Senior Scientist I (PS&T)
Abbott
5 - 10 years
nan
Posted: 22/11/2024
Job Description
JOB DESCRIPTION:
Purpose of Role
Injectables, Biosimilars expertise required, In addition, expertise on Oral dosage forms (Technology transfer & Project Management).
- Providing technical support to Abbott manufacturing facilities and Third-Party Manufacturers (TPM' s) in the region. Collaboration with Manufacturing, Supply Chain, Commercial, Quality Assurance and Regulatory Affairs is critical to the success of this role.
- End to end project management of technology transfers and Alternate source qualifications in the region METAP-CIS
- Troubleshoot the commercial manufacturing issues to avoid the supply chain disruption.
- Support the product localization considering cost estimates// regulatory requirement, business plans, timelines and contingency plans for responsible projects in areas of CIP/ Alternate Vendor Development/ Gross Margin Improvement/ Supply
Minimum Education Qualification for the role
Post Graduation in Pharmacy (Pharmaceutical Science)
Minimum Experience/ background for the role
- Sound knowledge of formulation development (Research & development), manufacturing process (understanding of commercial equipment), Hands on experience with Alternate source qualification for API, Excipients (functional & non-functional) and packaging materials of Injectable formulations, Biosimilars and Oral Dosage forms.
- Have the basic understanding and expertise of the formulation / product behavior to mitigate the process related risk.
- Keeping up good contacts with CFT team members and work closely to meet the role responsibility.
- Can exhibit smart working capabilities, be Agile, to meet the expectation.
Core Responsibilities
- Expertise in Injectables, Biosimilars as primary requirement and experience in handling Oral dosage forms as additional requirement.
- Providing technical support to Abbott manufacturing facilities and Third-Party Manufacturers (TPM' s) in the region. Collaboration with Manufacturing, Supply Chain, Commercial, Quality Assurance and Regulatory Affairs is critical to the success of this role.
- Lead project management activities across Egypt to ensure product reliability, support portfolio growth, cost improvement (ASQs, Tech Transfers, Compliance and Continuous Improvement)
- The responsibilities of this role include the technical support for internal and external manufacturing within the region as below:
- Support business decision-makers in terms of resource allocation, risk management, collaboration, and prioritization.
- Operational technical support to ensure product reliability, support portfolio growth, cost improvement by optimize.
- Lead Technology transfers, ASQ (API Supplier) qualifications, Localization Programs, Gross Margin Improvements, etc.
- Responding to technical issues resulting from manufacturing, compliance, or regulatory CMC deficiencies (Biowaiver, IVIVC & technical justification based the regulatory query).
- Lead technical Due diligence of products, Third party manufacturing sites before selection of manufacturing sites of finalising a product deal.
The base pay for this position is
N/AIn specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Manufacturing
DIVISION:
EPD Established Pharma
LOCATION:
India > Salcette : Goa Factory
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 25 % of the Time
MEDICAL SURVEILLANCE:
Not Applicable
SIGNIFICANT WORK ACTIVITIES:
Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)
About Company
Abbott is a global healthcare company developing medical devices, diagnostic tools, nutritional products, and medicines. It focuses on improving health outcomes across areas like heart disease, diabetes, and infectious diseases, with a strong emphasis on research and innovation.
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