Senior Executive/Executive-Engineering OSD (Process)

Job content

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients.

Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively.

The manufacturing location at Mysore is spread over 69 acres and it’s a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets.

• KEY ACCOUNTABILITIES
  

Accountabilities

Scope of work

• Control
• To ensure timely execution of preventive maintenance of machines as per schedule.
• To ensure minimum break down and schedule condition monitoring and proper selection of spares.
• Analysis of breakdown, failures, corrosion and chronic problems in the Plant.
• To co-ordinate with various contractors, consultants to ensure smooth and fast working.
• Conceptualize the schemes related to energy conservation, cost reduction.
• Standardization
• Reduction of inventory by standardization of spares.
• Maintenance
• To maintain the preventive maintenance and B/D maintenance records as per SOP’s.
• To impart training to all subordinates related to Safety, Health and Environment and Effective maintenance practices and tools.
• Employee Training and Development
• To prepare the complete cGMP and SOP compliances documents related with engineering departments.
• KEY INTERFACES
  

External Interfaces

Internal Interfaces

• Vendors
• Auditors
• Equipments
• Instruments
• EDUCATION & EXPERIENCE
  

Education Qualification (Highest) with target Institution(s) :

B.E (Mechanical)

Desired Certifications :

Experience Range :

5-8years

No. of years post Highest Qualification :

Desirable Experience :

5-8years of experience in Validation and Maintenance of Production Machinery

• SKILLS REQUIRED
  

Skills

Description

Proficiency Level

(General Awareness; Working Knowledge; Functional Expert; Mastery)

Functional Skills :

• Good knowledge of preventive & breakdown maintenance of Production Machineries.
• Knowledge of Validation of Production machinery,
• Exposure towards cGMP requirement as per regulatory norms like USFDA, MHRA etc.
  

Functional Knowledge

Behavioral Skills :

• Multitasker who can work independently
• Ability to clearly explain technical subject matter to a wide range of audiences
• Good Interpersonal skills
• Desire and ability to learn new skills
• Knack for problem solving
  

Working Knowledge

• General Awareness : Knows the fundamental or general understanding of concepts.
• Working Knowledge : Has broad job knowledge; knows and applies the full range of concepts and practices. Has broad / working knowledge of the subject. Candidate should use these concepts in day to day practices.
• Functional Expert: Candidate is certified functional expert with strong knowledge on concepts.
• Mastery: Candidate is subject matter expert and has command over the subject/ concepts.
  

Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R&D works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services.

JGL’s full-fledged Regulatory Affairs & IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market.

Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18.

Kindly refer www.jubilantpharma.com for more information about organization.