| 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 |