2.0 - 5.0 years

4 - 6 Lacs

Pune

Work from Office

Long Description 1. Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. 2. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. To maintain the stability chamber and tracker. 5. To maintain the stability chamber and tracker. 6. To ensure charging and withdrawal of stability samples as per approved protocols. Competencies Education Others Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs.

Posted 5 months ago

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Officer- QC AMNEAL PHARMACEUTICALS COMPANY (INDIA) PRIVATE LIMITED

1.0 - 6.0 years

4 - 7 Lacs

Ahmedabad

Work from Office

Responsible for testing of Raw material,IP/ FP and Stability sample as per method of analysis Should have knowledge for the Method Verification/validation and Method Transfer analysis Have an exposure on operation, calibration, Qualification and maintenance of laboratory instruments / equipments. Have an exposure for the preparation of calibration & PM schedule of laboratory instruments / equipments. Should have knowledge for the preparation, handling & management of working/reference standards etc. Testing of In-process, stability and Finished product samples Should have awareness of Caliber LIMS system operation.

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Team Member - Quality Control (Analyst) Dr Reddys

7 - 12 years

35 - 50 Lacs

Hyderabad

Work from Office

Roles & Responsibilities 1. To perform In-process and Finished product tests for Assay, Related substance, Residual solvent, UOD, Dissolution, and Water content. 2. To perform Exhibit, Hold time and process validation samples analysis. 3. To Handle HPLC, GC, Dissolution, UV and KF systems and its maintenance. 4. To handle Empower software, sample sets loading and processing independently. 5. Good experience in chromatography. 6. Knowledge on Investigations, Deviations, OOT and OOS. 7. To handle SAP, LIMS and DCMS activities. 8. To follow good laboratory practices (GLP) and good documentation practices (GDP). Qualification Educational qualification: MSC chemistry, B-Pharm Minimum work experie...

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Amneal Pharma Walk-in Drive @ Rajoda | 18th May '25 (Sunday) Amneal Pharmaceuticals

2 - 7 years

2 - 7 Lacs

Ahmedabad, Rajoda, SEZ Matoda,Rajoda

Work from Office

Walk-in Drive @ Ahmedabad on 18th May'25 (Sunday) for Quality Control Department We are looking for suitable candidates for OSD Quality Control for Ahmedabad location Unit Interview Venue Details: Date: 18th May 25 (Sunday), Time: - 9:00 AM to 1:00 PM Venue : Amneal Pharmaceuticals Pvt. Ltd Survey No. 634,637-641 Village: Rajoda Tal: Bavla Dist: Ahmedabad -Gujarat - 382220 1) REQUIREMENT FOR OSD QUALITY CONTROL DEPARTMENT Total Experience: 02 to 7 years (Pharma experience only) Qualification: B.Sc./ M.Sc/ B. Pharm/ M. Pharm Designation: Officer/ Sr. Officer /Executive/ Sr. Executive Department: Quality Control Desired Profile: Test RM, PM, in-process, finished & stability samples (various do...

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Qc Manager Shreeram Job Service

8.0 - 10.0 years

8 - 10 Lacs

dahej

Work from Office

Oversees QC processes, ensuring products meet specified std. Developing and implementing QC procedures, conducting audits, and resolving qc-related issues. trains the QC team, maintains records, and ensures compliance with regulatory standards

Posted Date not available

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Dy. Project Director / Team Leader ( Civil ) Aecom

17.0 - 22.0 years

30 - 35 Lacs

bengaluru

Work from Office

Serves as lead engineer on mid- to large size projects. Provides specialized technical input to studies and design for staff's specific area of expertise. Approves and signs off on work. Provides technical expertise for studies and design efforts. Presents complex technical solutions to clients. Performs quality control reviews of work developed by others. Participates in development of technical proposals. Provides estimates for the engineering budget and schedule to meet requirements on large projects.

Posted Date not available

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Research Associate Cadila Pharmaceuticals

2.0 - 7.0 years

3 - 7 Lacs

gujarat

Work from Office

Position: Pre-Clinical Designation: Research Associate Job Location: Dholka, Gujarat 1. Study Sample Analysis- Clinical studies 2. Method Development and Method Validation - Preparation of STP And MVP 3. Coordinate with QA & QC department for timely completion of Projects reports 4. Preparation of SOP and method development and method validation documents 5. Maintaining GLP & ensure 100% compliance

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