Company Description Althea Pharma Private Limited is a leading manufacturer specializing in IV Fluids using FFS Technology. The company is expanding its product line to include Sterile IV Drugs, available in glass ampoules and vials. Althea Pharma is WHO-GMP approved and holds certifications from the NDA (Uganda) and Yemen MOH. Role Description This is a full-time, on-site Mechanical Engineer role located in Daman. The Mechanical Engineer will be responsible for designing and developing machinery, overseeing the implementation of machine design projects, and utilizing Computer-Aided Design (CAD) software for drafting and modeling. The role includes project management responsibilities, such as planning, organizing, and managing resources to bring about the successful completion of specific project goals and objectives. Additionally, the Mechanical Engineer will be involved in research and development to innovate and improve existing products and processes within the manufacturing environment. Qualifications Mechanical Engineering, Machine Design, and Computer-Aided Design (CAD) skills Experience in Project Management Research and Development (R&D) abilities Strong problem-solving and analytical skills Ability to work collaboratively in a team environment Bachelor's degree in Mechanical Engineering or a related field Experience in the pharmaceutical manufacturing industry is an advantage Effective communication and documentation skills
Company Description Althea Pharma Private Limited specializes in the manufacturing of IV Fluids using FFS Technology. The company is expanding into the production of Sterile IV Drugs in both glass ampoules and vials. Althea Pharma is WHO-GMP approved and holds certifications from NDA (Uganda) and Yemen MOH. The company's commitment to quality and innovation drives its mission to provide essential pharmaceuticals. Role Description This is a full-time, on-site role for an IPQA at Althea Pharma, located in Daman. The IPQA will be responsible for day-to-day quality assurance activities, monitoring of manufacturing processes, and ensuring compliance with established quality standards. The role involves conducting in-process quality checks, reviewing batch records, and collaborating with the production team to maintain high-quality standards. Qualifications Experience in quality assurance and quality control Knowledge of GMP regulations and quality standards Strong attention to detail and analytical skills Ability to work collaboratively with production teams Excellent communication and problem-solving skills Relevant experience in the pharmaceutical industry Degree in Pharmacy, Chemistry, or a related field
Company Description Althea Pharma Private Limited is a leading manufacturer of IV Fluids using FFS Technology, and it is expanding its operations into the production of Sterile IV Drugs in glass ampoules and vials. The company is approved by WHO-GMP, demonstrating its commitment to international quality standards, and holds certifications from the National Drug Authority (NDA) of Uganda, PIC/S and the Ministry of Health (MOH) of Yemen. With a robust reputation in the pharmaceutical industry, Althea Pharma is dedicated to delivering high-quality healthcare solutions. Role Description This is an on-site, full-time Quality Assurance Executive role located in Daman. The Quality Assurance Executive will be responsible for implementing and monitoring quality assurance and quality control systems, conducting quality audits, and ensuring compliance with regulatory standards, including WHO-GMP and other applicable certifications. The role involves collaborating with cross-functional teams to address quality-related issues, document processes, and ensure that manufacturing operations meet quality and safety standards. Qualifications Proficiency in Quality Control, Quality Assurance, and Quality Management practices Knowledge and experience in Quality Auditing and regulatory compliance processes Background or education in Pharma for quality and safety assurance Strong analytical and problem-solving skills, with attention to detail and accuracy Experience in the pharmaceutical or healthcare manufacturing industry is a plus Bachelor's degree in Pharmacy or Masters in Pharmacy or a related discipline Need 7-8 years of experience The candidate should have knowledge about CAPA plan submissions, Root Cause Analysis, Investigation Methods etc. Candidate should have worked on the shop floor before. Please apply only if you are actually interested. We have had enough jokers who accept the offer and then don’t join. We are now accepting candidates who will be legally committed for 2 years once they accept the offer.