Senior Scientist for Pharma Candidates @ Johnson & Johnson

0 141

Johnson & Johnson

Caring for the world, one person at a time, inspires and unites the people of Johnson & Johnson. We welcome innovation—bringing ideas, products and services to life to advance the health and well-being of people around the world. We believe in collaboration, and that has led to breakthrough after breakthrough, from medical miracles that have changed lives, to the simple consumer products that make every single day a little better. Our over 125,000 employees in 60 countries are united in a common mission: To help people everywhere live longer, healthier, happier lives

In India, J&J operates as a single legal entity and consists of the 3 strategic business units: Consumer Products, Pharmaceuticals and Medical Devices, which are independently handled and report into their respective Global business segments

Job Title  Senior Scientist

Job Description:

  • Preparation of technical documents e.g. stability reports, method transfer and method validation protocol and reports, global change control, procedures, etc.
  • Review of analytical data for accuracy, compliance to quality requirements and completeness e.g. lab notebooks, raw data, LIMS entries, technical reports, etc.
  • Review of technical documents such as analytical reports, method transfer /method validation protocols, reports, etc as required.
  • Connect with internal groups, global cross functional partners for collating all information and documents required for preparing technical documentation.


Skill and Behavioral
· Excellent technical writing skills: Drafting, articulation, correctness of language, word/excel/power point formatting and use of appropriate features

· Adequate knowledge related to chemistry, analytical techniques, stability study assessment and research technologies

· Technical skills related to data review, interpretation of analytical data and accurate documentation of laboratory investigations, NC and CAPA, change control, impact assessments, etc.

· In depth knowledge of GMP, quality systems, SOPs, latest regulatory trends, and global regulations as appropriate

· Technical skills related to interpretation of analytical data and accurate documentation of laboratory investigations and non-conformances

· Ability to independently plan, prioritize and execute assigned deliverables

· Ability to connect with cross functions and global partners and collate information.

· Excellent oral and written communication skills

· Ability to connect with cross functions and global partners and collate information.

Education: Minimum Masters in Chemistry/Pharmaceutical sciences or similar technical discipline
Reporting Structure/ Reportees if any: None

Application Instructions / How to Apply:  

Internal Applicants: If you wish to apply, please consider the following information from our Policy:

We require you to have spent at least 18 months in your current position, and in good standing.

As our employee you may apply for a position without informing current manager. However, when invited to interview, then, to the extent that this is consistent with local law or practice, you are required to notify your manager prior to the interview. This notification is inspired to promote development discussions between the managers and our employees.

If you want to refer external talent for this position, please review our Global Referral Policy and submit your referral through My Career Opportunities by following the appropriate process.

External Applicants: Login to, search job matching you profile by location, keywords, requisition number.


View Notification

Leave A Reply

Your email address will not be published.