33 Intermediates Jobs

About Us Scimplify is a specialty chemicals manufacturing company offering a full-stack solutionfrom R&D and custom synthesis to large-scale manufacturing and doorstep delivery. Headquartered in Bengaluru, India, we serve multiple industries ranging from pharmaceuticals to agrochemicals and industrial chemicals to personal care and fragrances. We enable 500+ businesses across 20+ countries to develop and scale innovative chemicals from lab to commercial production. We have raised over $54 million from top tier investors such as Accel and Bertelsmann, We are a team of 250+ professionals with entities in India, Japan, USA, UAE, and Indonesia. Learn more about why Forbes thinks we are the top 1...

Role & responsibilities : Some of the key responsibilities include, but are not limited to: 1. Sales Execution & Business Development Develop, manage, and grow sales of APIs, Intermediates, KSMs, and Specialty Chemicals across Pan-India markets Identify and pursue new business opportunities independently, with a focus on strategic customers Conduct regular customer visits, technical discussions, presentations, and customer engagement to support business development Build and maintain strong relationships with key accounts, including API manufacturers, generic companies, CROs, and CDMOs. Achieve sales targets while ensuring sustainable long-term business partnerships Support in pricing, negot...

As a member of the team, you will be responsible for performing qualitative and quantitative analysis of raw materials, intermediates, and finished goods according to approved specifications, SOPs, and test methods. Your role will involve conducting testing using analytical instruments like HPLC and ensuring the accurate documentation of results in laboratory records. Key Responsibilities: - Perform qualitative and quantitative analysis of raw materials, intermediates, and finished goods - Conduct testing using analytical instruments such as HPLC - Prepare and standardize reagents, solutions, and reference standards for testing - Ensure accurate documentation of results in laboratory records...

You will be working as an Officer at AMGIS Lifescience Ltd., located in Bharuch, in a full-time on-site role. Your main responsibilities will include handling day-to-day tasks related to Pharma API's, Veterinary APIs, Human Health API's, and Intermediates for international corporations and startup clients. To excel in this role, you must possess knowledge of Pharma API's, Veterinary APIs, and Human Health API's. Experience in managing Intermediates for pharmaceutical products is crucial. Your attention to detail and organizational skills will play a vital role in executing tasks efficiently. You should be able to work independently and collaborate effectively with international clients. Prev...

As a Quality Management professional at Pillar Chemicals Private Ltd., your primary responsibility will be to conduct quality testing on raw materials, intermediates, and finished goods. In case of any abnormalities, it is crucial to report to the department in charge promptly. You will also be responsible for ensuring that all instruments in the laboratory are well-maintained and notifying the department in charge of any irregularities. Moreover, you will need to guarantee that all batches are tested in accordance with the specified procedures. Upon the approval of finished goods batches, it is essential to release the Quality certificate, panels, and samples from Quality Control. You must ...

Key Responsibilities: 1. Intermediates BD • Contribute to the API , Intermediate BD on Global Accounts growth objectives • Determine the strategies for the selected Accounts • Build the wallet share of business for Biocon API business in India 2. Leading Sales and Account Management • Lead operations and day to day activities to ensure smooth functioning of the businesses and in the monthly order forecasting for production planning • Grow the share of business, as well as expand the relationships within the customer identifying influencers, gatekeepers, decision makers within the region of India, but also to direct and align with Global and Regional KAM's to further penetrate the client orga...

The job involves conducting sampling, analysis, and reporting of raw materials, intermediates, in-process samples, finished products, and stability samples. You will be responsible for maintaining precise and comprehensive records of all quality control (QC) activities. Your role will include ensuring the safety, efficacy, and quality of drugs through test performance, data analysis, record-keeping, and adherence to regulations and standards. This is a full-time position that offers benefits such as food provision and a yearly bonus. The work location is in person. If you need further assistance or information, please feel free to reach out.,

As a Sourcing Specialist at a leading CDMO of active pharmaceutical ingredients (APIs) and an end-to-end solution provider for the pharmaceutical industry's chemistry needs, your primary responsibility will be to source raw materials, critical/key starting materials, intermediates, solvents, R&D, and QC chemicals for API Contract Research Organizations. You will be required to review purchase requests in collaboration with the planning team to ensure 100% On-Time In-Full deliveries. Additionally, you will need to plan for input materials and strategically evaluate risks to maintain adequate supplies on hand. The ideal candidate for this position should possess a BSc in Chemistry and have rel...

Science Graduate / Commerce Graduate with 5+ Years of Experience in Chemical / Pharma Manufacturing Unit as Sales Coordinator. From mail correspondence to finalizing the order & post sales coordination with factory and documentation. B2B Sales. Required Candidate profile Look after the export as well as domestic sales. Coordination with customer and plant for various communication related to pricing, quality, logistics, after sales service, inquiry, etc. Perks and benefits Negotiable - Depending Upon Candidate & Experience

You will be working as a Sourcing Specialist for a leading CDMO of active pharmaceutical ingredients (APIs) and an end-to-end solution provider for the pharmaceutical industry's chemistry needs. This organization operates in over 80 countries, with a significant portion of its revenues coming from exports, particularly from key markets like the US and Europe. Your main responsibilities will include sourcing raw materials, critical/key starting materials, intermediates, solvents, R&D, and QC chemicals for API Contract Research Organizations. You will be required to review purchase requests in collaboration with the planning team to ensure 100% On-Time In-Full deliveries. Additionally, you wil...

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