Qc Officer

**Job Title**: QC Executive / QC Officer **Location**: Sachin GIDC, Surat, Gujarat **Key Responsibilities** - **Sample Collection & Testing**: Collect and test raw materials, packaging components, in-process samples, finished products, and stability samples, following SOPs. - **Instrumental Analysis**: Perform chemical and physical analyses using HPLC, UV,...

To enhance and implement the Quality assurance system in order to achieve Quality standard. - To motivate and train the sub-ordinates and colleague to improve quality system and current GMP/GLP/GDP/GEP standards in the plant. - To remain updated regarding the recent international and regulated guidelines. - To establish, lay down, implement and approve...

**Job description: - ** **Instrumental Analysis**: - Perform routine and stability analysis of raw materials, intermediates, and finished products using **HPLC, UV-Vis Spectrophotometer, FTIR**, etc. - Operate and calibrate analytical instruments as per SOPs and regulatory guidelines. - Troubleshoot HPLC and other lab equipment in coordination with...

**Location**: Sachin **Company**: Navitas Alpha Renewables Pvt Ltd **Shift**: 3 Shifts (8 hrs) **Reporting to**: Quality Manager/Technical Manager **Probation Period**: 6 Months **Responsibilities**: - On-line checking. - Ensure a defect free product move to finish goods. - Training to helpers and winder person about defect. - Catching defects...

**Job Title**: Production Officer **Company**: Trident Lifeline Limited **Location**: Sachin G.I.D.C., Surat, Gujarat **Department**: Production **Employment Type**: Full-Time **Job Summary**: Trident Lifeline Ltd. is looking for a dedicated and enthusiastic **Production Officer** to support pharmaceutical manufacturing operations. The role involves...

**Job Summary**: **Key Responsibilities**: - Handle and manage the entire **production department** including **20-30 female workers** on the shop floor. - Prepare and implement **SOP-based work plans** to ensure compliance with manufacturing protocols and GMP guidelines. - Develop and execute **daily and weekly production plans** based on order...

To monitor compliance of GMP and GLP requirements. - To active participate and compliance of the client, regulatory audit and self-inspection. - To handle and maintain the QMS Documents, such as Change control, Incident, Deviation, CAPA, OOS, Recall, Cleaning validation and Market complaints. Maintain annual trends of it. - To give training to new employees,...

Job description: - To monitor compliance of GMP and GLP requirements. - To active participate and compliance of the client, regulatory audit and self-inspection. - To handle and maintain the QMS Documents, such as Change control, Incident, Deviation, CAPA, OOS, Recall, Cleaning validation and Market complaints. Maintain annual trends of it. - To give...

Key Responsibilities Supervise and execute production activities in the formulation department as per batch manufacturing records BMR and standard operating procedures SOPs Ensure compliance with cGMP GDP and regulatory requirements during manufacturing Handle granulation compression coating and packing activities in oral solid dosage OSD ...