Jobs for Microbiologists "A"

Claris Otsuka Private Ltd. (Claris Otsuka) is a Joint Venture between Claris Lifesciences Ltd., India, Otsuka Pharmaceutical Factory, Inc., Japan, and Mitsui & Co. Ltd., Japan, for Claris’ Infusion Business in India and Emerging Markets. We primarily manufacture & market products across multiple markets and therapeutic segments. Being a leader in intravenous nutrition products, we are committed to being the best partner of patients and healthcare professionals in the field of clinical nutrition.
Job Title : Microbiologist
Eligiblity : B.sc / M.sc Microbiology

Experience : 1 – 5 Years




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Career in Food Industry "A"

Institute of Good Manufacturing Practices India, registered as a non-profit society with Government of India and approved (as a higher/professional Education Institute) by Quality Council of India(QCI) – which is an autonomous body and an accreditation authority for education & vocational training providers under the Department of Industrial Policy & Promotion, Ministry of Commerce & Industry, Government of India -presents unique, friendly and interactive platform to get rid of all your GMP related glitches. IGMPI is also affiliated with Life Sciences Sector Skills Council (SSC) and Food Industry Sector Skills Council set up by National Skill Development Corporation (NSDC).



For counseling by our experts or prospectus, you may call/write on , +91 8587838177, +91 8130924488, 0120-2427175, 0120-4375280  ffsq@igmpiindia.org mentioning the name of the course and your phone number.

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Job as Scientific Officer "A"

On line applications are invited for the Posts of the Scientific Officer (Biology), Class-II, in General State Service under the Director of Forensic Science, Home Department (Advt. 47 /2016-17) between date: 18/10/2016, 13.00 Hrs. to date 03/11/2016, 13.00 Hrs.

Post : Scientific Officer

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B.Pharm, M.Pharm candidates required at Chantilly BioPharma "A"

Job Description
1. Need to do literature search for new projects and for writing patents.
2. market research for new products
3. Documentation
4. SOP write up
5. Identification of materials suppliers and manufacturers, specification and material status.


Forward your CV to : hr1.vsp@gmail.com  

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Opening for Regulatory Writing/ Medical Writing at Indegene, Bangalore "A"

Job Description

1.Responsible for authoring regulatory/ safety documents such as Protocol, CSR,PBRER/PSUR, Subject Narratives, Aggregate Reports, RMPs and others
2.Responsible for the entire life cycle of the document and accountable for maintaining quality and timeliness, and compliance to internal/client SOPs and regulations
3.Ensure that clinical documents adhere to current global standards, FDA, ICH and GCP guidelines and are in accordance with electronic publishing standards. Update SOPs and other job aids for completeness as needed

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Business Executive_metabolics_cardio-diabetic at BIOCON "A"

Job Description

• To attain or exceed the targeted sales volume in the assigned territory.
• To develop relations with the selected doctors in the assigned territory.
• To implement HO strategies on the field.      

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Job for Senior Medical Writer in Novartis "A"

Job Description
1.Write/edit regulatory documents (e.g. CSRs, DSURs, RMPs, contribute to CTD summaries).
2.Participate in planning of analysis and data presentation to be used in study reports or summary documents.
3.Act as a member of clinical trial teams following protocol finalization
4.Act as documentation consultant in clinical trial teams to ensure compliance of documentation to internal company standards and external regulatory guidelines.
5.Act as project medical writer for various programs in clinical development and ensure medical writing resource allocation to studies within these programs.
6.Contribute to process improvement initiatives
7.Supervise outsourcing to external medical writers.
8.Follow and track clinical trial milestones and resource requirements for assigned projects
9.Training and mentoring of associates as required.



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Jobs in CIPLA "A"

Note : Only for experienced candidates

Interested candidates can Walk-in with their updated CV, CTC /Salary Break-up and one photograph between 09.00 am to 03.00 pm on Sunday 23.10.2016 at below mentioned address:

Cipla Ltd.
Bommasandra Industrial Area
Bannerghatta - Jigani link Road
Landmark : Next to HCL
Bangalore - 560 105

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Massive Recruitment Drive "A"

Eligible candidates are required to apply ONLINE through Central Silk Board website www.csb.gov.in. Candidates after successfully submitting application online are required to take print out of the same, put his/her signature at the specified space, enclose photocopies of certificates with regard to educational qualifications, age, experience, Caste Certificate in the case of SC/ST/OBC etc. issued by Competent Authority in the prescribed proforma and Disability Certificate in respect of Persons with Disabilities [Certificate issued by Medical Board] etc.
Duly signed application alongwith all relevant documents be sent by Speed Post/Registered post to the Member-Secretary, Central Silk Board, Ministry of Textiles, Government of India, Hosur Road, B.T.M. Layout, Madiwala, Bangalore – 560 068 so as to reach this office on or before 11th November, 2016.

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Dell hiring Medical Coders "A"

Job Description : 

• To work with a variety of medical records and assigns appropriate codes based on medical documentation using CPT-4 and/or ICD-9 and ICD-10 coding guidelines
• Handle a team of 50 medical coders and responsible for their deliverables.
• Develop training materials and update the contents that are relevant to the specialty.

Job Requirement :

• 6+ years of team handling experience along with coding expertise.
• Strong knowledge in human anatomy and physiology along with any speciality of Medical coding
• Active CPC certification is mandatory.
• Excellent communication and presentation skills.
• Leadership skills in working with extended teams.
• Should have very good attitude flexible to work in shifts.
• Understand business requirements and cooperate when needed.
• Any life science graduate (BPT, nursing, medical transcription preferred)

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Novartis hiring for Pharmacovigilance team lead "A"

Job Description

Performs Pharmacovigilance activities for all assigned Novartis projects or products including identifying and analyzing safety signals based on a comprehensive evaluation of post-marketing data and Serious Adverse Events (SAEs) from clinical trials.
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 inquires 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 CPO 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 causal- ity/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.

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Novartis jobs for Regulatory CMC "A"

Job Description :
1. Author high-quality CMC documentation for HA submission, with support and guidance, applying agreed CMC global regulatory strategies, assuring technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements throughout project lifecycle.
2. Prepare CMC responses to health authority questions during development, registration and product lifecycle.
3. Identify the required documentation for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines.
4. Identify content, quality and/or timeliness issues with source documents, or any other potential au-thoring issues that may impact submission quality or timelines, as early as possible.
5. Keep knowledge up to date with regard to regulatory guidelines and requirements in all global re-gions as well as for new technical trends.
6. Actively participate as a member of the global Reg CMC team by contributing to the regulatory strategy, identifying the critical issues and lessons learned.
7. Establish and maintain sound working relationships with partners and customers.
8. Assume activities in support of the general department such as DRAGON support, annual and product renewal writing, coordination/collection/storage of source documentation needed for direct submission to HAs, other database entry activities (specialized department functions).



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Executive / Senior Executive required at Biocon "A"

Biocon is an integrated biotechnology enterprise focused on the development of biopharmaceuticals. With successful initiatives in drug discovery and development, bioprocessing, manufacturing and global marketing, Biocon delivers products and solutions to partners and customers in over 75 countries. Biocon has the defining science, world class capabilities and a focused vision to deliver the promise of innovative and affordable medicine to a waiting world.
Job Title – Mabs Production (Executive/ Senior Executive)



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Medical Writers required at Parexel "A"

Job Description

Essential Function
The Senior Medical Writer researches, creates, and edits all documents associated with clinical research. Responsibilities also include: acting as primary client contact for medical writing projects, working with other PAREXEL departments and clients to set and meet internal and external deliverable timelines, leadership, training and support of junior medical writing staff.

Relationships
Reports To Departmental Line Management, Medical Writing Services
Directly Supervises None
Provides Work Direction to Medical Writers, Associate Medical Writers, Medical Writing Assistants
Works Closely with Project Managers/ Leaders, Physicians, Biostatisticians, Data Managers, Regulatory Associates, Medical Writing staff
External Relationships Client technical representatives

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Roche Inviting Online Job Applications "A"

Roche Diagnostics India, with a sales turnover of INR 150 crores, nurtures an open, flexible and challenging work environment, which allows for rapid career progression. Roche is an equal opportunity employer.
Job Title : Assistant Consultant – Application
Job Description :

• Installations and Commissioning
• Customer complaint management
• Customer enrollment-QCS program
• Support to customer for Accreditation program
• Key Account Management
• QMS Adherence
• Customer call logging and closing
• Reporting – MIS

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Jobs @ Pepsico "A"

Job Description

• To deliver quality on all parameters (perceived and internal) and to ensure that trade sampling score is as per the target
• Provide support to MU / BU, for implementation, stabilization and sustenance of Quality
• Best Practice Tools.
• Provide ongoing problem solving and SME support to the Manufacturing team to help Plant / MU / BU sustain and continuously improve Quality results.
• Track Quality Scores basis the specified Physiological, Analytical, Microbiological & Sensory parameters.
• Provide SME support for and facilitate the development of local problem identification and process improvement.
• Ensure that Customer Perceived Quality product is manufactured and dispatched for the customer / consumer.
• Support the vendor qualification requirements for BU based materials procurement and verify raw material quality from vendor.
• Be the BU custodian for the Pepsi trademark and ensure compliance to PCC Quality policies.
• Plan and execute Market sampling campaign to ensure ready availability of product within quality specifications.

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Indegene hiring for Analyst Research Analytics "A"

At Indegene, we look to change healthcare for the better. Being an Indegene employee is not just doing a job, but it is about real contribution and outcomes. We are a global team of over 1,200 employees across 14 global locations. Our singular focus is to deliver real outcomes that are measurable, impactful, and sustainable. This has made us a recognized global leader and partner to some of the largest and most respected healthcare organizations.
Job Title : Analyst Research Analytics & Insights (HEOR)



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Abbott Laboratories Jobs, Mumbai "A"

Job Description:
Job Holder is accountable & responsible for overall milk quality management and leading the Aflatoxin monitoring project at site. The area of focus includes: Transparency in testing, Setting up Aflatoxing testing facilities, Milk & fodder samples management, Testing proficiency, Mapping milk & feed/fodder test results, GAP analysis, Trend Analysis, Coordination, Contaminants  Prevention and Education.



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Walk in Interview at Zydus Cadila "A"

Zydus Cadila is one of India's leading healthcare companies and a global healthcare provider with strengths all along the pharmaceutical value chain. The group’s state-of-the-art manufacturing infrastructure is spread across five states of Gujarat, Maharasahtra, Goa, Himachal Pradesh and Sikkim and the R&D Centers are spread across Ahmedabad, Baroda and Mumbai (Thane).

Post : Executive/Senior Executive / Assistant Manager

Walk-in-Interview 
Time : 9th October, 2016
Location: Hotel Sree Krishnaa Grand, Miyapur "X” Roads, Hyderabad, Telangana 500049
Timings : 9.30 a.m. - 5.00 p.m

Interested candidates may also email their resume to hr.mfg@zydusmail.com

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Scope of Clinical SAS "A"

Business intelligence’s growth in developed economies is much faster than in developing economies. The current trend in Business Intelligence is in transition or towards 3rd generation BI tools that involve less IT involvement and allowing business owners to do their own business intelligence analysis.

The future of BI lies with the evolution of Embedded Analytics that is poised to help organizations in every sector or industry in cementing ties with their customer and suppliers. Career wise BI Analytics are most sought after employees with companies paying BI Analysts huge salary package.

For instance, in the United States, the median salary of BI Analyst is around $102,000, which is higher than industry average of any technology job. In India, the base salary for a beginner level of business intelligence job starts around Rs.350,000 that increases by around 20% with every additional year of experience.

The career as a Business Analyst is quite lucrative with BI emerging as a fast growing function for companies in sectors such as e-commerce, retail, finance, food, public transport and in many other sectors. The dependence of data requires the services of BI analysts with their role becoming strategic in driving business data availability for end users.

source:https://www.quora.com/What-is-scope-of-SAS-in-future

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