Job Summary L ooking for a Development Quality Assurance Executive/Sr. Executive with a minimum of 5 years experience in the pharmaceutical industry. Responsibilities and duties Review and approval of development-related documents (e.g., process development reports, analytical method validation, exhibit batch records). Quality oversight of lab-scale, pilot-scale, and exhibit batch manufacturing to ensure GMP compliance. QA support during technology transfer from R&D to manufacturing. Management of change controls, deviations, and CAPAs for development activities. Review of process validation and analytical method validation data. Ensure data integrity and documentation compliance (as per ALCOA+). Support for audits, inspections, and regulatory submission readiness. Cross-functional coordination with R&D, QC, Production, and Regulatory Affairs. Required Experience, Skills and Qualifications B.Pharm / M.Pharm / M.Sc. in Chemistry, Pharmaceutical Sciences, or related field. 5–9 years of experience in Development QA (preferably in an API manufacturing environment). Strong understanding of cGMP, ICH guidelines, and regulatory requirements (USFDA, EMA, etc.). Excellent documentation, communication, and analytical skills. Benefits Competitive wages and benefits Increments every year based on performance Training Show more Show less
As an Assistant Manager or Manager in our organization, your primary responsibility will be to focus on the business development and marketing of APIs to Generic Pharmaceutical Companies in domestic, emerging markets, and EU markets for a few products. You will be tasked with identifying and engaging new customers, distributors, and agents within the relevant market. Your role will be instrumental in charting the strategic roadmap of the company by establishing a structured product selection process, designing the product pipeline, and prioritizing for future planning. The ideal candidate for the position of Assistant Manager should possess 5-7 years of relevant experience, while a Manager should have 8-10 years of experience. Prior experience in sales, business development, or corporate strategy within the Pharma industry is a prerequisite for this role. In terms of educational qualifications, candidates with a background in B.Pharmacy, M.Pharmacy, or MBA will be given preference for this position. It is essential to have a strong understanding of the pharmaceutical industry landscape and a proven track record of driving business growth and market expansion strategies. If you are passionate about business development, marketing, and strategic planning within the pharmaceutical sector, this opportunity offers a platform to showcase your skills and contribute to the growth and success of our organization. Join us in shaping the future of our company and making a meaningful impact in the healthcare industry.,
As a member of our team, your responsibilities will include manufacturing of Intermediates and Active Pharmaceutical Ingredients, operating and cleaning equipment, executing batches and cleaning as per Batch Manufacturing Record, calibrating weighing scales and other measuring devices, maintaining equipment logs for all equipment, performing process validation, conducting in-process sampling, and investigating process-related deviations. The ideal candidate should have 0-15 years of experience in the production department of a pharmaceutical company with a degree of M.Sc./B.Sc. in Chemistry or M.Tech/B.Tech in Chemical Engineering. Experience in manufacturing APIs or intermediates is required. Strong communication skills are essential, including good written and verbal communication skills to document procedures, draft reports, and collaborate effectively with team members. In return for your contributions, we offer a competitive salary and benefits package, yearly bonuses, increments based on performance, training opportunities, lunch service, and commuting support. Join our team and be a part of our exciting journey in the pharmaceutical industry.,
The responsibilities and duties of this role include: - Performing sampling and analysis of Raw materials, Packing materials, In process, Intermediate, and Finished products. - Conducting calibration of Quality Control instruments. - Carrying out Stability/Holding time studies. - Managing Reference Standards and qualifying Working Standards. - Ensuring Analyst qualifications are met. - Conducting Analytical Method Validation. - Managing Control samples (Retain sample). - Conducting OOS investigations (Phase-1). The ideal candidate should have: - 2-3 years of experience in Pharmaceutical Quality Control. - Educational background in M.Pharmacy/B.Pharmacy/M.Sc. (Chemistry)/B.Sc. (Chemistry). - Preferred experience in handling HPLC, GC, and other Quality Control instruments. - Good documentation skills with exposure to GLP, GDP, and cGMP practices. - Experience in Sampling and analysis, Calibration, Stability/Holding time studies, Analytical Method Validation, and OOS investigations. Benefits: - Competitive wages and benefits. - Yearly bonus. - Increments every year based on performance. - Training opportunities. - Lunch service. - Commuting support.,
Responsibilities Business development and marketing of APIs and Intermediates to generic pharmaceutical companies in the domestic market. Finding and selecting new customers and distributors in the concerned market. Playing a significant role in planning the strategic road map of the organization by setting up a product selection process in the company and designing the product pipeline and prioritization for planned future. Qualifications : B. Pharmacy/ M.Pharmacy/ MBA 5-7 years of experience for Assistant Manager and 8-10 years for Manager. Experience of marketing and corporate strategy in the Pharmaceutical industry is required Excellent verbal and written communication skills
Role Overview: As a Production Operator in the pharmaceutical industry, your main responsibility will be the manufacturing of Intermediates and Active Pharmaceutical Ingredients. You will be in charge of operating and cleaning equipment, executing batches as per Batch Manufacturing Record, calibrating weighing scales and other measuring devices, and maintaining equipment logs for all equipment. Additionally, you will be responsible for performing process validation, in process sampling, and investigating process-related deviations. Key Responsibilities: - Manufacturing of Intermediates and Active Pharmaceutical Ingredients - Operation and cleaning of equipment - Execution of batches and cleaning as per Batch Manufacturing Record - Calibration of weighing scales and other measuring devices - Maintaining equipment logs for all equipment - Performing process validation - In process sampling - Investigation of process related deviations Qualifications Required: - 0-15 years experience in the production department of a pharmaceutical company - M.Sc. /B.Sc. (Chemistry), M.Tech/B.Tech (Chemical Engineering) - Experience in manufacturing APIs or intermediates - Good written and verbal communication skills for documenting procedures, drafting reports, and collaborating effectively with team members,
As a Quality Control Analyst in the pharmaceutical industry, you will be responsible for sampling and analyzing a variety of materials including Raw materials, Packing materials, In process, Intermediate, and Finished products. Your role will also involve the calibration of all QC instruments, conducting Stability/Holding time studies, and handling Reference Standards while qualifying Working Standards. Key Responsibilities: - Sampling and analysis of Raw materials, Packing materials, In process, Intermediate, and Finished products - Calibration of all QC instruments - Conducting Stability/Holding time studies - Handling Reference Standards and qualification of Working Standards Qualifications Required: - 2-3 years of experience in Pharmaceutical Quality Control - Education Qualification: M.Pharmacy/B.Pharmacy/M.Sc. (Chemistry)/B.Sc. (Chemistry) preferred,