Maharashtra

Vacancy for Scientific Assistant at Tata Memorial Center

Vacancy for Scientific Assistant at Tata Memorial Center

SCIENTIFIC ASSISTANT ‘B’ (RADIO-DIAGNOSIS) : 1 POST (UR)
Qualification & Experience
B.Sc./B.Pharm. with minimum 50% marks and 2 years Diploma in Medical Imaging Technology OR B.Sc.(Physics) with minimum 50% marks and 2 years Diploma in Medical Radiography OR H.S.C. and 3 years degree course B.Sc. in Medical Radiography Should have atleast 01 year experience as Medical Radiographer in a large Hospital with CT and MRI.

Age : Upper Age limit as on 26.12.2016 : 30yrs

Pay Band : PB-2 (Rs.9300-34800)
Initial Pay & Grade Pay: Rs.9300 + 4200
Approximate total emoluments: Rs.35,876/-

GENERAL CONDITIONS :
1.Age & experience will be reckoned as on 26.12.2016
2. Age Relaxation
(a) Upper age is relaxable for persons belonging to Reserved Categories such as SC/ST/OBC/PWD/Ex-servicemen & Other categories as per the instructions of Govt. of India as under
05 Years : SC /ST
03 Years : OBC
10 Years : PWD [additional 5 years in case of SC/ST & 3 years in case of OBC]
Ex-servicemen : length of service in Armed forces plus 3 years (additional relaxation in case of SC/ST/OBC as per the instructions of Govt. of India)

(b) Age relaxation maximum by 5 years for Departmental candidates, candidates with additional qualification and higher experience  and candidates working in TMC on temporary basis / under project / on contract basis

Application Fee :
(i) Candidate shall pay the application fee of Rs.300/- online using  Debit Card / Credit Card.
(ii)SC /ST / Female Candidates / Persons with Disabilities / Ex-servicemen (1st time applying for civil post after serving any rank)  are exempted from paying application fees.
(iii) The application fee paid  will not be refunded under any circumstances.

Benefits
(a)Allowances : In addition to pay, other allowances including DA, HRA, TA etc. will be admissible as per the prevailing rules of TMC.
(b)Training & Development : All officers will be eligible for institutional financial support for active participation in National and International Medical Meetings, Workshops and Conferences after their probation is closed.
(c)Medical Facility : All officers will be covered by a Contributory Health Service Scheme for self and dependants
(d)Accommodation : Residential accommodation will be provided subject to availability
(e)Retirement Benefits : All are eligible for retirement benefits and pension under the New Pension Scheme.

Non Receipt of Application : Tata Memorial Centre does not take any responsibility for non receipt of application through Online / By post for whatsoever be the reason.

Late and incomplete applications will be rejected.  Canvassing in any form will disqualify the candidature.

Legal jurisdiction for any dispute will be at Mumbai.

Last date for online application is 26.12.2016 ­upto 05.30 p.m. & receiving hard copy of online applications within 7 days from last date of Online application i.e.  02.01.2017.

For more information, Click here.

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Opening at Quintiles for the post of Medical Writer

Opening at Quintiles for the post of Medical Writer

Job Description
PURPOSE
Prepares, or contributes to the preparation of straightforward clinical documents, for either internal Quintiles customers or external clients, for investigational drugs, biologicals, or medical devices, under the guidance of senior staff. Participates in project teams and may lead specific tasks, consulting senior staff as necessary.

RESPONSIBILITIES
• Acts as Lead Medical Writer and performs competently on straightforward projects, with guidance from senior staff as required. Takes responsibility for preparation of assigned documents to a high standard, working in accordance with
Quintiles SOPs and the customer’s requirements. Identifies project needs, tracks project timelines and implements client requests with senior review.
• Participates in both internal and external project team meetings and liaises directly with the customer on medical writing issues, as appropriate and with senior support as needed.
• Arranges appropriate internal review of assigned documents and takes responsibility for on-time delivery.
• May perform QC review of documents or parts of documents prepared by more senior staff.
• Takes responsibility for managing day-to-day workload for assigned tasks and projects, in collaboration with senior staff.
• Keeps abreast of current data, trends, medical writing/regulatory knowledge, developments and advances in area of drug development/medical writing.
• Complies with Company SOPs and participates in the implementation of new SOPs.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
• Excellent standard of written English, and ability to communicate fluently and effectively in English, both in writing and verbally.
• Familiarity with the structural and content requirements of clinical study reports, protocols, and similar documents.
• Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner.
• Competence in completing a good first draft clinical study report in a routine therapeutic area within a reasonable time frame with limited guidance.
• Good understanding of common statistical methods used in clinical trials and interpretation of their results.
• Ability to give a simple presentation to a project team and/or customer, e.g. on Medical Writing processes.
• Ability to identify inconsistencies and deficiencies in statistical output.
• Ability to work on several projects at once while balancing multiple and overlapping timelines.
• Ability to assess workload and suggest prioritization to senior staff.
• Demonstrated abilities in collaboration with others and independent thought.
• Demonstrates confidence and maturity in most routine Medical Writing situations.
• Behaves professionally and responds appropriately to feedback from internal and external sources.
• Knowledge of regulations relevant to medical writing.
• Careful attention to detail and accuracy.

Candidate Profile
• Must be computer literate.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
• Bachelor’s degree in a life science-related discipline, plus at least 1.5years experience as a medical writer within a pharmaceutical environment; or equivalent combination of education, training and experience

PHYSICAL REQUIREMENTS
Extensive use of telephone and face-to-face communication requiring accurate perception of speech
Extensive use of keyboard requiring repetitive motion of fingers
Regular sitting for extended periods of time
May require occasional travel.

Additional Information:
Experience: 1.5 years
Location: Mumbai, Maharashtra
Education: B.Pharm, B.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Medical Writing
Job Code: 1612335
End Date: 31st December, 2016

To apply online, Click here.

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Opening for Area Business Manager – Panacea Vaccines BU

Opening for Area Business Manager – Panacea Vaccines BU

Job Description
The candidate should have at least five year of experience in Pharma sales with minimum two years in man- management in specialty division.
Candidate who are presently working with Vaccines or with Top  MNC’s in Acute / Chronic / Pharma Business with past experience in Vaccines wants to further pursue their career and passion to excel in Vaccines Business.

Work Profile:
1) Sales target achievement.
2) Brand Building & Increase market  share
3) Implementation of marketing strategies.
4) Stockiest ,Dealer, People, Customer  Management.
5) KOL / KBL Management

The candidate should have good communication skills.
The candidate should have good people management skills.

Additional Information:
Experience: 5-15  Years
Age: 27-38 years
Location: Nagpur
Education: B.Sc, B.Pharm, M.Sc, M.Pharm
Industry Type: Pharma/Biotech/Vaccines
Compensation: Competitive salary
Functional Area: Sales
Last Date: 10th December, 2016

Apply/Forward your Resume, saleshr@PANACEABIOTEC.COM

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Career as Executive Sales and Market Development @ Panacea Biotec

Career as Executive Sales and Market Development @ Panacea Biotec

Job Description
The candidate should have at least one year of experience in Pharma sales in super specialty division or in Vaccines division.
Candidate who are presently working with Vaccines Division or with Top  MNC’s in Acute / Chronic / Pharma Business, wants to further pursue their career and passion to excel in Vaccines Business.

Work Profile:
1) Sales target achievement.
2) Coverage of listed Drs for brand promotion.
3) Implementation of marketing strategies.
4) Stockist management, Dealer Management.
5) KOL / KBL Management
The candidate should be localite.
The candidate should have good communication skill.

Additional Information:
Experience: 1 to 5 years
Age: 21-29 yrs
Location: Kanpur, Kolkata, Vizag, Hyderabad, Trichur,Chennai, Salem, Malad, Dombivali, Bhopal, Ahmedabad, Bispur, Valsad, Bangalore, Coimbatore, Mumbai
Education: B.Sc, B.Pharma, M.Sc, M.Pharma
Industry Type: Pharmaceutical
Compensation: Competitive salary
Functional Area: Sales
Last Date: 15th December, 2016

Apply/Forward your Resume to saleshr@PANACEABIOTEC.COM

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Opening for Manager Group Procurement in Merck Pharma

Opening for Manager Group Procurement in Merck Pharma

Job Description:
Your possibilities to develop in our growing company are just as manifold as our product portfolio. We offer a modern and international working environment to unleash your innovative potential in diverse teams, and take responsibility for our employees, products, the environment and society.
As Manager Group Procurement ‘Contract Manufacturing’ you are part of Merck’s Global Procurement Organization. Your role is positioned in the Healthcare Procurement team.
You are familiar with the contract manufacturing category, ideally in pharma, and you have gained a deep understanding of the current market trends. You have gained experience in global projects and you are comfortable working with different cultures. You are looking for challenges to establish best industry practice and innovative ideas in this procurement category.
You are working in close collaboration with different Merck stakeholders with focus on senior management level. This includes Manufacturing, Supply Chain, Quality, Regulatory and other functions.
You are partner of choice and in charge of the procurement of contract manufacturing services for a broad range of our pharmaceutical products. This includes the management of established business relationships, the optimization of our supply base aiming for improved service level, quality and cost. For new products, you will be part of the launch team, ensuring supply during the market entry phase and building a sustainable base for growing demands.

Candidate Profile:
•You are a Pharma graduate or Science graduate with Masters in Business Administration, Economics or related disciplines and you have 8+ years relevant professional experience.
•You are a procurement professional, having experience in RFI/RFP/RFQ processes, in coordinating pitches with external suppliers and commercial discussions.
•Negotiation of international contracts is substantial element of your expertise.
•Ideally you have worked in the manufacturing environment of the pharmaceutical industry.
•You have strong communication skills in an international environment and you are comfortable working in interdisciplinary teams.
•Strong problem solving attitude is part of your nature.
•You are a strong team player as well as being able to work independently
•You are fluent in English.
•You are willing to travel.

Additional Information:
Location: Mumbai
Industry Type: Pharma
Last date: 10th December, 2016

To apply, Click here.

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Medical Representative required @ REGALIZ MEDICARE

Medical Representative required @ REGALIZ MEDICARE

Job Description :
•  To promote, position & market existing Brands of Regaliz
•  New Product development
•  Brand building, Marketing Strategy Planning
•  Training Field Force, Motivating them
•  And other routine PMT work

Candidate Profile :
•  Derma.Background
• Hard worker with good market knowledge
•  Self starter with Initiative and Result Oriented Leader
• Positive Attitude
•  Good Communication &Good Documentation skills
• Good Analytical & Interpersonal Skills
• Committed & Ambitious Person who would be ready to take challenging responsibilities

Additional Information:
Experience: min 2 years

Qualification: B.Pharm & MBA / B.Sc.-M.Sc. & MBA
Location: Mumbai
Job Type: Marketing
Industry Type: Pharma

Email your Resume : info@regalizindia.com

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Walk Ins for Pharmacist at RRAP/CCRAS

Walk Ins for Pharmacist at RRAP/CCRAS




Essential: Diploma in Pharmacy /D. Pharm. (Ay.) from recognized University /Institution with two years’ experience in recognized Ayurveda Hospital or B. Pharm.

Age limit : Maximum 27years

Remunerat ion (Fixed) : Rs. 16,000/- per month

Interested Candidates fulfilling the qualifications prescribed above are requested to appear for written test /interview at the above mentioned address, date and time along with the originals for verification. Applicants should submit their application in the prescribed format, two passport size photographs and selfattested photocopies of the certificates on or before 09/12/2016.

General Conditions:-
1. The eligibility of the candidate in respect of age will be determined as on 01.01.2016 (relaxable in the case of SC/ST/OBC as provided in the Govt. of India orders)
2. The engagement would be purely on contractual basis and co-terminus with project. No claim for continuance or regular appointment will be entertained.
3. No T.A/D.A. will be admissible for attending the written test/ interview.
4. The formats for submission of bio-data may be downloaded from the Council’s website www.ccras.nic.in
5. Extension of tenure may be considered on need basis and performance of the incumbents.

Date and Time of Written Test/ Interview : Written Test on 15/12/2016 at 9.30 a.m

For application form, Click here.

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Career for Solution Consultant – Life Sciences in Thomson Reuters

Career for Solution Consultant – Life Sciences in Thomson Reuters




Job Description
JOB SUMMARY
Solution consultant will be involved in Pre Sales technical demonstration to Government and Academic and Pharmaceutical clients to assist sales team to progress open opportunities and also assist in post sales training with current and new customers to ensure customers are using our solutions effectively and renew their subscriptions year on year. This position is responsible for revenue generation, retention and identifying new business opportunities for existing customers

ESSENTIAL DUTIES AND RESPONSIBILITIES 
• Ensure the successful and optimum utilization of Thomson Reuters IP & Science products and solutions, particularly products from the Pharma (Cortellis, Integrity) and Scholarly & Scientific Research (Web of Science, EndNote) portfolio
• Deliver Onsite & Online training sessions.
• Support sales of Scholarly and Scientific literature products including Research data analytics, work-flow, measure & management.
• Support sales of Pharma products in the Academic and Government segment
• Acquire and develop deep insight into the client and Thomson Reuters objectives, projects, and activities with the goal of improving relationships and producing results.
• Leverage knowledge of Thomson Reuters, Industry, people, products, services, resources and activities, to continually strengthen the knowledge and business relationships with assigned clients.
• Develop good understanding of the research workflow at Universities, Research institutions and Pharmaceutical corporations
• Demonstrates an understanding of each assigned firms’ critical success factors and future direction while communicating Thomson Reuters’ goals and strategic direction.
• Provides high-level consulting services and solutions that focus on the mutual goals of Thomson Reuters Systems and the client firm.
• Promotes and participates (as appropriate) in projects to ensure that Thomson Reuters meets and exceeds client expectations.
• Deliver additional projects that may be assigned

Candidate Profile
• Post Graduate, preferably from science background.
• Candidates with PHD in Biological Science would get a preference
• Background and depth of knowledge in Biomedical Research, Drug discovery preferred
• Presentation skills and the ability to relate at all levels of an organization
• Experience with in-person client interaction
• Experience in working with online scientific solutions will be an added advantage.
• Experience in customer training will be an added advantage
• Ability to effectively perform business needs analysis
• Demonstrated planning and organization skills
• Ability to travel
• Consultative and problem-solving skills
• Client service and solution oriented thinking
• Sufficient exposure to and high level of comfort with online/ digital/ technology products and environments

Additional Information:
Location: Mumbai
Education: Post Graduate
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Consultant
End Date: 5th December, 2016

To Apply Online CLICK HERE

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Openings for Clinical Research Associate at Quintiles

Openings for Clinical Research Associate at Quintiles




Job Description
Purpose
Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. If applicable, Clinical Research Associates may be accountable for development of project subject recruitment plan on a per site basis. Support work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.

RESPONSIBILITIES

  • Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.
  • If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
  • Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
  • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
  • Build awareness of features and opportunities of study to site.
  • Collaborate and liaise with study team members for project execution support as appropriate.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES 

  • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Strong therapeutic and protocol knowledge as provided in company training
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer
  • Strong written and verbal communication skills including good command of English language
  • Strong organizational and problem-solving skills
  • Effective time management skills
  • Ability to establish and maintain effective working relationships with coworkers, managers and client

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

Bachelor’s degree in a health care or other scientific discipline or educational equivalent and 1 year of on-site monitoring experience; or equivalent combination of education, training and experience

PHYSICAL REQUIREMENTS 

  • Extensive use of telephone and face-to-face communication requiring accurate perception of speech
  • Extensive use of keyboard requiring repetitive motion of fingers
  • Regular sitting for extended periods of time
  • Requires frequent travel to sites

Additional Information:
Qualification:   Bachelor’s degree health care
Location: Mumbai, Maharashtra
Industry Type: Pharma
Functional Area:  CRA
End Date: 5th December, 2016

To apply online, Click here.

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Opening for Clinical Safety Scientist @ Johnson & Johnson

Opening for Clinical Safety Scientist @ Johnson & Johnson




Job Description:

Job Responsibilities :
· Literature search & clinical/safety data collection for product evaluation.
· Literature review for hazard assessment of new ingredients intended to be used in consumer products.
· Assessment of fragrances and flavors used in consumer products.
·Risk assessment for formulations for cosmetic applications including ingredients classification.
· Review of formulae at different stages of product development cycle
· Preparation of technical justification reports for data leverage.
· Assessment for Studies for Claim substantiation

Candidate Profile:
Master’s degree in toxicology, pharmacology or relevant science discipline. Diploma in clinical sciences preferred
1-2 years of experience in the field of consumer product risk assessment or other relevant Toxicology experience. Experience in clinical safety assessment preferred.

Additional Information:
Experience: 1-2 years
Qualification: M.Pharm
Location: Maharashtra-Greater Mumbai
Job Function: Toxicology Research
Requisition ID: 1600128511W

To apply online, Click here.

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