Chemistry & Pharma Team Member Post Vacancy @ Dr Reddy’s

Chemistry & Pharma Team Member Post Vacancy @ Dr Reddy’s

Chemistry Application for Team Member Position @ Dr Reddy’s. Team Member position at Dr Reddy’s, Chemistry jobs at Dr Reddy’s, Chemistry jobs at Dr Reddy’s. Applications are invited for the Team Member Position temporary position. Interested and Eligible candidates with chemistry filed may apply for this position at Dr Reddy’s. Check out all the details on the same below:

Job Title: Team Member – Ar&d, OSD- COE Formulation

Educational Qualification & Experience Required:

M. Pharm with 2-5 years of relevant experience or PhD with 1-2 yrs of relevant experience in Analytical R&D.

Key Responsibilities:

• Reverse engineering Physical and chemical analysis required for the proposed product and excipients.
• Develop analytical methods for drug substance as well as drug product.
• Technical evaluation of filed products- Conduct literature study, collect and Strategisation for identified product.
• Identification of critical material attributes- Perform intrinsic dissolution of API having differ solid state properties,
• Physical characterization of RLD or competitor formulation for particle size & shape analysis, Polymorph/form identification, amorphous/crystallinity assessment; API excipient distribution & interactions.
• Work in collaboration with experts and different labs (with in DRL/Outside CRO) on thermal, spectroscopy, imaging techniques to elucidate understanding on characteristics and interaction of API and excipients.
• Analyze and interpret analytical data; summarize and report with recommendations on the various analyses performed
• Validate methods developed for reverse engineering with cluster team or outsourced
• laboratory based on the scope & regulatory submission needs
• Perform physicochemical drug substance characterization including crystallinity assessment, solubility determination and morphological characterization
• Perform pre-formulation related activities such excipient compatibility studies on need basis
• Develops understanding on process induced transformation on solid state and bulk properties on drug substance and in drug excipients combination
  Develop/ screen new method using specialized chromatographic technique such as GPC/MALS, GPC/RI HPLC-RI etc., for quantitative estimation of excipients in the RLD formulation
• Extraction & deformulation of functional & non-functional excipients in RLD or competitor product for quantitative analysis
• Develop discriminatory dissolution method on need basis for problem solving in Bio study and in dosage form design
• Preparation of working standards for method development purposes.
• Prepare and execute the method validation protocols as per SOP for reverse engineering techniques established.
• Maintenance of lab compliance such as calibration schedules etc,
• Preparation of SOPs and other documents.

  Skills Required:

• Should be capable of handling different techniques like GC,HPLC-RI,GPC, XRD etc for method development activities. Hands on experience on NIR,Porosimeter etc is an added advantage.
• Works closely with a team of high-performing scientists responsible for the development.
• Working knowledge of common analytical methods and procedures, and expertise in
• calibrating and operating analytical instruments required.
• Ability to learn new technologies and strong computer, scientific, and organizational skills, along with necessary skills for investigation, evaluation, and analyse the project related issues at early development stage.
• Should perform additional tasks as required for the position.
• Should have the knowledge on both formulation as well as analytical aspect.
• Should be able to prioritize tasks and manage multiple tasks simultaneously.
• Should have sound knowledge on instrumentation and wet analysis principles.
• Should have basic knowledge on method development.
• Should have hands on experience on Method validation and analysis of various dosage forms.
• Should have capability to handle the analytical trouble shooting during the analysis.
• Should have experience and capable of online documentation and monitoring lab compliance.
• Should have good knowledge of cGMP and cGLP and other regulatory guidelines such as ICH etc.

  Key Personal Attributes:

• Should have good communication & interpersonal relationships and writing skills.
• Flexibility to work with cross functional teams
• Should be good team player, patient and good listener
• Should have positive attitude and Analytical thinking and innovative thinking for trouble shooting.
• Ability to work independently and as part of a team.

Apply Online

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