Job as Pharmacist (50 Posts) in Apollo Pharmacy, Bangalore

Post: Pharmacists

No.of posts: 50

Job Description:
* Dispensing the drugs as per prescription / Indents.
* Raising the Pharmacy Requisition slips as per requirements.
* Receive the stock from Stores and check against the Issue Slips, for quantity, batch no, expiry etc.
* Doing physical verification of stocks with computer data daily.
* Taking the stock of short-expiry medicines once a month.
* Taking the stock of non-moving medicines once in 6 months.
* Building customer relationship for effective service towards total patient care.

LOCALS PREFERRED.

Candidate Profile:
MUST BE REGISTERED IN KARNATAKA PHARMACY COUNCIL.
READY TO RELOCATE IN BANGALORE.
LOCALS ARE GIVEN PREFERENCE.
ONLY B.PHARM/D.PHARM CAN APPLY.

Thermo Fisher Scientific Antibody Scholarship Program

SCHOLARSHIP PROGRAM DESCRIPTION:
The Thermo Fisher Scientific Antibody Scholarship Program “(“Program”) will award scholarships to eligible life science students, to be used for the 2016 academic year. Entries will be accepted beginning on or about 12:00:01 a.m. Central Time (CT) on 1-Feb-2016 through 11:59:59 p.m. CT on 30-Jun-2016 (“Application Deadline”). By submitting a scholarship application, each applicant unconditionally accepts and agrees to comply with and abide by these Official Rules and the decisions of Thermo Fisher Scientific Inc. (“Sponsor”), which shall be final and binding in all respects.

ELIGIBILITY: 
Applicants must be individual persons who
(a) are legal U.S. residents age 16 or older at time of application;
(b) are enrolled as a Graduate Student, or Undergraduate Student at an accredited U.S. college or university for Fall 2016; and
(c) have a declared major of biology, chemistry, bio-chemistry or a related life science field.In addition,
(i) Undergraduate Sophomores, Juniors, and Seniors must have a cumulative college GPA of 3.0 or greater on a 4.0 scale;
(ii) Undergraduate Freshmen must have a cumulative high school GPA of 3.0 or greater on a 4.0 scale; and
(iii) Graduate Students must have a cumulative graduate GPA of > 3.0 on a 4.0 scale and have received cumulative undergraduate GPA of > 3.0 on a 4.0 scale. Sponsor, its subsidiaries, affiliates, distributors, sales representatives, and each of their respective officers, directors and employees (collectively, the “Program Entities”), as well as the immediate family members and/or those persons living in the same households of the foregoing are not eligible to apply or win a scholarship in this Program. This Program is void where prohibited by law.

SCHOLARSHIP AWARDS:
This Program will award two (2) $10,000 scholarships and four (4) $5,000 scholarships. All scholarship award payments will be made directly to the college or university at which the recipient is enrolled, upon receipt of all documentation from the recipient necessary to process payment. Any unused scholarship funds will be due and returnable to Sponsor.

Recruitment of Product Specialist in Novo Nordisk | B.Pharm/B.Sc

Post: Product Specialist - India Affiliate

Job Description
About the department
Sales is responsible for the successful implementation of long term and short term marketing strategies in the field and establish true diabetes leadership in all therapies which caters to every segment in the society. Also ,the department maximises sales force effectiveness by implementing robust tools and processes. 

• You will join an ambitious team of field executives responsible for promoting our brand to doctors and conducting prescription audits.
• You will especially focus on increasing sales and market share by educating the users about benefits of our products.
• You will be given a number of different responsibilities and experience a variety of tasks,working with both internal and external stakeholders.

Qualification
You hold an academic degree in B Pharmacy /B Science with 1+ years of pharmaceutical sales experience. You have excellent communication & influencing skills. You are flexible and result oriented with a 'can-do' attitude. You must be prepared to invest significant personal effort in your work and proactively take ownership of your areas of responsibility. You are fluent in both written and spoken English.

Additional Information:
Experience: 1+ Years
Qualification: B.Pharm, B.Sc
Industry Type: Pharma/ Biotech/Clinical ResearchFunctional Area: Field Sales 
Location: Faridabad-Haryana
Requisition ID: 38634BR
Last Date: 2 April 2016

Job as Pharmacists (5 posts) in NHM - Govt Job

Post: Pharmacist (RBSK)

No.of post: 05
ST: 04, OBC:01

Eucational Qualification: 
Degree  or  Diploma  in  Pharmacy (50%)  &  Registration  in Pharmacy  Registration  council.

Consolidate Salary: 10,000/- Per Month

Age: 18 - 64 years (as on 1 January, 2016)

Documents may needed -
10th marksheet
12th marksheet
all marksheets of Degree or diploma
Degree
Certificate of registration in pharmacy council
Caste certificate
Domicile certificate
Experience Certificate
Employment Registration certificate
Other related certificates

Last Date for Submission of Application is: 30/03/2016

Career as Country Approval Specialist in PPD Pharmaceuticals

Post: Country Approval Specialist - Mumbai - 130508

Job Description:
• Prepare, review and coordinate local regulatory and ethics committee submissions (and additional special national local applications if applicable for clinical trials) in alignment with global submission strategy for new and ongoing clinical trials
• Provide local regulatory submissions strategy advice (MoH & EC both) to internal clients and possibly to external client
• Provide project specific local submission strategy, technical expertise and coordination oversight for projects in collaboration with relevant internal departments, may represent PPD to external client
• Primary contact for internal teams during discussion with investigators, site study team and with the local regulatory authorities (in collaboration with the local regulatory or startup manager for complex issues) to ensure submissions are managed in a timely manner
• Ensures guidelines and processes are followed for effective internal PPD team communications as well as communications with investigators (sites), and with the country regulatory authorities to ensure submissions are managed in a timely manner
• Act as a key-contact at country level for all submission-related activities
• Participate as required in Submission Team Meetings, Review Meetings and Project Team meetings
• Coordinates with internal functional departments to ensure various site start-up activities are aligned with submissions activities and mutually agreed upon timelines; ensures alignment of submission process for sites and study are aligned to the critical path for site activation
• Achieves PPD’s target cycle times (study startup timelines) for site activations
• Develop country specific Patient Information Sheet/Informed Consent form documents for the study and sites, obtains translations from translation vendor
• May assist with grant budgets(s) and payment schedules negotiations with sites.
• Support collection of trial commencement documents.
• Ensures that trial status information relating to SIA activities (study startup activities) are accurately maintained in the database (clinical trial management system) and is current at all times.
• Maintain knowledge of and understand PPD SOPs, Client SOPs/ directives, and current regulatory guidelines as applicable to services provided
• Direct/mentor other Clinical and SIA individuals assigned to support projects of responsibility, as appropriate
• Preparation and maintenance of country master document templates and other PPD regulatory intelligence systems, as may be required and assigned
• Performs the function of mentor for junior clinical team members.
• Works in conjunction with the other Country Approval Specialist(s) and Contracts Specialist(s) to activate sites in timely manner.
• Represents PPD in the global medical research community and develops collaborative relationships with investigational sites and may assist with the feasibility process.
• Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
• Responds to company, client and federal regulatory requirements/ audits.
• Provide feedback on country environment/sites for RFP, Bids and feasibilities
• Perform feasibilities for India and any other country as applicable

Qualifications
- Bachelor’s degree in a science related field or Pharmacy graduate or equivalent certification/licensure. In some cases an equivalent combination of education, professional training, and experience that provides the required Knowledge, Skills and Abilities may be considered.
- Previous experience as a study startup specialist or submission specialist that provides the knowledge, skills, and abilities to perform the job or completion of PPD Drug Development Fellowship.
- Having prior experience of site monitoring may be beneficial.

Additional Information:
Location: Mumbai - Maharashtra
Industry Type: Pharma/ Biotech/Clinical Research
Job Code: 130508

Vacancy for Sr. Officer Engineering Purchase in Client of Nurture Consultancy

Post: Sr. Officer Engineering Purchase

No. of Posts: 06

Job description
Engineering Consumables Monthly Requirement
Engineering Spares Requirement
Co-Orindation with Accounts for Pending GRN, Pending PO, Payments
New Vendor Development
PO Making - Enquiry, RFQ generation, RFQ Comparative, Approval, PO Making
Follow Up - Deliveries in Time
Vendor Evaluation & Vendor Rating
Identify New Vendors/ Manufacturers/ Traders/ Distributors for Project Items
Co-Orindation with Accounts for Pending GRN, Pending PO, Payments
PO Making - Enquiry, RFQ generation, RFQ Comparative, Approval, PO Making
Follow Up - Deliveries in Time
Vendor Evaluation & Vendor Rating

Candidate Profile:
Diploma in Mech. Engg. With 5 to 7 years experience or Degree in Mech. Engg. With 3 to 5 years experience.
Atleast worked in SAP system for minimum 3 years in Engg. Purchase
Skill in Comparing Technical Specification & Art of Negotiation
Age - 27 to 35 years
Dynamic Personality
Honest & Straight Forward Person
Commitment towards work
Writing & Reporting Communication Skill
Located & Staying Close-by
Gender - Male

Additional Information:
Experience: 3-12 years
Education: Diploma Or Degree in Mecha. Engg
Industry Type: Chemical
Job Type: Engg Purchase
Location: Rabale (Maharashtra)
Salary: 4 L PA
Last Date: 18^th April, 2016

Forward your CV to: hr2@nurtureconsultancy.com

Opportunity for freshers Formulation R&D and QC Manager/supervisor at Chantilly BioPharma

Post: Formulation R&D and QC Manager/supervisor in Pharma

No. of Posts: 02

Formulation Method development:
SCOPE: The Formulations development Scientist, product development provides support to the product development department by Dispensing and compounding of Dosage forms for clinical supplies. Additionally, the SCIENTIST product development is responsible for assisting in development and implementation of quality control systems and procedures.

Duties/Responsibilities: 
• Checking and identifying correct actives and excipients to overcome incompatibility 
• Weighing/ dispensing of actives and excipients for making solid dosage forms 
• Blending/ mixing of actives and excipients for making solid dosage forms 
• Making the formulations by sophisticated instruments 
• Film coating of Tablets, Capsule filling, Packaging of the dosage forms 
• Check for Material Safety Data Sheets for all incoming materials before dispensing 
• Formulation of Pharmaceuticals of Novel drug delivery systems 
• Evaluation and modify existing processes as part of continuous improvement 
• Equipment qualification, participate on technical team to justify, specifies and starts up new  
• Development of Controlled Release Dosage forms 
• Development of Batch Manufacturing records for processing of pharmaceuticals 
• Assisting in analytical development work for pharmaceuticals 
• Maintain and follow CGMP practices and OSHA regulations.
• processes.

Quality control Manager:
Scope: The quality control provides support to the quality control department by performing functions, which aid assurance of GMP compliance. The quality control is responsible for assisting with quality control operations are performed according to written Sops, GMP and FDA guidelines. Additionally, the quality control is responsible for assisting in development and  implementation of quality control systems and procedures. 

Job for Associate Manager, Medical Writing Services in Parexel

Post: Associate Manager, Medical Writing Services

Job Description
Essential Function 
The Manager, Medical Writing Services, will research, create, and edit documents associated with the clinical sections of regulatory submissions and other clinical documents. This is a billable position (65%). The Manager is also responsible for all line management of assigned medical writing staff, either at the local site or remotely. The Manager inputs to medical writing resources for proposals. The Manager provides project management of the medical writing aspect for their projects and those of their line reports.

Key Account abilities include the following main areas: 
Writing and consultancy
Project management
General management
Line management
Process improvement
Training
Client liaison/service
Resource planning
Proposals

Skills
• Excellent interpersonal, negotiating, verbal and written communication skills.
• Professional attitude.
• Client focused approach to work.
• Client liaison.
• A flexible attitude with respect to work assignments and new learning.
• Logical thinking.
• Attention to detail.
• Self-motivated to work consistently in a fast-paced, rapidly changing environment.
• Able to work independently.
• Able 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.

Opening Various position in Nimar Institute of Pharmacy

Post: Asst. Professor, Lecturer, Lab Technician, Accountant, Store Keeper 

- Asst. Professor: 03 (Professor In pharmacology/Pharmacognosy/ Pharma. Chemistry)
- Lecturer: 03
- lab Technician: 03
- Accountant: 01
- store keepar: 01

Job Description
1) The candidate is expected to establish their corresponding departments and expected to lead the team.
2) The candidate is expected to extend his/her support to the Principal in administrative works as well day to day activities.
3) He/She is expected to involve actively in research
4) He/She is expected to apply novel projects for getting funding from resources like AICTE, UGC etc.,
5) He/She is expected to organize seminars/guest lectures and work shops to elevate the image of organization.

Candidate Profile:The candidate should posses sound academic tract record. Also expected to a strong inclination towards research. Having administrative skills and having experience as an administrator will be an added advantage. He or She should have impeccable personal character and should be a role model for adhering moral principles, ethics and self discipline.

Education:
Asst.Professor: M.Pharm., Ph.D(Pharmacology, Pharmacognosy, Pharma. Chemistry)
Lecturer: M.Pharma
Lab Technician: B.Pharm, D.Pharm, B.Sc
Store Kepar: D.Pharm, B.Sc
Accountant: M.Com

Additional Information:
Experience: As per AICTEIndustry Type: College
Job Type: Professor In Pharmacology/Pharmacognosy/Pharma. Chemistry
Location: Dhamnod, MP
Salary: As per AICTE
End Date: 20^th April, 2016

Interested candidate can send their biodata to the following e-mailprincipalnip@gmail.com

NIMAR INSTITUTE OF PHARMACY DHAMNOD
OPP- ITI MAHESHWAR ROAD DHAMNOD DIST DHAR

Recruitment of Pharmacist & Trainee Pharmacist at My Health Pharmacy - 20 Posts

No.of post: 20

Job Description
• Customer Engagement
- Clinical scrutiny of the prescription and counseling patients on usage of right medicine, consuming right dosage, right method of administration, cold chain management etc.
- Screening of symptomatic and asymptomatic customers and suggest them for diagnosis

• Follow-up
- Focused tracking on consumption of medicines of customers and follow-up according to their replenishment schedule (Ensure enhancement of sales by at least 10% per month thru’ follow-ups)
- Upon customer order, adhere to delivery time committed to customers

Candidate Profile
Candidate Should be well groomed, Go and getting ability,  Be a Good Professional to do customer engagement, follow up and patient counselling.

Additional Information:
Exprience: 0-2 years
Qualification: B.Pharm, M.Pharm
Location: Kukatpally - Chandanagar, Hyderabad
Industry Type: Pharmaceutical Care & Retail
Job Type: Medical Retail
Salary: Based on Candidate Experience and Skills and as per the Company Norms
Last Date: 9^th April, 2016

Email-ID: venkatesh_hr@rajeretail.in , hr@myheathpharmacy.in   

National Institute of Pharmaceutical Education and Research (NIPER)

Applications are invited for following two project positions. projects for a period of one year (extendable upto three years maximum or the completion of project, whichever is earlier) sponsored by DBT, GOI (GP-411) and DIHAR, DRDO (GP-409).

Post: Junior Research Fellow, Project Assistant

Junior Research Fellow (01)
Project positions under Dr. Inder Pal Singh in a project titled " Isolation and characterization of Xanthine oxidase inhibitors from endophytic fungi for treatment of hyperurecemia and gout" for a period of one year (extendable upto three years maximum or the completion of project, whichever is earlier) sponsored by DBT, GOI (GP-411).

Qualification 
M.Sc. Organic Chemistry/(M.S.Pharm./M.Pharm) Natural Products or Medicinal Chemistry, Pharmaceutical chemistry. The candidate should have qualified UGC/CSIR/ ICMR NET.
Desirable: Experience in isolation and characterization of natural products.

Project Assistant (01)
One temporary position (project assistant) in a Project titled  "Biologically active secondary metabolites from Codonopsis clematidea" (for a period of two years or the completion of project, whichever is earlier) sponsored by DIHAR, DRDO (GP-409)

Qualification:M.Sc. Organic Chemistry/(M.S. Pharm./M.Pharm) Natural Products or Medicinal Chemistry, Pharmaceutical chemistry.
Desirable: Experience is isolation of natural products

Age Limit: 35 years (age relaxation for SC/ST/PH is as per GOI rules)

Salary: Rs. 25000+HRA (10%) for JRF and 10000.00 consolidated for project assistant

Interested candidates with consistently good academic record may apply on plain paper containing name, address, telephone number, email address, educational qualifications and research experience supported with attested copies of certificates along with demand draft of Rs. 50/- (Rs.25/ for SC/ST) favoring Director, NIPER payable at Mohali/Chandigarh. Applications superscribing 'position applied' and 'project title' should reach the Registrar, NIPER within 21 days from the publication of this advertisement. The institute will not be responsible for any postal/ courier delay.
No TA/DAwill be paid for attending the interview.

NATIONAL INSTITUTE OF PHARMACEUTICAL EDUCATION AND RESEARCH NIPER, PUNJAB

Application are invited for the post of Research Associate Or Senior Research Fellow (Project) in National Institute of Immunology

The National Institute of Immunology, New Delhi, is a leading research Institute in India with a long-standing reputation for scientific excellence. The institute is equipped with state-of-the-art infrastructure for pursuing research in immunology and allied sciences. The Institute also imparts vigorous long-term research training leading to a Ph.D degree.

Applications are invited for the pos ition  of  Research  Associate or  Senior Research Fellow(Project)  for the following time-bound sponsored project as per the details given below.

Post: Research Associate Or Senior Research Fellow (Project) (One Position only)

Name of the project & Duration: “Identification and characterization the role of Retromer-complex in haemoglobin endocytosis in Leishmania” funded by DBT

Qualifications:
Research Associate:  Ph.D in any branch of Life Sciences
Senior  Research  Fellow (Project): M.Sc  in  any  branch  of  Life  Sciences  with  at  least  two  years of research experience.      

Emoluments: The selected candidates will draw consolidated emoluments as per Institute Rules, depending upon qualifications & experience.
Research Associate: Rs.22,000/- per month plus 30% HRA
Senior Research Fellow (Project): Rs. 18,000/- per month plus 30% HRA if qualified NET otherwise Rs. 14,000/- per month plus 30% HRA
(*Emoluments are likely to be revised to Rs. 36,000/- per mo nth plus 30% HRA for RA and Rs. 28,000/- per month plus 30% HRA for SRF)

Job description & Desired Knowledge: 
The candidate should be aware about  the molecular biology techniques and should have experience about tissue and cell culture techniques. Candidates with adequate experience with microscopy are preferable. Must  have knowledge about host-pathogen interaction.

Name of the Project Investigator: Dr. Amitabha Mukhopadhyay Staff  Scientist -VII (amitabha@nii.res.in)

GENERAL TERMS AND CONDITIONS: 
1. The candidates selected for the above posts will be on contract for one year or duration of the project whichever is shorter, at a time.
2. No hostel/ housing facility will be provided.
3. Applicants may clearly mention the category they belong to i.e. SC/ST/OBC/PH and attach documentary proof of the same.
4. No TA/DA will be paid for attending the interview, if called for.
5. Apart from sending application in the prescribed format given below, candidates should send complete Curriculum Vitae along with the names of three referees. Curriculum Vitae should contain details of the experimental expertise and list of publications.
6. Canvassing in any form will be a disqualification.

HOW TO APPLY
Interested candidates may apply directly, STRICTLY IN THE PRESCRIBED FORMAT GIVEN BELOW, through e-mail, to the Investigator of the project, clearly indicating the name of the project along with their complete C.V., e-mail id, fax numbers, telephone numbers. Only Short listed candidates will be called for interview and they required to submit attested copies of all their certificates and a Demand Draft of Rs. 100/- drawn on Canara Bank or Indian Bank payable at Delhi/New Delhi in favour of the Director, NII (SC/STPH and Women candidates are exempted from payment of fees) subject to submission of documentary proof), at the time of interview.

LAST DATE OF RECEIPT OF APPLICATIONS: 22^nd March, 2016

Recruitment for Technical Trainer (M.Pharm) in Apollo Pharmacy, Bangalore

Apollo Pharmacy is a leading retail chain of pharmacy and is a unit of - Apollo Hospitals Enterprise Ltd. - Asia's largest healthcare group.
Our growing Retail Pharmacy network touches lives across the length and breadth of Indiaca and we serve 150000+ customers a day. With over 30 years of retailing experience, customer-focused service and brand value our network spans out to  2200+ retail pharmacies through which we have been serving our customers for their healthcare needs 24x7.

Post: Technical Trainer (M.Pharm)

No.of posts: 01

Job Description:
• Training Need Identification and Analysis; customization of Training Methodology.
• Preparation of Monthly Training Calendar.
• Coordinate and deliver Training (Internal) in supervisory development, soft-skills, technical and process driven for frontline associates and achieving. Training man days.
• Plan and deliver induction to new hires on bi-monthly basis.
• Plan and deliver new hire’s training program monthly once.

Coordinate with HR
a) To receive the list of new joinees eligible for induction and new hire training as per the training calendar.
b) To submit the attendance of trainees undergoing induction and new hire training.
c) To track three monthly assessments of trainees and carry out counseling whenever required.
d) To help solve SAP issues related to attendance, ID card, uniform etc.

Budget & MIS:
1. Generate and maintain training related employee database.
2. Prepare monthly training MIS Report.
3. Record actual monthly training expenditure in training MIS

Operations & customer service:
1. Encourage and direct supervisors for collecting customer feedback forms.
2. Collect relevant SAP issues during SAP visit and coordinate with concerned in operations for solutions.
3. Liaison with the concerned in operations modules during New hire training.

Candidate Profile:
MUST BE REGISTERED IN KARNATAKA PHARMACY COUNCIL.
READY TO RELOCATE IN BANGALORE.
LOCALS ARE GIVEN PREFERENCE.
FACULTY EXPERIENCE IS ALSO COUNTED

Additional Information:
Experience: 2+ Years of relevant experience
Qualification: M.Pharm
Location: Bangalore
Functional Area: Trainer
Industry Type: Apollo Pharmacy, Retail Pharmacy
Employment Type: Full Time
Job Type: Regular
Last Date: 30^th March, 2016

Looking for for DGM - API Quality Assurance in Mylan

Mylan is one of the world’s leading generics and specialty pharmaceutical companies, providing products to customers in more than 150 countries and territories. The company maintains one of the industry’s broadest and highest quality product portfolios, which is regularly bolstered by an innovative and robust product pipeline. With a workforce of more than 16,000, Mylan has attained leading positions in key international markets through its wide array of dosage forms and delivery systems, significant manufacturing capacity, global commercial scale and a committed focus on quality and customer service.

Post: DGM - API Quality Assurance

Job Description: 
• Prepare controlled documents and distribute, retrieve, archive and destruct controlled documents. Support for DMF/ANDA filing and regulatory queries and prepare new documents as per cGMP requirement, as and when required.
• Prepare employee training curriculum, annual schedules and coordinate with internal trainers and execute the training as per schedule. Maintain, check and update the training records. Assess the training evaluation questionnaires and conclusion of re-training requirements.
• Track and highlight deviations in manufacturing operations to the supervisor and provide line clearances after satisfactory review. FDF: Perform in-process sampling as per production schedule.
• Initiate the change control with necessary document support and execute the approved changes as per the action plan. Prepare the validation protocols and reports and verify documents with current equipment capability. Execute the validation/qualification processes at each stage of manufacturing.
• Prepare and update the vendor list as per the schedule and initiate the vendor evaluation documents. Maintain master data SAP related to vendor.
• Prepare the APQR report and summarize the data collected in APQR preparation, as well as assist the supervisor in preparing recommendations based on APQR evaluation.

Candidate Profile
- Graduate degree in Pharmacy/ Chemistry
- Minimum 4 years of experience in pharma industry
- Application knowledge of Regulatory requirements; Qualifications and Validations
- Knowledge of Quality Management System
- Knowledge of GMP Requirements
- Knowledge and experience of regulatory audits (USFDA, EUGMP etc) 
- Proficiency in speaking, comprehending, reading and writing English

Additional Information:
Experience: 4 years
Qualification: Degree in Pharmacy/ Chemistry 
Location: Andhra Pradesh-Hyderabad
Industry Type: Pharma/Biotech/Clinical Research

https://mylan.taleo.net/careersection/myl_usajobs/jobdetail.ftl?job=153163

Opening in Various position in Omics International (100 posts) and Macleods Pharmaceutical (60 posts) | walk in interview

Post: Program Co-ordinator & Asst Managerial Editor for Journals (Omics International); Production, QC & QA (Macleods Pharmaceuticals Ltd.)

No. of Posts:
100 Posts - Omics International
60 Posts - Macleods Pharma. Ltd

Job Description
Invite speakers / committee liaison

FOR OMICS INTERNATIONAL:
• Coordinates program related events such as workshops, symposia, national and international Scientific Events etc.
• Plan and organizes logistics for events, ensuring their smooth operation. Arranges for travel accommodations, transportation, displays and other event needs.
• Negotiates event-related fees and honoraria agreements. Creates event programs and agendas.
• Ensure the smooth operation and that all logistics and other event details are implemented as planned.
• Be main point of contact for Program chairs, session chairs, scientific committee and invited speakers for conference content/for all conference related communications
• Manage timelines for Program chairs, session chairs, scientific committee and invited speakers Abstract management and abstract book production
• Compile conference specific abstracts and update on Abstracts database
• Liaise with chair to confirm abstract review procedure and compile review instructions accordingly
• Pro-actively work with internal and external teams to ensure that deadlines are meet
• Compile abstract review data, send to chair and mark-up Abstracts database
• Update Abstracts with dates, times and numbers and notify speakers of their presentation times
• Coordinate poster program details, update presenters and supply guidelines
• Request presenters/speakers to register by Speaker registration deadline
• Collate abstracts, invited speaker bios and abstracts, artwork and sponsor files
• Compile all files into conference abstract book proof and send for printing

FOR MACLEODS PHARM. LTD.:
To handle production units, Pharmaceutical analysis & quality assurance works in the plant.

Candidate Profile
Must have strong and polished interpersonal, written and oral communication skills. Able to balance competing priorities, complex situations, and tight deadlines. Creative, strategic and analytical thinker with the ability to manage multiple projects. Should work with a team in order to accomplish monthly & yearly targets. Knowledge of Microsoft Office and Windows based computer application and database management

Please send your C. V. to placementcellcps@gmail.com before 09.03.2016 to attend interview by Omics International and Macleods Pharmaceutical Ltd. 

Additional Information:
Experience: 0-5 years
Qualification: D.Pharm, B.Pharm, M.Pharm, M.Sc
Industry Type: Pharma/Biotech
Location: HYDERABAD
Job Type: PRODUCTION, QA, QC, PC, AME

Date, Time & Vanue of Interview:
Omics Internatjional10^th March, from 3:00 PM onwards
11^th March  from 9:00 AM onwards 

Macleods Pharmaceutical Ltd12^th March, from 9:00 AM onwards

Venue: Hotel Moti, Gandhinagar Main Road, Berhampur, Odisha  For more info contact: 09439868992