Zydus Cadila walk-in for API Unit for DABHASA located unit for Production, Quality Control , Quality Assurance on date 15th October 2017 at Ankleshwar

Company Name: Zydus Cadila 

About Company: Zydus Cadila is one of India’s leading healthcare companies and a global healthcare provider with strengths all along the pharmaceutical value chain. The group’s state-of-the-art manufacturing infrastructure is spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim. The group’s formulation manufacturing hub at Moraiya, Ahmedabad has received approvals from several regulatory authorities.

Job Type: WALK-IN API Unit

Departments: Production, Quality Control , Quality Assurance

Designation: Executive / Sr.Executive / Assistant Manager

Job Responsibility & Profile:  For Quality Control :  Candidate should have hands on experience and relevant exposure in handling instruments like HPLC, GC, UV , wet lab, micro lab and chemical analysis of Raw Material . Must be familiar with cGMP requirements. Shop floor Operation in API / Bulk Drug Manufacturing.

Job Responsibility & Profile:  For QUALITY ASSURANCE: Candidate must be familiar with cGMP requirements, Data Integrity, Document Cell, Batch release process, Trending APR shop floor Operation in API / Bulk Drug

Manufacturing.

 a) Data Integrity - Responsible to review of HPLC and GC , QC Sop Compliances, Investigation activities , OOS and OOT and quality control instruments.

 b) Document Cell -Review of documents before DMF submissions, distribution / Issuance of BMRs, Master Formulae, SOPs and Formats to the respective departments and controlling all master documents.

 c) Batch Release - Knowledge of ICH guidelines and should review of BMRs and Validation documents and to give usage decision and dispatch of all APIs and salable intermediates in LIMS and SAP.

 d) Technology transfer documents - Review R&D process & TTD, evaluation of CPP & CQA and comparison with batch record , review of master batch record also review of specification and STP of API, Intermediate, RM, In-process.

 e) Trending and APR - Knowledge of Market complaint, Deviation, Incident, Change control for trending of Systems, Review of Master SOPs, BMRs, PCRs, validation Protocols and reports and Annual Review reports.

Job Responsibility & Profile: For  PRODUCTION: Candidate should have experience and relevant exposure in API / Bulk Drug Manufacturing. Should also have knowledge of GMP documentation. Must be familiar with cGMP requirements.

Candidate should possesses excellent communication & interpersonal skills. Hands on exposure with software like SAP, LIMS, MS Office etc.

Candidates having experience of working in regulatory approved plants and possesses sound knowledge of documentation, cGMP and SAP will be preferred.

Qualification Required:

QUALITY CONTROL (M.Sc / B.Sc)

QUALITY ASSURANCE (M.Sc / B.Sc)

PRODUCTION (B.E Chemical)

Experience required: 2 to 7 years API Pharma Candidates only

Interview Date: 15th  October 2017 (Sunday)

Time of Interview: 9.30 am to 5 pm

Interview Location: Hotel Shalimar ,Valia Road, Near G.I.D.C. Reservoir, Ankleshwar, Gujarat 393002

Job Location: API Manufacturing located at Dabhasa, Gujarat

Contact Person & Details: Cadila Healthcare Limited- Dabhasa

Email : dkpatel@zyduscadila.com