QC Chemist

India, Haryana

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Quality management system following in QC department for compliance of Control of documents, Sampling, Testing , Labelling ofIncomingmaterials as per defined time schedule(Raw and Packaging material) , Calibration, Testing of Validation sample, Solution managements analysis of Finished Products , all type of water and other materials. Quality management system following in QC department for compliance of Control of documents, Sampling, Testing , Labelling ofIncomingmaterials as per defined time schedule(Raw and Packaging material) , Calibration, Testing of Validation sample, Solution managements analysis of Finished Products , all type of water and other materials.

Key Responsibilities

• Sampling of all Raw materials, all Packaging material, Water and In-process check.
• To carry out the testing of incoming in process check (gel charge) raw materials & packaging materials & water & finish capsules for chemical & Instrumental analysis: No misses & on time testing required.
• Keeping all records pertaining to testing activities.
• Ensure all test reports of RM & PM & Finish Capsules and profiles of capsule are made in accordance with the requirement.
• Preparation and standardization of volumetric solution and update the records with proper identification.
• Routine verification of all Instruments related to Chemical lab.
• Various data collection pertaining to testing.
• Identification labeling of Raw and Packaging material (all the Labeling should be as per requirement):No miss and on time .
• Update the logbooks & records as per procedure. Keeping all records of various QC activities follow the Data Integrity.
• Ensure Test reports of all Raw & PM & Finish capsule and profiles of capsule are made in accordance with the requirement.
• On- time material sampling, Testing, Labelling and all related records and logbooks of related instrument updated & Identification labelling.
• To perform the daily verification and Internal calibration of Equipment’s.
• Maintenance of the laboratory equipment’s & inventory, records for chemicals, spares, glassware and keeping all records pertaining to testing activities related to chem. Lab.
• To get’s ready for audits any time as per requirements
• Strictly follow procedures laid down in the quality manual & SOP’s and STP’s.
• Meeting Statutory / mandatory requirement of the customer and local FDA.
• Key requirements:
• Degree in Pharma/M.pharma/B.Pharma
• Good Communication skills.
• Work experience in similar role for 3 years to 7 years.
  
  

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Reference: R60746

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