Thursday, March 11, 2010

Pharmacist/Chemist/Bio Chemist, D.Pharm/B.Pharm; Surya Health Care Limited

Job description: Dispensing prescription medicine to the public,
Checking dosage and ensuring that medicines are correctly and safely supplied and labelled(pharmacist are legally responsible for any dispensing errors);
Liasioning with doctors about prescriptions
Selling over the counter medicines
Counseling and advicing the public on the treatment on minor ailments
Advising patint of any adverse side effects of medicines or potentials interactions with other medicines/ treatments
Preparing dosette and cassette boxes, usually for the elderly but also for those with memory/learning difficulties where tablets are placed in compartment for specified days of the week
Providing the reange of speacialist healthj check services
Overseeing the ordering and save storage of medical products
Keeping up to date with current pharmacy practice, new drugs and their uses
Maintaing computerized records
Managing, supervising and training pharmacy support staff
Promoting sales and developing the business


send resume to:
resume@vivayourfamilychemist.com

Bengaluru/Bangalore, Chennai, Delhi, Kolkata, Mumbai ; Executive - Scientific Services; M.Pharm Freshers; USV Limited

Catering to the request from the Doctors/Field personnel/Product Management Team for any brands specific topics for continous medical education.

Scientific reference search - disease & product specific and making scientific circulars based on this for the field.

Journals search, scanning and selection of relevant articles.

Devising Brand Stratrgy and support to Marketing team.

Making Powerpoint presentations.

Handling queries about products & related diseases

Taking active role in Theme meetings.


send resumes to : hrd@usv.co.in

Mumbai; B.Pharma/ M.Pharma, Executive/Sr Executive-Regulatory Affairs, Intas Pharmaceuticals

1.preparation of registration dossiers for semi regulated and regulated markets.

2.Compilation and review of plant and R&D documents

3.Response to letters from various health authorities

4.Checking/reviewing of documents as per regulatory requirements

5.guide site for regulatory filing documentation

6.maintenance of lists/documents/records

7.co-ordinate with QA/production

Send resume to:
hrd@usv.co.in

Mumbai; B.Pharm/M.Pharm; Pharmacist/ Associate Pharmacist - Drug Delivery Research Laboratory; USV limited

Technology transfer of formulation for Regulated Markets.
Good knowledge of process development and
Trouble shooting of pharmaceutical dosage forms
Candidate must have experience in Process Development & Technology Transfer.
Candidate having experience in manufacturing will be desirable.

Experaince:5 - 10 Years

send resumes to: hrd@usv.co.in

All India; AREA BUSINESS MANAGER; B.Pharm; Piramal Health care

Team Player / Customer Sentivity / Sales Oriented / Problem Solver / Market Analysis

To promote diagnostics products like instruments and reagents in the allocated territory. Follow up with the existing customers and provide the service if need. To interact with the disstributors for promoting the product and collection of payments. To achieve sales targets.

Exp: 3 years

Register and send resume to: http://cop.mynpil.com/ERecruitment/jsp/ViewJobs.jsp#

Baddi; EXECUTIVE-QUALITY ASSURANCE;B.Pharm; Piramal health care

Experience in Inprocess Quality assurance and candidate should be in formulation unit. Knowledge of SAP;

Ex: 2 years;

Register and send resume: http://cop.mynpil.com/ERecruitment/jsp/ViewJobs.jsp#

Mumbai; B.Pharm+MBA;BRAND MANAGER - SARIDON; Nicholas Piramal

Plan & deliver business objectives for the brand(s) assigned Develop & implement marketing plans which addresses brand requirements – short term & long term Lead and generate consumer insights, to enable brand extensions and/or NPD Create new insightful communication(s) and manage overall communication process on his/her brand in conjunction with the creative agency Possess comprehensive knowledge of media planning & buying and execute efficient, impactful media bursts to deliver successful brand performance Have in-depth knowledge & understanding of the entire gamut of market research – U&As, Tracks, Audit, CPTs, Link, BAR tests, etc Lead & generate MIS on brand(s) assigned, category, competition and trade at regular intervals so as to result in effective brand management.

Exp: 6 years

Send Resume to: http://cop.mynpil.com/ERecruitment/jsp/ViewJobs.jsp

All India; Medical Representatives; B.Pharm; Glaxo Smithkline

Responsibilities • Achieve and exceed sales target as per the company’s guidelines & policy
Promote Company’s brand & make products available at Chemist / Retail outlet, etc.
Increase and generate prescription base in a defined area.
Use strategically inputs and promotions materials given by Marketing Dept. from time to time to customers.
To conduct market research and to identify potential market and transfer market information.
Organise events, seminars, etc. for promoting brands.


Requirements Excellent Interpersonal skills & Communication skills
Planning and Analytical Skills
Flair for selling (Pharma selling)
Aggressive for meeting targets / deadlines
Good understanding of Pharma Market & strong network
Excellent Scientific Knowledge

Resume should send by regestring the site:
http://impact-in.jobstreet.com/jobs/jobs.asp?eid=14066169&fil=1

Hyderabad; M.Pharm; Team Member; R&D; Dr.Reddy's

Academic Background and Key Experience Requirements : 1. Required Education: M. Pharma
2. Minimum Experience:1-3 years of experience

Send resumes to: talent@drreddys.com

Hyderabad; Professional Service Representative

Academic Background and Key Experience Requirements : 1. Required Education: Graduate (Science/Pharmacy) with MBA
2. Minimum Experience:
• 3 to 4 years of work experience in Pharmaceutical industry
• Product Management experience is desirable

Send resume to: talent@drreddys.com

Hyderabad; M.Pharm; Regulatory Affairs(EU)-TM,Hyd; Dr.Reddy's

Job Responsibilities
• Providing regulatory guidance throughout R&D and mfg processes.
• Compiling / Writing & submitting regulatory documents in an efficient and timely manner.
• Integrate the relevant regulatory policies, guidance’s and procedural requirements into the developmental phase of the multi functional teams.
• Follow-up on submissions to ensure final approval in the shortest possible time.
• Auditing at various phases of development to ensure regulatory compliance.
• Responsible for responding to any regulatory queries on behalf of the project team with inputs from other team members.
• Anticipate issues from a reviewer perspective and proactively ensure actions.
• Ensure project work is auditable, complete & error free
• License applications-Test license, BE NOC, CT NOC, M&M application, Mfg license etc.
• Ensuring availability of documents like WHO GMP Certificates
• Interaction with RA counterpart of bulk suppliers.
• Develop/Review of SOP's, Checklists


Job Requirements
M.Pham with 2-5 yaars of relevant experience

Send resume to: talent@drreddys.com

Hyderabad; Quality / QC / QA / Quality Management; Dr Reddy's

Job Responsibilities
-For IPQA, documentation, annual product review, vendor qualification, analytical assurance


Job Requirements
Qualification : B. Pharm
Experience : 1-5 Years

send resume to: talent@drreddys.com

Hyderabad; Quality / QC / QA / Quality Management; Dr Reddy's

Job Responsibilities
-For IPQA, documentation, annual product review, vendor qualification, analytical assurance


Job Requirements
Qualification : B. Pharm
Experience : 1-5 Years

send resume to: talent@drreddys.com

Hyderabad; Team Member TTG/AVD; Dr.Reddy's

Job Responsibilities
Justification: Development of Alternate vendors for APIs and Excipients
for US, Europe, Row, National markets for approved and commercialized products.

Job responsibilities:
• Review of existing formulation, open part of DMF, Product dossier , Specifications, STP etc.
• Evaluation of alternate vendor material, establishing equivalency with existing material
• Execution of Feasibility , Pre exhibit and Exhibit batches
• Technology transfer from one manufacturing location to other
• Transfer from development lab/pilot plant to commercial locations
•Preparation of master batch documents, validation protocols, reports for filing supplement variation.
• Trouble shooting

Job Requirements
Academic Background and Experience:
• Should be M.Pharm/B.Pharm graduate.
• 1 - 3 years of experience in Process development/Tech transfer / formulation development areas.
• Having good knowledge and hands of experience on the equipment, process, materials, and specification etc of Solid dosage forms.
• Additional exposure in other dosage forms is desirable.
• Knowledge on formulation development, GMP, Regulatory requirements will be an added advantage.




Key performance Indicators:
• Number of Alternate vendor materials or CIP materials developed and got approval.
• Addressing trouble shooting through root cause analysis.
• Ensuring smooth transfer of technology in the defined time frame

Key personal attributes:
• Should have good communication & interpersonal relationships.
• Ability to work with cross functional teams
• Should have positive attitude and problem solving ability.

Operating Network:
•The position shall work at shop floor of different plants and interact with different departments like Supply chain, RA,QC, QA, Production etc.

send resume to: talent@drreddys.com

Hyderabad; M.Pharm; Regulatory Affairs-TM; Dr.Reddy's

Job Responsibilities
• Participate in the regulatory activities of full spectrum of formulation development, from clinical trials to marketing to post approval activities.
• Ensure the appropriate licensing, marketing and legal compliance of the finished dosages.
• Review the documents at each stage of formulations development.
• Highlight the regulatory issues that can be there and try to resolve them.
• Coordinate with R&D, AR&D, QA, etc. to collect the complete set of documents.
• Compile the ANDA document to be submitted to FDA.
• Ensure the documents are error free and have minimum deficiencies.
• Prepare annual reports and send them to FDA.
• Manage change controls and deviation controls.
• Keep themselves abreast of international legislation, guidelines and customer practices
• Develop and write clear arguments and explanations for new product licenses and license renewals.
• Advise PDTs on regulatory requirements.
• Respond to the queries of Regulatory authorities and customers on time.
• Review the process change proposals and provide guidance on change proposals.

Exp:

M.Pham with 2-4 years of relevant experience supporting Europien or RoW Region

send resume: talent@drreddys.com

Scientist / Sr. Scientist - RND - ANF; Biocon

Designation: Scientist / Sr. Scientist - RND - ANF
No Of positions: 1
Education Qualification: M.Pharm/M.tech
Experience: 1-4 years


Job Description:

Conducting analytical characterization
Pre-formulation studies and indicative stability programs of biologicals
Coordinating activities between the formulation group and purification/quality control groups

Resumes should send: careers@biocon.com

Bengaluru; Formulation Development - Dy.Manager/ Sr. Scientist; Biocon

Profile: Candidate who have Successfully developed, scaled and launched the varied dosage forms for ROW and Regulated markets; Qualification: B.Pharm, M.Pharm; Exp: 8-12 years; Telephone enq: 080-28082216; website: http://www.biocon.com/

Hyderabad/Bengaluru: Research Director- Chemistry / Biology

Qualification: UG - B.Pharma,B.Sc - Bio-Chemistry, Biology, Botany, Chemistry, Microbiology, Zoology
PG - M.Pharma,M.Sc - Bio-Chemistry, Biology, Botany, Chemistry, Microbiology, Zoology; experaince:8 - 13 Years; position: Research Scientist; Package: Rupees 35,00,000 - 50,00,000 & above
resume should send to: careers@aurigene.com