As an experienced professional with over 10 years in Solid Dosage formulation for Regulated Markets, you will play a crucial role in the development and manufacturing of pharmaceutical products at our company. Your expertise in this area will be essential in ensuring the quality and compliance of our products for regulatory approval. Key Responsibilities: - Develop and optimize Solid Dosage formulations for Regulated Markets - Conduct thorough research and analysis to ensure product efficacy and safety - Collaborate with cross-functional teams to meet project timelines and goals - Evaluate and improve existing formulation processes for efficiency and cost-effectiveness - Stay updated on industry trends and regulatory requirements to ensure compliance Qualifications Required: - Bachelor's or Master's degree in Pharmacy (BPharm/MPharm) - Minimum of 10 years experience in Solid Dosage formulation for Regulated Markets - Strong knowledge of regulatory guidelines and requirements for pharmaceutical products Please send your resume along with your contact number to hr@elysiumpharma.com or info@elysiumpharma.com. Rest assured that all resumes and communication related to employment will be treated with strict confidentiality.,
Role Overview: As an experienced professional with 3+ years of expertise in document review within the pharmaceutical industry, you will play a crucial role in ensuring the accuracy and efficiency of reviewing various documents. Your ability to analyze and assess documents will contribute significantly to the overall quality control process. Key Responsibilities: - Conduct thorough reviews of documents to identify errors, inconsistencies, and compliance issues - Collaborate with cross-functional teams to ensure the accuracy and completeness of all documentation - Maintain detailed records of document reviews and any necessary revisions - Follow established protocols and guidelines for document review processes - Provide feedback and recommendations for improving document review procedures Qualifications Required: - Bachelor's or Master's degree in Pharmacy (B.Pharm/M.Pharm) or Science (B.Sc/M.Sc) - Minimum of 3 years of experience in document review, preferably within the pharmaceutical industry - Strong attention to detail and excellent analytical skills - Ability to work effectively in a fast-paced environment and meet tight deadlines - Excellent communication and interpersonal skills Please note that all resumes and employment-related correspondence sent to hr@elysiumpharma.com or info@elysiumpharma.com will be treated with the utmost confidentiality. Be sure to include your contact number in your resume for easy communication.,
As an experienced candidate with 2-5 years of experience in HPLC/GC in the pharmaceutical industry, you will be responsible for the following key responsibilities: - Conducting HPLC and GC analysis as per industry standards - Analyzing and interpreting test results accurately - Maintaining and troubleshooting laboratory equipment - Ensuring compliance with safety regulations and quality standards To qualify for this role, you must have the following educational background: - Bachelor's or Master's degree in Pharmacy (B.Pharm/M.Pharm) or Science (B.Sc/M.Sc) If you are interested in applying for this position, please email your resume to hr@elysiumpharma.com or info@elysiumpharma.com. Kindly ensure that your resume includes your Cell number. Rest assured, all resumes and employment-related correspondence will be handled with utmost confidentiality.,