

UV-Vis Spectrophotometer

Dissolution Tester

pH Meter

Raman Analyzer

Conductivity Meter

Microscope

Job description

Job title: clear, with recognizable and searchable terms

• Grade: (only for internal Job description): L1-1
• Hiring Manager: (only for internal Job description): Bhanudas Bhor
• Location: Goa Parma
• % Remote working and % of travel expected: 100% on site
• Job type: Permanent

About the job

Our Team: We at Goa Pharma are involved in producing oral solid dosage and supplying it to domestic and regulated markets. The position is in the Quality Control department involved in testing raw materials and finished products.

Main responsibilities:

• Sampling: Sampling of Raw Material, intermediate, and Finished Product as per the relevant SOPs. Ensure proper storage as per Storage conditions for Raw Material, intermediate, stability samples, and Finished Product as per the relevant SOPs.
• Analysis: Analysis of stability samples and finished goods as per the required specifications in time. Ensure cGLP in the laboratory activities. Checking of chemical stores for proper storage and labeling. Analysis of Raw materials as per specification and test procedures. Analysis of Miscellaneous samples like cleaning validation and process validation samples. Carry out instrumental analysis of stability samples, Raw materials, Finished Goods such as potentiometer, IR spectrophotometer, Raman Analyzer, Dissolution tester, Disintegration tester, Microscope, UV-Vis Spectrophotometer, Conductivity meter, pH Meter, Sieve shaker, Karl Fischer, HPLC.
• Documentation: Prepare and maintain raw data and analytical records in compliance with current regulatory requirements. Maintain the raw data as per regulatory requirements. Scanning and Proper Storage of Raw Material ATR in documentation store. Filling and documentation of ILI/Deviations at site.
• Qualification/Calibration/Validation: Carry out the validation of analytical methods as per the testing procedure. To perform Calibration and PM of instruments like Dissolution tester, UV.

About you

• Experience: 1-2 years
• Soft skills: Communication Skills
• Technical skills: UV, Dissolution
• Education: MSC (not mandatory)
• Languages: English

Pursue progress, discover extraordinary. Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

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