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Tuesday, 31 July 2018
Pharmacy graduates required as Scientist in Union Public Service Commission
Post : Scientist B (Toxicology)
No of Posts : 02 (UR-02)
Pay Scale
Level – 10 (Rs.56100-177500/-) in Pay Matrix as per CCS (R.P.) Rules, 2016 (Pre – revised pay scale PB - 3 Rs.15,600-39,100/- with Grade Pay Rs. 5,400/-) Total emoluments excluding T.A. and HRA at the time of initial appointment will be Rs. 56,100/- plus DA as admissible p.m. approximately.
Level – 10 (Rs.56100-177500/-) in Pay Matrix as per CCS (R.P.) Rules, 2016 (Pre – revised pay scale PB - 3 Rs.15,600-39,100/- with Grade Pay Rs. 5,400/-) Total emoluments excluding T.A. and HRA at the time of initial appointment will be Rs. 56,100/- plus DA as admissible p.m. approximately.
Age
Not exceeding 35 years as on normal closing date. Relaxable for regularly appointed Govt. servants upto five years as per the instructions issued by the Govt. of India from time to time. For age concession applicable to some other categories of applicants, please see relevant paras of the ‘Instructions and Additional Information to Candidates for Recruitment by Selection.’
Not exceeding 35 years as on normal closing date. Relaxable for regularly appointed Govt. servants upto five years as per the instructions issued by the Govt. of India from time to time. For age concession applicable to some other categories of applicants, please see relevant paras of the ‘Instructions and Additional Information to Candidates for Recruitment by Selection.’
Essential Qualificaiton (s)
EDUCATIONAL - Master’s Degree in Chemistry / AIC by examination / Biochemistry / Pharmacology / Pharmacy / Forensic Science with Chemistry as one of the subjects at Bachelor of Science level from a recognized University.
EDUCATIONAL - Master’s Degree in Chemistry / AIC by examination / Biochemistry / Pharmacology / Pharmacy / Forensic Science with Chemistry as one of the subjects at Bachelor of Science level from a recognized University.
EXPERIENCE- Three years experience of analytical methods and research therein in the field of Toxicology in any Central Government or State Government organization or recognized research institute or Forensic Science Laboratory under the Central or State Government. Note- Qualifications are relaxable at the discretion of the UPSC in case of candidates otherwise well qualified
Desirable Qualificaiton (s)
Experience of working in a Forensic Science Laboratory.
Experience of working in a Forensic Science Laboratory.
Duty(ies)
Crime Scene Management, Crime Case Examination, bestow expert testimony/de’facto in the courts of law on subject matter under the provision of Cr. P.C. and Indian Evidence Act/Information Technology Act, R&D activities on Forensic Activities and imparting training in their respective field of forensic specialization to the trainees from different investigating agencies / forensic science labs and other organizations.
Crime Scene Management, Crime Case Examination, bestow expert testimony/de’facto in the courts of law on subject matter under the provision of Cr. P.C. and Indian Evidence Act/Information Technology Act, R&D activities on Forensic Activities and imparting training in their respective field of forensic specialization to the trainees from different investigating agencies / forensic science labs and other organizations.
Clinical Research Associate at Medpace @ Apply Now
Post: Clinical Research Associate
Job Responsibilities
• Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP;
• Maintain ongoing site correspondence and site files;
• Complete visit reports and maintaining study-related databases;
• Oversight and interaction with clinical research sites; and
• Review of patient charts and clinical research data.
• Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP;
• Maintain ongoing site correspondence and site files;
• Complete visit reports and maintaining study-related databases;
• Oversight and interaction with clinical research sites; and
• Review of patient charts and clinical research data.
Candidate Profile
• University degree in health-related field;
• 2- 4 years of monitoring experience gained from a global CRO and /or other related clinical research environment is preferred;
• Proven track record of demonstrating experience in clinical patient management, protocol, CRF, preparing of ISF, documentation to be submitted to competent authorities, project management;
• Computer literacy;
• Excellent verbal and written communication skills in English.
• Should be both a team worker and self-motivated professional ;
• Detailed-minded & well-organized;
• Strong determination to grow with the organization
• University degree in health-related field;
• 2- 4 years of monitoring experience gained from a global CRO and /or other related clinical research environment is preferred;
• Proven track record of demonstrating experience in clinical patient management, protocol, CRF, preparing of ISF, documentation to be submitted to competent authorities, project management;
• Computer literacy;
• Excellent verbal and written communication skills in English.
• Should be both a team worker and self-motivated professional ;
• Detailed-minded & well-organized;
• Strong determination to grow with the organization
Assistant Manager/Manager-Market Research required at Panacea Biotec
Panacea Biotec is a leading research based Health Management Company, with an annual turnover of approx. Rs. 830 Crores. We are engaged in research, development, manufacture & marketing of Vaccines, Bio-Pharmaceuticals and Pharmaceuticals (Rx & OTC) of international quality and Health Services. All Panacea Biotec plants are accredited by international agencies and they follow current Good Manufacturing Practices, as per WHO guidelines.
Post : Assistant Manager/Manager-Market Research
Job Description
- Identifying appropriate research methodology & supporting techniques to meet defined business objective.
- Development of brand plans & next 5 year forecast aided by business intelligence to cater to stratified markets thereby improving access & therapy’s footprint
- Conducting primary & secondary research and communicate defined opportunities, challenges and recommendations for the stakeholders
- Deliver insight driven action, aided with thorough understanding of brands, market space & industry benchmarking to enable better decision making
- Review & Interpret the collected data, writing reports and make business oriented actionable recommendations.
Technical Assistant required at National Institute for Research in Tuberculosis
Project titled : “Impact Evaluation of Antiretroviral Therapy (IE-ART) under NACO”
Place of posting : Karnataka and Kerala (ART centres are yet to be decided)
Note: The candidate is required to work in Karnataka and Kerala at the respective ART Centres as per the directions of Principal Investigator of the project.
No of Posts : 3 (Three) – UR-1, SC-1, OBC-1
Essential qualification
Graduate in science from a recognized university with three years’ work experience from a recognized institution in life science
OR
Master’s Degree in Life Science preferably Microbiology / Biotechnology / Bacteriology / Biochemistry
Graduate in science from a recognized university with three years’ work experience from a recognized institution in life science
OR
Master’s Degree in Life Science preferably Microbiology / Biotechnology / Bacteriology / Biochemistry
Walk in interview for Research Assistant at CSIR institute of Himalayan Bioresource Technology
CSIR Project: “CSIR Mission Project on Nutraceuticals and Nutritionals”(HCP-0019) [upto 31-03-2020].
Project Assistant Level - II (Sr No 1)
No of Posts : 05 Posts
Stipend (Per Month) [Consolidated] : Rs.25,000/- p.m.+ HRA
Maximum Age (As on date of interview) : 30 years as on 09-08-2018
Educational Qualification
Essential Qualifications: Master Degree with 55% marks in Chemistry / Chemical Sciences / Pharmaceutical Sciences.
Desirable Qualifications: Candidates having experience in the area of natural product chemistry, isolation and chemical profiling and separation of biomolecules from plants will be preferred
Essential Qualifications: Master Degree with 55% marks in Chemistry / Chemical Sciences / Pharmaceutical Sciences.
Desirable Qualifications: Candidates having experience in the area of natural product chemistry, isolation and chemical profiling and separation of biomolecules from plants will be preferred
Project Assistant Level - II (Sr No 2)
Monday, 30 July 2018
Recruitment for M.Pharm in research at AIIMS @Last date 3 August 2018
Detailed Advertisement: Advt.No: AIIMS Bhopal/CDCHICC/2017-18/03
Applications are invited from eligible candidates for contractual post for Research Associate III on purely temporary basis in the ICMR Funded Research Project entitled “AIIMS Bhopal:Initiating Antimicrobial Stewardship activities in hospitals in India” at General Medicine department AIIMS Bhopal. Details are as follows
S.no.
|
Name of the
post
|
Pay scale
|
Number
of posts
|
Essential Qualifications
|
Age limit
|
1.
|
Research
Associate III
|
Rs. 48,000/-
consolidated per month (40,000 + HRA 20%)
|
1
|
M.Pharm with 3 years’ experience and at
least one publication in science citation index journal.
|
40 years
(Relaxed by 2 years for
woman candidate)
|
Interested candidates may download the application form from the AIIMS Bhopal website. Scanned copy of filled applications should be emailed at icmraiimsbhopalamsp2018@gmail.com
Medical Rep (Area Sales Executive ) Chandigarh Location Dept Oncology
Job Summary
» Medical Rep (Area Sales Executive ) Chandigarh Location Dept Oncology by Gatik Consulting
» Salary: ₹ 600000/- per annum
» Job location: IndoreIndore, Chandigarh, Delhi, Other Kerala, Patna &
» Job type: Full time work from office job
» Working days: 5 days working (Sat/Sun/ off)
» Job title: Pre-Sales,Sales / BD
» Employment type: On company payroll job
» Hiring process: Interview
» No. of vacancies: 1
Job Description
SkillSet: medical representative, medical rep.
Dear Friends
I have job opening for my Pharma client job location is Chandigarh ,patna,kerala tvm and delhi. Dept is Oncology
PHARMALYTICA 2018 #10 & 11 August 2018 @Hyderabad
After a very successful 4th edition, PharmaLytica 2018 will be held on 10th and 11th August at the HITEX Exhibition Centre in Hyderabad, India. In the 5th edition of this international trade fair and conference Pharmaceutical community can pick up on the latest industry trends, innovations and do business with Analytical, Laboratory, Machinery and Packaging Industry.
PharmaLytica conference, collocated with the exhibition is the knowledge forum and important industry gathering that brings you entire range of topics in analytical, outsourcing, laboratory, scientific & biotechnology sector. PharmaLytica is evolving as the leading marketplace for products and services along the entire value chain in niche segments within the Pharma industry.
Top 5 Reasons to Attend PharmaLytica.
PharmaLytica is making it easier than ever to network with new suppliers and existing, source new technologies, products and services to help you cost effectively develop and manufacture quality product.
- Discover New Technologies at the Innovation Gallery
- 8 Innovative products from these companies were at display in 2017 Innovation Gallery: Spraytech Systems India, Hindustan Inox, NORD Drivesystems, Fuji Electric, NIHVA technologies, Starco Meta Plast, June Enterprise, Himsan Polymer, PR Packaging. Visitors attended the gallery for free and at one location got to see a wide range of new products and technologies in the market.
R&D Associate at Unilever @ Apply Now
Post : R & D Associate
Job Description
Responsibilities
• Deliver all technical elements of Skin Care Innovations with highest delivered quality, OTIF against all project brief requirements.
• Ensure compliance to Internal Unilever protocols, External regulatory environment, while developing product solutions with respect to commitment to safety, environment, claim support, specification management etc.
• Understanding the consumer habits and needs as required by the Project team while articulating the needs of business
• Work with extended teams to align on innovation plans and ensure smooth delivery of the projects
Job Description
Responsibilities
• Deliver all technical elements of Skin Care Innovations with highest delivered quality, OTIF against all project brief requirements.
• Ensure compliance to Internal Unilever protocols, External regulatory environment, while developing product solutions with respect to commitment to safety, environment, claim support, specification management etc.
• Understanding the consumer habits and needs as required by the Project team while articulating the needs of business
• Work with extended teams to align on innovation plans and ensure smooth delivery of the projects
Merck Limited require Specialist in Bio Regulated Materials
Post : Specialist - Bio Regulated Materials
Job Description
PURPOSE OF THE POSITION
The Sales support/Technical support engineer manages on a daily basis product and application inquiries to support sales directly or indirectly and ensures these are treated with the level of reactivity according to the needs.
PURPOSE OF THE POSITION
The Sales support/Technical support engineer manages on a daily basis product and application inquiries to support sales directly or indirectly and ensures these are treated with the level of reactivity according to the needs.
Senior Associate required at Novo Nordisk
Post : RA Senior Associate
Job Description
As RA Senior Associate, you will be responsible for compiling and supporting the submission of manufacturing sites globally. The key responsibilities are: facilitation of submission planning meetings with RA colleagues in different countries, compilation of National Table of Contents TOCs based on the countries’ local requirements, request additional documentations from RA colleagues in HQ, as per the local requirements, coordination of registration samples when samples are required, quality Check of the registration dossiers, follow up with RA Affiliates on final submission to Health Authority You will be delivering high quality registration dossiers, which require a good understanding of Regulatory guidelines, Regulatory CMC documentation, different registration file formats and the Regulatory dossier compilation process.
As RA Senior Associate, you will be responsible for compiling and supporting the submission of manufacturing sites globally. The key responsibilities are: facilitation of submission planning meetings with RA colleagues in different countries, compilation of National Table of Contents TOCs based on the countries’ local requirements, request additional documentations from RA colleagues in HQ, as per the local requirements, coordination of registration samples when samples are required, quality Check of the registration dossiers, follow up with RA Affiliates on final submission to Health Authority You will be delivering high quality registration dossiers, which require a good understanding of Regulatory guidelines, Regulatory CMC documentation, different registration file formats and the Regulatory dossier compilation process.
Requirement of Pharmacist at Southern Railways
Online Applications are invited from eligible candidates for the engagement of various Para Medical Categories on full time contract basis. Applicants may submit Online Application by login to rrcmas.in.
Post : Pharmacist
Level in VII CPC Pay Matrix : Level 5
No of Posts : 01 (1 UR)
Age as on 01.01.19 : 20 to 35 years
Medical Classification : C2
Educational Qualification :
10+2 in Science or its equivalent with Diploma in Pharmacy from recognised institution and registered as Pharmacist under the pharmacy act 1948,
OR
Bachelor degree in Pharmacy from a recognised university or equivalent and registered as a Pharmacist under the pharmacy act 1948
10+2 in Science or its equivalent with Diploma in Pharmacy from recognised institution and registered as Pharmacist under the pharmacy act 1948,
OR
Bachelor degree in Pharmacy from a recognised university or equivalent and registered as a Pharmacist under the pharmacy act 1948
Sr Manager - Regulatory Affairs For A Pharma
Sr Manager - Regulatory Affairs for a Pharma Hyderabad Hiring for A manufactures and markets a comprehensive portfolio of Oncology products 10 - 15 YearsHyderabad Job Description Job Descripton Provide responses to regulatory agencies regarding product information or issues. Develop and maintain standard operating procedures or local working practices. Maintain current knowledge of relevant regulations, including proposed and final rules. Manage activities such as audits, regulatory agency inspections, or product recalls. Participate in the development or implementation of clinical trials, BE studies and other protocols. Direct the preparation and submission of regulatory agency applications, reports or correspondence. Formulate or implement regulatory affairs policies and procedures to ensure that regulatory compliance is maintained or enhanced. Provide regulatory guidance to departments or development project teams regarding design, development, evaluation or marketing of products Communicate regulatory information to multiple departments and ensure that information is interpreted correctly. Develop regulatory strategies and implementation plans for the preparation and submission of new products. Implement or monitor complaint processing systems to ensure effective and timely resolution of all complaint investigations. Investigate product complaints and prepare documentation and submissions to appropriate regulatory agencies as necessary.
Ug and Pg Pharmacy Freshers Physician,BPT,MPT,MLT Grads Wanted for Medical Codin
ISKILLS - Conciergerie d'entreprise Responsable
Cuddalore, IN
Designation :Medical Coder Trainee/ Medical
Coder/Sr.Medical Coder/Team lead Medical Coding
Specialization : EM In_Patient/ Out Patient/ Observation/
ED/ Surgery/ Multi specialty
Requirement
- Experience in Medical Coding (or) knowledge in Anatomy and Physiology.
- Good communication and interpersonal skills.
- Basic Computer Skills.
Salary : Negotiable (Incentives Benefits as per Corporate
Standards)
Hiring Process :Face to Face Interview, Telephonic
Interview
Technical Writer from Pharma required at Jekson Vision
Jekson Vision Pvt. Ltd.
Bhopal, IN
Job description
Develop documentation for end users; including User
Manuals, Online Help, Installation Guide, Technical Admin Guide, Release Notes
Validation of system according to cGMP Guidelines Preparation of qualification
documents such as IQ, OQ, PQ, DQ; Preparation of User Requirement Specification
Standard Preparation of the Manual like Product, Operational, Installation,
Maintenance, Trouble Shooting and Training Preparing Product Qualification Documents
Product Development Planning and Tracking Documentation as per requirements
This job is provided by Shine.com
Sunday, 29 July 2018
Pharmacists required at Bhavnagar Municipal Corporation (BMC)
BMC is a local government committed to provide basic infrastructure facilities to the people of the city. BMC is very well known for the managing the city by using private sector participation as well as introduction of innovative mechanism in management to serve people efficiently. City has prepared different plans for improving services and to nullify gap between services and demands.
Post : Pharmacist
No of Posts : 12 posts (ST-01, SOBC-03, UR-08)
Qualification :
1) D.Pharm or B.Pharm (From recognized university by Indian Government or State government) and experience as Junior Pharmacist in Government or Semi Government hospital as dispenser
1) D.Pharm or B.Pharm (From recognized university by Indian Government or State government) and experience as Junior Pharmacist in Government or Semi Government hospital as dispenser
Research Associate require at CENTRE FOR DNA FINGERPRINTING AND DIAGNOSTICS (CDFD)
Research Associate
Minimum Qualifications : Minimum qualifications: Ph.D. in Physics / Chemistry / Life Science / Biotechnology / Genetics / Biochemistry / Microbiology / Bioinformatics from recognized University / Institute.
OR
M.V.Sc./ M.Pharm./ M.E./ M.Tech. having three years of research, teaching and design and development experience
Minimum Qualifications : Minimum qualifications: Ph.D. in Physics / Chemistry / Life Science / Biotechnology / Genetics / Biochemistry / Microbiology / Bioinformatics from recognized University / Institute.
OR
M.V.Sc./ M.Pharm./ M.E./ M.Tech. having three years of research, teaching and design and development experience
Project – Junior Research Fellow/ Project Assistant /Research Assistant
Minimum Qualifications : M.Sc. in Physics / Chemistry / Life Science / Biotechnology / Genetics / Biochemistry / Microbiology / Bioinformatics / Medicinal Chemistry / M. Tech from recognized University / Institute.
Minimum Qualifications : M.Sc. in Physics / Chemistry / Life Science / Biotechnology / Genetics / Biochemistry / Microbiology / Bioinformatics / Medicinal Chemistry / M. Tech from recognized University / Institute.
Desirable Qualifications: Experience in research as demonstrated by the successful completion of a research project in a reputed Institute / Centre.
CGHS Recruitment 2018: 125 Pharmacist & ECG Technician (Junior) Posts
CGHS Recruitment 2018: Central Government Health Scheme is ambitious to engage new employees for a probation period of two years. For a total of 125 posts of Pharmacist and ECG Technician (Junior), the application form filling procedure has already been commenced. Before enrollment, aspirants must read out notification and check whether they are eligible for the recruitment or not. Application forms must be submitted before 27th August
CGHS Recruitment 2018 Eligibility Criteria
Educational Qualifications:
- Applicant must have passed 12th class exams with Physics, Chemistry and Biology subjects.
- Must have completed a diploma in pharmacy and catalogued as pharmacist under the Pharmacy Act, 1948.
- Should have two years experience as pharmacist in any of the recognised hospitals or pharmacy.
Saturday, 28 July 2018
Require Drug Safety Associate in Icon Clinical Research
Post: Drug Safety Associate
Job Description
• As a DSA, you will be expected to prepare regulatory documentation packets and coordinate the timely completion and submission of required reports to Health Authorities, Ethic Committees, Principal Investigators and business partners.
• Ensure compliance with regulatory reporting requirements for safety reporting in clinical trials.
• Ensure all ICON, Sponsor, and regulatory timeframes are met for the reporting of safety information.
• Ensure the completion of all departmental project activities accurately in accordance with ICON standards, regulatory requirements, and contractual obligations to sponsors
Job Description
• As a DSA, you will be expected to prepare regulatory documentation packets and coordinate the timely completion and submission of required reports to Health Authorities, Ethic Committees, Principal Investigators and business partners.
• Ensure compliance with regulatory reporting requirements for safety reporting in clinical trials.
• Ensure all ICON, Sponsor, and regulatory timeframes are met for the reporting of safety information.
• Ensure the completion of all departmental project activities accurately in accordance with ICON standards, regulatory requirements, and contractual obligations to sponsors
Job for Junior Research Fellow at CSIR-IHBT, Palampur
Post : Junior Research Fellow
No of posts : 02
Maximum Age (As on date of interview) : 28 years as on 10-08-2018
Stipend (Per Month) [Consolidated]
Rs.25,000/- p.m. + HRA
Rs.25,000/- p.m. + HRA
Educational Qualification(s) Essential / Desirable
Master Degree in Biotechnology / any branch of Biological Sciences / Bioinformatics with 55% marks and CSIR / UGC - NET-LS qualified.
Desirable: Experience in molecular markers / NGS / high-throughput genotyping.
Master Degree in Biotechnology / any branch of Biological Sciences / Bioinformatics with 55% marks and CSIR / UGC - NET-LS qualified.
Desirable: Experience in molecular markers / NGS / high-throughput genotyping.
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Regulatory Compliance Information Specialist at Merck Limited