Clinical Research Job seekers Submit Resume here

October 28, 2008

Great News for everyone looking for a job in the feild of Clinical research, Analytical Science, Biotechnology, Microbiology QA QC etc in India. If you stay in India then you are invited to submit your resume on Google groups. All resume posted to this Official Guide2make.com-Google group will be open for everybody to veiw. You can upload your C.V. directly if you have a google account. If you dont have one then you can mail your resume to guide2make@googlegroups.com and your C.V. will be online instantly. However, you must copy paste your CV in the mail body itself. Dont send CV as an attachment. Also dont use tables in your resume.

You have to keep few things in mind though. Such as giving appropriate title to your resume in following format

 Field-Name-Post applied for-Highest qualification-Total Relevant experience in years-Relevant experience-Current location

eg: Bioanalytical-Rahul Sinha-Clinical Research Associate-M.Sc. Bioanalytical Science-3yr-Analyst on mass spectrometer-Mumbai.

More instructions are available on the parent website www.guide2make.com that maintains the database.

Vist the database at http://groups.google.com/group/guide2makecom?lnk=srg . You can also access the database through the main website.

Besides having this database the parent site has latest bioanalytical and clinical research jobs. Some of the major employers in this industry are Reliance life Science, Biocon , Dr Reddys , Macleod , Sun Pharma , Lambda , Cipla , Glenmark etc. The list is very long.

Most of these organizations have their own database too where you can post your Biodata.

All placement agencies are welcome to access Resume from this database and contact candidates for clinical research associate and other jobs directly.

QA QC job Opening in a leading pharma company in Bandra – Mumbai

October 31, 2008

We have opening in a leading pharma, distillery, textile, water purification , 

tannery, chemical etc company for the post of QA QC in Bandra.

Designation :- QA QC 
Qualification :- Bsc Chemist / Bsc Environmental Science / Bsc Biotechnologist
Experience :-  0 3 years  (Fresher can apply)
Location :-  Bandra 
Package :-  Upto 1.4 lac

Send resume in following format. 
Current Company :-
Current Designation :-
Current CTC :-
Expected CTC :-
Highest Education :-
If interested sent your updated CV on tnmniraj@gmail.com 

Niraj
HR Recruiter
T&M Services Consulting Pvt. Ltd
Mumbai

Also dont forget to forget to upload your C.V on the online resume database  by sending your resume to guide2make@googlegroups.com .

Please dont send attachment. Type or copy paste you resume in mail body while sending it to database

Bioanalytical Jobs in India (from Guide2make.com)

October 13, 2008

Dear friends,

Here are some jobs shown on Guide2make.com

You can visit this link to get contacts http://guide2make.com/Bioanalytical-jobs-in-India.htm

Please do not send mails to me since it is not me who has the job opening. I am only providing links for you collected from different websites. Hope you find this useful.

All the best.

Research Scientists/Research Associates (Bioanalytical CRO)

Responsible for Bioanalytical functions with high proficiency level in Method Development, Method Validation, Subject sample analysis, Review of protocols and reports. The person should be well versed with operation of LCMS/MS, UPLC, HPLC and having advanced knowledge of GLP requirements, method development and validation related to regulated markets.
 

Sr Research Associate-Bioanalytical for Females only

Responsibilities: Manage document approval process of a project or Quality system from checking to approval Document Check / review for complete, correct and online entries Report non-compliances/ GAPs and organise / conduct trainings to implement established procedures Co-ordinate with project groups, quality assurance and audit teams during data review / approval Prepare SOPs and technical documents as and when required Challenge the performers data at regular intervals to re-verify the result…
 

Sr. Research Associate – Bioanalytical, M.Pharm Compulsoary

Responsibilities: Manage document approval process of a project or Quality system from checking to approval.Document Check / review for complete, correct and online entries. Report non-compliances/ GAPs and organize / conduct trainings to implement established procedures. Co-ordinate with project groups, quality assurance and audit teams during data review / approval .Prepare SOPs and technical documents as and when required.Challenge the performers data at regular intervals to re-verify the res…
 

Research Associate ( Bioanalytical ), fresh Ph.d candidates for MNC CRO, Client of Elixir Web Soluti

Job Description: Preparation and review of Method SOPs, Method Validation Reports and Bio-analytical project reports.Supervision of laboratory instruments, calibration and maintenance programs.Co-ordinate Bio-analytical & Bio-equivalence studies. Development and implementation of efficient and compliant systems for Bio-analytical laboratory. Theoretical and operational knowledge of API -LCMSMS Co-ordination of Bio-analytical method transfer from method development and validation group to Bio-ana…
 

Research Scientist – Bioanalytical,with MPharm/PHD for Renowned Pharma

Manage document approval process of a project or Quality system from checking to approval Document Check / review for complete, correct and online entries Report non-compliances/ GAPs and organise / conduct trainings to implement established procedures Co-ordinate with project groups, quality assurance and audit teams during data review / approval Prepare SOPs and technical documents as and when required Challenge the performers data at regular intervals to re-verify the results Training and men…
 

Opportunity in a Leading CRO (Bio-Analytical)

This individual will be responsible for establishing and running LC-MS/MS-based bioanalytical methods for the quantitation of drug discovery candidates and related substances in a variety of biological matrices. This individual will be responsible for providing input into the design of multiple component bioanalytical procedures, for the analysis of samples, and for the evaluation, interpretation, and distribution of bioanalytical results using LC-MS/MS-based methods. SKILL SET : This individual…
 

Research Associate II /Scientist

Novartis is currently seeking a Master or Ph.D. level Scientist in Analytical Chemistry that is to support our research efforts at our facility in Shanghai, China. The position has two primary areas of responsibility. You will be responsible for developing high throughput methods to analyze biological samples to support in vitro ADME and in vivo PK studies using LC/MS/MS and other technology. For the area of NMR, Mass Spectrometry / Separation structure elucidation of small molecules (organic) i…
 

Biomarker Expert (Lab head)

Be responsible for the generation and application of bioanalytical tools for preclinical and clinical studies to support R&D programs. Perform Validation of analytical methods according appropriate quality standard and BM analysis for multiple preclinical and clinical studies. Interpret and report the biomarkers analysis data to support clinical studies. Explore and develop core capabilities in Biomarker analysis with classical and cutting edge technology (such as ELISA, Luminex, multiplexed ass…
 

Research Associate

Responsible for Method Development and Validation of molecules by LCMSMS tecniques Bioequivalence projects for analytes by LCMSMS techniques Calibration for HPLC instruments& maintaining its Records Documentation as per USFDA & WHO Requirement Responsible for making SOPs , EOPs, Protocols, Method Validation Report, Bioanalytical reports Hnadling of Bioanalytical Instruments
 

Senior Scientist I

Ensure project support with generation and application of bioanalytical tools for Biomarker analysis in preclinical and clinical studies. Support projects with state of the art in Biomarker analysis using classical and cutting edge technology (such as ELISA, Luminex, multiplexed assays, biochip, etc). Be responsible for validation of analytical methods according to appropriate quality standard and Biomarker analysis for multiple preclinical and clinical studies. Contribute the internal and exter…

Latest Clinical Research jobs shown on Guide2make.com

October 13, 2008

Dear friends,

Here are some jobs shown on Guide2make.com

You can visit this link to get contacts http://guide2make.com/clinical-research-jobs-in-India.htm

Please do not send mails to me as it is not me who has the job opening. I am only providing links for you. Hope you find this useful.

All the best.

Clinical Research Associate

Clinical Research Associate (CRA ) SUMMARY OF POSITION: The Clinical Research Associate (CRA) is part of the Global Clinical Research Professional Pathway that defines Clinical Research positions. It is a mid-level rung in a ladder that steps from Clinical Research Assistant to Clinical Research Associate to Senior Clinical Research Associate. Colleagues in these positions monitor clinical trials Phase II through Phase IV within a country. MAJOR ACTIVITIES AND RESPONSIBILITIES: Site Management: …
 

Clinical Research Associate

Our client is an established clinical research organization. In line with their expansion plans, there are now openings for the following positions. Clinical Research Associates Philippines Clinical Research Associates Malaysia Clinical Research Managers Philippines Clinical Research Managers Malaysia Clinical Research Associates Your main responsibility will be to ensure the setting up, management, monitoring and closeout of investigator sites in the country assigned; undertaking clinical trial…
 

Associate Manager Clinical Research Associate

Associate Manager, Clinical Research Department : Medical Reports to : Clinical Research Manager Responsibilities: Lead and manage one of two Clinical Research sub-teams Conduct feasibility assessments and select appropriate investigational sites for assigned trials Conduct contract negotiation with investigational sites Oversee implementation and conduct of assigned trials in accordance with ICH GCP guidelines, applicable local laws and regulations and all internal SOPs Develop informed consent…
 

CLINICAL RESEARCH ASSOCIATE (M.D PHARMACOLOGY ONLY)

CLINICAL RESEARCH ASSOCIATE/EXECUTIVE (M.D PHARMACOLOGY ONLY) We are placement consultants in Mumbai, recruiting candidates on All India basis for the Indian companies + for the Gulf Countries + African Countries.Some of our clients are:- Pfizer Ltd,Reliance Life Sciences, Serdia,UCB India Ltd,B.Braun Medical India,Merck Ltd, Emcure, Elder Pharmaceuticals Ltd, Merck, Matrix Labs,Meyer Organics, Roche, Molekule India Limited, Healthprime International, Unichem, Shreya Lifesciences, Glenmark Pharm…
 

Clinical Research Associate (Consultant)

The Clinical Research Associate (CRA) is consultant position based in the International AIDS Vaccine Initiative India, New Delhi. He/she refers directly to the Medical Director of IAVI India, New Delhi. In close collaboration with the medical investigators and laboratory and site staff from TRC (Tuberculosis Research Center), Chennai and National AIDS Research Institute (NARI), Pune, the CRA provides assistance in organizing and coordinating preparedness and implementation activities related to …
 

Clinical Research Associate II / Senior CRA / Technical Assistant

Clinical Research Associate II / Senior CRA Job Functions: Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators for participation in clinical trials Negotiate study budgets with investigators Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites Review draft protocols for completeness and feasibilit…
 

Senior Clinical Research Associate

A leading Indian Multinational Clinical Research Organisation which provides full clinical development services and has steadily built its reputation as a specialist in late stage clinical development solutions is looking out for Senior Clinical Research Associate. Job Description:- Experience : Minimum two year clinical trial monitoring experience Exclusively on the conduct of Phase II and Phase III clinical trial as a Clinical Research Associate.Kindly note candidates working in BE/BA or other…
 

Clinical Research Associate

Our client is an international CRO a strong presence in Asia. They have vacancies for experience Senior Clincial Research Associates and Clinical Research Associates to be based in the Singapore. The CRA/SCRA will be responsible for the assigned clinical studies from study initiation, coordinating & track, and ensuring the quality of the studies. Responsibilities include and not limited to: Conduct pre-study, initiation, monitoring, and close-out visits for research sites; Source document verifi…
 

Senior/Clinical Research Associate (Beijing)

Our client is a US-base CRO with a growing presence in Asia. To support their expansion of clinical operation in North Asia, they are seeking to recruit an experienced Senior/Clincial Research Associates to be based in Beijing, PRC. Responsibilities include but not limited to: Initiate study start-up of sites Management and monitoring of assigned studies Assist in the recruitment of patients within the study criteria Ensure effective resource management and in ensuring time lines are met Ensure …

Clinical Research Associate

We are interested in recruiting Clinical Research Associates for Mumbai, Chennai, Bangalore & Gurgaon. The Job Description is as follows: Key Accountabilities Responsible for identification of PI s & collection of necessary documents to be forwarded to study managers, in order to check the feasibility of site and approval from authorities. Responsible for training of team at site regarding the monitoring plan, recording & maintenance of essential documents and assisting study managers for start …

Job for Research Scientists /Post-Doctorate at China Novartis Institutes for BioMedical Research Company, Ltd (Beijing)

August 15, 2008

Minimum quantification requirement for the post is

PhD and/or MD degree in relevant domains, such as Biology Sciences, Animal Sciences, Biochemistry, and Pharmacology, etc. The company is looking for people with Two to three years of direct research experience along with good publication of workin reputed journals is needed. The job applicant must have wide knowledge and experimental skills are necessary. The successful job applicant will posses demonstrated Capability to work in group-oriented matrix structures, and posses strong communication skills in both oral and written English.

Details

Experience: 3 – 8 years
Job Opening (vacancy) Category: Pharmaceutical/ Biotechnology
Job Opening (vacancy) Location: Beijing
Important Skills: “biology sciences”, “animal science”, biochemistry
Job Opening (vacancy) Ref code: 42339BR
Role: Basic Research Scientist

apply here

Trainee – Microbiology (Mumbai) Colgate Palmolive (India) Limited

August 11, 2008

Colgate Palmolive (India) Limited
— Advertised on 6-8-08. — Application deadline on 4-10-08.

Trainee – Microbiology
(Mumbai)

Requirements:

Applicant would work as a Trainee in the Microbiology group of the India Global Technology Centre (IGTC). After 12-18 months the individual could be considered for permanent job based on performance and adapatability while the traineeship duration.

Minimum qualification needed – Masters in Science (M.Sc.) (Microbiology)
Kindly apply on internet against the Position. We do not promote candidates to send Biodatas through E-mails.

Come to our website http://www.colgate.co.in for information on more opportunities.

Biotechnology Manufacture

August 11, 2008

Biotechnology Manufacture (HEAD)
Experience/Skill:
10 – 16 Yrs

Workplace:Pune
Educational qualification:
UG – Bachelors in Technology/B.E. – Any Specialization, Bio-Chemistry/Bio-Technology, Biomedical

POST GRADUATE – Any POST GRADUATE Course – Any Specialization;Post Graduation Not Needed;M.Sc – Any Specialization, Bio-Chemistry, Biology;Masters in Technology – Any Specialization, Bio-Chemistry/Bio-Technology, Biomedical

Industry Type:
Pharmaceutical/ Biotechnology/Clinical Research
Work domain:
Manufacture, Maintenance, Quality
Posted Date:
07 Aug

Vacancy Details
Position will be leading the complete manufacturing activities of a biotechnology plant manufacturing therapeutic genetically modified (recombinant) proteins and monoclonal antibodies.

Major Responsibilities are as under,
Guides the monthly/daily manufacture plan and manufacture activities for the different Domains to achieve the monthly manufacture target, including managing variances in the manufacture plan of Microbiological & Mammalian Cell lines.

Provides technical inputs and ensures execution of up-gradation and expansion projects for specified Domain.

Sets, establishs and reviews STANDARD OPERATING PRACTICE (SOP)s for the plant(s) to achieve quality/Current Good manufacturing Practices (cGMP) and productivity targets.

Ensures latest product operationalisation to meet manufacture plan and ensure product availability as per specified timelines.

Manages the operations of the plant(s) to ensure they adhere to the budgets.

Ensures compliance with different regulatory and Current Good manufacturing Practices (cGMP) requirements with respect to facility, quality, validation, documentation and safety.

Represents the organization in regulatory audits and is responsible for getting plant related regulatory sanctions from different regulatory agencies.

Desired Applicant Profile
Must have 10-15 yrs of Experience/Skill in manufacture of Biological/Biotechnology products in well-known companies with 4-5 yrs hands on Experience/Skill of therapeutic genetically modified (recombinant) proteins and mammalian cell culture.
Must have sound knowledge of different regulatory and Current Good manufacturing Practices (cGMP) requirements.

Corporate profile
One of the leading Pharmaceuticalceutical organization.

Contact Details

Organization Name:
Customer of Fact Personnel.

Executive Name:
Pramod Deshmukh

Address:
3/823 To 828, Navjivan Society
Lamington Road
Near Minerva Cinema, Mumbai Central (East)
Mumbai,Maharashtra,INDIA 400008

Email Address:
pt@factVacancys.com

Telephone:
91-022-66500718

Reference ID:
PD – Biotechnology Manufacture

HIMEDIA Chemist Job vacancy in Mumbai

August 9, 2008

Chemist

The candidate must be MSc /B Tech in Inorganic or Organic chemistry or biochemistry.
The candidate must have experience with laboratory reagents and mus be able to handle packing material

Female candidates are preferred for this position

Contact:
HIMEDIA
Vadhani industrial estate,
LBS marg
Ghatkopar (W)
Mumbai 400086

tel: 2500 1607

HIMEDIA Diagnostic< Biotechnology Molecular Biology

August 9, 2008

Stores Assistant post

Qualification MSc / BSc / B.Tech /B Chem,
Specialization in material management warehouse and other logistics.

Exp: Must have 2-4 years of experience in handling store operations, chemicals and raw materials. The candidate must be able to maintain records and co-ordinate with the purchase dept.

Candidate having similar profile in other company will be preferred.

The position requires one to have good command over english and good computer skills

Contact:
HIMEDIA
Vadhani industrial estate,
LBS marg
Ghatkopar (W)
Mumbai 400086

tel: 2500 1607
2500 0809

Officer/ExecutiveCorporate Quality Assurance

July 25, 2008

We are looking for an Officer/Executive–Corporate Quality Assurance for one of our esteemed client in
Mumbai. If you want any more information regarding this company then please reach me on 9328191491

Location : Worli, Mumbai (Free Transport Facility from Dadar station provided by the company)

Qualification : M. Sc Analytical Chemistry (Preferably)

Gender : Male Candidate

Experience : Minimum 3- 4 years

Job Profile : Should have experience of analysis of Pharmaceutical products and substances.

Monitoring and review of Process Validations, Qualification of equipments and utilities, and handling
f Non-conformances, analytical method validations.
Exposure/ Experience of Inspections ad conducting Audits for evaluation and monitoring of desired
quality systems for API/ Bulk Drug Manufacturing facility.
: Readiness for extensive traveling across manufacturing facilities at different location.

Varun Menon
Recruitment Consultant,
Universal Hunt.

email: varun.menon@universalhunt.com


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