Job Description

JOB DESCRIPTION:
Work Experience (Total number of years/ experience/ background or equivalent):

• Total experience (in years): 15
• Experience in current role (in years): 6.5 Years
• Work Background: Formulation Development, Technology Transfer, Root Cause Investigations, Project Management

Primary Job Function

• To drive technology transfer for Third party manufacturing, Loan license projects, Abbotts own manufacturing plants.
• To support Abbott site MS&T team as per requirements.
• To support Alternate supplier qualification of raw materials & API.
• To comply with the regulatory, quality, statutory, EHS and Pharmacovigilance requirements.

Core Job Responsibilities -

• To perform effective gap analysis between sender & receiving site in process & equipment and to provide solution for smooth technology transfer.
• To prepare Master formula record & Technology transfer protocol for products identified for transfer.
• To Review receiving sites draft documents pertaining to manufacturing, process validations & analysis of product under transfer & executed documents post validation.
• To execute validation batches and to ensure validation batch reproducibility is demonstrated in commercial batches.
• To review executed process validation batch documents & support FLQR approvals. To service, trouble shoot and solve production process problems at manufacturing site.
• To acquire sufficient process understanding at current manufacturing site to enable effective investigations of commercial batch failure or market complaints and to contribute towards appropriate CAPA.
• To carry out due diligence of new sites with focus on formulation and required infrastructure and support new product acquisitions & product certifications.
• To work towards improving knowledge base for handling of Parenteral products in addition to the other dosage forms such as Oral solids, Oral liquids, Topicals, etc.
• To extend technical support and batch execution (as applicable) to activities like Alternate Supplier Qualification and Material Harmonization. To initiate, review & approve change controls in Soltraq.
• To author, review & approve technical documents in Darius. To extend support to NPI activities like Dossier review, Product certification & FLQR approval.
• To extend support to I&D for new product launches, review & approval of technical documents, batch monitoring & FLQR approval.
• To keep track of ongoing projects and update senior management beforehand.

The base pay for this position is N/A
In specific locations, the pay range may vary from the range posted.
JOB FAMILY: Manufacturing
DIVISION: EPD Established Pharma
LOCATION: India
Mumbai : BKC Building
ADDITIONAL LOCATIONS:
WORK SHIFT: Standard
TRAVEL: Not specified
MEDICAL SURVEILLANCE: Not Applicable
SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)