Walk in at USFDA & MHRA approved manufacturing facility of Inventia Healthcare

Pharma Admission

pharma admission

 

Inventia Healthcare Ltd is a pharmaceutical development and manufacturing company headquartered in Mumbai with over 30 years of operations. Our focus is on development of value added oral solid dosage formulations (“OSDF”). We have fully integrated manufacturing support systems at Ambernath which is approved by prominent regulatory authorities. Our facility is focused on manufacturing of value added OSD including capsules, tablets, DC Granules and pellets. With an ever-growing portfolio of niche products, Inventia’s presence has progressively increased to 28 countries globally. We intend to leverage our existing relationships and our business experience to explore opportunities in the high growth injectables business. Inventia also intends to leverage its capabilities to explore growth opportunities in the nutraceuticals segment by developing and manufacturing branded nutraceutical ingredients as well as finished nutraceutical products in the domestic and international markets.

As a part of expansion phase for state or art USFDA & MHRA approved manufacturing facility

 

Post: Production: Technician/Machine Operator/Senior Technician

Education & Experience: ITI /D.Pharm with 2-5 years of experience

No. of position & Area: 15 (Tablet), 10 (Pellet), 5 (Packaging)

Experise required:
Tablet: Sejong (Bl-Layer), Compression, Coating
Pellet: Capsule Filling, , APEG machine, Coating Pan
Packaging: Hoonga, Coaster, Elmac, cartonator, Strip Pack, PG super, Rotovac

Technical Skill: Knowledge about Tablet, Capsule and Pellets manufacturing Awareness of Regulatory guidelines, GLP & GMP

 

Post: QA: Analyst/Chemist: 25 Position; Reviewer: 5 Position

Education & Experience: BSc. / MSc / B.Pharm
Analyst/Chemist: 1-4 years of experience
Reviewer: 6-10 years of experience

Instrument Knowledge: HPLC, GC, UV & others

Area: API, Stability, in process and finished products

Technical Skill: Experience in analysis of API, excipients, tablets and capsules. Exposure to modified release products preferred, Good documentation skills. In addition to the above; Experience in handling and leading Laboratory errors and 005 investigations. Coordination with QA and Regulatory for submissions. Understanding of GLP & GMP is required.

Date: 17th Nov, 2019 (9 AM - 5 PM)
Venue: Hotel Woodlands, NH No. 8, Balitha, Vapi, 396 191

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