Quality Jobs

Work Schedule Other Environmental Conditions Office Job Description Summarized Purpose: We are offering an outstanding opportunity to join Thermo Fisher Scientific as an Engineer III, Software Quality

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Radiometer, one of Danaher’s 15+ operating companies,

Assist in routine microbiological testing of samples (water, food, pharma, or clinical). Perform culture preparation, staining, and basic microbial identification. Maintain sterile laboratory conditio

Quality Control & Analysis: Conduct and oversee microbiological testing, including bioburden, sterility, endotoxin, and environmental monitoring for raw materials and finished products. Regulatory Com

Good skill in investigation and investigation report writing. Stability management and finished product analysis planning. HPLC and other laboratory instrument knowledge. Documentation skill. Knowledg

Review of the Finished product / Raw material / stability / calibration of instrument, hands on LIMS, Investigation and documentation.

Preparation of Qualification protocol and report Review of document and compilation of document execution of qualification documents

Review of change control ,deviation, OOS and OOT documents Assign change control, deviation and CAPA to user department involve in investigation and market complain Self inspection management and plan

Analysis of Drug Product using HPLC, Particle size analyzer, Autotitrator, Chcmical testing, Documentation. Knowledge of LIMS.

Experience of documentation, calibration of instrument & equipment, LIMS, chemical testing, working standard qualification.

Review of batch manuafcturing record and line clearance of area and equipment Inprocess check and sampling of bulk , finshed product AQL sampling . Packing and manufacturing sampling.

To perform accurate and reliable analysis of Raw Material as per method of analysis or protocol. To perform method transfer, method verification, analytical method validation and protocol base study.

Sr. No. Responsibilities 1.0 Handling of Overall QMS (Quality Management System) activities 1.1 Change Management 1.1.1 Initiation of Change control for QMS related changes, implementation and closure

Sr. No. Responsibilities 1.0 Issuance and Retrieval of Log Book and Loose Annex. 1.1 Issuance and Retrieval of Log book as per request given by concern department. 1.2 Issuance and Retrieval of Loose

Sr. No. Responsibilities 1.0 Handling of Signature Log. 1.1 To maintain signature log for New Employee and Left Employee. 2.0 Document Preparation. 2.1 To prepare the qualified trainer list. 2.2 To pr

Job Description Summary Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue