Participate in DMM activities including data review and query management, assist with quality database design including documentation, testing, validation, and ...
Why Patients Need You Were looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local a...
Why Patients Need You Were looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local a...
ROLE SUMMARY This position will provide statistical support for clinical Phase I-IV projects in Vaccine Research and Development. The successful candidate will ...
To function as regulatory team lead for Annual Report (AR) team, working with Global Product Owners (GPO) and Cross Functional Team to ensure quality preparatio...
Understanding of pharmaceutical manufacturing, packaging, quality assurance. Understanding of visual inspection operation. Good interpersonal skills. Good peopl...
Why Patients Need You Were looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local a...
Why Patients Need You Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated...
Graduate or Diploma Engineer in Electronics and Instrumentation Engineering / Electrical and Electronics Engineering with specialization in Instrumentation. Kno...
Position Purpose Individual filling the position are responsible for the project management of safety aggregate reports submitted to regulators that include the...
Why Patients Need You Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, ...
Why Patients Need You Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated...
Role Summary The Assistant Manager, Regulatory Affairs CMC, Upjohn, possesses CMC regulatory knowledge and quality expertise to independently prepare regulatory...
Role Summary Develop CMC regulatory strategies, submissions and compliance activities for pharmatherapeutic development programs and commercial products support...
Why Patients Need You Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated...
ROLE SUMMARY summarize the primary purpose & key accountabilities of the role. Summary should be concise and include strategic information that would attract ca...
Having Good hand and IN and Out knowledge of SAP system. Having knowledge on SAP troubleshooting, stock clearance, WH SAP management etc. Troubleshoot and solve...
Why Patients Need You Were looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local a...
What You Will Achieve You will represent Upjohn Pfizer as CMC Author/Strategist in the regulatory affairs team. Your understanding of regulatory procedures...
ROLE SUMMARY Will be technically responsible for working on the synthetic organic Chemistry projects involves optimization of small molecules, macromolecules an...
