337 Lab Jobs - Page 5

About the Role Are you searching Medical Officer Job to grow your career in healthcareJoin our team and build a rewarding future in Medical Officer! Experience Required 4 yrs Responsibilities Assist fertility specialists in patient consultations and treatment planning Monitor patient responses to IVF protocols and medications Perform or assist in minor procedures (e.g., ultrasounds, follicular monitoring) Provide pre- and post-procedure counseling to patients Ensure accurate documentation and maintenance of medical records Coordinate with lab and nursing staff for smooth workflow Support patient education about fertility, treatment options, and

Performing QA activities, Analytical testing organic as well as inorganic, and Documentation.

Job description: Leadership role to manage team size of 20+ scientists (Ph.D. and M.Sc.) Extensive knowledge in E&L Planning and excution of projets in Analytical services Extractable and Leachable experience in CCS as per USP monograph and medical devices as per ISO guidelines Ensuring the compliance related to all the activities Method development/Validation experience in LC-MSMS, GC-MSMS and ICPMS instrument Preparation and Implementation of SOPs related to E& L,Stability studies, general laboratory processes and best guidance. Good knowledge of 21 CFR part 11, Data Integrity principals, good documentation practices in cGMP lab Monitor and management of day-to-day laboratory activities Subject Matter Expert for guiding extractables and leachable studies, Stability studies, Nitrosamine studies, PSD, PXRD, HPLC, GC-MS/MS, LC-MS/MS, ICP-MS, IC, Dissolution, UV-Vis, etc., including designing the preparation of protocols and report Extensive knowledge of preparation, reviewing and approval capability for standard operating procedure (SOP) and COA Sound knowledge of structural elucidation and interpretation using analytical techniques such as NMR, IR, HPLC, GC, LC-MS etc. Resolving the team conflicts and provide training to the team for development and empowers team members Provide scientific and leadership direction to team members Knowledge on LIMS Supporting in setting up lab facility and instrument distribution Good knowledge of laboratory safety and be a strong promoter of SHE activities in the lab. Skills Required: For M.Sc, 20-25 years of Analytical R&D/QC experience in CRO environment Excellent technical, problem-solving, writing, influencing and communication skills Strong leadership with excellent interpersonal skills, proven success of analytical projects and managing cross functional teams Demonstrative communication skills and confident in conveying information to internal/ external customers Skill for resolving the team conflicts and provide training to the team for development and empowers team members Behavioral Competencies: Excellent oral / written communication skills and flexibility to work in a dynamic environment Excellent in Knowledge sharing at all levels. If you're a fit, send your resume to . Please share only relevant profiles. Qualifications M.Sc -Analytical Chemistry/Organic Chemistry/General Chemistry/Industrial Chemistry

Requirements / Prerequisites Has Lean implementation and change management experience, preferably in a lab/ pharma/ life sciences context Has or can acquire deep knowledge of local lab processes and resources, and has quick learning ability, excellent influencing & project management skills Has been a responsible Project Manager on an end-to-end Lean transformation under the coaching of a Lean Program Leader Has successfully delivered key training modules during the Lean project Has the ability to coach and steer local lab teams in Lean transformations and continuous improvement initiatives Has successfully completed Lean certification from a reputed institute Roles & Responsibilities Acquire deep knowledge of local lab processes and resources, assess and arrive at cost reduction / Lean opportunities Prepare and manage local Lean implementation roadmap Promote Lean methodology by circulating regular snippets on lean tools and techniques Carry out the Lean projects / transformations independently with zero conflicts by utilizing change management and project management skills Manage performance management infrastructure, namely the definition, tracking and reporting of KPIs, adequate structure of meetings and performance dialogues and definition and implementation of corrective action Coach/ train local Lean teams in Lean methodology and toolset inline with the Lean Academy curriculum or local requirements Work with Global teams and coach / steer local lab teams in Lean transformations and continuous improvement initiatives Independently manage IDEA generation program from generation until implementation and ensure sustenance Implement and sustain 5S in relevant businesses / locations Implement Daily Management and Kaizen circles in relevant businesses and locations Conduct internal satisfaction surveys for relevant departments / sections to understand the scope for improvements in stakeholder satisfaction and implement appropriate corrective actions Conduct new joiners induction as per HRs calendar Present the completed projects locally as well as globally during the Lean Network calls for wider awareness and horizontal deployment Participate in development of training modules and methodology Document and share best practices Qualifications Qualification Min. Bachelors degree

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. With over 30 years of GLP compliance and certification, Eurofins Advinus serves diverse industries such as Biotech, Pharmaceutical, Biological, Agrochemical, Nutraceutical and Cosmetic. Eurofins Advinus is the only contract research organization (CRO) in India to have developed data in support of 90+ end-to-end IND enabling packages to be submitted to global regulators such as USFDA, EMA, MHRA, Health Canada and others. Role to manage team size of 1 to 3 scientists (M.Sc.) Good team player, should be able to lead the team of 1-3 scientist (M.Sc.) and monitor their day-to-day activities along with his own to complete the time bound tasks Strong interpersonal skill and managing cross functional teams Sound knowledge in synthetic/Medicinal chemistry Niche area chemistry experience is preferred Performing fundamental literature & patent searches related to project activities and develop alternative strategies Sound knowledge of scientific search engine such as SciFinder, Reaxys etc. Sound knowledge of structural elucidation and interpretation using analytical techniques such as NMR, IR, HPLC, GC, LC-MS etc. Good knowledge of laboratory safety and be a strong promoter of SHE activities in the lab Qualifications For M.Sc, 7-10 years of Discovery/Medicinal Chemistry R&D experience and for PhD, 2-4 years of experience in discovery/medicinal Chemistry CRO. Additional Information Excellent technical, problem-solving, writing, influencing and communication skills Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude. Demonstrative communication skills and confident in conveying information to internal customer

1) Understand the CTQ for a process 2) Ensure complaince of process parameters and product parameters for the responsible area 3) Educate the operators and ensure adherence of GMP/quality systems in the process 4) indentify non conformances, Deviations- segeregate and quarantine the materials and reporting 5) Basic quality trouble shooting guidelines implementation to assist production to ensure Quality 6) System updation in ERP/ material clearance process completion 7) Deviation process controls 8) customer CTQ CAPA implentation points checking for effectiveness 9) maintaining of the correspoding Lab equipments and testing as per audit plan and reporting and taking actions on NC 10) Reporting of abnormality on Machine quality automations like EVS, magnetic separator etc.,

Business Unit / Function Department - Quality Control Location Bharuch; SEZ;;; Reports to Lab In charge-QC Summary of Job (Purpose/ objective of the job Department Organogram to be enclosed) candidate is required having complete experience in API/Bulk/ Intermediates industries as per global regulatory requirements and responsible for implementation and compliances of ICH-Q7A, cGMP, WHO-GMP, ISO9001, FSSC, HACCP / global QMS requirements at SEZ site. Key Responsibilities (Performance Indicators) Knowledge about IMS system (ISO 9001:2015, ISO 14001:2015 OHSAS 18001:2007, and cGMP, USFDA, FSSC - 22000, NABL . Analytical skill for QC instrument, i.e. GLC, HPLC, UV-Visible, FTIR, ICP, K/F, Melting point etc. Regularize the QC activities as per cGMP requirements. RM, PKG, In-process and FG sampling and Analysis. Co-ordination with QC staff, R and D, Commercial and production for quality and dispatch related activities for on time dispatches. Day to day monitoring and execution online all IPQC and FG analysis activities. Resolve the trouble shooting related to QC activities. Knowledge about 21 CFR Part 211, 111 with data integrity (Part-11) Awareness about responsible care (Environment, Health, Safety and Security) No. of Reportees Qualification and Experience M.Sc. (Chemistry) with 2 - 6 yrs. Key Competencies (Technical, Functional and Behavioral) Handling, Calibration and Hand-on experience of all QC instruments. Compliance of 21 CFR Part-11. Troubleshooting related to QC analytical instrument

Title Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Cardiologist - Medical Director to join our Core Labs in Mumbai office. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Responsibilities Participate in oversight of assignments, training, and management of central reader s of cardiac imaging and EKG Collaborat e with Core Lab management on technical aspects of cardi ac study assessments Participat e in sponsor site visits and audits related to cardiac assessments as requested Participati e in training and subsequently demonstrating competency in the operation of independent central review of EKG and cardiac imaging for clinical trials Review protocols, Image Review Charters and associated clinical and technical study documents as required Complete source documents accurately and promptly, according to the specific protocol requirements and Medpace’s SOPs Blinded independent central review of EKG and cardiac imaging according to study endpoints as specified in clinical trial protocol, charter and according to GCP and standard Medpace SOPs Participate in IntraReader and InterReader variability assessments Participate in the development, review and evaluation of SOPs and study specific procedures. Other duties as assigned Qualifications Must have an M.D. and current medical licensure Board Certification preferred. Experience with EKG and most cardiac imaging modalities and expertise interpreting EKG, Holter-EKG and one or more cardiac imaging modality and therapeutic application Experience with various EKG and cardiac image analysis and viewing software (including PACS) Experience working with computer software including Word, Excel, Access and Project preferred Board Eligibility in Cardiology or equivalent training demonstrating competency People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets

We are hiring for the role of Admin associate cum Materials Management Specialist R&D - for FMCG MNC , position based at Chembur East, Mumbai . You'll be hired on the payroll of Ashkom Media India Pvt. Ltd. Kindly go through the attached JD and if interested revert me back with your feedback and updated resume. Job description : Admin associate cum Materials Management Specialist R&D We are seeking a detail-oriented and organized individual to join our research and development (R&D) team as a Material management Specialist. In this role, person will be responsible for managing and maintaining the inventory of chemicals, reagents, laboratory supplies, admin supplies and equipment required for our R&D activities. Expertise in inventory management, documentation, and adherence to safety guidelines will be crucial in ensuring the smooth functioning of our R&D stores. Responsibilities: Oversee the daily operations of the R&D stores, including receiving, inspecting, and organizing incoming supplies and equipment. Collaborate with R&D scientists and other stakeholders to understand their material requirements and ensure timely availability of supplies. Coordinate with vendors to get quotation, place purchase requisitions, coordinate with procurement to place purchase orders, track deliveries, and resolve any issues or discrepancies. Maintain accurate inventory records, including stock levels, expiration dates, and batch numbers. Involved in managing housekeeping supplies and depute responsibilities to HK team member Inform GR owner about receipt of material for updation in inventory and follow PoP process. Implement and maintain proper storage conditions for sensitive materials, including temperature-controlled. Engage with customs, procurement team, courier agencies to manage incoming and outgoing shipments in R&D. Ensure compliance with guidelines, safety protocols, and quality standards in all aspects of R&D stores management. Perform routine inventory audits to identify discrepancies, analyze usage patterns, and recommend appropriate stock levels. Provide support during internal and external audits by ensuring proper documentation, traceability, and adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Collaborate with cross-functional teams to identify process improvements and implement best practices for R&D stores management. Required Qualification & experience: Bachelor's degree in a scientific discipline or a related field. Strong understanding of laboratory supplies, chemicals, and equipment commonly used in pharmaceutical R&D. 4-5 years of experience Previous experience in inventory management, preferably in a pharmaceutical/ Personal Health/Chemical R&D environment.

Role: Lab Test Resource Location : KOTHUR MANDAL , Telangana 509228 Education: Person should preferably have a Bachelors degree (okay with 12th qualification as well). Software: Can use Microsoft Office (preferred but not mandatory) Work Experience: The person should have 0-1 year of experience and be able to do admin work. Lab Test Scope: The person should be able to collect powder samples in process and perform lab tests called Particle Size Distribution and Density. Training will be provided. Required period: 2 months depending on project need and skills and performance. Working days: 6 days a week, (flexible to work in shifts when required), standard working hours Communication: Telugu, Hindi or English Warm Regards, ______________________________________ "Your Manpower Managers" Varun Executive - TA | HR ASHKOM MEDIA INDIA PVT. LTD. (An ISO 9001:2015 Certified Company) "Ashkom House" Dk -2/6 , Danish Kunj, Kolar Road Bhopal Pincode - 462042 Madhya Pradesh Mobile : +91-6262600059 / 8989271488 Website: www.ashkom.com

Role: Lab Test Resource Location : KOTHUR MANDAL , Telangana 509228 Education: Person should preferably have a Bachelors degree (okay with 12th qualification as well). Software: Can use Microsoft Office (preferred but not mandatory) Work Experience: The person should have 0-1 year of experience and be able to do admin work. Lab Test Scope: The person should be able to collect powder samples in process and perform lab tests called Particle Size Distribution and Density. Training will be provided. Required period: 2 months depending on project need and skills and performance. Working days: 6 days a week, (flexible to work in shifts when required), standard working hours Communication: Telugu, Hindi or English Warm Regards, ______________________________________ "Your Manpower Managers" Varun Executive - TA | HR ASHKOM MEDIA INDIA PVT. LTD. (An ISO 9001:2015 Certified Company) "Ashkom House" Dk -2/6 , Danish Kunj, Kolar Road Bhopal Pincode - 462042 Madhya Pradesh Mobile : +91-6262600059 / 8989271488 Website: www.ashkom.com

Role & responsibilities The individual has to follow safety/quality procedures of lab. Any other relevant task assigned by the lab leader. The individual must have the capability to visually inspect, collect, and analyze samples of raw material, packaging material, finished goods, intermediates according to standard analytical procedures. Follows procedures for basic calibration and maintenance of equipment Maintains the laboratory in a clean and organized manner. Skill Required The individual is responsible to work in QC Lab compliant with Good Laboratory Practice (GLP) and current Good Manufacturing Practice (cGMP). Knowledge & Skills: Able to do understand basic principles of analytical tests & instruments. Person must also have knowledge and capability to operate Lab instruments. Digital Skills: Effectively use MS tools, i.e., Word, Excel, PowerPoint, in day-to-day operations. If required, need to operate company software.

Role & responsibilities The individual should be able to perform Microbial daily monitoring (sampling and testing) of water, compressed air, and environmental air (for manufacturing area, warehouse, and Micro-lab) as per site matrix after. Preparation of media as per requirement and performance of growth promotion tests. The individual should be able to receive, issue, store, use, and reconciliation of media, cultures, disinfectant solutions, cleaning solutions, consumables, and accessories. Operation & Management of Micro-lab equipment and instruments. To perform internal verification and calibration of Micro-lab equipment and instruments as per work instructions. Daily monitoring of temperature, relative humidity, and differential pressure in the Micro-lab. Preparation and documentation of disinfectant solutions for Micro-lab cleaning as per procedure to maintain the Micro-lab in a clean and organized manner. Update and maintain the status labeling of all equipment and instruments in the Micro-lab as required by the laboratory system and SOP. Timely reporting of any laboratory incidents, out-of-specification (OOS), and out-of-trend (OOT) results to the immediate supervisor and investigating the same. Recording of activities as per procedure and instruction in the Micro-lab and maintaining the documents follow GLP, cGMP, GDP, and EHS practices. Skill Required The individual is responsible to work in Micro-Lab compliant with Good Laboratory Practice (GLP) and current Good Manufacturing Practice (cGMP).Knowledge & Skills: Able to do understand basic principles of Microbiological procedures & instruments used in Micro-lab. Person must also have knowledge and capability to operate instruments by following aseptic practices. Digital Skills: Effectively use MS tools, i.e., Word, Excel, PowerPoint, in day-to-day operations. If required, need to operate company software. The individual must have good communication skill with team.

Role & responsibilities The individual should be able to perform Microbial daily monitoring (sampling and testing) of water, compressed air, and environmental air (for manufacturing area, warehouse, and Micro-lab) as per site matrix after. Preparation of media as per requirement and performance of growth promotion tests. The individual should be able to receive, issue, store, use, and reconciliation of media, cultures, disinfectant solutions, cleaning solutions, consumables, and accessories. Operation & Management of Micro-lab equipment and instruments. To perform internal verification and calibration of Micro-lab equipment and instruments as per work instructions. Daily monitoring of temperature, relative humidity, and differential pressure in the Micro-lab. Preparation and documentation of disinfectant solutions for Micro-lab cleaning as per procedure to maintain the Micro-lab in a clean and organized manner. Update and maintain the status labeling of all equipment and instruments in the Micro-lab as required by the laboratory system and SOP. Timely reporting of any laboratory incidents, out-of-specification (OOS), and out-of-trend (OOT) results to the immediate supervisor and investigating the same. Recording of activities as per procedure and instruction in the Micro-lab and maintaining the documents follow GLP, cGMP, GDP, and EHS practices. Skill Required The individual is responsible to work in Micro-Lab compliant with Good Laboratory Practice (GLP) and current Good Manufacturing Practice (cGMP).Knowledge & Skills: Able to do understand basic principles of Microbiological procedures & instruments used in Micro-lab. Person must also have knowledge and capability to operate instruments by following aseptic practices. Digital Skills: Effectively use MS tools, i.e., Word, Excel, PowerPoint, in day-to-day operations. If required, need to operate company software. The individual must have good communication skill with team.

Role & responsibilities The individual should be able to perform Microbial daily monitoring (sampling and testing) of water, compressed air, and environmental air (for manufacturing area, warehouse, and Micro-lab) as per site matrix after. Preparation of media as per requirement and performance of growth promotion tests. The individual should be able to receive, issue, store, use, and reconciliation of media, cultures, disinfectant solutions, cleaning solutions, consumables, and accessories. Operation & Management of Micro-lab equipment and instruments. To perform internal verification and calibration of Micro-lab equipment and instruments as per work instructions. Daily monitoring of temperature, relative humidity, and differential pressure in the Micro-lab. Preparation and documentation of disinfectant solutions for Micro-lab cleaning as per procedure to maintain the Micro-lab in a clean and organized manner. Update and maintain the status labeling of all equipment and instruments in the Micro-lab as required by the laboratory system and SOP. Timely reporting of any laboratory incidents, out-of-specification (OOS), and out-of-trend (OOT) results to the immediate supervisor and investigating the same. Recording of activities as per procedure and instruction in the Micro-lab and maintaining the documents follow GLP, cGMP, GDP, and EHS practices. Skill Required The individual is responsible to work in Micro-Lab compliant with Good Laboratory Practice (GLP) and current Good Manufacturing Practice (cGMP).Knowledge & Skills: Able to do understand basic principles of Microbiological procedures & instruments used in Micro-lab. Person must also have knowledge and capability to operate instruments by following aseptic practices. Digital Skills: Effectively use MS tools, i.e., Word, Excel, PowerPoint, in day-to-day operations. If required, need to operate company software. The individual must have good communication skill with team.

Role & responsibilities The individual has to follow safety/quality procedures of lab. Any other relevant task assigned by the lab leader. The individual must have the capability to visually inspect, collect, and analyze samples of raw material, packaging material, finished goods, intermediates according to standard analytical procedures. Follows procedures for basic calibration and maintenance of equipment Maintains the laboratory in a clean and organized manner. Skill Required The individual is responsible to work in QC Lab compliant with Good Laboratory Practice (GLP) and current Good Manufacturing Practice (cGMP). Knowledge & Skills: Able to do understand basic principles of analytical tests & instruments. Person must also have knowledge and capability to operate Lab instruments. Digital Skills: Effectively use MS tools, i.e., Word, Excel, PowerPoint, in day-to-day operations. If required, need to operate company software.

Role & responsibilities The individual has to follow safety/quality procedures of lab. Any other relevant task assigned by the lab leader. The individual must have the capability to visually inspect, collect, and analyze samples of raw material, packaging material, finished goods, intermediates according to standard analytical procedures. Follows procedures for basic calibration and maintenance of equipment Maintains the laboratory in a clean and organized manner. Skill Required The individual is responsible to work in QC Lab compliant with Good Laboratory Practice (GLP) and current Good Manufacturing Practice (cGMP). Knowledge & Skills: Able to do understand basic principles of analytical tests & instruments. Person must also have knowledge and capability to operate Lab instruments. Digital Skills: Effectively use MS tools, i.e., Word, Excel, PowerPoint, in day-to-day operations. If required, need to operate company software.

Applications are invited for the Post of, QC Analyst VIT Samsung Data Lab SCOPE at Vellore Institute of Technology (VIT), Vellore, T N, India, Job Title : QC Analyst VIT Samsung Data Lab SCOPE Qualification : Sc Mandatory Skills : Basic understanding of Microsoft Office tools (Excel, Word, etc ), Quality control and assurance knowledge with hands-on experience in data validation, of Vacancies : 2 Posts Experience : 1 to 2 Years experience Sponsoring Agency : Samsung R&D Institute India-Bangalore, Job Description : Analyse and validate annotated data to ensure accuracy, consistency, and compliance with project guidelines, Perform detailed quality checks on data (images, videos, text) to identify errors and suggest corrective actions, Develop and maintain quality standards by conducting regular audits and monitoring task outputs, Collaborate with annotators and provide constructive feedback to enhance data quality, Assist in defining quality control processes and updating guidelines as required, Ensure structured management of reviewed data, maintaining version control and secure storage, Participate in periodic training to stay aligned with evolving quality standards and annotation processes, Good communication and teamwork skills, ability to learn quickly and adapt to project-specific requirements, Send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc through online http://careers vit ac in No TA and DA will be paid for appearing the interview, Shortlisted candidates will be called for an interview at a later date which will be intimated by email, The selected candidate will be expected to join at the earliest,

NUTRIS CROP SOLUTIONS INDIA PVT.LTD is looking for LAB ANALYST to join our dynamic team and embark on a rewarding career journey. Perform analytical testing of samples to ensure quality and compliance. Record and interpret test results, maintaining accurate documentation. Calibrate and maintain laboratory equipment for optimal performance. Follow safety and regulatory guidelines for laboratory procedures. Collaborate with teams to develop new testing methods and protocols.

PrimeGen Healthcare Laboratories Private Limited is looking for Phlebotomist to join our dynamic team and embark on a rewarding career journey. Collect blood samples from patients using a variety of techniques, including venipuncture, fingerstick, or heelstick. Ensure the proper identification of patients and their blood samples, and accurately label each sample with the patient's name and other relevant information. Transport blood samples to the laboratory for testing and analysis, ensuring proper handling and storage to maintain sample integrity. Monitor patient reactions and provide appropriate care and support during and after the blood collection process. Maintain accurate records of all blood collections and patient interactions, and ensure compliance with all relevant regulations and guidelines. Collaborate with physicians, nurses, and other healthcare professionals to ensure that blood samples are collected and handled appropriately for each patient. Maintain cleanliness and sterility of equipment and work area, and dispose of all used needles and other materials in accordance with safety protocols.

Greetings from Thyrocare! We are looking Consultant MD BIOCHEMISTRY- (Full Time ) for our Navi Mumbai Lab of *Thyrocare Technologies Ltd. Qualification Required - MD Biochemistry & DNB Shit Timing- 10 PM TO 6 AM Address : D-37/1, TTC Industrial Area, MIDC, Turbhe, Navi Mumbai - 400703 . If any one is interested kindly share your resume : tereza.nerson@thyrocare.com Or whatsaap : +91 83558 89455 Regards, Mrs.Tereza Nerson Contact No: 8355889455 Sr. HR | Talent Acquisition Thyrocare Technologies Ltd.

We are seeking motivated and detail-oriented trainees to join our pathology lab or X-ray. This is an excellent opportunity for individuals looking to gain hands-on experience in a NABL laboratory. Trainees will assist in various laboratory tasks and learn about the processes involved in pathology. Assist in specimen collection and processing. Support laboratory staff in performing tests and experiments. Maintain laboratory equipment and ensure cleanliness. Document and report test results accurately. Follow safety protocols and standard operating procedures. Educational Background : Bachelors degree in medical laboratory technologist. Experience : Prior internships or clinical experience in a lab setting is advantageous but not mandatory.

We are seeking a qualified Medical Laboratory Technician to join our diagnostic team The role includes collecting and processing patient samples, performing various laboratory tests, and ensuring accurate and timely results Candidates should have a diploma or degree in medical laboratory technology and relevant certification Attention to detail, technical proficiency, and the ability to work independently are crucial for this position Experience in a healthcare setting is preferred

Role & responsibilities Conceptualizing visuals based on requirements Develop illustrations, newspaper ads, leaflets, newsletters, pamphlets, and other marketing collaterals using software Prepare rough drafts and present ideas Use the appropriate colors and layouts for each graphic Work with the marketing team to produce the final design Test graphics across various media platforms Amend designs after feedback Ensure final graphics and layouts are visually appealing and on-brand Skills Required: Familiarity with design software and technologies, like photoshop, CorelDraw, illustrator, after-effects, etc Capable of doing all types of designing, like graphics, multimedia, web, creative artworks, basic videos, newspaper ads, print ads, t-shirts, leaflets, etc Degree in Design, Fine Arts, or a related field Creativity Artistic talent Branding Time management A keen eye for aesthetics and details.

Ensure the daily visits to prospective clients, quality of pitch, and profile of on boarded clients are per the organizations expectations. Analyze market in the territory to identify new opportunities. Keep an eye on competition and help strategize against the changing dynamics of market. Maintain a comprehensive knowledge of the product portfolio including technical aspects and marketing tactics. Complete sales cycle starting from database building, lead generating, client onboarding, to assisting in receiving payments