Submitting more applications increases your chances of landing a job.

Here’s how busy the average job seeker was last month:

Opportunities viewed

Applications submitted

Keep exploring and applying to maximize your chances!

Looking for employers with a proven track record of hiring women?

Click here to explore opportunities now!
We Value Your Feedback

You are invited to participate in a survey designed to help researchers understand how best to match workers to the types of jobs they are searching for

Would You Be Likely to Participate?

If selected, we will contact you via email with further instructions and details about your participation.

You will receive a $7 payout for answering the survey.


User unblocked successfully
https://bayt.page.link/4N8RTD33Yx78jsjTA
Back to the job results
Other Business Support Services
Create a job alert for similar positions
Job alert turned off. You won’t receive updates for this search anymore.

Job description

Use Your Power for Purpose



As a Senior Associate, you will play a crucial role in improving patients' lives while working at Pfizer. Your contributions will directly impact the development and delivery of innovative solutions that enhance the quality of life for patients worldwide. Join us in our mission to bring breakthroughs that change patients' lives.




What You Will Achieve



In this role, you will:



  • Perform analytical method transfer strategies from site to site and PSci to site.



  • Prepare & execute study protocols/reports for AMTEs



  • Stratification of data from engineering/EB/PVs for CQA trend analysis.



  • Theoretical & practical knowledge on working principle of analytical instruments- FTIR, UV, IR, HPLC, GC with minimum 5 years of relevant experience.



  • Understanding on the purpose of different method validation parameters and ICH guideline requirements.



  • Reviewing/providing feedback and technical/scientific support on project deliverables, i.e. remediation initiatives, plan reports, etc.



  • Theoretical knowledge on titration, LOD and understanding the working principle of DSC and TGA etc.,



  • To be able to perform the compilation of methods and its requirements.



  • Ensure compliance to cGMP/ cGLP, organizations procedures and practices.



  • Ensure effective safety systems are implemented in the premises.



  • Partnering with manufacturing to meet the production schedule, ensure commercial supply and uphold quality standards.



  • Perform & review trending and monitoring of critical quality attributes/critical process parameters to maintain product quality and to control process drift.



  • Identifying and implementing potential process improvements in conjunction with manufacturing operations.



  • Assisting in documenting changes/updates to manufacturing processes and working with manufacturing, engineering, and validation to implement those changes.




Here Is What You Need



  • M. Pharm/M.Sc with minimum 5 years of pharma experience



  • Experience in Analytical Development/ validation / Technology Transfer of Injectable formulations to cater regulated markets, essentially experience in Plant Technology Transfer support in Injections including process validation.



  • Understanding of DMAIC methodologies (M1/M2/M3)



  • Trained on Minitab tools







Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.





Engineering


This job post has been translated by AI and may contain minor differences or errors.

You’ve reached the maximum limit of 15 job alerts. To create a new alert, please delete an existing one first.
Job alert created for this search. You’ll receive updates when new jobs match.
Are you sure you want to unapply?

You'll no longer be considered for this role and your application will be removed from the employer's inbox.