Takeda PhD Freshers Job Opening 2020 – Apply Online
Takeda PhD Freshers Job As one of the world’s leading biopharmaceutical companies, Takeda is committed to bringing Better Health and a Brighter Future to people worldwide. We aspire to bring our leadership in translating science into life-changing medicines to the next level, in our core focus areas; oncology, gastroenterology, neuroscience, rare diseases, plasma-derived therapies, and vaccines.
Job ID SR0050555
Location Lexington, Massachusetts
Job Title: Scientist
Responsibilities include:
Takeda PhD Freshers Job
- Execution of laboratory experiments to support development and validation of analytical methods for process-related impurities
- Author, review and/or approve technical documents or regulatory filings ensuring high technical standards and compliance with applicable regulatory guidelines to support analytical impurity methods. (protocols, reports, test methods, regulatory filings, etc)
- Evaluation / Implementation of new technologies
- Development, validation and transfer strategy of analytical impurity methods to support biological product release.
Responsibilities Breakdown:
Takeda PhD Freshers Job
- 50%: Planning, designing, and conducting experiments and data analysis to support the development and optimization of process-related impurity methods.
Responsible for documentation of experimental data, generation of high-quality written study protocols/development reports, and oral presentations - 30%: Design and participate in the validation and transfer strategy of analytical impurity methods to support biological product release.
- Responsible for execution and documentation of validation data, generation of high-quality written validation protocols / validation reports, and participation /leading cross-functional meetings
- 20%: Participate or lead technology working groups to evaluate and implement new technologies related to impurity related methods.
Key Skills & Competencies:
- Independently prepare, execute and document complex laboratory experiments per established company guidelines
- Takeda PhD Freshers Job Independently design and implement scientifically sound and creative solutions to a variety of problems of moderate to complex scope
- Understands and applies scientific principles, theories, concepts, practices and standards to method development
- Author and review technical documents such as protocols, reports, internal presentations
- Ability to manage externalized activities such as: method development, method validation
- Ability and willingness to gain an in-depth understanding of new technologies, method platforms, and scientific concepts.
- Hands-on experience with qPCR, ELISA, Octet/Biacore
- Effective communication skills, oral and written
- Proficient with standard computer applications
- Ability to work effectively both independently and in a collaborative cross-functional environment with internal and external partners.
- Complexity and Problem Solving
- Has sufficient expertise in multiple laboratory technologies to be a functional area resource and/or trainer
- Uses an understanding of project timelines and Pharm Sci deliverables to plan and coordinate project work with departmental and cross-functional peers (maybe outside PS)
- Takeda PhD Freshers Job Lead method development, validation, and technology transfer activities
- Identify and analyze technical problems and proactively explore/implement solutions
- Independently plan, design, execute, and analyze experimental data and provide succinct conclusions and/or recommendation
- Work closely with his/her supervisor and coworkers in managing multiple workstreams and projects. Make sound and timely decisions based on project priorities. Provide expert input to internal and external sub-teams.
- Sound knowledge of applicable regulatory guidance
Required Education and Skills:
Degree in Biology, Biochemistry or other related disciplines with minimum to some years of relevant industry experiences in analytical development.
- PhD: 0+ years
- Takeda PhD Freshers Job Key areas of expertise are the development of process-specific host cell protein (HCP)
- ELISA, DNA, residual process impurity methods and critical reagent generation/characterization with respect to regulatory guidelines
- Demonstrated experience working with plate-based immunological and molecular biology methods including ELISA, Octet protein binding assays, Host Cell Protein assays, immunogenicity assays and qPCR is essential.
- Proven record of technical expertise and troubleshooting. Proven ability to work in a fast-paced environment with demonstrated capacity to juggle multiple competing tasks and demands.
- Effective communication skills (oral and written) are essential.
Other Job Requirements
Please note that some domestic travel may be required to work with collaborators
