Deputy Manager

7 days ago


Indore, India Par Formulations Full time

Description

To perform product transfer activities of injectable and complex injectable assigned by Manager/Sr. Manager /Designee. Execution /Supervision of Trial, Engineering/Scale-up & Submission/ Exhibit batches. To perform all activities related to Technology transfer at site (As applicable) To compile and interpretation of Scale up trials/Scale up batches/Submission batches results, drawing conclusions. Prepare & review technology transfer documents i.e. Product risk assessment, Batch manufacturing & packing records, Hold time study protocol & report, Scale-up batch protocol & report etc. (as applicable). Handling of QMS documents like Change control, Investigations, Deviation, CAPA, etc., (As applicable) Initiation of request for Creation / Extension of Material code & prepare RM & PPM. Day to day work on SAP, document compliance manager and track wise or other relevant software which are used for documentation work. Bachelor of Pharmacy / Masters of Pharmacy (Full Time) Required Experience: 8 – 12 yrs. Good exposure on technology transfer of Simple & Complex Injectable / sterile products. Technology transfer experience for regulated market in simple and complex injectable / sterile products. Hands on Experience with GMP Documentation and QMS activities.

Commitment to Diversity, Equity, and Inclusion:

At Endo, our diversity unites and empowers us as One Team, and we are committed to cultivating, and valuing, each person’s unique perspective. We actively promote a culture of inclusion that draws strength from our broad spectrums of diversity, including race, ethnicity, religion, gender identity or expression, national origin, color, sexual orientation, disability status, age, and all our other unique characteristics, qualifications, demonstrated skills, achievements, and contributions, backgrounds, experiences, cultures, styles, and talents.



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