Key Responsibilities:Perform routine and non-routine chemical analyses of raw materials, in-process samples, and finished products using various laboratory instruments (e.g., HPLC, GC, UV-Vis, FTIR).Calibrate, maintain, and troubleshoot laboratory instruments to ensure accurate and reliable results.Prepare and review Standard Operating Procedures (SOPs) for analytical methods and ensure compliance with quality standards.Analyze data from testing and document results in reports, ensuring proper record-keeping and traceability.Conduct stability studies and product testing to ensure that products meet specifications.Work closely with production teams to resolve any quality-related issues and recommend corrective actions.Assist in the development and validation of new analytical methods.Ensure compliance with Good Laboratory Practices (GLP) and relevant regulatory requirements (e.g., GMP, ISO).Perform equipment maintenance and troubleshooting to ensure continuous operation of testing instruments.Assist in the preparation for internal and external audits and inspections. Qualifications:Bachelors degree in Chemistry, Biochemistry, or a related field.Proven experience (2+ years) in a Quality Control role within a laboratory or pharmaceutical/chemical industry.Familiarity with lab instruments such as HPLC, GC, UV-Vis spectrophotometer, and other analytical techniques.Strong understanding of GLP, GMP, and regulatory standards.Excellent attention to detail and ability to work independently.Strong analytical and problem-solving skills.Good communication and documentation skills.Ability to work under pressure and meet tight deadlines.

Role & responsibilities Documentation is the key to GMP compliance and ensures traceability of all development,manufacturing, and testing activities. Documentation provides the route for auditors toassess the overall quality of operations within a company and the final product.Quality Management System (QMS) is ensuring that drugs are safe, effective, and of highquality is fundamental, as these factors directly impact patient health. Quality managementsystems are essential across the industry to uphold these stringent standards.• Officer - Documentation & QMS ensures that all documentation is clear and concise,and that it's followed by all personnel. This helps to ensure that the manufacturingprocess is consistent and safe. • Officer - Documentation & QMS play a critical role in ensuring that thepharmaceutical industry complies with a wide range of regulatory requirements andinternational standards. This involves preparing and submitting regulatory documentsand conducting audits and inspections to ensure compliance with regulations.• He/she should have familiarity with guidelines such as GLP, FDA and cGMPregulation and principles of Quality Management.• Officer - Documentation & QMS will provide technical and general administrativesupport to this department and ensure that tasks are carried out in a timely manner,Preferred candidate profile Perks and benefits

Role & responsibilities Develop and implement targeted marketing strategies to increase the awareness and sales of our APIs in the domestic market.Identify growth opportunities and key trends in the pharmaceutical industry, focusing on API markets and related sectors.Collaborate with senior leadership to align marketing strategies with company goals and objectives.Oversee the digital marketing strategy for promoting APIs, including SEO, SEM, email marketing, and social media campaigns.Work with the digital marketing team to develop educational content, blog posts, case studies, and white papers that highlight product features and industry trends. Collaborate closely with the Sales team to support business development efforts, lead generation, and customer acquisition strategies.Work with the R&D team to gain a deep understanding of new product developments and translate technical information into effective marketing communication. Stay informed on regulatory requirements related to the marketing of pharmaceutical ingredients and ensure that all marketing activities comply with industry standards and regulations.Ensure marketing materials accurately represent product specifications and adhere to pharmaceutical industry regulations.Prepare regular reports on marketing campaign performance, market trends, customer feedback, and competitive intelligence.Present insights and recommendations to senior management for continuous improvement in marketing efforts.Preferred candidate profile Bachelors degree in Marketing, Pharmaceutical Sciences, Business, or a related field (Masters degree preferred).3-5 years of experience in domestic marketing within the pharmaceutical or chemical industries, with a focus on Active Pharmaceutical Ingredients (APIs).Strong understanding of the pharmaceutical industry, including API manufacturing, regulations, and market dynamics.Proven experience in developing and executing integrated marketing campaigns across digital and traditional channels.Excellent communication, presentation, and interpersonal skills.Proficiency in CRM tools, marketing automation software, and analytics platforms (Google Analytics, HubSpot, etc.).Ability to work collaboratively with cross-functional teams (Sales, R&D, Regulatory Affairs).Strong analytical skills and ability to interpret data to inform decision-making.Knowledge of regulatory standards in the pharmaceutical and API sectors (e.g., GMP, FDA regulations, etc.).