Jubilant Generics Limited Pharma Job Opening – Executive
Jubilant Generics Limited Pharma. MSc Job. Research Job. Application is invited along with complete bio-data for the one post of Officer. Interested and Eligible candidates may apply Online. Check out all the details on Rasayanika.com.All the latest jobs related to chemistry & Pharma can be found.
LOCATION: Roorkee – Plant, IND
COMPANY: Jubilant Generics Limited
FUNCTION: Technical Services
JOB-DESCRIPTION:
Jubilant Generics Limited (‘JGL’) is a wholly-owned subsidiary of the Company through Jubilant Pharma. JGL owns two manufacturing facilities; one at Nanjangud, Karnataka and another at Roorkee, Uttarakhand which are engaged in APIs and Dosage Forms business, respectively.
The manufacturing location at Nanjangud spread on 69 acres is engaged in manufacturing of APIs and caters to the sales worldwide. API portfolio is focused on Lifestyle driven Therapeutic Areas (CVS, CNS) and also targets complex and newly approved molecules. The company is market leader in four APIs and is amongst the top 3 players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand with 5 acres of infrastructure is USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA audited and approved. This
business focusses on B2B model for EU, Canada and emerging markets. It has capabilities to develop multiple dosage forms including Oral solid, injectable and ophthalmic dosage forms. Revenue of the company during the Financial Year 2016-17 was 10,726.09 Million as compared to 9,197.82 Million during the Financial Year 2015-16.Summary of Job
To ensure smooth manufacturing operation with international regulatory standards & to build a team capable of delivering Business Goals in Formulation Business.
Key Responsibilities
- Responsible for planning, coordinating and managing process and packing validation activities to ensure successful and timely launch of approved products.
- Responsible for overseeing the execution of post approval batch manufacturing and packaging activities on the shop floor. This includes scale-up, verification, validation batches etc.
- Responsible for preparation and review of documents such as Batch record, Protocols, reports etc. pertaining to post approval activities involving process scale-up, verification, validation, stability and hold time study.
- Responsible for conducting and reviewing investigations results from OOS results and deviation involving batch failures at validation and commercial stage.
- Review of batch manufacturing and packaging records for Exhibit, scale-up, verification and validation batches.
- Preparation and review of SOPs related to Technical Services and validation department.
- Responsible to meet defined compliance procedures related to validation activities as per cGMP and laid down standard.
- Responsible to impact and evaluate training of Technical services and validation department.
- Coordination with different department to meet the timely execution of validation batches.
Qualification & Experience
M Pharma in Pharmaceutics/Pharm. Technology/Industrial Pharmacy with 5-7 years of experience in Validation/Technology Transfer of Pharma unit with strong exposure to all regulatory requirements.
Key Competencies
Exposer of different regulatory guidelines such as ICH, USFDA, MHRA, ANVISA.
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