48 Intermediates Jobs - Page 2

Role & responsibilities Equipment Operation: Operate and monitor equipment used in the manufacturing of OSD products, such as granulation equipment, blending machines, tablet presses, Set up machines according to standard operating procedures (SOPs) and batch records. Ensure equipment is properly cleaned and maintained to prevent cross-contamination and ensure product quality. Production Execution: Follow batch records, work instructions, and SOPs to manufacture OSD products in accordance with regulatory requirements (GMP, FDA, etc.). Monitor production processes to ensure products are produced within specifications regarding quality, yield, and output. Perform in-process checks and sampling...

The job involves performing sampling, analysis, and reporting of raw materials, intermediates, in-process samples, finished products, and stability samples. It is essential to maintain accurate and complete records of all quality control (QC) activities. As part of the role, you will be responsible for ensuring the safety, efficacy, and quality of drugs by conducting tests, analyzing data, maintaining records, and ensuring compliance with regulations and standards. This is a full-time position with benefits such as food provided and a yearly bonus. The work location is in person.,

M.Sc. - Organic Chemistry with 5 to 8 years of experience in Pharma Manufacturing Industries. Having Pharma Company experience in APIs & their Intermediates. Literature Search via Scifinder, chemical abstract, Free Patent online & Journals. Required Candidate profile Communication with IPR & Regulatory Affairs & DQA Dept. Development with Extraction, Purification & Distillation of product. Preparation of Process safety report & data analysis of Intermediate & APIs Perks and benefits Negotiable - Depending Upon Candidate & Experience

Role & responsibilities HPLC Analyst, Operation of HPLC, Troubleshooting, Analysis of all In-process, Intermediates, RM, PM, Finish Product, Stability samples and other analytical samples of lab. Operation of GC, IR, UV, KF, Auto titrator, SOR and Wet Lab analysis. Preferred candidate profile Minimum 3 to 8 years of experience required.

Conduct market research to identify potential customers Promote & sell chemical products (Pharma) to customers & Provide technical advice Maintain records & sales reports Will work independently & will be handling South Region Required Candidate profile Excellent communication and organizational skills Ability to coordinate multiple projects Excellent customer service skills Strong problem solving and analytical skills Excellent negotiation skills

BE - Environment Engineer with 2 to 5 years of experience related field. CTE / CCA Application. Notice Reply. Form - 4/5. Environment Audit Report. Environment Related Data Preparation. HE Management - Manitest. GPCB Related Work. CGWA Related Work. Required Candidate profile Maintaining Legal & GMP documents related to ETP Operation, Laboratory & Hazardous waste generation & disposal. Handling Biological Wastewater Treatment. Knowledge About ETP & Environmental Audit. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / M.Sc. - Chemistry with 02 to 03 years of experience in Pharmaceutical Industries (API – Intermediates). Must be aware of the working conditions in an API / Intermediate unit. One who is able to handle all pharma reactors. Equipment handling. Required Candidate profile Monitoring production planning to meet production targets. To ensure that the production records are maintained and recorded at the time of performance. Knowledge of GMP & GDP procedure to follow. Perks and benefits Negotiable - Depending Upon Candidate & Experience

BE - Environment Engineer with 2 to 5 years of experience related field. CTE / CCA Application. Notice Reply. Form - 4/5. Environment Audit Report. Environment Related Data Preparation. HE Management - Manitest. GPCB Related Work. CGWA Related Work. Required Candidate profile Maintaining Legal & GMP documents related to ETP Operation, Laboratory & Hazardous waste generation & disposal. Handling Biological Wastewater Treatment. Knowledge About ETP & Environmental Audit. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / M.Sc. - Chemistry with 02 to 03 years of experience in Pharmaceutical Industries (API – Intermediates). Must be aware of the working conditions in an API / Intermediate unit. One who is able to handle all pharma reactors. Equipment handling. Required Candidate profile Monitoring production planning to meet production targets. To ensure that the production records are maintained and recorded at the time of performance. Knowledge of GMP & GDP procedure to follow. Perks and benefits Negotiable - Depending Upon Candidate & Experience

BE - Environment Engineer with 2 to 5 years of experience related field. CTE / CCA Application. Notice Reply. Form - 4/5. Environment Audit Report. Environment Related Data Preparation. HE Management - Manitest. GPCB Related Work. CGWA Related Work. Required Candidate profile Maintaining Legal & GMP documents related to ETP Operation, Laboratory & Hazardous waste generation & disposal. Handling Biological Wastewater Treatment. Knowledge About ETP & Environmental Audit. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / M.Sc. - Chemistry with 02 to 03 years of experience in Pharmaceutical Industries (API – Intermediates). Must be aware of the working conditions in an API / Intermediate unit. One who is able to handle all pharma reactors. Equipment handling. Required Candidate profile Monitoring production planning to meet production targets. To ensure that the production records are maintained and recorded at the time of performance. Knowledge of GMP & GDP procedure to follow. Perks and benefits Negotiable - Depending Upon Candidate & Experience

BE - Environment Engineer with 2 to 5 years of experience related field. CTE / CCA Application. Notice Reply. Form - 4/5. Environment Audit Report. Environment Related Data Preparation. HE Management - Manitest. GPCB Related Work. CGWA Related Work. Required Candidate profile Maintaining Legal & GMP documents related to ETP Operation, Laboratory & Hazardous waste generation & disposal. Handling Biological Wastewater Treatment. Knowledge About ETP & Environmental Audit. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / M.Sc. - Chemistry with 02 to 03 years of experience in Pharmaceutical Industries (API – Intermediates). Must be aware of the working conditions in an API / Intermediate unit. One who is able to handle all pharma reactors. Equipment handling. Required Candidate profile Monitoring production planning to meet production targets. To ensure that the production records are maintained and recorded at the time of performance. Knowledge of GMP & GDP procedure to follow. Perks and benefits Negotiable - Depending Upon Candidate & Experience

BE - Environment Engineer with 2 to 5 years of experience related field. CTE / CCA Application. Notice Reply. Form - 4/5. Environment Audit Report. Environment Related Data Preparation. HE Management - Manitest. GPCB Related Work. CGWA Related Work. Required Candidate profile Maintaining Legal & GMP documents related to ETP Operation, Laboratory & Hazardous waste generation & disposal. Handling Biological Wastewater Treatment. Knowledge About ETP & Environmental Audit. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / M.Sc. - Chemistry with 02 to 03 years of experience in Pharmaceutical Industries (API – Intermediates). Must be aware of the working conditions in an API / Intermediate unit. One who is able to handle all pharma reactors. Equipment handling. Required Candidate profile Monitoring production planning to meet production targets. To ensure that the production records are maintained and recorded at the time of performance. Knowledge of GMP & GDP procedure to follow. Perks and benefits Negotiable - Depending Upon Candidate & Experience

BE - Environment Engineer with 2 to 5 years of experience related field. CTE / CCA Application. Notice Reply. Form - 4/5. Environment Audit Report. Environment Related Data Preparation. HE Management - Manitest. GPCB Related Work. CGWA Related Work. Required Candidate profile Maintaining Legal & GMP documents related to ETP Operation, Laboratory & Hazardous waste generation & disposal. Handling Biological Wastewater Treatment. Knowledge About ETP & Environmental Audit. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / M.Sc. - Chemistry with 02 to 03 years of experience in Pharmaceutical Industries (API – Intermediates). Must be aware of the working conditions in an API / Intermediate unit. One who is able to handle all pharma reactors. Equipment handling. Required Candidate profile Monitoring production planning to meet production targets. To ensure that the production records are maintained and recorded at the time of performance. Knowledge of GMP & GDP procedure to follow. Perks and benefits Negotiable - Depending Upon Candidate & Experience

We are looking for a passionate and skilled M.Sc. Chemistry graduate (Organic/Analytical) to join our R&D or Quality Control team. The candidate will assist in routine chemical and instrumental testing, synthesis, method development.

Role & responsibilities HPLC Analyst, Operation of HPLC, Troubleshooting, Analysis of all In-process, Intermediates, RM, PM, Finish Product, Stability samples and other analytical samples of lab. Operation of GC, IR, UV, KF, Auto titrator, SOR and Wet Lab analysis. Preferred candidate profile Minimum 3 to 8 years of experience required. Perks and benefits Best in the Industry

Manufacture the product as per the production guidelines And SOPs Monitor the manufacturing activity such as calibration /production of finished goods labelling / Packing / cleaning / shop floor activities Responsible Safety And Environment policies Required Candidate profile Candidate must have experience in Intermediate - Pharma API And Agro Technical - As well As Agro And Pharma Formulation.. Must aware with production report preparation Ready to work in All Shift

Manufacture the product as per the production guidelines And SOPs Monitor the manufacturing activity such as calibration /production of finished goods labelling / Packing / cleaning / shop floor activities Responsible Safety And Environment policies Required Candidate profile Candidate must have experience in Intermediate - Pharma API And Agro Technical - As well As Agro And Pharma Formulation.. Must aware with production report preparation Ready to work in All Shift

Role & responsibilities Role & responsibilities:- Responsible for identifying and developing new business opportunities in Africa & CIS regions. Responsible for Sales and marketing of APIs, Specialty Chemicals, Intermediates, Excipients, Medical equipments & Finished Products on above regions. Maintaining Strong relationships with existing customers and updating clients with new products. Driving new business by developing new international customers. Meetings with new clients to finalize the products and negotiate prices and quantity. Following up with buyers for orders and maintaining payment tracks accordingly. Sending quotations, samples, and other technical and regulatory documents to r...

Manufacture the product as per the production guidelines And SOPs Monitor the manufacturing activity such as calibration /production of finished goods labelling / Packing / cleaning / shop floor activities Responsible Safety And Environment policies Required Candidate profile Candidate must have experience in Intermediate - Pharma API And Agro Technical - As well As Agro And Pharma Formulation.. Must aware with production report preparation Ready to work in All Shift