For all the positions, it is essential for candidates to have exposure in Injectable Sterile plant and regulatory requirements of documentation as per cGMP/GLP.
Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.
Eurofins Scientific is a group of international life sciences companies which provide a unique range of analytical testing services to clients across multiple industries. The Group believes it is the global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
Color Tunable Thermally Activated Delayed Fluorescent Emitter for OLED Applications. Candidates with MSc., Chemistry with GATE, NET and Master of Pharmacy.
Experience must include analysis of Raw Material, In-Process, finished goods. Stability Testing and Stability sample handling Tablets / Capsules. Handling of HPLC, dissolution & other sophisticated instruments.
Preparation of quality system related, Instrument operation related SOPs, Specification, STPs, GTPs, raw data sheet, certificate of analysis. Preparation, review, execution of method transfer and method validation protocols and reports etc.
As Regulatory Professional II, the candidate will be responsible for making the timely submissions to the Health Authorities worldwide. The candidate is expected to establish and maintain the CMC part of the core regulatory file.
Execute shift packing activity by managing available resources and reduces micro stoppage of machine to achieve shift target. Review documentation related to packing activity and monitor standard packing parameters as per BPR to meet regulatory requirement
Chemical or Physical testing analysis of raw materials, finished products, stability or request samples. Documenting and submitting all raw data and results in LIMS