Lonza QC Chemist Job Openings – Apply Online Now
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 of Incoming materials 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 of Incoming materials 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.
Link to apply: Apply Now
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