Saturday, August 6, 2016

Vacancy of Area manager and Medical Representative at "Gynaec DIVISION"

2 Medical Representative and 1 Area Manager required in "Gynaec DIVISION" for North Gujarat H.Q.
Experience: Min 3-5 year experience for Medical Representative and 10 years for Area Manager in Gynaec Division.

Package: Negotiable
Interested candidates can contact 
Yash Patel on 9825055073
Or email the C.V. on yash@saffronhealthcare.co.in

Troikaa Altius Div Require Young and energetic Medical Representative


We at Troikaa Altius Div Require Young and energetic Medical Representative for Maninagar Ahmedabad Fresher with science Background can Apply 
Jainendra Jani ZBM 
97240 40203

Friday, August 5, 2016

SPC IIPC & IDMA GSB coorganized state level seminar on Quality Management Systems at PERD Centre





Organisers:

AICTE sponsored Industry Institute Partnership Cell (IIPC) at Shri Sarvajanik Pharmacy College, Mehsana

Indian Drugs Manufacturers’ Associations – Gujarat State Board (IDMA-GSB).

Day and Date: Sunday -7th August 2016.

Venue: B. V. Patel Pharmaceutical Education and Research Centre (PERD Centre), Opp. Zydus Hospital, Nr. Thaltej

Cross Road, Sarkhej Gandhinagar Highway, Ahmedabad.

Learning Objectives: 1) To provide technical guidance to develop and sustain Quality Culture and Data Integrity by

adopting Quality Management Systems in the pharmaceutical industry and to ensure regulatory compliance 2) To

provide technical guidance to academic institutes to upgrade their knowledge on Quality & Technical Systems, Six

systems approach to GMP inspection.

Who will benefit: COO of companies, factory managers, quality managers, production department heads, RA

personnel, Personnel involved in Quality documentation and Regulatory inspection.

Faculty members, PG and Research Students in all subjects particularly Pharmaceutics, Quality Assurance and

Regulatory Affairs.

Registration: 2.00-2.30 pm

Registration fee: Rs. 200

Contacts for registration:

1. Shri Sarvajanik Pharmacy College, Near Arvind Baug, Mehsana-384001. Telephone: (L) 02762-247711/12,

Coordinator of Seminar: Varsha B. Chaudhary; Email: varshavijay10@gmail.com

2. Indian Drugs Manufacturers’ Associations–Gujarat State Board, 4-Park Avenue, Parimal Garden, Near Gujarat

GAS, Ellis Bridge, Ahmedabad-380006, Telephone : (L) 079-26406680, Contact: Dr. R. S. Joshi; Email:idmagsb@gmail.com

Vacancy of Quality Control Manager

    Handling all testing activity of Raw material, finished product and documentation work as per GMP/ISO & WHO-GMP. EDQM & USFDA requirements.

    Expertise in handing of sophisticated instruments like AAS,GC,HPLC & IR etc.

    cGLP implementation in QC.
Salary:INR 2,00,000 - 6,00,000 P.A
Industry:Pharma / Biotech / Clinical Research
Role Category:Production/Manufacturing/Maintenance
Role:Quality Assurance/Quality Control Executive

Apply Now

Source: http://www.naukri.com/job-listings-Quality-Control-Manager-Pharma-QC--Crystal-Fact-Ahmedabad-6-to-11-years-010616004631?src=jobsearchDesk&sid=14704134066615&xp=22&qp=pharma&srcPage=s



Vacancy of Research Executive/ Sr. Research Executive

Job Description

    -Knowledge of Formulations of Tablet / Ointment for Regulated Market.
    - Literature Search & carrying out pre-formulation studies.
    -Knowledge of QbD (preferable) & DOE based process optimisation (preferable).
    - Understanding of USFDA, EU guidelines.
    - End to end responsibility to support the multiple formulation projects.
Salary:INR 3,50,000 - 5,50,000 P.A
Industry:Pharma / Biotech / Clinical Research
Functional Area:Engineering Design ,R&D
Role Category:R&D
Role:R&D Executive

Desired Candidate Profile

Education-
UG:B.Pharma - Pharmacy
PG:M.Pharma - Pharmacy
Doctorate:Doctorate Not Required
    Source: naukri.com
    http://www.naukri.com/job-listings-Research-Executive-Sr-Research-Executive-pharma-Formulation--Sarthee-Consultancy-Ahmedabad-4-to-6-years-300716003653?src=jobsearchDesk&sid=14704134066615&xp=3&qp=pharma&srcPage=s




Vacancy of Pharmacovigilance Officer at Cadila Pharmaceuticals Limited

Job Description


    Major Purpose of the Job:
    Single Point of Contact for all Pharmacovigilance activities for International (Formulation) business.
    Principal Accountability:
    Doing research work on adverse events or product complaints or with an inquiry about the human health product;
    Receiving calls from consumers and health care professionals with reports and respond to inquiries;
    Verbal Probing for necessary information including but not limited to the adverse event(s),
    the patient's medical history, Suspect product, concomitant drugs involved if any, and medication history
    of patient;
    To be responsible to the Medical Head for day-to-day processing of incoming adverse event reports and reporting to regulatory authorities, with the objective of achieving a high level of regulatory compliance;
    To ensure that all Pharmacovigilance activities are conducted in accordance with SOP's, Work Instructions, Good Clinical Practice guidelines and regulatory requirements;
    To assist the Medical Head in preparation for any internal audits or external inspections on CPL Pharmacovigilance function;
    To liaise with Clinical Research personnel in the preparation of safety data required in support of the clinical research program.

Desired Candidate Profile
Education-
UG:B.Pharma - Pharmacy
PG:M.Pharma - Pharmacy
Doctorate:Any Doctorate - Any Specialization, Doctorate Not Required
    Please refer to the Job description above
Company Profile:
Cadila Pharmaceuticals Limited
Cadila Pharmaceuticals Ltd. (CPL) is one of India's most reputed, research-based, techno-savvy pharmaceutical companies with a focus in the area of Formulations & APIs and having its corporate office at Bhat, Ahmedabad and State-Of-Art manufacturing facilities compliant with USFDA, MHRA, TGA, MCA, MCC & WHO norms at Dholka, Ankleshwar, Kadi and Jammu.

With Diversified operations including Manufacturing of Hospital Disposables, Diagnostics, Laboratory Chemicals,Pharmaceutical Machinery, Animal Health Formulations, Feed Supplements and Bio-fertilizers, CPL is all set to forge ahead, rising to new challenges, in its quest for excellence.

The present volume of the group is Rs. 650 Crore and strategic business plans are aggresively to double up the volume of business over the next three years

CPL invites Young, DynamicProfessionals with proven competencies such as Excellent Analytical Abilities, Strong Communication and Interpersonal Skills for building up a strong team of Quality Control, Quality Assurance, API, Contract Manufacturing, Central Packaging, Supply Chain Management, F&D and Bioanalytical.

View Contact Details:

Website:http://www.cadilapharma.com