Openings in Jubilant for Dy Manager in Quality Assurance

 

About the Company  :

The firm is one of the integrated Company having relations with top MNC's delivering them high class medicine and pesticides. The company is equipped with around 8000 employees with 2400 in North America and ~1100 in R&D. It is having its footprints in USA, India, Europe, North America and China. while connected to the top MNC's this is delivering the products with quality and competitive prices. The company have sales in about 100 countries.

The Portfolios of the firm include Solid Dosage Formulations, APIs, Radio pharmaceuticals, Advance Intermediates, Fine Ingredients, Allergy Therapy Products, Life Science Chemicals, Crop Science Ingredients and Nutritional Products. 

Jubilant is having a strong expertise in chemistry and in bio-sciences, and is continuously improving its values and strategies to deliver the ultimate outputs. The efforts of this are reported from 2003. The company having the strengths of Strong R&D team and facilities, non infringement process for product development. The company having the title of "Partner of Choice" for the TOP MNC's.

Training and Experience:

M.Sc., Training Capability

10-12 years of involvement with Pharma industry

Quality Administration framework:

Treatment of Progress The executives, Deviations, Out of Pattern, Out of Determination and CAPA connected with Plant-5 and conclusion of a similar before the item discharge.

Treatment of QMS exercises in Track Wise framework and archives through SAP framework, as appropriate. Track and complete all the QMS exercises of Plant-5 inside the due date.

Fabricating Compliances:

Checking of Assembling Interaction to distinguish the main driver for item disappointment and cleaning occurrence.

Will be answerable for performing spontaneous review on shop floor.

Yearly Item Quality Survey's:

Planning of PPQR and APR of the items produced in Plant-5.

SOP Consistence:

Planning of Value Confirmation SOPs and audit of SOPs connected with Plant-5.

Risk Evaluation:

Readiness and survey of Chance Evaluation Reports connected with Plant-5.

Item Quality Measurements:

Planning of Plant Measurements, Item Measurements for Plant-5 items and to accomplish laid out Quality measurements.

Documentation Authentic:

Authentic of progress control and other related records.

Abilities Required:

Useful Abilities:

Great Information on Administrative Rules like USFDA, MHRA ANVISA, TGA, MCC and so forth.

Information on cGMP and Quality frameworks.

Conduct Abilities:

Having great logical, correspondence and relational abilities

Apply from here