Indian Institute of Technology Indore located in Madhya Pradesh, known as IIT Indore or IITI, is an institute of national importance established by the Government of India in 2009. It is one of the eight new IITs, started by the Ministry of Education, Government of India. The institution started functioning from 2009-10 in a temporary campus at Institute of Engineering and Technology of Devi Ahilya University under mentorship of IIT Bombay.
Post : Junior Research Fellow (JRF)
Project Title : “Combating Pandemics through textiles : An Approach to Ease Viral/ Bacterial Infections using advanced Nano Fibrous fabrics” (NTTM-Ministry of Textiles) Indian Institute of Technology Indore invites applications for 2 JRF position in the above NTTM-Ministry of Textiles, Govt of India project with the following details.
Eligibility Criteria : Master’s degree in Life Sciences / forensic science / Bio-Tech or relevant (with first division as defined by the awarding Institute/ University) from recognized Universities/Institutes, with CSIR/UGC- NET (Equivalent qualification/fellowship) or valid GATE score.
Age limit : 28 years on the date of application, with relaxation to SC/ST/OBC candidates as per Government of India norms.
Candidates experience in the areas of nanomaterial synthesis, heterostructure fabrications and their characterizations with very good track record and have excellent research experience will be given preference. Good communication skills are essential for the sponsored research project
Fellowship and Duration : The amount of JRF fellowship will be as per funding agency norms and following the IITI institute policy. The appointment will be for one year initially, or completion of project whichever is earlier.
How to Apply
The applicants should send their complete CV (with official transcripts, email address and cell phone number), copies of all academic certificates (single PDF file) to Dr. Shaikh M. Mobin (xray@iiti.ac.in) by email. The subject of the email should be : Application for JRF position for NTTM Project. Only the shortlisted candidates will be called for seminar and/interview and will be informed by email. Interviews may happen remotely through virtual conferencing.
Note : CV should include details of academic grades starting from X standard onwards with details of the year of passing, university or institute, etc. and work experience and nature of work if applicable. Complete details of NET/GATE such as year of passing/validity, discipline, marks. Incomplete applications will be rejected.
Address for Correspondence :
Dr. Shaikh M. Mobin
Discipline of Chemistry
Indian Institute of Technology Indore (IITI)
Email: xray@iiti.ac.in
Last Date of Application : April 26, 2024 by 5pm.
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Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world. Today, Intas is present in more than 85 countries worldwide and is growing at 20% CAGR. Around 70% of its revenues come from the international markets, particularly the highly regulated markets of EU and US. At Intas, every day and everyone works to create a world of good health, happiness and hope.
Officer / Sr. Officer
Department : Parenteral (Sterile) Complex Skid / NDDS
Qualification : B.Pharma / M.Pharma
Experience : 2-5 Years
Skills : For Staff Level require good knowledge in "Complex Skid / NDDS
Technician
Department : Parenteral (Sterile) Complex Skid / NDDS / Aseptic / Manufacturing Clean Area / Lyphilizer/ Visual
Qualification : ITI / Diploma Eng / D.Pharma
Experience : 2-7 Years
Skills :
• For Technician Level require good knowledge in Skid / NDDS / Aseptic (PFS / Vials Liquid) / Manufacturing Clean Area / Lyphilizer /Visual Inspection.
Job Location : Intas Pharmez, Ahmedabad
Walk in Interview
Date : 25th April, 2024 (Thursday)
Time : 09:00 am
Venue : Intas Pharmaceutical Limited Plot no. 05 to 14, Pharmez, Near Village Matoda, Sarkhej - Bavla Highway 8-A, Taluka- Sanand, Dist- Ahmedabad.
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More than 30,000 Takeda employees working in more than 70 countries are committed to improving quality of life for patients, who remain at the center of everything we do. Takeda Pharmaceutical Company Limited is a global, research and development-driven organization working internally and with external partners to translate science into life-changing medicines. Takeda focuses on the core therapeutic areas of oncology, gastroenterology, neuroscience and providing vaccines that address the most important infectious diseases. Novel products, especially in oncology and gastroenterology, as well as our presence in emerging markets, fuel our growth.
Post : Senior Clinical Research Associate
Job Description
Objectives
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and Takeda requirements
Accountabilities :
• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with study protocol and applicable regulatory requirements
• Work with CROs to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
• 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 as appropriate.
• 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. May support start-up phase.
• Ensure site documents are available for filing in the Trial Master File (TMF) and verify that documents are maintained in accordance with GCP and local regulatory requirements
• Ensure 100% adherence to monitoring and study plan
• Support clinical quality in managing CAPAs and other study audit observations
• Support Clinical Operations Lead/ Clinical Operations Manager in performing CRO oversight as per agreed parameters
• Ensures adherence to study budget through constant monitoring for allocated study(ies)
• Ensures dissemination of study updates to relevant stakeholders as per agreed timelines
Candidate Profile
• Master’s or Ph. D degree in scientific discipline or healthcare with >5 years’ experience in clinical trials industry as Clinical Research Associate
• Good working knowledge of GCP and local clinical trial rules and regulations
• Organizational and problem-solving skills
• Superior communication, strategic, interpersonal, and negotiating skill
• Proven/ stable performance records over past 2-3 years
Additional Information
Experience : >5 years
Qualification : Master’s or Ph. D degree in scientific discipline or healthcare
Location : Mumbai, Maharashtra
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Research & Development
End Date : 20th May 2024
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Pfizer is the world's premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support.
Post : Associate I – Regulatory Conformance
Job Description
As an associate, your focus on the job will contribute in achieving your team’s tasks and goals. This is a multifaceted role that will offer you a number of opportunities to enhance your skills. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.
Job Description
• Committed to quality and excellence in compliance and conformance
• With the reasonable understanding of regional regulations, would perform the evaluation of the notifications assigned.
• Accountable for maintaining the HA status in corporate change and dossier management system for the allocated Regions / Markets
• Contributes independently and manages own time to meet the timelines.
• Work in collaboration with GRA colleagues to ensure the gaps are identified and escalated on time.
• Independently Perform accurate updates in system for most of the cases and consult with TL/Designee for clarification of any discrepancies in complex cases, before updating the system.
• Makes informed decisions on straight cases within guidelines and policies
• Support for updates in system for License withdrawals
• Operate in line with internal SOPs and policies
• Adhere to standard turnaround timelines
• Escalate any potential compliance issues to management
• Support periodic and ad-hoc system reports to estimate metrics
• Contribute to local and regional regulatory initiatives promoting a culture aligned with Pfizer values
• Assist in ensuring internal regulatory processes and procedures are well documented
• Assist in remediation activities
• Support the teams in ADHOC activities
• Shares the learning time to time with the team colleagues
Technical Skills
• Theorotical Knowledge on Regulatory Affairs / Compliance
• Experienced in Regulatory / Quality Assurance/ Production or any other functions in Pharmaceutical or related industries
• Diligence and attention to detail
• Good communication skills
• Understanding stakeholder needs
Behavioral/Any other Skills – An assertive, results oriented, positive “can do” attitude, and Time management skills. Preferred
Candidate Profile
Qualification – Master’s / Bachelor’s degree or equivalent i.e. degree in Chemistry, Pharmacy, or a related life sciences. Preferred Year Of Experience - 2 to 4 years of experience
Type of Experience – Any relevant experience in Pharmaceutical or relevant industry. Experience in Regulatory or Quality or Compliance roles is preferable.
Additional Information
Experience : 2 to 4 years
Qualification : Master’s / Bachelor’s degree or equivalent
Location : Chennai
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory
End Date : 20th May 2024
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