R&D Knowledge and Learning Manager (Content Development) Job at Amgen (Hyderabad)

R&D Knowledge and Learning Senior Manager (Content Development)

As a Senior Manager – TA/Product Knowledge & Learning (Content Development), you...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree with 10+ years of clinical/scientific affairs experience
Master’s degree with 12+ years of experience
Bachelor’s degree with 15+ years of experience
Strong experience in learning content development, visual storytelling, and instructional design
Proven ability to create infographics and visually compelling learning assets
Excellent scientific writing, editing, and presentation skills
Experience supporting global stakeholders in a matrixed environment
Strong project management and attention to detail

Job Responsibility

Support U.S. Senior Managers (Product/TA Learning Leads) by developing learning content aligned to product strategy and learning objectives
Work closely with the global K&L Sr Managers to create new learning materials while also refreshing and updating existing content
Design and develop a wide range of learning materials, including: Slide decks, facilitator guides, and participant materials, Infographics, visual summaries, and quick-reference tools, Content to support congress-related trainings
Translate complex scientific, clinical, and product information into clear, concise, and visually engaging content
Apply adult learning principles and instructional design best practices to enhance learner engagement
Incorporate interactive elements to support learning calls and virtual learning sessions
Manage content development timelines, version control, review cycles, and documentation
Review and edit content to ensure scientific accuracy, consistency, compliance, and alignment with Amgen standards
Incorporate feedback from U.S. Senior Managers and learners to continuously improve content quality
Maintain organized repositories of approved learning content and updates

R&D Learning Enablement Specialist

Part of Amgen's R&D Strategy & Operations organization, the R&D Knowledge & Lear...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 2 years of related experience
Master’s degree and 6 years of related experience
Bachelor’s degree and 9 years of related experience
Experience in regulated learning environments
Familiarity with AI-enabled learning operations or digital learning tools
Strong organizational and project coordination skills
Knowledge of LMS and learning logistics
Knowledge of project management and continuous improvement methodologies
Data and reporting literacy
proficiency in dashboards and analytics

Job Responsibility

Lead the design and delivery of onboarding, development, and upskilling programs for CfDA teams in direct partnership with CfDA Subject Matter Experts
Build structured, role-specific onboarding experiences that accelerate time-to-productivity and deepen engagement
Continuously refine onboarding and learning pathways using learner feedback, data insights, and business priorities
Partner with local learning enablement team and CfDA Subject Matter Experts to coordinate end-to-end delivery of learning events and programs, ensuring alignment with CfDA needs
Collaborate with content owners and subject matter experts to update, localize, and sustain learning content
Apply data and analytics to monitor participation, effectiveness, and impact of learning experiences
Partner with CfDA teams and global Learning Business Partners to identify learning needs and implement targeted enablement solutions
Serve as a key point of contact for onboarding and learning initiatives within CfDA, ensuring consistent communication and alignment
Manage learning calendars, scheduling, and logistics in partnership with the R&D Learning Enablement team
Leverage automation and AI-enabled tools (e.g., scheduling bots, analytics dashboards) to improve efficiency and learner experience

Working Student Digital Learning – R&D Product Support

As a working student you will have the opportunity to substantially shape the le...

Location

Germany , Munich

Salary:

Not provided

Brainlab

Expiration Date

Until further notice

Requirements

Currently enrolled student of media design, technical documentation, education management, or other content creation or education related program
Fluent written and spoken English communication skills
Basic MS Office knowledge
Knowledge on Adobe premiere, Camtasia or Articulate 360 is a plus
Ability to support the design and development of a new learning program
Image and video editing skills
Basic knowledge of Learning Management Systems and how they work.

Job Responsibility

Create and update media assets for internal training material
Explore and implement new and existing digital training formats
Participate in projects.

What we offer

A mutually supportive, international team
Opportunity to build career experience in an exciting international company with a lasting impact on medical technology based in Munich
Flexible working hours
Parking garage and safe underground bike storage
Award-winning subsidized company restaurant and in-house cafes
Variety-rich fitness program in our ultra-modern 360m2 company gym
After work and company events

Working Student Digital Learning – R&D Product Support

As a working student you will have the opportunity to substantially shape the le...

Location

Germany , Munich

Salary:

Not provided

Brainlab

Expiration Date

Until further notice

Requirements

Currently enrolled student of media design, technical documentation, education management, or other content creation or education related program
Fluent written and spoken English communication skills
Basic MS Office knowledge
Ability to support the design and development of a new learning program
Image and video editing skills
Basic knowledge of Learning Management Systems and how they work

Job Responsibility

Create and update media assets for internal training material
Explore and implement new and existing digital training formats
Participate in projects

What we offer

Flexible working hours
Parking garage and safe underground bike storage
Award-winning subsidized company restaurant and in-house cafes
Variety-rich fitness program in our ultra-modern 360m2 company gym
After work and company events

Parttime

Clinical Genomics Scientist, Oncology

BillionToOne is looking for a Clinical Genomics Scientist, Oncology to help driv...

Location

United States , Menlo Park

Salary:

158401.00 - 179521.00 USD / Year

BillionToOne

Expiration Date

Until further notice

Requirements

Ph.D. in Human Genetics, M.S. in Genetic Counseling, or related field
2+ years of experience in somatic variant interpretation based on ACMG/AMP guidelines in a clinical setting (alternatively, 1+ years of germline variant interpretation and 1+ years of somatic variant interpretation experience)
Hands-on experience working with human mutation databases (COSMIC, ClinVar, OncoKB), functional annotation sources (dbSNP), and genome browsers (UCSC)
Familiarity with IGV and BAM file analysis and data-minded willingness to learn to use basic bioinformatics tools, with technically minded insights
Knowledge of cancer somatic mutation and signaling pathways (e.g., which mutations have FDA approved drugs, Phase II/III clinical trials, which mutations are considered “hot targets” for drug development, etc.)
Exceptional attention to detail to follow highly detailed SOPs and strong organizational skills to track and manage clinical reporting and product improvement projects
Excellent communication skills and ability to work collaboratively with cross-functional teams
Operationally-defined flexible schedule, including weekends, as dictated by clinical reporting needs

Job Responsibility

Somatic variant interpretation and data review: Perform somatic-based variant interpretation, diving into the literature and databases to classify variants and match treatments for reporting, performing verification as required with BAM file analysis
Clinical report drafting: Carefully draft reports for each requisition primarily using in-house reporting API, working closely with the engineering and QA teams on reporting, and the laboratory directors on report language
Somatic mutation interpretation and reporting policy development: Work closely with lab directors, R&D, medical, and other related functions to develop and modify the somatic interpretation SOPs in accordance with ACMG/AMP guidelines, and the latest published literature
Content curation: Contribute to curation of gene-level content such as domain and critical residue curation
Molecular tumor board: Serve as a subject matter expert in consulting with the medical science liaison team, and presenting in molecular tumor boards to facilitate knowledge sharing
Contribute to oncology R&D: Work closely with the R&D team to help with somatic oncology based projects, providing expertise on variant interpretation, biological pathways/mechanisms, and other gene/variant-level reviews and analyses

What we offer

Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients
Open, transparent culture that includes weekly Town Hall meetings
The ability to indirectly or directly change the lives of hundreds of thousands patients
Multiple medical benefit options
employee premiums paid 100% of select plans, dependents covered up to 80%
Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%)
Supplemental fertility benefits coverage
Retirement savings program including a 4% Company match
Increase paid time off with increased tenure
Latest and greatest hardware (laptop, lab equipment, facilities)

Fulltime

Senior Manager, Hub Labeling

Is responsible for executing the content management of LPDs, LLDs and PLDs for n...

Location

Australia , Sydney

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Life sciences, pharmacy graduate or equivalent
or equivalent relevant professional experience
Advanced academic qualifications/degree such as PhD
Demonstrated ability to develop strong and positive working relationships across multiple cultures and locations
Demonstration of attention to detail and problem-solving skills
Proven technical aptitude and ability to quickly learn new software
Proven technical aptitude and ability to quickly learn regulations and standards
‘Hands on’ registration experience associated with development, maintenance and commercialization activities within Regulatory Affairs
preferably from the perspective of a Country office or Regional Regulatory Strategy important and advantageous especially with the perspective of the implications of a Core Data Sheet on LPDs
Ability to understand, assess and manage the regulatory implications of product strategy with regard to the product label

Job Responsibility

Is responsible for executing the content management of LPDs, LLDs and PLDs for nationally registered products for their assigned products across multiple countries/regions
Acts as a subject matter expert for local labeling throughout the organisation, leading or assisting in the most complex labeling projects or initiatives, and contributing to the use and development of current and new tools, technologies and processes to support global label development, submission and approval
Sharing of intelligence and contribution to knowledge resources is also a key part of the role
The Senior Manager is proactive in gathering, assessing and disseminating regulatory intelligence for use by the labeling managers as well as for use in strategic decision-making at the global group level
The Senior Manager will insightfully seek technology solutions leveraging process automation and Artificial Intelligence (AI)
May lead/manage projects
May supervise/lead colleagues/teams
May act as delegate/deputy for the TLs
To utilize regulatory labeling expertise to review, develop and deliver labeling documents for submission to the Regulatory Authorities across markets/regions, requesting medical advice and input from other functions as appropriate
To support provision of other deliverables within the scope of ILG responsibilities e.g. readability testing

What we offer

Paid parental leave
Access to Health & Wellness apps
Career Growth Experiences program
Recognition & rewards program
Paid volunteer days
Life Insurance Benefits
Pfizer Learning Academy access to top content providers
Access to flu vaccines & skin checks
Options to purchase additional leave
Salary packaging & novated lease options

Fulltime

Field R&D Lead Data Scientist - Industrial Focus

Our global Field R&D team is a central part of the company strategy. The team fo...

Location

United States , Remote

Salary:

149665.00 - 269396.00 USD / Year

Cloud Software Group

Expiration Date

Until further notice

Requirements

5+ years of experience in advanced data analytics and delivery of demonstrations, projects, engagements or deployed software applications
5+ years of experience in applying analytics to industry verticals such as Energy, Manufacturing, or similar
Superior communication and storytelling skills with data
Capability to formulate a real-world problem into a mathematical equivalent, propose various solutions, compare and contrast them, deploy the solution, validate the results, and present the results to technical and non-technical stakeholders
5+ years of experience with Python or R and some knowledge of SQL
Excellent communication and collaboration skills, with the ability to work effectively in a team environment and communicate technical concepts to non-technical stakeholders
Strong problem-solving skills, with the ability to identify key areas for improvement and develop data-driven solutions to address them
A Master’s or higher degree in STEM (Computer Science, Statistics, Data Science, Engineering, Science, or related analytical field of study) with graduate classes in statistics and data mining

Job Responsibility

Delve deep into energy, manufacturing, or similar types of analytical and data science challenges
Engage with customers through presales support and post-sales success projects
Perform and guide R&D topics in the field of applied machine learning and AI
Create reusable data models, workflows and test suites in order to streamline project delivery
Provide input into product management and engineering for the product roadmap
Innovate in the areas of application and deployment of machine learning
Tool Kit Development: create demos and templates with data science libraries
Technical marketing: create white papers, blogs and content for the Spotfire user community
Represent the team as a speaker or instructor in industry events and external conferences
Participate in technical customer engagements through understanding Spotfire use cases, providing guidance, and building prototypes

What we offer

Healthcare
Life insurance
Disability benefits
401(k) plan and company match

Fulltime

Non-Pharma Global Regulatory Affairs Specialist

The Global Regulatory Non-Pharma Specialist manages regulatory documentation and...

Location

Italy , Bologna

Salary:

Not provided

Alfasigma

Expiration Date

Until further notice

Requirements

At least 5 years’ experience in Regulatory Affairs preferably within the food supplements, medical devices, and cosmetics sectors
Exposure to regulatory operations or documentation in EU and/or RoW markets or similar experiences is preferred
Advance degree in Life Sciences, Pharmacy, Chemistry, or a related field
Relevant certifications in Regulatory Affairs are considered a plus
Good knowledge of EU regulations for medical devices (MDR, MDD) and relevant legislation for food supplements and cosmetics
Strong attention to detail, time management and organizational skills
Willingness to learn and ability to work effectively in a team-based environment
Strong communication and interpersonal skills
Proficiency in Microsoft Office Suite and familiarity with document management systems
Fluent in English, both written and spoken

Job Responsibility

Contributing in a cross-functional team to provide the necessary regulatory input for the development of new projects
Support regulatory strategies by providing impact assessments
Collaborate actively with the Research & Development team to integrate regulatory requirements during the design and development of assigned products
Prepare, organize and submit regulatory documentation for submission and maintenance of dossiers for the projects assigned
Coordinate with local affiliates and global stakeholders to ensure submissions are aligned with timelines and business priorities
Manage multiple tasks in a fast-paced environment while keeping on task and to the company’s quality standards
Contribute to the preparation of regulatory project updates in internal meeting and governance committee providing regulatory input and flagging risks
Assist colleagues with administrative tasks
Execute defined regulatory tasks within scope and deadlines under the guidance of the Head
Review and validate commercial artwork, packaging, and labeling in compliance with EU Regulations, ensuring timely product launches

What we offer

Competitive salary
Comprehensive benefits
Extensive opportunities for professional growth and development

R&D Knowledge and Learning Manager (Content Development)

Amgen

Location:
India , Hyderabad

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
May 14, 2026

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