Senior Research Associate/ Associate Scientist- Genomics by Syngene International Private Limited, BBRC in Bengaluru/Bangalore Experience: 1 to 6 yrs -"D1"

Senior Research Associate/ Associate Scientist- Genomics

by Syngene International Private Limited, BBRC in Bengaluru/Bangalore

Experience: 1 to 6 yrs.  |  Opening(s): 2 Posted on: 22 Jun

Job Description

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Position/ Designation:- Associate Scientist
Qualification:- M.Sc./M.V.Sc/M.Tech. in Biological sciences (Biochemistry/Molecular Biology/Cell Biology/Biotechnology)
Experience:- 1-7 years industrial or academic research
Location:- Bangalore
Job Profile:-
Candidate is expected to have very good understanding of cloning and mutagenesis processes
Perform de novo and sub cloning using various molecular biology techniques
Document the data and generate reports
Collaborate with other scientists from various functions in understanding the reagent requirements
Skills Set:-
He/She must have a very strong technical background in various molecular biology techniques such as cloning, PCR, Gateway cloning system, RACE and mutagensis.
Experience in quantitative real-time PCR/ microarray techniques for gene expression studies and data analysis is desirable.
Candidate should possess strong scientific aptitude.
He/She should be a good team player with excellent communication skills. Candidate should be able to handle multiple time bound projects simultaneously

APPLY

Apply for Clinical Research Operation job in Quintiles with 6 month experience in Gurgaon, Banglore, Mumbai "D6"

Job description

PURPOSE

Serve customers of Centralized Clinical Operations by determining requirements, answering inquiries, resolving problems, fulfilling requests, maintaining Contact Center database.

RESPONSIBILITIES

· Answer international Calls, Emails, assess customers' technical support needs related to Centralized Clinical Operations and handle/ route inquiry accordingly.

· Provide first level support for customer issues including documented procedures and available tools. Fulfill requests by clarifying desired information, completing transactions, forwarding requests for second level support.

· Maintain Contact Center database by accurately entering information.

· Keep tools, applications & equipments operational by following established procedures and reporting malfunctions.

· Enhance organizational reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES



· Strong customer focus and customer service skills

· Clinical Research/Life Sciences Background would be an added advantage

· Strong listening and phone & email management skills

· Strong verbal and written communication skills

· Good data entry skills



Qualifications :

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

· High or Secondary School diploma/certificate or country's educational equivalent plus 6 months to 2 years of relevant experience; or equivalent combination of education, training and experience

P.S: Applicants should be open to working in shifts & if required on weekends as this is a 24*7 support model. Also, they must be willing to support global customers.

Apply directly

Walk in for drug safety associate for freshers

Walk in for drug safety associate for freshers
employer- synowledge
qualification- bpharm/mpharm/bds
date- june 3

walk in add
‪#‎120P‬-122P, Belagola Industrial Area,
K.R.S. Road,, Metagalli,
Near GRS Fantasy Park,
MYSORE,
Karnataka - 570017,India

To start career in Clinical Research as a Fresher , Apply for- Clinical Trial Analyst Position- "D5"

Job Title: Clinical Trial Analyst

Experience : 0 to 2 years

Position Type : Full Time

Functional Area: Scientific Content

Education : B.D.S, M.Pharm, MBBS

Work Location : Bangalore

Job Description

1.To Review of various clinical trial protocols and source documents.

2.Clinical trial data analysis, tagging and updating the database.

3.Advise data management staff on trial parameters, database designs, and validation of
critical data.

4.Reports progress and changes in clinical trials.

5.Statistical analysis and competitive analysis of trial results.

Desired Profile

1.Should have a qualified MBBS, BDS, M Pharm Degree.

2.A strong educational background in clinical research.

3.Computer skills including use of Microsoft word, excel and power point.

4.In depth therapeutic and clinical research expertise as well as knowledge of
GCP/ICH and applicable regulatory guidelines.

Soft Skills

·Client focus

·Result orientation

·Communicating with Impact

·Team player

·Process oriented

Apply Now

Clinical Research Coordinator/ Associate openings in I5 Clinical Research for B.Pharmacy/M.Pharmacy freshers @ Chennai/Bangalore/Ahmedabad "D5"

Education:

Experience: 0-1 year
Industry: Pharma/Biotech
Department: Clinical research
Designation: Clinical Research Coordinator / Clinical Research Associate/executive
Job Location: Chennai/Bangalore/Ahmadabad
Salary: 2,00,000 - 4,00,000 P.A
Candidate should have knowledge on
Regulatory affairs
Site Management
Clinical Operations
Clinical Study Coordinating
Site Monitoring
Clinical Study Preparation
Clinical Data Management

Company profile: http://www.i5clinicalresearch.com/

Interested candidates send your updated resumes to
Recruiter Name:Mohamad
Email ID: mohamad.sagadh@i5clinicalresearch.com
            hr@i5clinicalresearch.com
            sankar@i5clinicalresearch.com
Contact NO: 91-44-7200017361
Address: Rajeshwari Nagar, Mudichur Road, West TAmbaram CHENNAI,Tamilnadu,India

Fresher vacancy in Quintiles Bangalore as CTA for trained Bachelor's degree holders - Apply now "D"

Clinical Trials Assistant-1314261

Description

 

Provide administrative support to clinical projects under direction of line manager, Clinical Team Leads and/or other

designated clinical team members. May assist with general administrative functions as required.

RESPONSIBILITIES

• Assist Clinical Team Lead (CTL) and Clinical Research Associates (CRAs) with accurately updating and maintaining

clinical systems that track site compliance and performance within project timelines.

• Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for

accuracy and completeness.

• Assist CTLs with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.

• Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.

• Act as a central contact for the clinical team for designated project communications, correspondence and associated

documentation.

• May perform assigned administrative tasks to support team members with clinical trial execution.

All responsibilities are essential job functions unless noted as nonessential (N).

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• Awareness of knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and

International Conference on Harmonisation (ICH) guidelines

• Knowledge of applicable protocol requirements as provided in company training

• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint

• Strong written and verbal communication skills including good command of English language

• Effective time management and organizational skills

• Attention to detail and accuracy in work

• Ability to establish and maintain effective working relationships with coworkers, managers and clients

PHYSICAL REQUIREMENTS

• Extensive use of telephone and face-to-face interactions, which require accurate perception of speech

• Extensive keyboarding involving repetitive motions with fingers

• Regular sitting for extended periods of time

• Packaging and lifting supplies for storage and shipping

• Occasional travel

Qualifications

 

 School diploma/certificate or educational equivalent; or equivalent combination of education, training and experience

Primary Location

: India

Organization

: India

APPLY HERE

* Drug Safety Asociate / Sr. Drug Safety Associate / Sr. Operations Specialist-1406098 job for 1 year exp. professionals - Quintiles - Bangalore "D"

Job Description 

* Drug Safety Asociate / Sr. Drug Safety Associate / Sr. Operations Specialist-1406098 Description   PURPOSE Review, assess and process Lifecycle Safety data and information, across all service lines received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOP's and internal guidelines. May provide oversight on projects with limited complexities for activities on small to medium service operational projects. RESPONSIBILITIES  Receive, triage, review and process Lifecycle Safety data from various sources on time, within budget and quality standards. Perform data entry for tracking and Lifecycle Safety databases, coding relevant medical terminology, writing descript narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations and ensuring reports are sent to the customer within assigned deadlines. Pre-process material for endpoint committee or core laboratory adjudication. Preparation of material for submission of secondary review.  Assess Lifecycle Safety data for report ability to relevant authorities, track reportable cases and report to regulatory authorities, ethics committees, institutional review boards, investigators, oversight groups per legislation, within timelines and in a format compatible to requirement. Liaise with local Quintiles offices to facilitate expedited reporting. Liaise with systems manager for regulatory tracking requirements and electronic reporting.  Contribute to individual deliverables in the field of Safety Publishing, Risk Management, Safety Surveillance and Medical Information or other service lines as appropriate.  Receive and document incoming telephone calls, faxes or emails from investigative sites or other sources reporting Lifecycle Safety data.  Process Lifecycle Safety data according to applicable regulations, guidelines, Standard Operating Procedures (SOPs) and project requirements.  Mentoring less experienced or newer staff members. May provide oversight on operational activities and have a sound understanding of project protocol, therapeutic indication, budget and scope of work (SOW) for assigned projects; set up and maintain project files, standards, templates, electronic forums, databases and workflow.  May provide oversight role to impart technical and process information to the LSM point of contact and members of operational team.  May provide an oversight role to perform operational and collaborative LSM tasks as directed by Lifecycle Safety Infrastructure.  Participate in team meetings and provide regular feedback to operations team manager and lifecycle safety management (LSM) on operational project metrics, out of scope work challenges/issues and successes.  Ensure compliance to Quintiles high quality standards and works with LSM constructively in a matrix framework to achieve project and customer deliverables.  Work with LSM constructively in a matrix framework to achieve project and customer deliverables.  Participate in training across Lifecycle Safety service offerings. Provide project-specific operational process training to junior team members, monitors and investigative site personnel, as appropriate.  Liaise with different functional team members, e.g. project management, clinical, data management, health care professionals e.g. investigators, medical monitors, site coordinators and designees to address operational project issues.  Contribute to achievement of departmental goals e.g. utilization realization and productivity metrics.  Read and acknowledge all necessary Quintiles standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented. Work towards ensuring your individual training plan and training transcript are reconcilable.  Perform other duties as assigned. REQUIRED KNOWLEDGE, SKILLS AND ABILITIES  Excellent knowledge of Lifecycle Safety processes; willingness and aptitude to learn new skills across Lifecycle Safety service lines.  Good understanding of applicable global, regional, local clinical research regulatory requirements; i.e. Good Clinical Practice (GCP) and International Conference of Harmonization (ICH) guidelines, Standard Operating procedures (SOPs)  Proven ability to meet strict deadlines; manage competing priorities and changing demands.  Proven ability to follow instructions/guidelines, work independently and on own initiative.  Good understanding of operational metrics, productivity and initiatives.  Excellent attention to detail and accuracy and maintain consistently high quality standards.  Effective mentoring skills.  Excellent written and verbal communication and report writing skills.  Ability to be flexible and receptive to changing process demands.  Sound judgment; decision making skills.  Ability to work effectively on multiple projects simultaneously. Organize own workload and effectively time manage competing priorities.  Ability to establish and maintain effective working relationships with coworkers, managers and clients. Qualifications   MINIMUM REQUIRED EDUCATION AND EXPERIENCE  Bachelor's Degree or educational equivalent in a Scientific or Healthcare discipline and 1 year's experience of Lifecycle Safety (Pharmacovigilance, CEVA, Medical Information, Safety Publishing, Risk Management etc) or equivalent combination of education, training. APPLY HERE

Clinical Data Analyst by Theorem Clinical Research India Private Limited in Bengaluru/Bangalore Experience: 2 to 5 yrs "D"

Clinical Data Analyst

by Theorem Clinical Research India Private Limited in Bengaluru/Bangalore

Experience: 2 to 5 yrs. 

 Understand and follow the Data Management Plan with regards to project specific activities related to the clinical data. Continually apply DMP changes to daily work activities. Reference data issues log to resolve questions whenever possible. - Good understanding of the protocol with specific concentration on the study purpose and design, and to the data being collected
- Independently perform data cleaning including query activity and EDC Status changes. Identify and report issues and data trends. Communication with CDM Team Lead with regards to issues and concerns along with suggested resolution. Completion of assigned tasks in a timely manner meeting assigned goals for tasks. Run reports as requested and needed for daily tasks.
- Actively participate in internal project meetings
- Complete SOPs, WPGs and other role related training within the required timeframe. Understanding of technical aspects of the assigned clinical database(s) as relates to the CDA role
- Completion, understanding and documentation of required Company and Sponsor project and non-project training (includes SOPs, WPGs and other role related training) within the required timeframe. Timesheet information entered in a timely manner

APPLY HERE

Clinical Trial Analyst job for freshers @ Bangalore Indigene "D"

                             Position Details : Clinical Trial Analyst

Designation  Clinical Trial Analyst  Experience  0 to 2 years  Position Type Full Time  Functional Area  Scientific Content  Education B.D.S, M.Pharm, MBBS  Work Location Bangalore  Job Description   1.To Review of various clinical trial protocols and source documents. 2.Clinical trial data analysis, tagging and updating the database. 3.Advise data management staff on trial parameters, database designs, and validation of   critical data. 4.Reports progress and changes in clinical trials. 5.Statistical analysis and competitive analysis of trial results. APPLY

Large no. of Job openings in Syngene Bangalore, Hyderabad for freshers B.Sc. Biochemistry/ Microbiology/ Zoology/ Life Science candidates @ Bangalore "D"

Syngene International is one of India's premier contract research and manufacturing organizations in providing customized service. Their services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area.

Job Title: Sample Coordinator, Test Material Coordinator

No. of Openings: 2

Job Description:

• Management and maintenance of samples and test material
• Maintain proper records of receipt and accessioning and storage and retrieval of samples and all GLP and GCLP related documentation
• Receipt of sample shipment and reconciliation as per SOP for samples and test material and storage under specified conditions
• Verification of samples and test material with the document provided and as per approved SOPs.
• Safe custody of samples and test material and timely communication to stake holders
• Daily Retrieval and relocation of samples and test material to and from analytical team
• Routine disposal of the expired samples and test material as per requirements
• Following GLP principles for operations

1. Qualification: B.Sc. Biochemistry/ Microbiology/ Zoology/ Life Science
2. Experience: 0-4 years
3. Desired Skills: Thorough experience in the relevant field

Location: Bengaluru/Bangalore, Hyderabad / Secunderabad, Chennai

How to Apply:

Interested candidates can send their CVs at cydwel.mascarenhas@syngeneintl.com

Cognizant Walk-In Drive For Freshers On 6th to 10th May 2014 - Bangalore "D"

Designation : Voice / Non-Voice / Semi-Voice Process

Experience:0 Yrs

Qualification: Any Graduates

Location: Bangalore

Job Details:

Good Communication Skills

Apply Mode : Walk In

Walk In Date: 5th to 10th May 2014

Venue:
Be Practical Tech Solutions Pvt Ltd
(Recruitment for our reputed client – MphasiS | Cognizant),
No.613/40/1, First Floor, Dr.Rajkumar
Road, Prakashnagar,
Bangalore.

Clinical Research Associate-1314280 @ Quintiles Bangalore for candidates with 3 months of monitoring exp. "D"

Job Description 

Clinical Research Associate-1314280 Description   Conduct monitoring visits for assigned protocols and study sites. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.   RESPONSIBILITIES    Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.  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 to Clinical Project Manager (CPM), Clinical Research Specialist (CRS) and/or line manager.  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.  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.  May provide assistance to less experienced clinical staff. All responsibilities are essential to job functions unless noted as non-essential (N). REQUIRED KNOWLEDGE, SKILLS AND ABILITIES  Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines  Good 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 lap top computer  Good written and verbal communication skills including good command of English language  Good organizational and problem-solving skills  Effective time management skills  Ability to establish and maintain effective working relationships with coworkers, managers and clients Qualifications   Bachelor's degree in a health care or other scientific discipline or educational equivalent and successful completion of a CRA Trainee Program or 3+ months of on-site monitoring experience; or equivalent combination of education, training and experience   APPLY HERE

Senior Clinical Research Associate @ PARAXEL BANGALORE "D"

Qualifications

• 4+ years of onsite monitoring experience.
• Strong ability to make appropriate decisions in ambiguous situations
• Ability to work independently and to proactively seek guidance when necessary
• Excellent presentation skills
• Client focused approach to work
• Ability to interact professionally within a client organization
• A flexible attitude with respect to work assignments and new learning
• Ability to prioritize multiple tasks and achieve project timelines, utilizing strong analytical skills to make decisions autonomously due to the unpredictable nature of the issues that arise
• Willingness to work in a matrix environment and to value the importance of teamwork
• Strong computer including but not limited to the knowledge of Clinical Trial Management Systems (CTMS), Electronic Document Management System (EDMS), EDC, IWRS, and MS-Office products such as Excel and Word
• Excellent interpersonal, verbal, and written communication skills

APPLY HERE

Urgent Job openings for post of Business Analyst/Patient Care Coordinator/Medical Coding & Billing associate @ Bangalore for Freshers/Exp. B.PHARMA, B.Sc. & M.Sc. candidates - "D"

Interested candidates can send their resume to dheeraj.awasthi@cliniindia.org, writing in Subject line the post they are applying for.

*Note: Candidates must have good communication skills & Basic knowledge about profession.
For training enquiry @ DELHI Location - mail your C.V. to same mail id writing "Enquiry" in subject line.

Job opening for fresher M.Pharma in Indigene Bangalore "D"

Designation - APPLY HERE Trainee
Experience	0 to 1 years
Position Type	Campus Full Time
Functional Area	Scientific Content
Education	M.Pharm
Work Location	Bangalore
Job Description
A. Operational Responsibilities 1. Develop scientific medical content for all projects, meeting international quality standards 2. Prepare Literature Review, Abstracts, Posters, Slide Sets and Manuscripts (complex), working from various data sources including clinical study reports, patient profiles, protocols etc. 3. Deliver medical content that is rated high on depth, comprehensiveness, quality and timelines 4. Develop innovative medical content products by leveraging on the depth of scientific content.

Medical Writing Job opening in Quintiles Bangalore for freshers - "D"

Job Description 

Medical Writing - Intern-1407773 Description   PURPOSE Assists senior medical writing staff in the preparation of study reports, submissions, or other documents for either internal Quintiles customers or external clients, for investigational drugs, biologicals, or medical devices. Participates in project teams and may lead specific straightforward or small tasks, consulting senior staff as necessary. RESPONSIBILITIES • Supports Medical Writing senior staff in managing client requests. Examples include but are not limited to the following: writing patient narratives, checking document edits, checking documents for consistency, adapting generic document shells to project specifications, assisting with document compilation, and entering numbers into in-text tables. May also draft text for simple documents or sections of documents, with guidance of senior staff. • Identifies project needs, tracks project timelines and implements client requests, with senior review. • Interacts with internal clients. May have some external interactions, mostly directed by senior staff. • Takes responsibility for managing day-to-day workload for assigned tasks, 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. All responsibilities are essential job functions unless noted as nonessential (N). REQUIRED KNOWLEDGE, SKILLS AND ABILITIES • Excellent standard of written English, and ability to communicate fluently and effectively in English, both in writing and verbally. • 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. • Knowledge of regulations relevant to medical writing. • Careful attention to detail and accuracy. • Must be computer literate. • Ability to establish and maintain effective working relationships with coworkers, managers and clients Qualifications   MINIMUM REQUIRED EDUCATION AND EXPERIENCE • Bachelor's degree in a life science-related discipline or equivalent combination of education, training and experience Primary Location : IND-Karnataka-Bangalore Organization : IND02 - India - CDS/Product Devel

 APPLY

 

Document Specialist I @ Parexel, Bangalore - Medical Writing - For freshers graduates, Also Click here to get some Interview Tips "D"

  Job Family
Requisition # pare-10033676
Location India - Karnataka - Bangalore

Key Accountabilities
• Compile appendices to clinical study reports in compliance with appropriate regulatory requirements, under the supervision of the project lead Medical Writer. Work with internal or external Clinical and/or Project Leadership functions to ensure that appendix documentation is complete and complies with the relevant guidelines.
• Perform all scanning/uploading of paper documents
• Be responsible for conversion of documents to PDF format
• Use departmental publishing software to produce electronic deliverables to ensure insertion of navigability features, and accurate intra-document hyperlinking, according to SOP/client/regulatory requirements
• Perform MS Word formatting of clinical documents according to SOP/client/regulatory requirements. Insert tables if requested.
• Coordinate production and distribution of draft and final documents to project team and client. Organize and track delivery of all deliverables.
• Ensure that all work is complete and of high quality prior to delivery
• Provide support on software and document related issues to MWS staff as required
Skills
• Excellent interpersonal, verbal and written communication skills, and good degree of initiative
• Client focused approach to work
• Flexible attitude with respect to work assignments and new learning
• Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
• Ability to work in a matrix environment and to value the importance of teamwork
• Advanced word processing skills in MS Word/Office. Ability to apply formatting to template documents, perform quality checks, edit tables and figures within templates, and verify template data against source documents
• Advanced PDF processing skills in Adobe Acrobat
• Advanced skills in other document editing software, such as design and application of styles/templates, graphics, and integration with other applications
• Proficient in document management systems and key publishing software
• Proficiency in basic grammar, punctuation, and spelling. Understanding of medical and pharmaceutical terminology desired.
• Advanced keyboard skills
Education
• Primary degree or a regionally acceptable equivalent qualification, either in health-related sciences with significant experience in document processing/publishing, and/or in computer science or technology
Language Skills
• Fluent in written and spoken English
Qualifications Good knowledge of word processing and publishing software with proven ability (15-17 pages per hour of formatting and post PDF work).  Experience with processing multiple clinical documents of varying complexity such as clinical trial submission dossiers, clinical study reports, etc., as an independent document technologist or specialist.

APPLY

 

 

 

CLICK HERE TO FILL COUNSELING FORM

Clinical Data Management - Executives & Associates @ Valycon Clinical Research Organization FOR Fresher graduates - Bangalore, Karnataka

WALK-IN
Date: 13th April-2014
Day: (Sunday)
Time: 10:00 am-04:30 pm
Valycon Clinical Research Organization
# 504, 3CM, HRBR Layout, Kalyan Nagar Bus stop, Landmark: Back Building of Tanishq Jewellery Showrooms, Bangalore - 43, Karnataka, India.
Position - Junior Data Entry Executives & Associates
Experience - 0 to 3 years
ROLES AND RESPONSIBILITIES
Minimum 1 year experience in Clinical Data Management (Rave/Inform/Oracle Clinical),
Perform data management activities on the assigned project in a timely and efficient manner.
Good Communication Skills is mandatory
Generate queries to clarify and improve the quality of the data
Test and execute validation procedures
Willing to work in multi task environment
Should have teaching skills
Functional Area: CDM Department
Location: Bangalore
Contact: Mr. Kumar
Ph: 080-60123460, Mobile: 8095934777
Url: www.valycon.com,
Company: Valycon CRO, Bangalore.
Job Posted: 4th April 2014



 

List of all Walk ins in Delhi NCR, Ahmedabad, Baddi, Mumbai, Pune, Hyderabad & Bangalore in April.14 - For Freshers/Experienced B.Pharma, M.Pharma, B.sc., M.Sc. Life sciences, Biotech & Medical Graduates - See full post to apply for Jobs as per your profile - All the best : Team CLINI INDIA -"D"

• 
  

  Walkin at Wipro BPO Sarita Vihar for Pharmacovigilance Graduates
  

  by Wipro BPO Solutions Ltd in Noida, Delhi, Delhi/NCR

  
  

  Experience: 0 to 1 yrs.  | Salary: INR 1,50,000 - 3,00,000 P.A  |  Opening(s): 25 Posted on: 05 Apr

   

  Job Description

  
  

  Highest Education :- ONLY B.Pharm and NO Master Degree or Diploma
  Experience :- 0-1years
  Language :- English
  Excellent communication skills (Written & Spoken)
  Salary : 11k-21k (in hand)+ incentives
  Need to be confortable 24*7
  Minimum skills required
  Registered pharmacist
  Written and spoken fluency in business English
  Experience working in a B2C environment
  Comfortable with a rapidly-changing environment
  Strong problem-solving skills
  
   
  Walkin To:A-29, Mohan Cooperative Industrial Area, Sarita Vihar
  Date- 7th April-11th April
  Timing: 1pm - 3pm
  Document Required:
  1)2 photograps
  2)1 govt. ID proof
  3)Updated CV
  Contact Person: Jigyasa Pahwa
  

  Salary: INR 1,50,000 - 3,00,000 P.A
   
• Opening for Freshers in Biotech and B.pharma in Evalueserve

by Evalueserve.com Pvt. Ltd in Gurgaon

Experience: 1 to 2 yrs.  | Salary: INR 3,00,000 - 5,00,000 P.A  |  Opening(s): 6 Posted on: 04 Apr

CLICK HERE FOR MORE DETAILS 

• Walkin 7 April 2014 for Ipr (f&d) by Mankind Pharma, Manesar - GURGAON

Experience: 3 to 6 yrs.
Posts: 1
1.Drafting of patent description & knowledge to study case laws. Prosecution & grant of patents etc.
2. Candidate have an exposure in patent drafting, Patent analysis. etc.
3. Preparing Patent search Reports for Regulated Markets.
4. Patent application Drafting and Prosecution.
5. Patent invalidation and infringement analysis.
B.Pharm, M.Pharm, Ph.D - Chemical
1. Min. Qualification is M.Pharma
2. PG Dip. in IPR.
Interested Candidate can Vist at
7th April from 11 AM
Mankind Research Centre,
191-E, Sector-4-II, IMT Manesar,
Gurgaon, Haryana
Ph:- 0124-2873900

• Walk in @ Crest, Pune for freshers  - 
• Education: B.Pharmacy/M.Pharmacy and M.Sc
  Experience: freshers
  No. of openings: 30
  Required skills: Good communication skill in English (Written and spoken)
  Technical skills: MS word
  Schooling should be from English medium only.
  Walk in details:
  Date: 4th-12th April
  Time: 10 AM to 2 PM
  Venue: Fifth Floor, Wing A , Tower 9,
  Magarpatta City SEZ, Hadapsar
  Pune 411013, Maharashtra, India

Walk - In for Quality Control, Quality Assurance and Production

by Dr. Reddys Laboratories Ltd. in Hyderabad / Secunderabad

Experience: 3 to 8 yrs.  |  Opening(s): 30 Posted on: 02 Apr

Walk in for Quality Control, Quality Assurance and Production  
Date of Walk in : 6-Apr-14 (Sunday)
 
Time : 9:30 am  - 11:00 am
 
Venue :
 
Dr. Reddy's Laboratories Ltd
Bachupally Campus
Qutubullapur
Ranga Reddy Dist - 500090
 
1) Quality Control :
 
B Pharm / M Sc with 2-10 years of experience in Formulations QC
 
Skill Sets Required

• RM & PM Analysis
• FG Analysis
• Stability Samples Analysis

 
2) Quality Assurance:
 
B Pharm / M Sc with 2-10 years of experience in Formulations QA
 
Skill Sets Required
 

• IPQA
• Manufacturing Assurance
• Analytical Assurance
• QMS

 
3) Production:
 
B Pharm / M Pharm with 3-10 years of experience in Pharma Production
 
Skill Sets Required

• Granulation
• Compression
• Coating

• Walk In Interview for IPCA Athal - Qa/qc/production/pkg./male Nurse

by IPCA Laboratories Ltd., Athal. in Dadra & Nagar Haveli / Silvassa

Experience: 2 to 7 yrs.  |  Opening(s): 30 Posted on: 02 Apr

1. Officers/Executives Quality Control / Quality Assurance: Candidates should be B.Pharma/B.Sc. (Chemistry) with minimum 2-8 years of relevant experience, on HPLC, GC, UV is required for Quality Control/ In-process QA, Validation including equipment qualifications and routine documentation for Quality Assurance.
2. Officers/Executive - Production & Packing: Candidates should be B.Pharma/B.Sc. with minimum 2-8 years of relevant experience in Tablet/Capsule manufacturing & packing, should have thorough knowledge on sophisticated granulation, Compression, Coating and Capsule Filling Machines for production position and Blister Packing and Cartonator Machines for packing position.
3. Male Nurse - Administration (Dispensary)
Experience of Male nurse having with minimum 1-3 years of relevant experience of Dispensary.
AT - Hotel Sovereign, Sea Face Road, Daman, Phone No. 0260-2250236/7, Date : 06.04.2014 (Sunday) Time : 10 a.m. to 6.00 p.m.
Fresh candidate should only send their resume on below email & Not attend interview. Those who are unable to attend the interview may email their detailed resume at hrd.athal@ipca.com

CLICK HERE FOR MORE DETAILS 

 

• Pharmacist 
  Education:B.Pharma - Pharmacy
  Experience:0 to 2 yrs

by MIOT Hospitals in Chennai

Experience: 0 to 2 yrs.  |  Opening(s): 2 Posted on: 13 Mar

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• Designation	Walk in Interview for Tablet Manufacturing & Packing on 07/04/14 - 10 Opening(s)
  Job Description	Walk in Interview for Tablet Manufacturing & Tablet Packing on 07th April 2014, Monday, Timings - 10:00 am - 02:00 pm at Cadila Healthcare Ltd, Sarkhej- Bavla N. H No.8A, Near Modern Denim, Moraiya, Tal Sanand, Dist- Ahmedabad 382 210.   Opening in Tablet Manufacturing & Tablet Packing for Technical Supervisor/ Sr. Techinical Supervisor/ Officer.   Job Profile for Tablet Manufacturing : Handling Manufacturing activities like Granulation, Coating, Compression, Inspection, Dispensing of Tablet according to cGMP Practice. Handling in process monitoring and documentation. To co ordinate with all department i.e. QC, QA, Warehouse Engg as per requirement. Required Education Qualification for Tablet Mfg : B.Pharm Graduate only     Job Profile for Tablet Packing : Handling Tablet Packing activities. Handling bulk packing lines (Blister / Bottle) Operating packing as per the requiement. Maintaining BPR & Log Books. Required Educational Qualification for Tablet Packing : Bsc / Msc / B.Pharma  Graduate   Preference will be given to candidate who has relevant experience from reputed organization and ready to relocate in Ahmedabad. Interested candidates can walk in along with latest salary slip & lncrement letter.
  Desired Profile	Refer Job description above. Candidate should have atleast 2 -5 years pharmaceutical experience in required field Candidate should have B.Pharm Graduate only for Tablet Mfg & Bsc/Msc/ Bpharm Graduate for Tablet Packing.
  Experience	2 - 5 Years
  Industry Type	Pharma / Biotech / Clinical Research
  Role	Outside Consultant
  Functional Area	Production, Manufacturing, Maintenance
  Education	UG - B.Pharma - Pharmacy PG - Any Postgraduate - Any Specialization, Post Graduation Not Required DOCTORATE - Any Doctorate - Any Specialization, Doctorate Not Required
  Compensation:	Best in the Industry
  Location	Ahmedabad
  Keywords	Granulation, Compression, Coating, Packaging
  Contact	Ms. Jigna Joshi Cadila Healthcare Limite

       CLICK HERE FOR MORE DETAILS

 

• Designation	Walk-in - Vadodara 12th April 2014 (2nd Saturday). - 10 Opening(s)
  Job Description	Walk-in Vadodara 12th April 2014 (2nd Saturday).   We have following vacancies at our API Manufacturing located at Baroda   Chemist/Sr. Chemist/Officer Production : Diploma/ BE - Chemical Engineer/M.Sc./ B.Sc. (Chemistry) with 1 to 10 years of experience and relevant exposure in shop floor Operation in API / Bulk Drug Manufacturing.   Chemists/Sr. Chemists/Officers: - Quality Control : M.Sc. / B.Sc.(Chemistry) with 1 to 5 years of hands on experience of HPLC, GC, Dissolutions Apparatus, UV-Visible Spectrometer, Weight analysis and Stability studies.   Chemists/Sr. Chemists/Officers: - Quality Assurance : M.Sc. /B.Sc. (Chemistry) with 1 to 5 years of experience and relevant exposure in quality assurance. Exposure to qualification, validations and GMP audits is required.   Chemist/Sr. Chemist/Officers VALIDATION : M Sc/B. Sc. (Organic Chemistry) having at least 2 to 6 years of experience in Analytical Method Validation.   Office/Executive TT/PE (Technology Transfer & Process Engineering) : Diploma/BE/B. Tech. - Chemical Engineering, having at least 2 to 6 years of experience on shop floor in Technology Transfer, Scale-up, Process Engineering.     Interested candidate may Walk-In for Interview along with their CVs and relevant documents between 09:00 AM to 05:00 PM   Venue : Baroda Productivity Council,               2nd Floor, Productivity House,               Alkapuri, Vadodara               Contact No of HR representative : 0266-2679121   Candidates having experience of working in regulatory approved plants, exposure to GLP and SAP Environment will be preferred. Those unable to attend the Personal Interview, may send their resume through e-mail to hr.dabhasa@zydusmail.com. Please mention the position applying for on the top of envelope / subject in case of e-mail.   Note : Fresher may not need to appear for for Personal Interview.
  Desired Profile	Qualification & Experience - Candidates interested in any of the above positions with relevance experience, in API Production in API Pharmaceutical industry / API manufacturing facility can appear for the Interview
  Experience	2 - 7 Years
  Industry Type	Pharma / Biotech / Clinical Research
  Role	Other
  Functional Area	Other
  Education	UG - B.Tech/B.E. - Chemical, B.Sc - Chemistry, Diploma - Chemical PG - M.Sc - Any Specialization, Chemistry DOCTORATE - Doctorate Not Required
  Compensation:	INR 2,00,000 - 3,00,000 P.A
  Location	Vadodara/Baroda
  Keywords	Api Manufacturing, Production, QC, QA, TT, Method Validation, Technology Transfer
  Contact	Ms. Pooja Thakkar
  Telephone	0266-2679121
  Email	hr.dabhasa@zydusmail.com
  Website	http://www.zyduscadila.com
  Job Posted	04 Apr
  Reference	API-DBH/Walk-In/2014-002

• Designation

  Walk-in for Production / QC / QA on 18th April 2014 @ at Tarapur.

  Job Description

  Walk-in for Production / QC / QA on 18th April 2014 @ at Tarapur .   Here is a chance to join us at our API Manufacturing located at Ankleshwar as.   Chemists/Sr. Chemists/Officers Production : Diploma Chemical Engineer/M.Sc./ B.Sc. (Chemistry) with 1 to 6 years of experience and relevant exposure in shop floor Operation in API / Bulk Drug Manufacturing.   Chemists/Sr. Chemists/Officers Quality Control : M.Sc./ B.Sc. (Chemistry) with 1 to 6 years of experience and relevant exposure in shop floor Operation in API / Bulk Drug Manufacturing.   Chemists/Sr. Chemists/Officers Quality Assurance :M.Sc./ B.Sc. (Chemistry) with 1 to 6 years of experience and relevant exposure in shop floor Operation in API / Bulk Drug Manufacturing.   Interested candidate may Walk-In for Interview along with their CVs and relevant documents at   Date :18th April 2014 (Friday)   Time: 10:30 to 04:00 PM   Venue : HOTEL SILVER EVENUE,               NEXT TO BIG BAZAR,               OSTWAL EMPIRE,               BOISAR(W), THANE 401501   Contact No of HR representative : 02646-660408/660507   Candidates having experience of working in regulatory approved plants and possesses sound knowledge of documentation, exposure to cGMP and SAP Environment will be preferred.   Those who are unable to attend the Personal Interview, may send their resume through e-mail to reema.patel@zydusmail.com Please mention the position applying for on the top of envelope subject in case of e-mail.   Preference will be given to only those candidates who are working in Pharmaceutical Industries - API .   Note : Other than B.E Chemical / Diploma Chemical, fresher may not need to appear for the Personal Interview.

   
• Walkin--IPQA Officers-acme Formulation Pvt. Ltd  

Walkin Interview from 7th April to 12th April from 11 AM 

• by Acme Formulation Pvt Ltd in Baddi
  

  Experience: 1 to 3 yrs.  | Salary: INR 80,000 - 1,25,000 P.A  |  Opening(s): 30 Posted on: 05 Apr

  APPLY 

  
  

  
  

  
  

  Junior Medical Writer

  
  

  by Digital A Plus Group in Bengaluru/Bangalore

  
  

  Experience: 0 to 1 yrs. Posted on: 05 Apr

  
  Qualification: Master in pharmacy, MBBS, Master in biological sciences, BDS, Ph.D

  CLICK HERE FOR DETAILS 

   

  Drug Safety Reviewer/Scientist

  Job Location:Bangalore

  Job Number:J3172

  Apply Online

  Job Description Qualifications

  Schedule: Full-time

  • Confirm that the information in the Global Safety Database is accurate and consistent with the Source Documents;
  • Confirm that the information has been data entered in accordance with applicable Guidelines and SOPs;
  • Perform medical coding for each ICSR in accordance with Guidelines and SOPs using MedDRA;
  • Confirm the accuracy of terminology and coding and manually recode any errors or inconsistencies as needed per Guidelines and SOPs;
  • Conduct the seriousness assessment and global expectedness (listedness) assessment and conduct a Local Assessment for cases that qualify for reporting to regulatory agencies in the US and Canada;
  • Prepare a Case narrative for each Case, which reflects the safety data. The Case narrative should be a concise summary of the facts of the case, and the format should follow applicable Guidelines and SOPs;

  Apply Online

  

   

  

  
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