Require Pharmacists (06 posts) in ESIC Hospital @ Central Government Job

Online Applications (through website of ESIC at (esic.nic.in) are invited for filling up the posts of Paramedical and Nursing Staff for ESIC Medical Education Institutions, Hospitals and Dispensaries in Haryana Region on regular basis by Direct Recruitment.

Pharmacist (Allopathy)

Post Code : 06

No of posts : 06 (UR-03, SC-01, OBC-02)

Pay Matrix (as per 7th CPC) : Rs 29200-92300

Educational & Other qualification : Degree in Pharmacy / Sr. Secondary with Diploma in Pharmacy from a recognized Institution and qualified & Registered as pharmacist under pharmacy Act, 1948.

Age : Not exceeding 32 yrs. (Relaxable upto 37 years in case of Govt. Servant & Employees of ESIC).

Note-
(i) Candidates who have not acquired/will not acquire the educational qualification as on the closing date of receipt of application will not be eligible and need not apply.
(ii) Experience gained after completion of requisite educational qualification will only be considered.
(b) Age Relaxation Upper age limit is relaxable for candidates belonging to reserved categories i.e. SC/ST/OBC/PWD/Ex-Servicemen in accordance with the instructions of Govt. of India as under:
(i) 03 years for OBC
(ii) 05 years for SC/ST.
(iii) 10 years for PWD (additional 05 years in case of SC/ST & 03 years in case of OBC). However, the upper age limit under PWD category shall be as per instructions of Govt. of India.
(iv) Ex.SM-Length of Service in Armed forces + 3 years (additional relaxation for SC/ST/OBC).
(v) Relaxation in age for other categories shall be as per instructions of Govt of India and Recruitment Regulations of concerned post.

NATIONALITY/ CITIZENSHIP
A candidate must be either:
(a) a citizen of India, or
(b) a subject of Nepal, or
(c) a subject of Bhutan, or
(d) a Tibetan refugee who came over to India, before the Ist January, 1962 with the intention of permanently settling in India, or (e) a person of Indian origin who has migrated from Pakistan, Burma, Sri Lanka, East African Countries of Kenya, Uganda, the United Republic of Tanzania (Formerly Tanganyika and Zanzibar ), Zambia, Malawi, Zaire, Ethiopia and Vietnam with the intention of permanently settling in India. Provided that a candidate belonging to categories (b), (c), (d) and (e) above shall be a person in whose favour a certificate of eligibility has been issued by the Government of India. A candidate in whose case a certificate of eligibility is necessary may be admitted to the Examination but the offer of appointment will be given only after the necessary eligibility certificate has been issued to him by the Government of India.

APPLICATION FEE:-
SC/ST/PWD/ Departmental Candidates, Female Candidates & Ex Servicemen *This fee of Rs. 250/- shall be refunded duly deducting Bank Charges as applicable, on appearing of the candidate in the Written Examination : Rs. 250/-*
All other categories : Rs. 500/-

(iii) Mode of payment: -
(a) ONLINE Fee Payment through Internet Banking/Debit/Credit Card etc. (as provided in the Online Application) will only be accepted.
(b) Fees paid by modes other than through Online Application will not be accepted and the applications of such candidates will be rejected forthright and the payment made shall stand forfeited.
(c) Detailed instructions for filling online application and ONLINE Fee Payment are available on the website.
(d) Female candidates, Departmental Candidates and candidates belonging to Scheduled Caste, Scheduled Tribe, Person with Disabilities (PWDs) and Ex-serviceman should provide the details of beneficiary account in which they would like to receive the refund viz. Beneficiary Name, Bank Name, Account Number and IFSC Code etc.

IMPORTANT NOTE: THE CANDIDATES MUST ENSURE THAT THEY HAVE MADE PAYMENT THROUGH STATE BANK COLLECT SYSTEM (SBI) AFTER 24 TO 36 HOURS OF SUCCESSFUL SUBMISSION OF THE APPLICATION FORM. MERE FILLING OF BENEFICIARY DETAILS IN THE APPLICATION FORM WILL NOT AUTO DEBIT THE APPLICATION FEE. THE BENEFICIARY DETAILS ARE CAPTURED ONLY FOR THE PURPOSE OF REFUND OF APPLICATION FEE TO EXEMPTED CATEGORY CANDIDATES AND NOT FOR AUTO DEBIT OF APPLICATION FEE.

HOW TO APPLY
1. Candidates must apply online through the website esic.nic.in. No other means/mode of application will be accepted. Applications received through any other mode will not be accepted and will be summarily rejected. To apply Online visit our website esic.nic.in or esicmaharashtra.qov.in
2. Detailed Instructions for filling online application are available on the website. Candidate should read the instructions carefully before making any entry or selecting options. 
3. After submitting the online application, the candidates are required to take print out of the finally submitted online application and retain the same with them.
4. Candidates are not required to submit to ESIC either by post or by hand the printouts of their online applications or any other document. They will be required to submit printout of online application along with documents in support of their eligibility etc.
5. ONLINE EXAMINATION MAY BE CONDUCTED BY HOLDING A SINGLE EXAMINATION. AS SUCH CANDIDATES MAY CAREFULLY APPLY FOR HIS/HER CHOICE OF POST AND REGION/STATE POST.
6. The candidates are advised to submit ONLY SINGLE ONLINE APPLICATION FOR A POST AS ONLINE EXAMINATION FOR A PARTICULAR POST FOR ALL THE STATES MAY BE HELD IN SINGLE EXAMINATION. However, if somehow, he/she submits multiple online applications, then he/she must ensure that online application with the higher “Application Number” is complete in all respects including fee. The applicants, who submit multiple online applications, should note that only the online application with higher “Application Number” and complete in all respect shall be entertained by the ESIC and fee paid against one “Application Number” shall not be adjusted against any other “Application Number”.
7. Application once submitted cannot be modified, hence utmost care should be taken to furnish the correct details before submitting the online application.
8. Candidates are required to keep active their Email-ID and Mobile Number registered in online application during the currency of this recruitment process. ESIC will also send Letters for Computer Test and other communication only at the registered email ID/Mobile of candidates. Hence under no circumstances, the candidates should provide email ID to anyone.
9. Candidates are advised in their own interest to apply online much before the closing date and not wait till the last date to avoid the possibility of congestion in server to log on etc.

CLOSING DATE: The Closing Date for submission of Online Application through ESIC website esic.nic.in is 21.01.2019.

EMPLOYEES’ STATE INSURANCE CORPORATION
Regional Office, Sector-16, Faridabad

Require Production Executive at Sanofi @ Apply Now

Post : Executive - Production

Job Description:
Production
Implementing monthly schedule with consistent quality, adhering to Regulatory, GQS, and HSE guidelines, with proper utilisation of resources and optimum cycle time.
Performing the production activities in assigned areas in order to achieve 100 % customer service.

ISO 14001 and SAP
Adhering to ISO 14001 activities and objectives in Pharma Mfg.
Performing all the SAP related activities as and when needed.

Compliance
Implementing and ensuring compliance to GQS, HSE and ISO guidelines / standards and maintaining documentation for the same including process validation and qualification

Coordination 
Coordinating with   Engineering department for preventive and break down maintenance, modifications etc.  Purchase for procuring and controlling auxiliaries.  Quality Operations for all quality related matters.  Performing the function related SAP activities.

Yield monitoring
Implementing and making efforts for continuous improvement of yield of assigned products

Training
Impart training to the operative staff on GMP, HSE, ISO requirement & process improvement and maintaining good industrial relation in the plant by effective grievance process.

Others 
• Carrying out any other assignments or projects like qualifications and validations as per the instruction of the Dept. Head to meet the organizational priorities.
• Identifying and correcting unsafe conditions or behaviours and promptly reporting other potentially hazardous situations.
• Maintaining plant assets in good condition and making optimum use of all resources.
Coordination with packaging department

Candidate Profile
Graduate / Post Graduate in Pharmacy
2.0 to 3.0 years in a Pharmaceutical Company

Additional Information
Experience : 2-3 years
Qualification :  B.Pharm, M.Pharm 
Location : Ankleshwar
Industry Type : Pharma
End Date : 15th January, 2019

Require Research Associate at Baxter @ Apply Now

Post : Research Associate III
Job Description
• Develop effective platforms and schedules to manage activities in/with our Indian partners.
• Contribute to the effective management of CRO resources (specifically staff, facilities and the relevant budgets).
• Apply best-demonstrated practices, team processes, and improve operational efficiency. Seek regular input and feedback from customers and take the appropriate action.
• Pro-actively prioritize and balance utilization of resources allocated to project. Develop recommendations for outside resources as required for the team/project.
• Implement Metrics to measure the quality and on-time delivery.
• Accountable for timely and effective completion of tasks to meet business milestones
• Build a professional network both internally within Business Unit, across Units and outside of Baxter
• Maintain current knowledge of relevant Quality System Regulations and other regulatory requirements related to research, development, and product lifecycle.  Effectively performs risk/benefit analysis for project identification and prioritization.
• Adhere to the Quality System, understand and apply applicable corporate, divisional and departmental procedures as relevant

Candidate Profile
• Master or Ph.D. degree in Analytical chemistry plus min 5 years of experience in leadership role (experience in developing and directing projects).
• Strong understanding of analytical validations per ICH and compendial guidelines.
• GMP experience are essential.
• Experience in Supply chain and international regulation on Chemical material shipment is an asset
• Has a solid background in a series of analytical techniques like GC, LC, KF, MS, FTIR, NMR….Based on significant technical expertise reviews, provides direction to technical staff.
• Manage laboratory documentation for compliance to quality.
• Ensure compliance with established standards, e.g. ICH, EP and USP.
• Keeps management informed of accomplishments, any technical challenges, and resource constraints
• Assess scientific data and interpret results in a clear and concise manner and provide interpretation of results to team members.

Additional Information
Experience : 5 years
Qualification : M.Sc, Ph.D
Location : Bangalore, KA
Industry Type : Pharma
Functional Area : R&D
End Date : 30th January, 2018

Apply as Pharmacovigilance Leader at Novartis @ Apply Now

Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.

Post : Pharmacovigilance Leader

Job Description 
1. Monitors the clinical safety of projects/products and responds appropriately.
2. Performs medical assessment and related activities for single cases, including collecting additional follow‐up information as necessary, medical evaluation of quality defects, review of line listings of single cases, and preparation of investigator notifications. Medical review of single case reports will be performed by associates possessing medical degree.
3. Identifies safety signals based on the review of solicited or unsolicited single cases and confirm that they are not overlooked. Performs signal detection, monitoring and evaluation based on single cases, aggregate data and signal detection tools.
4. Provides input into responses to inquiries from regulatory authorities or health care professionals on safety issues. Prepares safety data for health authority review boards. Provides input to responses for legal queries and CO requests involving safety issues.
5. Provides pharmacovigilance input to initial development of basic prescribing information and is responsible for pharmacovigilance input into updates of this information.
6. Prepares medical input to aggregate clinical safety regulatory reports.
7. Provides input to safety profiling and risk management plan.
8. Provides guidance as appropriate to Clinical Safety Operations for the coding and causality/expectedness assessment of adverse event reports.
9. Provides expert evaluation on the clinical context of adverse event reports, assessment on the medical conditions, and the implications on Novartis drugs.
10. Collaborates productively with colleagues from Clinical Research, Regulatory Affairs, Medical Affairs, Medical Information, Statistics, Safety Data Management, Epidemiology and other related departments.
11. Participates in review of clinical study protocols/reports/other regulatory documents as needed.
12. Provides relevant input for Global Program/Brand Team (GPT/GBT), Global Clinical Team (GCT), and CTT meetings as needed.
13. Provides support as needed for licensing activities, regulatory authority inspections and for project/product recall activities

Candidate Profile
Bachelor of Science in Pharmacy /Bachelor of Science in Nursing / PharmD/PhD in relevant field or Medical Degree (MBBS or MD) required Medical degree with specialization preferred. Medical degree is e Fluent in spoken and written English. Understanding in another major language (e.g. French, German, Spanish) preferred. - 3 years clinical experience postdoctoral - At least 3 years in drug development in a major pharmaceutical company including 2 years in drug safety at an operational or medical position - Proven ability to analyze, interpret, discuss, and represent safety information both in writing and orally - Experience in preparing or contributing to preparation of clinical safety assessments and regulatory reports/submissions involving safety information - Experience with (safety or others) issue management - Experience in drug development, clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing of publications

Additional Information
Experience : 2 years
Qualification : Pharm.D/Ph.D
Location : Hyderabad, AP
Industry Type : Pharma
Functional Area : Research & Development
End Date : 20th January, 2019

International Conference on Nanotechnology and its Application to Ocular Drug Delivery Systems at Uka Tarsadia University Surat, Gujarat, India @ 28-30 January 2019

Uka Tarsadia University (UTU), established in 2011, by Gujarat State Private University amendment act 25 of 2011, is located on the Bardoli- Saputara state highway at Bardoli, Di: Surat, Gujarat, India. The university has taken rapid strides and is emerging as one of the leading universities in the field of higher education in Gujarat. UTU leads a culture that supports teaching learning excellence and has 15 constituent institutes, 4 departments under 7 faculties offering 76 career oriented academic programmes at diploma, undergraduate, postgraduate & doctoral level. The university offers a comprehensive array of academic programs across the disciplines of Management, Commerce, Engineering & Technology, Architecture, Design, Applied Science (Chemistry, Physics, Mathematics, Biotechnology, Micro-biology), Computer Science, Pharmacy, Nursing and Physiotherapy. University is committed to provide need based, industry focused education nurturing in an inclusive environment.

ABOUTTHE CONFERENCE
This International Conference aims to provide a knowledge sharing experience in the area of “Nanotechnology and Ocular Drug Delivery.” It is with utmost happiness to stretch out our warm temptation to join the International Conference on “Nanotechnology and its Application to Ocular Drug Delivery Systems”, on 28 - 30th January 2019 at Maliba Pharmacy College, Surat, Gujarat, India. This conference incorporates keynote introduction, plenary lectures, invited talks, oral presentations and poster presentations. This conference would unite people occupied with fields of nanotechnology, ocular drug delivery, ocular pharmacology, ophthalmology and drug delivery systems. The highlights of the conference include nanotechnology, drug delivery through contact lens, challenges in ocular pharmacokinetics and modalities in ophthalmology. The conference would also have open panel discussions with experts from academia and industry to discuss on current challenges in nanotechnology and ocular drug delivery.

The conference will also provide the opportunity to scientists, students, academician and research scholars from various organizations to put forth their innovative ideas and research findings by means of deliberations, discussions, oral and poster presentations.

International Conference on

"Nanotechnology and its Application to Ocular Drug Delivery Systems"

28 - 30th January 2019

Thrust Areas

• Advances in Ocular Drug Delivery
• Pharmaceutical Nanotechnology
• Colloids & Interfaces Medical Devices & Related Technologies
• Computer Aided Drug Design, Synthesis of Drug & Drug Discovery
• Pharmaceutical Biotechnology
• Pharmacology, Clinical Pharmacy
• Pharmacovigilance & Pharmacy Practice
• Impurity Profiling
• Standardization of herbal drugs

Call For Paper 
The abstracts (research only) in the mentioned thrust areas are invited. The paper must be an original contribution that has not been published previously or not under consideration for publication or presentation elsewhere. Abstract can be submitted by email to scicom.maliba@utu.ac.inon or before December 31, 2018 as per the format available on the conference website (utu.ac.in/mpcon). All abstracts will be reviewed by the Scientific Review Committee and intimation of the acceptance will be sent to the presenting author through email by January 05,2019. All accepted posters will be presented at Poster presentation session during the conference. Presenting authors have to register themselves for the conference on receipt of acceptance mail, if not, the abstract will be cancelled and will not be considered for publication in the abstract book. Authors of the selected posters will be called for Oral presentation on day-2 of the conference. The best paper will receive exciting prizes. All the accepted abstracts will be published in the special issue of Journal of Pharmacy and Applied Sciences (JAPS) [ISSN 2395 - 6097(PRINT), ISSN 2395 - 6100(ONLINE). All the presenting authors will also be invited for submission of full paper.
Winner : Rs 11,000/-
Runner's Up : Rs 5000/-

Registration Details
Regular registration upto 10 January, 2019
Foreign Delegates : $100
Indian Delegates Academia/lndustry : Rs 2500
Indian Delegates Students : Rs 1200

On Spot Registration After 22 January 2019 (Subject to Availability)

Foreign Delegates : $150

Indian Delegates Academia/lndustry : Rs 3000

Indian Delegates Students : Rs 1500

• Registration entitles you to Registration kit, attendance in all sessions and proceedings of the symposium and hospitality during the conference. Online registration is also available at utu.ac.in/mpcon
• Registration fee is non-refundable. However, change in nomination can be permitted only on request.
• Registration fees would be accepted either cash or DD/Cheque to be made in favor of "Maliba Pharmacy College" payable at bardoli.
• Electronic Transfer NEFT/RTGS: Maliba Pharmacy College. HDFC Bank A/c: 02091000008509.
IFSC: HDFC0000209. Submit Transaction Details/ScreenShot of payment to registration.maliba@utu.ac.in

ORGANIZED BY
Maliba Pharmacy College,
Uka Tarsadia University
Bardoli,Gujarat,
INDIA-394350
+91 82386 51055
utu.ac.in/mpcon
registration.maliba@utu.ac.in

For registration: You can contact Dr. Bhavin Vyas [Joint Secretary] by Cell + WhatsApp
at (+91) 9879629765 or by email at registration.maliba@utu.ac.in

Last date of registration: 10th January 2019

GPAT Test Series 2019 #3

Require Pharmacist at ESIC @ Apply Now

Online Applications through website of ESIC at (esicmaharashtra.gov.in/ esic.nic.in) are invited for filling up the posts of Paramedical and Nursing Staff for ESIC Medical Education Institutions, Hospitals and Dispensaries in Maharashtra Region on regular basis by Direct Recruitment

Pharmacist (Allopathy)

Post Code : 06

No of posts : 35 (UR-20, SC-02, ST-03, OBC-10)

Pay Matrix (as per 7th CPC) : Rs 29200-92300

Educational & Other qualification : Degree in pharmacy/ Senior Secondary with diploma in pharmacy from a recognised institution and qualified and registered as pharmacist under Pharmacy act , 1948.

Age : Not exceeding 32 yrs. (Relaxable upto 37 years in case of Govt. Servant & Employees of ESIC).

Note-
(i) Candidates who have not acquired/will not acquire the educational qualification as on the closing date of receipt of application will not be eligible and need not apply.
(ii) Experience gained after completion of requisite educational qualification will only be considered.
(b) Age Relaxation Upper age limit is relaxable for candidates belonging to reserved categories i.e. SC/ST/OBC/PWD/Ex-Servicemen in accordance with the instructions of Govt. of India as under:
(i) 03 years for OBC
(ii) 05 years for SC/ST.
(iii) 10 years for PWD (additional 05 years in case of SC/ST & 03 years in case of OBC). However, the upper age limit under PWD category shall be as per instructions of Govt. of India.
(iv) Ex.SM-Length of Service in Armed forces + 3 years (additional relaxation for SC/ST/OBC).
(v) Relaxation in age for other categories shall be as per instructions of Govt of India and Recruitment Regulations of concerned post.

NATIONALITY/ CITIZENSHIP
A candidate must be either:
(a) a citizen of India, or
(b) a subject of Nepal, or
(c) a subject of Bhutan, or

(d) a Tibetan refugee who came over to India, before the Ist January, 1962 with the intention of permanently settling in India, or (e) a person of Indian origin who has migrated from Pakistan, Burma, Sri Lanka, East African Countries of Kenya, Uganda, the United Republic of Tanzania (Formerly Tanganyika and Zanzibar ), Zambia, Malawi, Zaire, Ethiopia and Vietnam with the intention of permanently settling in India. Provided that a candidate belonging to categories (b), (c), (d) and (e) above shall be a person in whose favour a certificate of eligibility has been issued by the Government of India. A candidate in whose case a certificate of eligibility is necessary may be admitted to the Examination but the offer of appointment will be given only after the necessary eligibility certificate has been issued to him by the Government of India.

APPLICATION FEE:-
SC/ST/PWD/ Departmental Candidates, Female Candidates & Ex Servicemen *This fee of Rs. 250/- shall be refunded duly deducting Bank Charges as applicable, on appearing of the candidate in the Written Examination : Rs. 250/-*
All other categories : Rs. 500/-

(iii) Mode of payment: -
(a) ONLINE Fee Payment through Internet Banking/Debit/Credit Card etc. (as provided in the Online Application) will only be accepted.
(b) Fees paid by modes other than through Online Application will not be accepted and the applications of such candidates will be rejected forthright and the payment made shall stand forfeited.
(c) Detailed instructions for filling online application and ONLINE Fee Payment are available on the website.
(d) Female candidates, Departmental Candidates and candidates belonging to Scheduled Caste, Scheduled Tribe, Person with Disabilities (PWDs) and Ex-serviceman should provide the details of beneficiary account in which they would like to receive the refund viz. Beneficiary Name, Bank Name, Account Number and IFSC Code etc.

IMPORTANT NOTE: THE CANDIDATES MUST ENSURE THAT THEY HAVE MADE PAYMENT THROUGH STATE BANK COLLECT SYSTEM (SBI) AFTER 24 TO 36 HOURS OF SUCCESSFUL SUBMISSION OF THE APPLICATION FORM. MERE FILLING OF BENEFICIARY DETAILS IN THE APPLICATION FORM WILL NOT AUTO DEBIT THE APPLICATION FEE. THE BENEFICIARY DETAILS ARE CAPTURED ONLY FOR THE PURPOSE OF REFUND OF APPLICATION FEE TO EXEMPTED CATEGORY CANDIDATES AND NOT FOR AUTO DEBIT OF APPLICATION FEE.

HOW TO APPLY
1. Candidates must apply online through the website esic.nic.in. No other means/mode of application will be accepted. Applications received through any other mode will not be accepted and will be summarily rejected. To apply Online visit our website esic.nic.in or esicmaharashtra.qov.in
2. Detailed Instructions for filling online application are available on the website. Candidate should read the instructions carefully before making any entry or selecting options. 
3. After submitting the online application, the candidates are required to take print out of the finally submitted online application and retain the same with them.
4. Candidates are not required to submit to ESIC either by post or by hand the printouts of their online applications or any other document. They will be required to submit printout of online application along with documents in support of their eligibility etc.
5. ONLINE EXAMINATION MAY BE CONDUCTED BY HOLDING A SINGLE EXAMINATION. AS SUCH CANDIDATES MAY CAREFULLY APPLY FOR HIS/HER CHOICE OF POST AND REGION/STATE POST.
6. The candidates are advised to submit ONLY SINGLE ONLINE APPLICATION FOR A POST AS ONLINE EXAMINATION FOR A PARTICULAR POST FOR ALL THE STATES MAY BE HELD IN SINGLE EXAMINATION. However, if somehow, he/she submits multiple online applications, then he/she must ensure that online application with the higher “Application Number” is complete in all respects including fee. The applicants, who submit multiple online applications, should note that only the online application with higher “Application Number” and complete in all respect shall be entertained by the ESIC and fee paid against one “Application Number” shall not be adjusted against any other “Application Number”.
7. Application once submitted cannot be modified, hence utmost care should be taken to furnish the correct details before submitting the online application.
8. Candidates are required to keep active their Email-ID and Mobile Number registered in online application during the currency of this recruitment process. ESIC will also send Letters for Computer Test and other communication only at the registered email ID/Mobile of candidates. Hence under no circumstances, the candidates should provide email ID to anyone.
9. Candidates are advised in their own interest to apply online much before the closing date and not wait till the last date to avoid the possibility of congestion in server to log on etc.

CLOSING DATE: The Closing Date for submission of Online Application through ESIC website esic.nic.in is 21.01.2019.

EMPLOYEES’ STATE INSURANCE CORPORATION
Panchdeep Bhavan, N.M. Joshi Marg, Lower Parel, Mumbai - 400013

Require Regional Training Manager at Novartis @ Apply Now

Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.

Post : Regional Training Manager

Job Description
Has primary responsibility for the sales training strategy and sales training activities across major geographical sector of country. To reinforce goals and standards within existing teams and support the implementation of existing and new programmes, products and structures.  Develops and implements training programs for entry level and experienced sales people. Develops training programs including sales techniques, presentations, project and product applications information and roleplay. Provides materials and development support to sales teams for presentations at sales meetings. Design and deliver training to in areas as required to support Sales Plans To construct, with training colleagues, the national Core Programmes, and strategic and operational plans. To manage the training budget. To analyse and actively respond to internal/external benchmarks and diagnostics; to respond actively to customer, employee and performance feedback. To input into and implement training which supports and enables EFFECT champions (area managers who additionally handle training responsibilities) To communicate plans, evaluation and achievements to the Head of Sales Training, Senior Sales Management Team and Marketing Team. Working with relevant personnel and agencies, devise and develop the product launch training packages for the sales force. Implement successful learning programmes to equip representatives with tools to launch products to Novartis standards. To develop the content for learning publications and Business Unit magazines capturing the achievement and successes of teams. To develop and implement distance learning modules which encourages participation of sales teams. Knowledge of other learning platforms like e-learning, video conferencing and teleconference.

Candidate Profile
B.Pharm, M.Pharm, B.Sc. Post graduate qualification related to training desirable. English + local language 3 years experience as a sales representative 3 years experience as a first line manager 2-3 years experience in training position. (Prefereble)

Additional Information
Experience : 2-3 years
Qualification : B.Pharm, M.Pharm, B.Sc
Location : Chennai
Industry Type : Pharma
Functional Area : Research & Development
End Date : 15th January, 2019

Apply as Regulatory Associate at Makro @ Click Here to Apply

Post : Regulatory Associate

Job Description
• Serves as an Associate RA representative on project team
• Supports senior Regulatory personnel in preparing new product marketing submission for the FDA (510k, PMA)
• Maintains Regulatory Affairs documentation & support international Regulatory requests
• Collaborate with the Clinical Functional Unit on projects requiring the collection of clinical data
• Provide support to currently marketed products & assit on change requests, etc.
• Maintain and organize appropriate regulatory records to demonstrate compliance with applicable regulations
• Evaluate the safety, efficiency, and effectiveness of biomedical equipment
• Perform analysis of data collected, root-cause sources of error in measurements, implement improvements in hardware, measurement methods, or signal processing
• Liaising with medical, engineering & scientific staff, literature search expert
• Train clinicians, life scientists, chemists, medical scientists and other personnel on engineering aspects of biological systems of humans and animals on the proper use of equipment.
• Basic understanding of FDA and EU regulatory process for different class devices.

Additional Information
Experience :  0-2yrs
Qualification : M.Pharm, B.Pharm, M.Sc
Location : Hyderabad
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory Affairs
End Date : 25th January, 2018