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MAJOR COMPANIES (BPO's)

SOFTWARE COMPANIES

CAREER RESOURCES

Manager - Regulatory Affairs,with a reputed Pharma Industry, Panchkula

Candidate should have good flair for laisoning with different dept. of state, central level, laisoning with DCGI, Good knowledge of excise and sales and other labour laws. Keywords: Regulatory Affairs, Laisoning, corporate communication, excise and sales and labour laws

HR Recruiter - Placement Consultancy - Mulund Mumbai

To follow with clients and candidates. To find out suitable candidate for the client To close the vacancies Keywords: HR executive

Executive / Sr Executive

Draft editorials for Pashudhan. Select, review and edit articles/research articles for Pashudhan. Co-ordinate with News Sources, Article Sources of Pashudhan. Publishing Pashudhan and inhouse journals viz., Naturally Ours, Moving Forward, etc Keywords: Journalism, Editor, Graduate, Mass Communication

GM Medical Service (Mumbai)

 Developing Product Profiles  Reviewing Market Survey & Compiling Feedbacks  Coordinating CLINICAL TRIALS  Developing Training Modules  Roll out of medico-marketing activities for the fore-mentioned therapy areas viz. support brand-related activities, designing of CME programs- preparation of resource books for use by faculty for the meeting, identification of interesting clinical case studies etc., training of field force (design the modules, contribute to medical sessions, assessment of trainees etc.).  Handling of adverse events (AEs), product complaints and off-label queries on marketed products in the TA.  Medical / clinical evaluation of new products for poten

RBM (Pharma) - Ahmedabad & Pune (2)

Under Supervision, Planning and controlling sales activities, developing sales force and ensuring sales through effective supply chain and customer relationship management, •Execution of sales Plans, •Field work - Traveling to all territories Keywords: Regional sales manager, Oncology

Project Quality Lead II, OpsQM

Provide quality oversight to project team management throughout the project. Specifically responsible for standard and risk-based quality interventions including: review of key project documentation, consultation, CAPA support, audit and inspection support, and collection and reporting of project quality metrics. Keywords: project documentation, consultation, CAPA support, audit and inspection support

Associate Medical Director (MD Radiologist)

Essential Function Provide medical expertise especially on imaging-related projects where imaging is used to evaluate the safety or efficacy of an investigational drug or device. Work closely with clients to develop strategies for the use of imaging in clinical trials. Key Accountabilities -Provide medical expertise to project teams conducting clinical trials that rely upon the results of medical imaging studies. -Assist in study design to ensure standardization of techniques in multi-center trials. -Provide consulting to clients on medical issues.

BUSINESS DEVELOPMENT MANAGER (MUMBAI, DELHI)

INITIATING CONTACT WITH DOCTORS, HOSPITALS, ORTHOPEDICS, GYNACS & POTENTIAL CUSTOMERS FOR DEVELOPING CELL THERAPY BASED PRODUCTS.IDENTIFYING NEW MARKET SEGMENTS & TAPPING PROFITABLE BUSINESS OPPORTUNITIES. BUILD COMPANY PROFILE & BRAND IMAGE. Keywords: ORTHOPEDIC SURGEONS, DENTAL PRODUCTS, GYNACS, BHMS

Medical Co-ordinator

Coordination between the Lab & Marketing Team. Calling & counseling the clients about stem cell banking.Following up with the leads & fixing up the presentations for the Mktg Team.Tracking & monitoring sample status. Keywords: co - ordination, biotech

Business Development Manager-Life science

Responsible to RFIs/RFPs,presentations,due diligences etc. Should generate new leads and conduct prospect research. Preparing & delivering solution based product presentations to meet customer business requirements. Financial modelling for clients. Keywords: Business dev.,RFI,RFP,clinical data mgt,Statistical programming.

Assistant / Deputy Genaral manager-Global Regulatory affairs- API

Should have international regulatory affairs experience from any reputed pharma company. Keywords: Regulatory affairs,RA,regulatory affairs API

DQA/Junior Manager

Planning and execution of activities related to the group. Review of intended MRPs and executed BRPs for exhibit & commercial batches. Ensuring cGMP and required Sops and followed during manufacturing and packing of the drug product. Ensure no delay in dispatch of finished goods. Release of batches. Review of cGMP compliance and adherence to norms. Verification of validation / sampling / stability protocols before and after approval. Responding to ANDA review comments. Investigation, handling disposal of incidents related to production and R&D. Handling of Market complaints and preparing responses to them. Internal & vendor audits. Monitoring of inprocess activities. Imparting training to Quality Assuranc

Officer/Executive-R&D - 4 Opening(s)

• Should be responsible for the improvements in the processes and for the commercialization of the developments. • Should be able to develop the process independently, able to transfer the processes of API'S and the intermediates through scale-up, piloting to plant floor. • Should be capable of data analysis/evaluation, Knowledge on regulatory/ICH norms and familiar to chem. software/computers. • Should have exposure related to operating & calibration of instruments like H.P.L.C, F.T.I.R, G.C, U.V etc. • Good Experience of various preparative organic reactions.

AGM-DRUG DEVELOPMENT- 5 Opening(s)

Development of formulations on a global basis.Manage Drug Development process by interacting with . RA, Clinical Research, Pre-clinical, Tech. Transfer, Quality & Compliance, Research Centres, IPR Keywords: research, general manager,drug development, formulations, scientist.pharma

MANAGER-SALES HR3 Opening(s)

Ensure manpower is recruited as per plan (Number, as per JD) Ensure enough resource pool is there in pipeline to fill the vacancy in 7 days. Keywords: Sales,Human resource,field operation

Microbiologist (4 - 9 yrs)

Experience of handling audits like WHO GMP (World Health Oraganisation Good Manufacturing Practices), EDQM (European Directorate for the Quality Medicine & Health Care) etc. Experience around 5 yrs in a reputed pharma company. Good Communication Skill. www.JobOshop.com

CHEMIST / R & D ASSISTANT / QUALITY CONTROL EXECUTIVE (2 - 5 yrs)

Q C / PRODUSCT DEVELOPMENT/PRODUCTION CHEMIST / REASEARCH AND DEVELOPMENT you will help and support manufacturing activity and involve in Analytical Chemistry Basic Research Chemical Research Chemist Formulation Quality Assurance/ Control, upkeep of records and data primary and secondry as per need of the organisation and maintain the lab as per the government compliances and the industry norms. you are also required to represent the products and industry appropiatly time to time.

Quality Control (0 - 1 yrs)

Quality Control handling R & D Candidate ,Bio Tech/R&D/Scientist Graduate in B.Sc/chemistry Salary 5 to 7 Location :- MICD Hingna Fresher / Experience Mail :- support@simplynaukri.in Quality Control handling R & D Candidate ,Bio Tech/R&D/Scientist

peptide chemist/organic chemist

Peptide Chemist is responsible for the manufacturing of peptide raw materials such as protected amino acids, functionalized resin supports etc. and to manage the synthesis, cleavage, purification and isolation of peptides. Keywords: peptide, amino acids, chemist, organic

GROUP LEADER - FORMULATIONS – R&D – INJECTABLES

Candidate with rich experience in professionally managed Cos is desired. They should be able to deliver results with accuracy and methods. Keywords: GLF

Sales Executive

The incumbent will be responsible for looking after sales of pharmaceutical tablet coating machine. His other responsibilities will include co-ordinating with universities and pharmacy colleges and identifying potential customers. Keywords: Sales Executive

Research Scientist

Will be responsible for : Product development of new formulation – preformulation studies, lab scale trials packaging material, compatibility studies protocol and carry out stability studies for US, EU, and Russia. Conduct regular literature search, patent search. Provide data and information required for registration of drugs. Execution of Pilot and scale – up batches, improvement and trouble shooting of existing formulations. Documentation of all R&D activities as per GMP & GLP and maintenance of the records. Develop Injectable and ophthalmic products for US, EU and Russia. Impart training to the Research Associate in all aspects of product development and related documentation.

Dr-Doctor Health Claims 1

Evaluation health Claims Ratio Evaluation of Healthcare Treatment & associated Costs Interaction with Health Care Providers Coordination with internal & external teams. Implementing new process to cut down on cost and improve client service Keywords: doctors, claims, TPA, clinical research, hospitals, claims,insurance claims,MBBS, Doctors,Dr,clinical research,

Dr-Doctor Health Claims 1

Key accounts manager-Life science

•Key Account Management • the key products to be handled are related to pharma •no team is to be handled •handle few key accounts for the company •to be a part of effective and efficient team •to contribute to healthy relations with the customer •maintain and encourage inter-departmental relations •retention of existing customers •team work Keywords: key account management

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