Purna Organics Recruits at BioTecNika | Research Position Vacant

Purna Organics invites application fromfresher's for the post of Research Associateto work on organic terrace gardening projects based at Bangalore, Karnataka.

Name of the Post :Research Associate (RA)

Company Name : Purna Organics Pvt Ltd

Qualification & Experience * 
UG/PG in Agriculture or Plant Biotechnology / Biotechnology / Life Science / Genetics.

Required Skills * 
Candidates must be strong in General aptitude, Agriculture/ Plant biotech, Organic farming basics & Good communication (written as well as oral). Candidates will be screened through Written exam, Technical interview, HR.

Salary: 10,000 – 12,000/- p.m

Contact Details :
Postal address :
#14, 16th cross, 20th main,
JP nagar 5th phase,
Bangalore- 78,
Karnataka, India.
Phone no:
080-26587680, 080-41722163
Web Site :http://www.purnaorganics.com

How to apply: Eligible candidates can send their resume to careers@purnaorganics.comon OR before 1st march, 2011.

Interview Date: 3rd march, 2011

BioTecNika recruiting M.Sc /B.Tech Biosciences for the post of Academic Support Specialist | Freshers Welcome

BioTecNika Info Labs Pvt Ltd, Bangalore – Parent Company which runs India’s Largest BioSciences Career & education Portal is looking for passionate candidates having sound academic qualifications, willing to join India’s Largest BioSciences Career & Education Portal www.biotecnika.org as Academic Support Specialist

Post : Academic Support Specialist
Essential Qualification : B.Tech or M.Sc BioSciences
Experience : 0-5 Years
Annual Salary : Rs 96,000 – 1,50000
Nature : Full Time
Location : Bangalore

Required Skills:1.Candidate must be well conversant with Biosciences and must be strong in academics
2.Candidate must be dynamic, having excellent Communication skills & Inter-personal skills
3.Must be ready to work under pressure and meet targets given
4.Must have good computer Knowledge & Troubleshooting skills as well as typing skills
5.Should be ready to serve & counsel Biotecnika members/ Students through his/her Knowledge, IQ & Passion

NB : This position is located in Bangalore only, hence the candidate should be willing to relocate to bangalore upon selection.

Desired Qualification:1.Must be passionate about Biosciences subject
2.Should be a fresher/ Experienced with a CSIR NET/GATE Qualification and/or DBT/ICMR Qualification
3.Experience in Teaching will be an added advantage
4.Should be multi- tasking
5.Should be ready to work for long hours in front of computer
6.Experience in online Teaching will be an added advantage

Interested candidates should send their resume to jobs@biotecnika.org  with subject Line: Academic Support Specialist | <Highest Qualification achieved> | < Experience if any > | <current Location>

NB: This is not a research position rather an academic Post, Hence candidateslooking for Research Position need not apply

Deadline: 

 Friday, March 4, 2011

B.Tech Biotechnology Freshers can apply for Biotechnology Trainee Engineers at RGCB

As part of its human resource developmentprogram, RGCB invites applications forBiotechnology Trainee Engineers inbiotechnology instrumentation operation, cell & molecular biology and bioinformatics. It is hoped that through this training program, the candidates will get better job offers placements in the Biotech Industry. A total of 4 positions will be available in the year 2011 – 12. The positions will be temporary, on project mode, and initially for one year.

Essential Qualification : Candidates must have a BTech/BE degree or equivalent engineering degree in Biotechnology from a recognized University with  first class.
Age : Below 35 years
Emoluments (Stipend) : Selected trainees with 0 – 2 year documented work experience in related fields will be paid a stipend of Rs.16,800 /- consolidated per month. Selected trainees with more than 2 years documented work experience in related fields will be paid a stipend of  Rs.19,200 /- consolidated per month.
Duration : One year.

Only those fulfilling the above criteria needapply and will be called for interview Suitably qualified candidates may send applications in the prescribed format (www.rgcb.res.in/downloads/adv.doc) with a copy of full resume and attested photocopies of credentials & experience to reach the undersigned on or before 15th March, 2011. The envelopes must be superscripted with abbreviated title of the project, theadvertisement number and job title. Selection to the position will not entitle the candidate to any future positions at RGCB (permanent or otherwise). As with all project positions at RGCB, the position will be co terminus with end of the project.

In the event of more than 10 candidates being short listed, a written test will be done before the selection interview.

Deadline : 15.03.2011

Graduates in Life Science can apply for Senior Medical Writer at Parexel

Senior Medical Writer opening at Parexel. Details include

Description : Senior Medical Writer
Division : CRS
Department : Medical Writing
Location : AS - India - Bangalore
Essential Function :The Senior Medical Writer researches, creates, and edits all documents associated with clinical research. Responsibilities also include: acting as primary client contact formedical writing projects, working with other PAREXEL departments and clients to set and meet internal and external deliverable timelines, leadership, training and support of junior medical writing staff.
Key Accountabilities :

• Write clinical documents for submission to North American and European regulatory authorities, including but not limited to: briefing documents, clinical development plans, previous human experience summaries, human pharmacology summaries, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, CTD clinical overviews and summaries, safety updates, integrated summaries of safety and efficacy.
• Act in the capacity of project manager for medical writing projects. This may entail serving as the primary client contact, negotiating deliverable timelines, and resolving project-related issues. Project management of contractual and financial aspects may only be performed with the guidance of medical writing management.
• Serve as the Medical Writing representative on assigned project teams, providing proactive support to Project Management for planning efficient work plans and timelines for medical writing deliverables, and medical writing input into other departmental deliverables. Identify any potential project challenges to departmental line management and project manager including changes in project plan, timeline or out of scope requests, and suggest possible resolution options.
• Provide medical editing review of draft and final documents prepared by other writers before internal or external distribution. This includes both copyediting and content review.
• Ensure document content and style adheres to FDA/EMEA or other appropriate regulatory guidelines, and complies with departmental and corporate or client SOPs and style guidelines.
• Coordinate and conduct interdivisional team review and sign-off of document deliverables
• according to PAREXEL guidelines/SOPs including: distribute drafts, chair review meeting, incorporate revisions, document key project events, and complete sign-off procedures.
• Coordinate production and distribution of draft and final documents to project team and client. Ensure that all work is complete and of high quality prior to team distribution or shipment to client.
• Perform literature searches/reviews as necessary to obtain background information and training for development of documents.
• Review statistical analysis plans to assist in determining appropriateness of content/format for clinical writing.
• Attend internal technical team and client team meetings as required.
• Provide training and guidance and act as a mentor to less experienced departmental members.
• Supervise collection of materials by the medical writing administrative assistant or associate medical writer for assembly of client deliverables and for filing appropriately in Central Files, department project files and medical writing archives. 
• Assist management as needed with preparation of resourcing estimates for potential new medical writing projects.
• Assist management as needed in reviewing request for proposal packages sent by clients to determine content and appropriateness of materials required for development of clinical documents.
• Initiate and participate in departmental or interdivisional process improvement and training initiatives.
• Initiate and manage development of formats, templates and general guidelines for clinical documentation and workflow procedures. Assist in the development of departmental SOPs.
• Keep abreast of professional information and technology through workshops and conferences, and assure the appropriate transfer of that information to the department.
Skills :
• Excellent interpersonal, verbal and written communication skills
• Client focused approach to work
• A flexible attitude with respect to work assignments and new learning 
• Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
• Willingness to work in a matrix environment and to value the importance of teamwork.
• Team leadership skills. 
• Demonstrated understanding of the drug development process and a broad knowledge of FDA and EMEA guidelines. 
• Extensive clinical/scientific writing skills.
• Sound clinical foundation (e.g. knowledge of immunology, oncology, cardiology, etc.) is essential. 
• Advanced word processing skills, familiarity with Word for Windows.
Education Experience:
• Bachelor's degree in Life Sciences/Health Related Sciences or equivalent.
• Fluent in written and spoken English.
Clinical research/medical writing experience: 
• Experience in writing multiple clinical study reports either CTD documents or similar, or study protocols.
• Specifically for this position, experience in writing of pharmacovigilance documents such as PSURs and/or PADERs is highly desirable.
Note : Candidate With Relevant Medical Writing Experience in above mentioned areas can directly forward their CV to Kirloskar.das@parexel.com
Deadline : 18.03.2011
Apply Online

Fresher can apply for post of Production trainees at Cipla

Cipla known for its innovative pharmaceutical products backed by latest in technologyand creative marketing practices, is enjoying a commanding position among the top pharma companies in the country. Several specialised therapeutic divisions and promising new products have been launched and many more are in the pipeline.

Designation : PRODUCTION TRAINEES (API /Bulk Drugs) - 2 Opening(s)
Job Description :

• Daily Bulk Drug production activities.
• Documentation

Desired Profile :

• Reponsible for the production shop floor activities
• Looking for the freshers with B.sc chemistry and Bio-chemistry.

Experience : 0 - 1 Years
Location : Bengaluru/Bangalore

How to Apply:

Interested & Eligible Candidates can apply to Goverdhan Reddy /adminbms@cipla.com

Deadline : 27.03.2011

Deadline: 

 Sunday, March 27, 2011

Try and Try until u succeed

Beginner- Pilot

Hi friends, my name is Eben. As i am pursuing my study in the field of biotechnology, i am using this tool of blogging to give my views on some of the hurdles that we come across in this field. I want to take this opportunity to create an interactive interface for better understanding and communication of your views.