Sandoz Chemistry Scientist Vacancy – Candidates Apply Online


Sandoz Chemistry Scientist Vacancy - Candidates Apply Online

Sandoz Chemistry Scientist Vacancy – Candidates Apply Online

Sandoz chemistry job opening. PhD.BSc and MSc Chemistry job opening, Sr scientist post vacancy. Chemistry scientist job opening 2022. Chemistry job. Candidates with master’s, bachelors, and PhD degree in chemistry may apply for the job vacancy at Sandoz for the post of scientist. Check out all the details on the same below:

Job Title: Senior Scientist

Job Id: 348187BR

Location: Hyderabad, AP

Eligibility Criteria & Experience: 

• PhD /Master of Science / Bachelor of Science (Chemistry or Pharmaceutical Analysis) Fluent in English (oral and written) Basic skills in local site language, as required for the position Technical expert studies with PhD and 3 years relevant experience or Master of Science with 8 years of relevant experience.

• Technical hands-on experience and expertise in handling dosage type expertise in Complex Injectables, such as Peptide-based Injections, Nanoparticulate/microparticulate Suspensions, microsphere, Liposomes. Experienced in Method development, Validation, and sameness package. Technical knowledge and experience in advanced-LC, HRMS, GC-MS/MS, IVRT & Dissolution testing, Solid State Characterization techniques etc., for complex dosage types. Knowledge on NMR and its application is good to have.

• Awareness for safe handling of chemicals, potentially dangerous materials and equipment.

• Broad theoretical and scientific knowledge in the relevant area (e.g. manufacturing, analytical, pharmaceutical)

• Proficient with laboratory and/or technical tools. Good knowledge of software and computer tools.

• Good documentation skills . Good knowledge of current Good Manufacturing Practices (cGMP)

• Good Presentation skills. Advanced scientific/technical writing skills.

Resposnibilties:

• Design, plan, perform/supervise and monitor all activities of assigned teams/ projects; handle several activities at a time; understand and meet customer needs.

• Technical hands-on experience and expertise in handling dosage type expertise in Complex Injectables, such as Peptide-based Injections, Nanoparticulate/microparticulate Suspensions, microsphere, Liposomes; support to drive & build inhouse injectable capabilities for complete physiochemical characterization; and also support global teams in project development.

• Subject Matter Expertise in defining and executing of complete characterization strategy for product development & sameness for complex injectable dosage type, identifying critical CQA for structural & physiochemical parameters; Experienced in Method development, Validation, and sameness package. Technical knowledge and experience in advanced-LC, HRMS, GC-MS/MS, IVRT & Dissolution testing, solid-state physiochemical characterization, etc. for complex dosage types. Knowledge on NMR and its application is a good to have.

• Identify, embrace, and adopt industry innovations on technology and advanced analytics, Regulation and Guidelines. Work in close collaboration with the multifunctional project team in designing project strategy. Collaborate with internal CFTs, CROs, CMOs, and academic institutes to carry out complex injectable characterization, including designing experiments and reviewing reports and data.

• Interpret & evaluate results and draw conclusions; write & review characterization, analytical method, protocols and associated validation reports to ensure suitability for regulatory submissions. Manage several projects needs simultaneously while learning to prioritize and execute towards timelines. Bring new technique(s) into lab increasingly proficient at supporting multiple activities in parallel and contribute to document and interpret scientific/developmental experiments.

• Should have the strong analytical problem-solving skill, learning, adaptability and innovative experimental aptitude. Demonstrate good communication and presentation skills, and team connection & collaboration. Work according to appropriate standards as defined in Quality Manual, SOPs, ethical, health, safety, environment (HSE), and information security (ISEC) guidelines; lead initiatives to ensure proactive compliance and continuous improvement; advise team members and ensure all own and team activities are aligned with the overall drug development process.

• For technical development units: Develop complex methods (lab or plant); lead the optimization of project-related scientific/technical activities or processes; co-ordinate local team(s); drive development and implementation of new technologies. For GMP units: ensure compliance to cGMP

• For technology-focused role: Provide scientific and technical guidance; perform information and literature searches; actively drive knowledge exchange. Develop, mentor and coach other scientific associates; present scientific/technical results internally and contribute to publications, presentations and patents

Apply Online

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