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Sun Pharma Walk In Interview

Sunpharma Walk-in Interview:

  • Quality Assurance ( Non OSD) - Executives/Officers: B.Sc/M.Sc/B.pharma /M.Pharma with 2 to 12 year of experience in Validation, Equipment Qualification, QMS, Compliance, Computer System Validation, Internal Quality Audit in regulatory approved formulation plant. 

  • QualityControl (Analysis/Reviewer) - Executives/Officers: B.Sc/M.Sc/B.Pharma/M.Pharma with 3 to 12 year of experience in Analysis, Review, Documentation in regulatory approved formulation plant. 

  • Production (Non OSD) - - Executives/Officers: B.Pharma/M.Pharma with 3 to 12 year of experience in Hormone /Cyto / Injectable production in regulatory approved formulation plant. 

Date: 31st May 2016 (Tuesday)
Time: 10.00 hrs to 17.00 hrs
Job Location : Sun Pharma - Halol

Lemon Tree Premier; The Atrium, Ahmedabad
Off Nehru Bridge, Sabarmati Riverfront, Ahmedabad, 380001, Gujrat
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Walk in interview at Piramal Enterprise Ltd-Pharmaceutical Development services

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Vacancy at Cadila Pharmaceutical Ltd

Vacancy at Cadila Pharmaceutical Ltd, Dholka for various post, 

Cadila Pharmaceuticals Excellence in manufacturing facilities is central to Cadila Pharmaceuticals. The company’s formulations manufacturing plant at Dholka near Ahmedabad, Gujarat is spread over hundred acres of land. This state-of-the- art facility is not only impressive in size, but is also USFDA approved.
Cadila Pharmaceuticals Limited
Required to

Cadila Pharmaceutical Ltd, Dholka

1. Executive - Validation
2. Officer Store - Desensing and RM /PM
3. Executive - CQA
4. Executive - IPQA
5. Executive - Regulatory Affairs (ANDA and Other Markets)
6. Diploma - Mechanical and Instrumentation  (Freshers)
7. B.Pharm - Freshers
8. M.Pharm - Freshers

Interested Candidate can send their Resume with Applicable Title on

Bhavik Patel
HR Department
Cadila Pharmaceutical Ltd.
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VACANCY IN Pharmacy and Science COLLEGE

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Recruitment of Faculty in CHARUSAT University

Here is i am giving information on Faculty recruitment in Charotar University Science and technology in various field
so get all information from following advertisement

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Urgent Requirement of Pharmacist

eSwasthya Mediserve Pvt Ltd

Company Details
Established in the year 2014, “E Swasthya Mediserve Pvt. Ltd.” has seen prodigious growth over the last few years and has quickly emerged as an affluent Trader and Supplier of premium quality Surgical Item, Medical Item, Surgical Products, Surgical Instrument, Medical Instrument, Pharmaceutical Medicine, etc. Our wide range of products also includes Surgical IV Set, Infant Feeding Tube, Surgical Steam Inhaler, Medical Vein-o-line, Leokoplast Tape, Hernia Belt, Elbow Brace, Paraffin Gauze, Skin Grafting Blade and many more items. Operating from Ahmedabad (Gujrat, India), we aim to list ourselves amongst the top pharmaceutical companies world-wide. In addition, our company intends to build long term value in this business via strong alliances with established vendors of the industry.
We are offering products of reputed brand such as Smith & Nephew, Diamond, Aquasonic, One Touch, 3M, North, Systane, veridean etc.

Urgent requirement of Pharmacist with licence

Qualification: B.pharm/M.pharm
Pay scale: No constraints of Salary for the right candidate
Location: Ahmedabad
Interested candidates can mail me resume on
Or share your resume by Whatsapp on 8460759686
Swati Chauhan
HR Administrator
eSwasthya Mediserve Pvt Ltd
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Vacancy at INTAS Pharma

Experience required for the Job: 2 - 10 years
Annual Salary of the Job: 2.0 - 6.0 Lacs
Job Location: Ahmedabad

Dear Candidate,

Routine stability sample analysis. Method Development by HPLC & GC. Calibration of Sophisticated instruments. Method Validation, Protocol & Report Preparation.
Routine Sample analysis by HPLC/GC/XRD/NMR Analytical Method Development Analytical Method Transfer & Validation Protocol & Report preparation for AMV & AMT Chemical Analysis by FT-IR, UV & Polarimeter.

Thanks & regards
Nutann Garg
Human Resource
Mobile: +91 9727443532
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Vacancy in Xylopia Lab Ahmedabad

here is I am giving information on vacancy in Xylopia labs.

Company Overview

Xylopia logo

Xylopia founded in October 2009 and established as a formulation CRO in January 2010. 

Xylopia established with the strength of mere 15 people, which is now more than 70 and still growing…

Xylopia offers comprehensive solutions for preformulation, formulation development of conventional and novel drug dosage forms, analytical method development and validation, stability and scale up. We also provide services for bioavailability, bioequivalence, bioanalysis, pharmacokinetics, biostatistics and clinical diagnostics. Add to the above, we offer solutions for commercial manufacturing by coordination of outsourced contract manufacturing services at locations where we enjoy a preferred customer status.

Formulation Development

  • Preformulation studies
  • Reference product characterization
  • Prototype formulation development
  • Full formulation development
  • Scale up at the manufacturing site
  • Technology transfer documentation
  • Expertise in the field of modified release dosage forms based on multi particulate systems as well as matrix based systems

  • Lab capable of handling products which requires low humidity (Lab can attain % RH of around 30% maintaining the temperature below 25°C)

  • Vacancy in Formulation Development Department

    We have vacancy in formulation development department for person having experience of 4 to 6 years for regulated market specially US and Europe experience is preferred first.

    Interseted candidates can send the resume to

    Xylopia labs is located in Ahmedabad and its Subsidiary of Zydus Cadila.

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    Walk In Interview for Zydus Cadila on 22nd May

    Walk In Interviews for Analytical Method Validationat PTC- Sigma, Ahmedabad for Zydus Cadila

    Zydus Cadila - Pharmaceutical Technology Center , Moraiya (Ahmedabad)

    Image result for Zydus CAdila ambali
    Job description:

    Officer / Executive / Sr. Executive / Assistant Manager - Analytical Method Validation:

    M.Sc. / B.Pharm / M.Pharm with 1-5 yrs experience in analytical or QC.

    Instrument Knowlegde required: HPLC, GC , UV & Dissolution testing for Regulated and Emerging Markets. Should have good knowledge of GMP/GLP.

    Interested candidates may Walk-in for an interview at the below mentioned address along with their updated CVs, latest salary slip, last increment letter, and relevant documents as per the below schedule.

    Date : Sunday, May 22, 2016

    Timings : 9 a.m. to 1 p.m.

    Walk-In-Interview Venue :
    Zydus Cadila Healthcare Ltd.
    Pharmaceutical Technology Centre.
    Sigma Commerce Zone,
    Opp. Iscon Mandir BRTS Bus Stand,
    Ambali - Bopal Road,
    Ahmedabad - 380015.

    Candidates can also send CVs on

    Seeking your support in forwarding this message to your contacts in pharma industry. Thanks.
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    Walk in on 20th May Cadila Healthcare Ltd

    Walk in Drive on 20th May, 2016 (friday)

    Cadila Healthcare Limited Careers

    2 - 7 yrs

    Zydus Cadila is a fully integrated, global healthcare provider, with strengths all along the pharmaceutical value chain. The group has state-of-the-art vertically integrated manufacturing facilities for APIs and Formulations, spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim. The groups API manufacturing units at Dabhasa and Ankleshwar have received approvals from the USFDA, AFSSAPS France, EDQM, KFDA.
    We, at Zydus are looking for young, dynamic and result oriented professionals for our Active Pharmaceutical Ingredients Manufacturing facilities based at Dabhasa, Vadodara, Gujarat.
      Dept : Quality Assurance  
      Designation: Officer to Assistant Manager
      Qualification : M.Sc. / M Pharm 
      Experience: 2-8 years of relevant experience In QA (API)
      Vacancy in Functions of QA mentioned below : 
      1. Site over Site, 
      2. Engineering Assurance, 
      3. Validations, QMS, 
      4. Analytical Compliance, 
      5. Documentation, 
      6. BMR Review and Audit & Compliance.
      Dept: Quality Control 
      Designation:  Officer to Assistant Manager 
      Qualification : M.Sc.
      Experience : 2-8 years of relevant experience in QC (API) 
      Job Description : 
      1. Handling HPLC, GC, Dissolution Apparatus, UV-Visible
      2. Spectrometer, wet analysis and stability studies.
      3. Knowledge of LIMS software will be preferred.

      Dept : Production 
      Designation :  Officer to Assistant Manager
      Qualification:  M.Sc / B.E./B.Tech (Chemical)
      Experience : 2 to 8 Year of Experience in API manufacturing
      Job Description: 
      1. Issuance and receive of blank Batch Manufacturing Record (BMR) from QA department.
      2. Issuance of Raw Material from Raw Material store as per BMR.
      3. Check and ensure that Raw material , packaging material and cleaning material is received as per requirement mentioned in material requisition slip from warehouse and keep it to the designated area in plant.
      4. Issuance of Cleaning materials & packing materials from warehouse.
      5. Maintaining the process parameters as per BMR.
      6. Keep the BMR updated for on-line production activity.
      7. Maintaining Usage, Cleaning & Maintenance log book of different equipment. 
      8. Daily calibration of electronic weighing balance..
      9. Compliance with the cGMP & safety norms.
      10. To ensure timely preventive / breakdown maintenance of equipment.
      11. To give the complete charge to reliever for pending and online activity and vice- versa in case of charge taker.
      Interested candidate may Walk-In for interview along with CV and Salary Structure and relevant documents on below mentioned details  

      Date     : 20th May, 2016 
      Time    : 9:30 am to 5.00 pm 
      Venue : Hotel Silver Avenue
                      Next to Big Bazar, 
                      Ostwal Empire, 
                      Boiser West,
                      Palghar 401501

      Candidates having experience of working in regulatory approved plants and sound knowledge of documentation, exposure of CGMP / GLP and SAP environment will be preferred.

      Those unable to attend may send their resume through e-mail to /
    GC, XRD, Calibration and handling of HPLC, QMS, QA documentation, UPLC, Analytical complaints, adl compliance.

    Desired Candidate Profile

    PG:M.Sc - Chemistry, M.Pharma - Pharmacy
    Doctorate:Doctorate Not Required
      Please refer to the Job description above
    Company detail Profile:
    Cadila Healthcare Limited

    Zydus Cadila is an innovative global pharmaceutical company that discovers, develops, manufactures, and markets a broad range of healthcare products. The group's state-of-the-art manufacturing infrastructure is spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim. The group has global operations in four continents spread across USA, Europe, 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 16500 employees worldwide, world-class research and development centres dedicated to discovery research and
    state-of-the-art manufacturing plants, the group is dedicated to improving people's lives.
    We are looking for young, dynamic and result oriented professionals for our API Manufacturing Facilities at Dabhasa, Vadodara, Gujarat.
    Recruiter Name:Pooja Thakkar
    Contact Company:Cadila Healthcare Limited
    Address:Zydus Tower Satellite Cross Road,AHMEDABAD,Gujarat,India 380015
    Reference Id:API-DBH/Walk-In/2016/0015
    Walkin Interview
     20th May  9 AM
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    Walk-In at Cadila Pharmaceuticals Ltd on 18th May

    Here is I am giving information on Walk in Interview at Cadila Pharmaceuticals :

    Quality Control Walk In Interview at Cadila Pharmaceuticals:

    Cadila Pharmaceuticals Limited

    Walk In Date: 18th May 2016
    Time: 3.00-5.00 pm.
    Position: Officer/ Sr.Officer/Executive
    Qualification: B.Sc./M.Sc./B.Pharm/M.Pharm
    Experience:  3 to 10 years
    Note: Pharmaceuticals (API) candidate preferable


    Cadila Pharmaceuticals Ltd.
    Plot No.294 Opp Atul Ltd GIDC,
    Ankleshwar, Dist: Bharuch, Gujarat

    Interested candidates will appear with their updated bio-data & CTC Proof.

    Mayur Dalal


    More than 38 APIs and intermediates including USFDA – certified products are manufactured at our ISO-9002 & ISO14001 accredited facilities at Ankleshwar, India
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    Opening for MIcrobiologist and HPLC Analyst

    Postion1: Microbiologist 
    Exp. 2 to 5 years 
    Company: Vapi care pharma
    Location: Kharauni, Baddi.  

      Responsibilities include:
      planning and carrying out trials,tracking environmental micro-organism development
      growing microbe cultures,collecting samples from a variety of locations,recording, analysing and interpreting data writing research papers, reports and reviews, keeping up-to-date with scientific and research developments,ensuring that data is recorded accurately in accordance to guidelines observing high health and safety standards inspecting food and drink manufacturing processes to check for possible contamination managing laboratories
      to comply with government food and safety regulations.

    Position2: Hplc analyst 
    Exp. 2 to 5 years
    Company: Vapi care pharma
    Location: Kharauni, Baddi.  


    * Perform all functions related to taking samples, sample receipt, control and sample disposal.
    * Perform analysis of routine samples and investigation of non-conforming samples, data evaluation and reporting.
    * Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols.
    * Be responsible for the operation, maintenance, training delivery as an expert and maintain operating procedure for at least one piece of laboratory equipment.
    * Perform technology transfer (method transfers) and critically evaluate data.
    * Maintain own training record for laboratory GMP, regulatory compliance and Health & Safety.
    Qualifications/education requirements
    * Bachelor's degree or more in Chemistry 
    * Preferred: 1 to 2 year experience in a pharmaceutical laboratory environment with cGMP requirements. 
    * Basic manual analytical technique and working experience with UV/VIS and FTIR
    * Working knowledge of tablet and capsule physical tests and tablet/capsule dissolution.
    * Familiarity with equipment such as HPLC, GC 

    To apply send resume to Send resume on or call 9805966955 Ramesh Shrivastav. Freshers can also apply
    Read More »

    Dr. Reddy's Walk-In Interview on 15th May

    Here is Opening in Dr.Reddy's lab Ltd
    Get all information through following advertising

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    Walk in Interview in Sun Pharma on 15th May

    Here is I am giving information on Interview in Sun Pharma on 15th May get all details through this advertise
    Vacancies in various position are given below

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    Walk In Interview Alembic Pharmaceutical Ltd on 11th may

    Here is I am giving information about walk in interview in Alembic Pharmaceutical Ltd on 11th may
    Get all details through this advertise

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    Opportunity in BHABHA ATOMIC Research Center For Pharmacist & Dental Technician

    Dr. Homi Jehangir Bhabha was the visionary who conceptulised the Indian Nuclear Programme and along with a handful of Scientists initiated the nuclear science research in India in March, 1944. He envisaged the vast potential of nuclear energy and its possible successful utilization in the field of power generation and allied areas. Dr. Bhabha started working with the goal of achieving self reliance in the fields of nuclear science and engineering and today’s Department of Atomic Energy which is a consortium of different and diversified fields of science and engineering is the final outcome of the farsighted planning of Dr. Bhabha. Thus, in his own words “When Nuclear Energy has been successfully applied for power production in, say a couple of decades from now, India will not have to look abroad for its experts but will find them ready at hand

                 1) Pharmacist 02 (St-01,Obc-01)
                 2) Technician/D [Dental Technician (Dental Mechanics)
                 3) Technician/D [Dental Technician (Dental Hygienist)
    All Details about Pharmacist Post:
    Job description for Pharmacist:
    Dispensing medicines, inspection of medicines in stores, raising indents, data entry and stock keeping of medicines etc.
    Educational / Technical Qualification:
    HSC  (10+2)  +  2  years  Diploma  in Pharmacy  +  3  months  training  in  Pharmacy + Registration  as a Pharmacist with Central or State Pharmacy Council.
    Persons With Disability [One Leg Affected (OL) or Part ially Deaf (PD)] can apply for Post No : DR/01  only. “Hearing  Impairment  (partially deaf)”  means loss  of  60  decibels or more in the better  ear in the conversational range of frequencies and physical deformity should not be less than 40 percentage.
    Applications will be accepted ON-LINE only. Facility for applying on-line will be available from 07/05/2016 to 27/05/2016. For detailed information, online submission of application and procedure for payment of application fee please visit the website
    AGE LIMIT : 18 years minimum and 25 years maximum. Age relaxation is not applicable for SC/ST/OBC candidates applying for Un-reserved posts.
    The Upper age limit prescribed will be relaxable :-
    1. Upto a maximum of five years if a candidate belongs to ST category
    2. Upto a maximum of three years if a candidate belongs to OBC category
    3. Relaxation in the upper age limit of 5 years shall be admissible to all persons who had ordinarily been domiciled in Kashmir division of the state of Jammu & Kashmir during the period from the 1st day of January 1980 to 31st day of December, 1989 provided that the relaxation in the upper age limit for appearing at any examination shall be subject to the maximum number of chances permissible under the relevant rules.
    4.  Relaxation in the upper age limit of 5 years shall be admissible to children/family members of those who died in the 1984 riots.
    5. Age relaxation to PWD (For Post No:DR/01 only) and Ex-Servicemen will be as per Govt. orders.
    6. For departmental candidates (Central Government employees) with 3 years continuous service in the same line or allied cadre, upper age limit will be 40 years for general candidates, 43 years for OBC candidates and 45 years for ST candidates.
    7. Widows, divorced women and women judicially separated from their husbands and not re-married are eligible for relaxation in the upper age limit as per Government orders.
    8.  Meritorious sportpersons are eligible for relaxation in the upper age limit as per Government orders.
    Note: Only date of birth indicated in School Leaving Certificate or equivalent certificate will be accepted. No subsequent request for change shall be allowed.
    SELECTION  PROCEDURE :There will be an initial screening written exam (first level) which will be objective type in   nature. The syllabus for the screening test shall be  as under : 
    No. of questions
    General intelligence and reasoning
    1 Hour
    Numerical aptitude
    General Science
    Questions based on the respective trade / discipline

    Candidates who score 50% and above in the screening written exam will only be considered for appearing in  the  next stages. The second level exam shall consist of  practical and theory exams of 50 marks each in the respective  trade  /  discipline.  Candidates  who  score  50%  and  above  both  in  practical  and  theory  exam  will  be  eligible  for  considering for empanelment based on the merit and n umber of vacancies. If two or more candidates obtain t he  same mark in the second level exam (theory + practical),  the merit will be decided by taking into consideration n one  more  criterion,  i.e,  percentage  of  marks  obtained  in  t he  minimum  educational  qualification  prescribed  for  the  particular post. Suitable relaxation in marks will be  given in the exams to scheduled tribe candidates applying for  the post of Pharmacist/B. 
    Candidates  will  have  the  option  to  write  the  paper  in  either  Hindi  or  English.  All  exams  will  be  held  in  Mumbai.
    APPLICATION FEE :    100 /-
    Fee is exempted for candidates belonging to SC/ST, E x-serviceman, PWD (for DR/01 only) and women categories. With regard to application fee, the candidates may download the three fold challan form from the BARC website and make payment in any branch of SBI. The portion of the challan marked “Institution copy” should be submitted by the candidate s at the time of initial screening written exam. Application fee should be paid on or before the last date of receipt of on-line applications . Fee once paid shall not be refunded under any circumstances and cannot be held in reserve for any other recruitment

    Important Insrtuction for all three post:

    Get all detail 
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    Walk-In Interview in USV Pvt. Ltd

    Walk-In Interview for QA, Q.C. Manufacturing, Eng.Jobs in USV Pvt Ltd on 8th may

    In India we are recognized for our leadership in the Oral Anti-Diabetic market where we rank No. 1 by Rx and Value. In the Cardiovascular diseases segment we are No. 1 by Rx and in the top 8 by Value. We also have a significant presence in the areas of Vitamins, Minerals, Nutrients, Dermatology, Gastroenterology and CNS. 
    We are 2000 carore  health care company with operations in India, US & EU, with leadership in diabetes and cardiovascular segments. We provide a supportive and learning, environment where personal growth is encouraged and nurtured. We have three plants based at Daman and Baddi manufacturing Tablets, Capsules: Sterile injectables & Ophthalmic Products, one API plant at Chiplun and biotechnology facility in Nerul Mumbai. All our plants are approved by US, EU, Health Canada and other leading country's regulators

     here is I am giving information about Interview on 8th may

    Dear Candidate,

    We have scheduled Walk-In for USV Pvt Ltd., Daman Plant on 8th May, 2016 (Sunday)


     USV Pvt Ltd.-Daman Plant

    Date: 8th May, 2016 - SUNDAY

    TIME: 10:00 AM to 04:00 PM

    Job Location: Daman

    Vacancy for Different Areas are:

    • Quality Control
    • Quality Assurance
    • Manufacturing
    • Engineering

    Candidates may Walk-In for an interview along with their updated Resume,updated salary slip

    Ajeet Singh
    Human Resources
    USV Pvt Ltd.
    Office no: 02606636229/232

    Great Place To Work

    Value addition at all levels of the organisation chain is essential and necessary for the growth and success of our company. To ensure this, USV provides an environment that:
    • Values people
    • Promotes learning
    • Nurtures innovation
    • Rewards collective excellence
    If you have a passion for achievement, if you enjoy working with a team of qualified young professionals and if it is challenge that excites you, USV is the place to make a difference!

    About USV
    We are a 53 year old leading healthcare company which began as a joint venture with USV&P Inc. USA, a subsidiary of Revlon. Our product offering today includes Active Pharmaceutical Ingredients (APIs), Fixed Dosages Formulations (FDF), Peptides, Biosimilars and Injectables. These are manufactured in our cGMP compliant plants located in India.
    We market our products globally to 75 countries. In the financial year 2013-14, our total income was Rs. 20,099 million. Our Indian business contributed 78% to the revenue and the rest was from export of APIs and Finished Dosages.

    Our international business consists of:
    • A large portfolio of small molecule APIs. Of the 52 products in our portfolio, 27 APIs are commercially available, while others are in various stages of development. Our special skills include production and characterization of polymorphs and particle sizing
    • A portfolio of Finished Dosages. These include immediate release, modified release and products with 'complex' characteristics which are promoted through ANDA filings and Dossiers linked to supply.
    Our spend of 7.35% of sales on R&D ensures that we are able to deliver on our research portfolio. We have over 100,000 sq. ft. of laboratory space with excellent infrastructure. Our research is driven by a team of 262 scientists including 2 doctors, 31 PhDs and 229 post-graduates, many of whom have studied in universities in USA, Europe and Japan. Our intellectual property portfolio consists of patent filings for 43 inventions of which 18 have been granted.
    Read More »

    Walk in Interview for Torrent Pharma

    Walk in Interview for INDRAD (Ahmedabad) Plant on 8th may

    Torrent Pharma, The flagship company of Torrent Group, is ranked amongst the top pharma companies of India. It is a dominant player in the therapeutic areas of cardiovascular (CV) and central nervous system (CNS) and has achieved significant presence in gastro-intestinal, diabetology, anti-infective and pain management segments. Torrent Pharma has a international presence spanning over 70 countries across five continents with over 1200 product registrations. Today Torrent Pharma, with it state of the art of manufacturing and research facilities and a global presence, is all poised to crave a niche itself in the international Pharma arena. It is well set on an exciting growth phase in all directions.   Torrent Pharma’s competitive advantage as a manufacturer stems from its world-class manufacturing facilities. Its manufacturing facilities at Indrad, Gujarat, comply with WHO, cGMP, MHRA and TGA norms and have received ISO 9001, ISO 14001 and OHSAS 18001.

    Here is all detail about job:

    Department:- Quality Control

    Job Location:- Indrad Plant (Ahmedabad)

    Section:-  Stability , Formulation,Method Validation and API

    Education Qualification: B.Sc./ M.Sc./B.Pharm./M.Pharm

    Jobs Requirement:
    • Analysis of finished product,stability samples and Raw material as per Method of analysis.
    • Analytical Method development, Verification and Validation.
    • Responsible for preparation of specification and STP, Data interpretation and troubleshooting.
    • Preparation of method verification protocols and Raw-data sheet.
    Specific:-Sound knowledge of operation/calibration of : HPLC/GC/UV/ IR

    Others: Knowledge of  Solid Orals manufacturing and quality process preferably USFDA/EU approved.


    1) Hotel Nami Residency
    Opp. V.S Hospital,
    Ellisbridge, Ahmedabad

    2) Hotel Budget INN Palm Regency
    NH-8,8/h 21st Century Hospital,
    Gunjan, GIDC, Vapi

    Date: 8th May, 2016 - SUNDAY

    TIME: 10:00 AM to 04:00 PM

    Contact Person: Mayur/Aswin (Cell No.:9909905477)


    Important Note: 
    • Minimum experience required 1 is year.
    • Please attend interview with latest resume, salary slips & Photograph.
    • USFDA, MHRA, ANVISA knowledge & good communication skill will be an added advantage.
    More detail Torrent Pharma:Torrent Pharmaceuticals Limited is a major player in the Indian pharmaceuticals sector with the vision of becoming a global entity. Torrent Pharma enjoys dominance in the niche therapeutic areas like, cardiovascular and central nervous system, gastro-intestinal, pain management and oral anti-diabetic segments. Torrent Pharma owes its success in the domestic market to its thrust on frontline research, strategic marketing and world-class manufacturing. It is among the largest spenders on R&D and has set up one of the most advanced research centers in the country at an investment of Rs. 200 crores so far. It has discovered and patented the AGE (Advanced Glycosylation End Product) Breaker Compound which has potential to treat heart diseases and diabetes related vascular complications. Its manufacturing facilities have received quality certifications from various international regulatory authorities. It is this success that Torrent Pharma attempts to replicate in the international market now. It has already established fully-owned subsidiaries in Australia , Brazil , Germany , Japan , Mexico , Philippines Russia and USA and has over 1000 product registrations in more than 50 countries worldwide
    Read More »



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