Walk-In for Quality Assurance - Zydus Cadila

By: Pharma Jobs | Views: 6150 | Date: 15-Aug-2012

Zydus Cadila is an innovative global pharmaceutical company that discovers, develops, manufactures and markets a broad range of healthcare products. The group's operations range from API to formulations, animal health products and cosmeceuticals. Headquartered in the city of Ahmedabad in India, the group has global operations in four continents spread across USA, Europe, Japan, Brazil, South Africa and 25 other emerging markets.In its mission to create healthier communities globally, Zydus Cadila delivers w

Walk-in for Quality Assurance on 18th August 2012 @ Moraiya, Ahmedabad - 20 Opening(s)




Zydus Cadila is an innovative global pharmaceutical company that discovers, develops, manufactures and markets a broad range of healthcare products. The group's operations range from API to formulations, animal health products and cosmeceuticals. Headquartered in the city of Ahmedabad in India, the group has global operations in four continents spread across USA, Europe, Japan, Brazil, South Africa and 25 other emerging markets.

In its mission to create healthier communities globally, Zydus Cadila delivers wide ranging healthcare solutions and value to its customers. With over 11,000 employees worldwide, a world-class research and development centre dedicated to discovery research and eight state-of-the-art manufacturing plants, the group is dedicated to improving people's lives.
Designation Walk-in for Quality Assurance on 18th August 2012 @ Moraiya, Ahmedabad - 20 Opening(s)
Job Description

Walk-in for Quality Assurance on 18th August 2012 @ Moraiya, Ahmedabad

We having opening in Quality Assurance at Formulation Mftg Unit located at Moraiya, Ahmedabad.

Officer / Executive: M.Sc / B.Phama / M.Pharma with 3 to 8 years of experience and relevant exposure in Formulation Mftg Unit of regulated pharma organization.

Vacancies are for IPQA-Parenteral, IPQA-Tablet, QA Validation, QA compliance

Details of vacancies are as under:

For IPQA (Parenteral):

IPQA - Line clearance, in-process checks, sterile,Liquid etc.

To issue of BMR/BPR as per production plan, cGMP documents.

To issue and retrieval of SOPs, RMS/SPS.

To prepare APQR.

Review of BMR and BPR.

Responsible for training of personnel.

To handle the incidents report, deviation, change control, CAPA, market complaint.

Responsible for handling mediafill activities

To handle inprocess checks.

For IPQA (Tablet)

IPQA - Line clearance, in-process checks, Tablet, Capsule etc.

Issuing of SOPs, BMR, BPR, MFR, Process Validation Protocols and Reports with preparation of standard.

Preparation, Review and Control of Documents related to BMR, BPR etc.

Preparation and Review of Annual Product Quality Review.

Market complaint investigation, Failure investigation and its CAPA.

Reconciliation and Reviewing of BMR before Batch Release.

To handle the incidents report, deviation, change control, CAPA, market complaint.

To handle inprocess checks.

QA-Validation

Review of filled batch process records

Preparation of process validation protocol and report

To monitor and support the validation activity in plant.

To support and provide the documents to regulatory affairs department timely.

QA Compliance

Should have good exposure in CAPA handling/tracking, audit compliance, handling market complaints , Annual product reviews and product failure investigation

Should have strong experience in handling QA Compliance of Formulation Mftg Unit

Interested candidate may Walk-In for Interview along with their CVs and relevant documents between 09:00 AM to 02:00 PM

Candidates having experience of working in regulatory approved plants and posses sound knowledge of documentation, exposure to cGMP/GLP will be preferred.

Preference will be given to only those candidates who are working in USFDA Approved Pharmaceutical Organization.

Interested candidates may Walk-In for an interview along-with their updated CVs and relevant documents on-

Date: 18th August 2012 (Saturday)

Timing: 09: 00 a.m. to 02:00 p.m

Venue : Sarkhej-Bavla, N.H No. 8A, Moraiya, Tal. Sanand, Ahmedabad.

NOTE : Candidates already appreared for the personal interview for the above position during last three months, need not required to reappear for the Walk-in

Desired Profile Please refer to the Job description above
Experience 3 - 8 Years
Industry Type Pharma, Biotechnology, Clinical Research
Role Quality Assurance/ Quality Control Executive
Functional Area Production, Manufacturing, Maintenance
Education UG - B.Sc - Any Specialization, B.Pharma - Pharmacy
PG - M.Pharma - Pharmacy, M.Sc - Any Specialization
Compensation: Best in The Industry
Location Ahmedabad
Keywords Quality Assurance, QA, Zydus, Cadila
Contact Ms. Ruchi Lal
Cadila Healthcare Limited
Zydus Tower Satellite Cross Road,
AHMEDABAD,Gujarat,India 380015
Telephone 91-2717-666590
Website http://www.zyduscadila.com/
Job Posted 14 Aug
Reference Walkin - Moraiya - Aug 2012
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