88 Job openings found

Candidate should have knowledge of purchasing of Row Material of Bulk Drug/Intermediate Unit from International Market. Propose improvements to the current purchasing system that will improve vendor relationships and lower the cost of doing business Collaborate with inventory control and sales to develop metrics for gauging inventory level needs and then maintaining ...

Job description: Responsible for overseeing manual production methods to make sure that the desired product yield is achieved. Responsible to maintain and improve housekeeping in all areas within the department. Ensure final product meets quality and customer specifications. Ensure that all products are manufactured with utmost efficiency and quality, according to planned protocols using ...

A Chemist in a Direct Reduced Iron (DRI) plant is responsible for chemical analysis of raw materials and finished products, quality control and assurance, monitoring chemical processes, and maintaining lab equipment to ensure the safe and efficient production of DRI for steelmaking. Key duties include conducting tests on raw materials like ...

Provide leadership planning and work assignment. Drug licence application and renewable of licence in State Drug Authority for different type of Formulation. Monitoring & Maintaining Quality Systems in the plant to meet State GMP requirements. To organize inspection & testing of Raw Material, In-Process & Finished Products. Planning and carrying out self-inspection of all ...

  Client Info: Exporters and Importers of Pharma/ Aroma Chemicals, Pharm Ingredients, Natural Essential Oils, Perfume Ingredients, Flavour Ingredients, Pharm Ingredients.   Qualification: Graduate, MBA or PG in Marketing would be an added advantage Gender: Male/Female Job Profile: a) A pharmaceutical marketing job can entail product and service development, research, communication projects, sales programs, customer relations ...

Job description for API Regulatory: Preparation, review and submission of Drug Master Files/CEP in eCTD format for the regions US, EU through ESG and CESP. Life cycle management of the Drug Master Files (Amendments, Annual Reports, CEP updates). Preparation, review and submission of Applicant's Part DMF (Open Part DMF) and Technical data ...

CORE JOB RESPONSIBILITIES: •Conduct comprehensive research of internal reports, scientific literature, databases, and regulatory documents relevant to formulation development, dosage forms, dissolution, biorelevant media, and drug disposition (ADME), pharmacokinetics (PK), pharmacodynamics (PD), pharmacology, and toxicology/toxicokinetics. •Extract, curate, and critically evaluate data from tables, figures, and published sources; organize datasets into standardized formats ...

Must have experience in Pharmaceutical industry. Knowledge of HVAC Filter cleaning, Preventive maintenance of AHU. Operation of Chiller Plant. Basic knowledge of HVAC Validation. Knowledge of pressure zoning. Troubleshooting of HVAC system. Knowledge of EMS system. Basic knowledge of GDP & DI(Data integrity) Lead internal quality audits and represent the organization as the technical QA lead during joint ...

Position:         EHS Officer Location:        Vapi Experience:     3 - 5 Years Industries:      Pharma API   Responsibilities: Assist in Compliance Reviews, General Risk assessment and support health, safety and environmental management Responsible for adherence to GMP-ICH-q7 guidelines, ISO 14001 & ISO 45001 guidelines with respect to approved SOPs. Prepare STD HSE ...

Surgical Oncologist Surgical Removal: Performs operations to remove solid tumors, surrounding tissues, and affected lymph nodes. Biopsies & Diagnostics: Conducts surgical biopsies (e.g., excisional, incisional, or needle-assisted) to diagnose, stage, and grade tumors. Minimally Invasive Procedures: Utilizes robotic, laparoscopic, or endoscopic techniques to remove tumors with faster recovery times. Palliative Surgery: Performs procedures to ...