118 Job openings found

Job Responsibilities :   Experience in pharmaceutical formulations- Minimum 3 years Job Description-  1. Artwork development with designers as per country requirements in accordance with pharmacopoeia. 2. Coordination with factories for artwork approvals. 3. Handling product permission and regulatory approvals with liaison agents.  4. Maintaining documentation as per SOP and guidelines.     Responsible for monitoring, inspecting and proposing measures to correct or improve ...

Responsible for: . Analyzing, collecting data, and providing accurate, documented information about the status of quality . Verifying the correctness of quality related development results in compliance with the Quality Management Plan & authorize their release for medical devices . Validation of compliance to basic requirements, e.g. ISO standards and regulations like Medical Device ...

Responsible for: . Analyzing, collecting data, and providing accurate, documented information about the status of quality . Verifying the correctness of quality related development results i n compliance with the Quality Management Plan & authorize their release for medical devices  Validation of compliance to basic requirements, e.g. ISO standards and regulations like Medical Device ...

Responsible for: . Analyzing, collecting data, and providing accurate, documented information about the status of quality . Verifying the c orrectness of quality related development results in compliance with the Quality Management Plan & authorize their release for medical devices . Validation of compliance to basic requirements, e.g. ISO standards and regulations like Medical Device ...

Responsible for: . Analyzing, collecting data, and providing accurate, documented information about the status of quality . Verifying the correctness of quality related development results in compliance with the Quality Management Plan & authorize their release for medical devices  Validation of compliance to basic requirements, e.g. ISO standards and regulations like Medical Device Regulation ...

Responsible for: . Analyzing, collecting data, and providing accurate, documented information about the status of quality . Verifying the correctness of quality related development results in compliance with the Quality Management Plan & authorize their release for medical devices . Validation of compliance to basic requirements, e.g. ISO standards and regulations like ...

Responsible for: . Analyzing, collecting data, and providing accurate, documented information abou t the status of quality . Verifying the correctness of quality related development results in compliance with the Quality Management Plan & authorize their release for medical devices . Validation of compliance to basic requirements, e.g. ISO standards and regulations like ...

REQUIREMENTS Education / Experience Education: BSC / MSC Chemistry   Experience: 2-3 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Qualification, Regulatory requirements   JOB PURPOSE Generic Implement Quality Assurance activities for Pharmaceutical at Dahej adhering to standard operating procedures with optimum utilization of resources to ensure consistent good quality of products to meet with ...

Job Description:? Should have strong communication skill? Handling & Calibration of instruments like HPLC, GC, KF, IR, UV, Viscosity,Tintometer? Sampling and analysis of of raw material as well as finish good? ETP sample analysis – pH, COD, TDS. MLSS , TS , TSS? Good Knowledge of physical as well as ...

1. Summary of the roleThe Role will assist Healthcare business growth by developing Biopharmaceutical and Biotechnology business development activities. A techno-Commercial role with good understanding of bio-pharma market and ability to establish the Bio-Pharma products Range. 2. Education and Experience: B. Pharmacy/BiotechExperience: 3 to 5 Years in B2B Pharma/Bio-Pharma SegmentsNotice Period ...