10 Lab Support jobs in India

Job Description

Position : Lab Assistant – Information Technology Department

Type : Urgent Hiring

Qualification:

• Graduation/Diploma in Computer Hardware & Networking

Experience:

• 1–2 years (CCTV Cameras experts will be given preference)
• Prior experience and hands-on knowledge of CCTV cameras will be highly preferred

Roles & Responsibilities:

• Installation, configuration, and maintenance of CCTV cameras (IP & HD cameras)
• Regular monitoring, troubleshooting, and performance checking of CCTV systems
• Knowledge of CCTV networking, DVR/NVR configuration, and video backup management
• Installation and testing of IT equipment such as routers, switches, and workstations
• Basic troubleshooting of Windows 10/11 and Microsoft Office 365
• LCD projector setup and maintenance
• ID card designing and creation
• Providing support for day-to-day IT-related assignments as directed

Selection Process:

Interested candidates are requested to share their updated resumes at .

Job Description-

Urgent Hiring for Lab Assistant in Fashion Design Department

Required Qualification-

Diploma in Fashion Design (B.Sc. in Fashion Design will be preferred)

Or Polytechnic in Fashion Design

Experience -

2 Years in academics as well as in apparel industry

Required Skills

Proven work experience as a tailor, lab assistant, or in a similar role, with basic computer knowledge preferred. Skilled in garment stitching and pattern creation, with expertise in handling industrial machines. Capable of guiding students on machine operations and various stitching techniques.

Roles and Responsibilities-

* Responsible for maintaining lab amenities, including machines and other inventories.

* Preparing and updating log books.

* Guiding students in stitching and pattern-making projects.

* Assisting students with machine operations.

* Supporting garment construction and pattern-making tasks for the university beyond the curriculum

Selection Process-

Interested candidate can share your cv at

Shortlisted candidate called for Physical Interviews.

Job Responsibilities :

Qualifications :

Company Overview

GOVIAFLY Cargo and Logistics Private Limited is a dynamic organization in the Transportation, Logistics, Supply Chain, and Storage industry. With headquarters in Bangalore, our team is committed to delivering exceptional service and innovative solutions. We are dedicated to fostering a collaborative environment where our employees can grow and contribute to our success.

Job Overview

The Market Research and Customer Support role is designed for freshers eager to embark on their careers. Based in Bangalore Urban, the position offers a full-time, internship opportunity with immediate joining. Candidates are expected to execute market research tasks and provide exemplary customer support services to ensure customer satisfaction and deliver strategic insights.

Qualifications and Skills

• Basic understanding of market research methodologies and the ability to collect and analyze data effectively.
• Proficiency in Microsoft Excel to handle data, perform calculations, and create reports efficiently.
• Excellent communication skills in English, Kannada, and Hindi to interact effectively with diverse customers.
• Strong problem-solving abilities to address customer queries and resolve issues promptly and courteously.
• Good organizational skills to manage multiple tasks and prioritize workload in a fast-paced environment.
• Eager to learn and adaptive to new technologies and methods related to market research and customer support.
• Must have skill to handle customer interactions via chat platforms and ensure satisfaction with strategic feedback.
• Ability to work independently and collaboratively within a team setting to meet business objectives successfully.

Roles and Responsibilities

• Conduct market research to gather data on customer preferences and trends to support strategic planning.
• Analyze research data and provide insights to improve product offerings and customer services.
• Assist customers by addressing their inquiries, resolving concerns, and ensuring a positive experience.
• Collaborate with internal teams to relay customer feedback and drive product and service improvement.
• Maintain accurate records of customer interactions and research data for future reference and analysis.
• Contribute to the development and implementation of customer support policies and procedures.
• Participate in regular training to enhance product knowledge and stay updated with industry trends.
• Work efficiently in a dynamic environment, maintaining a high level of professionalism and commitment.

contact at

• Coordinate patient participation in clinical trials, ensuring all study procedures are followed.
• Schedule patient appointments and manage study-related documentation.
• Educate patients and their families about study protocols, procedures, and expectations.
• Monitor patients for adverse events and report them to the appropriate personnel.
• Facilitate communication between patients, investigators, and sponsors.
• Collect and manage clinical data accurately and efficiently.
• Ensure compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Assist with study site visits and audits.
• Provide ongoing support and guidance to trial participants.
• Troubleshoot and resolve issues related to patient participation and data collection.
• Maintain accurate and up-to-date patient records and study files.
• Contribute to the improvement of clinical trial processes and patient experience.

• Bachelor's degree in Nursing, Pharmacy, Life Sciences, or a related healthcare field.
• Minimum of 3 years of experience as a Clinical Research Coordinator or in a similar role.
• Strong understanding of clinical trial processes and Good Clinical Practice (GCP).
• Excellent organizational, time management, and multitasking skills.
• Proficiency in using Electronic Data Capture (EDC) systems and clinical trial management software.
• Exceptional communication and interpersonal skills, with a focus on patient empathy.
• Ability to work independently and manage workload effectively in a remote setting.
• Detail-oriented with a high level of accuracy in data management.
• Familiarity with various therapeutic areas is a plus.
• Ability to maintain confidentiality and handle sensitive information.

• Coordinate and manage all aspects of clinical research studies related to patient support programs.
• Recruit, screen, and enroll eligible participants, ensuring informed consent procedures are meticulously followed.
• Schedule and conduct participant visits, collect and manage study data accurately and efficiently.
• Monitor participant adherence to study protocols and provide ongoing support and education.
• Liaise with healthcare providers, investigators, and study sponsors to ensure seamless study operations.
• Maintain accurate and organized study documentation, including case report forms (CRFs) and source documents.
• Ensure compliance with all relevant ethical guidelines, regulatory requirements (e.g., ICH-GCP), and institutional policies.
• Assist in the development of study protocols, informed consent forms, and other research-related documents.
• Track study progress, identify potential issues, and implement corrective actions as needed.
• Communicate effectively with participants, providing them with clear information and support throughout their study involvement.
• Contribute to data analysis and the preparation of study reports and publications.
• Mentor and provide guidance to junior research staff or volunteers involved in patient support initiatives.
• Act as a key point of contact for participants and stakeholders related to ongoing research projects.

• Bachelor's degree in Nursing, Public Health, Life Sciences, or a related field. Master's degree preferred.
• Minimum of 5 years of experience in clinical research coordination, preferably with a focus on patient support or community health programs.
• In-depth knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Experience with electronic data capture (EDC) systems and clinical trial management software.
• Strong understanding of patient recruitment strategies and participant engagement techniques.
• Excellent organizational, time management, and problem-solving skills.
• Exceptional interpersonal and communication skills, with a compassionate and patient-centered approach.
• Ability to work independently and manage multiple priorities in a remote environment.
• Proficiency in Microsoft Office Suite and data management tools.
• Certification as a Clinical Research Professional (e.g., CCRP, CCRA) is a strong asset.
• Experience working with vulnerable populations is highly desirable.