The Analyst must: Proficient in operating HPLC Ensures that all work is carried out in compliance with company Safety policies, Good Manufacturing Practices (GMP/GLP) and Standard Operating Procedures (SOPs). Analyse API, Raw Materials and Finished products for Assay, Impurities & Dissolution study using HPLC instrument with minimum supervision. Review technical data, documents, and proposals as required. Troubleshoot technical issues/ difficulties with methods. Coordinate with team members to perform method transfers between R&D group to QC group. Promote and maintain a safe and healthy working laboratory environment in compliance with established health and safety procedures. Strong interpretation of routine analysis or tests. Be able to write lab reports. Ability to work directly from the USP or EP pharmacopeia to write protocols and execute methods. Be able to work under GMP guidelines and be proficient with USP and pharmaceutical testing. Competent research and study skills to learn about innovative methodologies and equipment used for problem-solving and troubleshooting. Design, preparation, and production of study materials including procedure manuals. Responsible for the testing of raw materials, finished products and stability samples by instrumental and wet chemistry methods and described in compendia references or in-house methods. Perform other duties as assigned by the Laboratory manager.Note : The Analyst will have over minimum 3 to 5 years of laboratory testing experience Education:MSc in Analytical Chemistry, or diploma in related filed.A solid background and understanding of Chemistry is mandatoryExperience working with Pharmaceuticals.
As the Head of Analytical the key responsibilities would be:* To plan and manage all the activities of the Analytical Research Department, To assure the quality of all products manufactured by the Company* Responsible for an Analytical team involved in Method development, Method Transfer and Validation for various stages of API development.* Responsible for Analytical Method Development activities of SM / RM/ Intermediate / API as per SOP, Pharmacopeia & ICH Guideline* Method Validation of analytical methods as per internal and country specific regulatory guidelines and execution through proper protocols.* Effective method development ensures that laboratory resources are optimized, while methods meet the objectives required at each stage of API development.* Participating with group members to explore innovative and improved ways for meeting the group's deliverables while contributing to the scientific depth of the group.* Demonstrated experience in designing and writing stability protocols for small- or large-molecules, investigational or registration studies, analysing and trending large sets of data.* Responsible for In-house method Development of in-process, intermediates, and API.* Responsible for Preparation of Specification, JOS, MSDS, AMV and AMT Protocol.* To co-ordinate for development of specifications, the analytical procedure in coordination with Quality Assurance Department and R&D.* To be responsible for instruments qualification as per the guideline and prepare protocols and reports accordingly.* Well versatile with ICH Quality Guideline & Pharmacopeial monograph.
HR Madhuri Kadam - 9326858835 email id - hr2@mubychem.cpmEssential Duties and Responsibilities: Sample preparation and Mobile phases preparation. Documentation: Ensuring accurate reporting in lab books. Using a wide range of sophisticated equipment and instruments to conduct analysis and research and troubleshoot instrumentation/methods. Perform other departmental tasks such as cleaning, supply ordering, assist with instrumentation training and maintenance, etc. Perform analytical tests utilizing HPLC and other laboratory instruments. Mentoring/training junior staff members and Imparting training to new recruits for operation, calibration and preventive maintenance of HPLC. Writing SOPs. Ensure that work is performed in compliance with good manufacturing practices (GMP), standard operating procedures (SOPs) and the current test method. Participates in general lab duties, including clean-up, administration, logbook review and operations support.
The Sales Executive is responsible for developing and maintaining relationships with customers in the API, Specialty Chemicals and Excipients industry. The ideal candidate will have a strong understanding of the industry and the products and services we offer. They will also be able to build rapport with customers and close deals Develop and execute sales plans to achieve revenue goals Prospect for new customers and develop relationships with existing customers Present and demonstrate products and services to customers Close deals and negotiate contracts Stay up-to-date on industry trends and competitor activity
Anmol Chemicals is a manufacturer supplier exporter of Pharmaceutical Excipients, Food Grade Chemicals and it offers materials as per IP BP EP Ph Eur USP NF JP FCC Food Grade as per the the latest monograph at best prices. Anmol Chemicals Group, established in 1976, is the pioneer manufacturer of Specialty Chemicals, Pharmaceutical Excipients, Some API, Food Chemicals in India. Anmol Chemicals Group has manufacturing facilities spread across Western India, representatives in Houston, Chicago USA and Dubai, UAE. We also have toll manufacturing units for processing chemicals in a few countries around the world. We make IP, BP, EP, USP, NF, Ph. Eur., JP, FCC or Food Grade, Analytical Reagent Grade, LR or Laboratory Reagent Grades and Pure Grades of various chemicals. All our items are analyzed to meet the required standards. We can supply the product in grams for your laboratory trial and in tons for your plant scale jobs.
Share your thoughts with other customers for Anmol Chemicals Private Limited