レベル: Mid-Senior level

ジョブタイプ: Full-time

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仕事内容

Jubilant Life Sciences Limited is one of the India’s leading corporate and a highly treasured brand throughout the world. The organization has a presence in the fields of Pharma and Life Sciences, Agri & Performance Polymers, Food & Retail, Oil & Gas and Services.

  • Jubilant Life Sciences Limited is an integrated global pharmaceutical and life sciences Company engaged in Pharmaceuticals, Life Science Ingredients and Other businesses including Drug Discovery Solutions and India Branded Pharmaceuticals.
  • The Pharmaceuticals segment, through its wholly owned subsidiary Jubilant Pharma Limited, is engaged in manufacturing and supply of APIs, Solid Dosage Formulations, Radiopharmaceuticals, Allergy Therapy Products and Contract Manufacturing of Sterile Injectable and Non-sterile products through 6 USFDA approved manufacturing facilities in the US, Canada and India and a network of over 50 radio-pharmacies in the US.
  • The Life Science Ingredients segment, is engaged in Specialty Intermediates, Nutritional Products and Life Science Chemicals through 5 manufacturing facilities in India.
  • The Drug Discovery Solutions business, provides proprietary in-house innovation & collaborative research and partnership for out-licensing through 2 world class research centers in India.
  • Jubilant Life Sciences Limited has a team of around 7,700 multicultural people across the globe and is committed to deliver value to its customers across over 100 countries.
  • The Company is well recognized as a ‘Partner of Choice’ by leading pharmaceuticals and life sciences companies globally.
  • Ranked No. 6 amongst top 10 Global Pharmaceutical outsourcing players as per UNCTAD World Investment Report 2011
  • Reputed and High Quality relationships with 19 out of the top 20 Pharmaceutical companies, and 6 out of the top 10 Agrochemical companies globally
Vision

  • To acquire and maintain global leadership position in chosen areas of businesses
  • To continuously create new opportunities for growth in our strategic businesses
  • To be among the top 10 most admired companies to work for
  • To continuously achieve a return on invested capital of at least 10 points higher than the cost of capital.
Our Promise

We will, with utmost care for the environment and society, continue to enhance value for our customer by providing innovative products and economically efficient solutions; and for our stakeholders through growth, cost effectiveness and wise investment of resources.

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

Position

Sr. Executive- FC-Batch Process

Grade – A4

Business Unit / Function

Production – Fine Chemicals

Location

Bharuch

Reports to

Section Incharge

Summary

Summary of Job

(Purpose/ objective of the job Department organogram to be enclosed)

  • This role is responsible to coordinate the GMP and regulatory compliance at plant level to ensure full compliance with ICH guidelines, FSSC and regulatory standards requirements.
Key Responsibilities

(Performance Indicators)

  • Preparation and review the system based SOP`s.
  • Preparation, Evaluation and closer of change controls, CAPA, Market complaint & deviations
  • Running the plan as per written SOP/WI.
  • Batch entry in ERP (SAP / BAAN)
  • Preparation of the daily production report and commercial report.
  • Compliance with company quality policy in all aspects.
  • Review raw material, intermediate, finished product specifications.
  • Generate, review, and approve GMP documentation such as Standard Operating Procedures, non-conformance reports, Out of specification results.
  • Participate in daily activities, ensuring cleaning, environmental monitoring and maintenance schedules are up to date and maintained to GMP standards. Area and equipment logbooks completed.
  • Implements the manufacturing plan and establishes procedures for maintaining high standards of manufacturing operations to ensure that all products confirm to established customer and company quality standards.
  • Sound Knowledge in Equipment qualification & Process Validation
  • Safety of man and machine and housekeeping of the plant.
  • Avoiding any abnormality in the plant by frequent checks.
  • Ensure the required quality and safety standards are achieved and maintained with respect to cGMP operating procedures, all cGMP batch manufacturing documentation, area housekeeping in cGMP suites, SHE (Safety, Health & Environment), and compliance with the relevant regulatory (ICH Guidelines/MHRA).
  • Training and development of team members.
  • To implement ISO 9001, ISO-14001, SMS -45001, TPM.
  • To implement 5S+1S in plant and office.
No. of Reportees

2-3

Qualification & Experience

  • B. Tech (Chemical Engineering) with 3 – 5 years or B.Sc. (Organic) with 6-7 of experience in Fine Chemical/ Bulk drug / API Plant.
Key

Competencies ( Technical, Functional & Behavioral)

  • Knowledge of Fine Chemical/ batch chemical process.
  • Practical experience in handling reactors, centrifuges, filters used in API / Bulk drug / Batch chemical plants.
  • Exposure in ERP or like software.
  • Computer proficiency
  • Technical knowledge.
Approval HoD / CoD Unit HR
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締切: 13-06-2024

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