We are hiring candidate for reputed company job location Mohali education min graduation in medical or b pharma fresher candidates preferred salary 17000/month day shift sitting job basic computer knowledge and medical knowledge require

This is a full-time on-site role for a Key Account Executive at Cryoviva Biotech Pvt Ltd. The Client Relationship Executive will be responsible for business relationship management, client relations, communication, relationship building, and account management on a day-to-day basis . Your primary task will be to educate pregnant women about stem cell preservation – explaining the importance and potential future benefits of preserving their child’s stem cells. You will act as a counselor, providing information, answering questions, and assisting clients in understanding the process of stem cell preservation. You will be working closely with doctors and hospital staff to build relationships and ensure smooth communication between our company and the clients. Your goal is to convince expectant mothers to opt for our stem cell preservation services Graduates/Post-graduates from life sciences background (Biotechnology, Microbiology, Pharmacy, Bioinformatics etc.) Job Types: Full-time, Permanent, Fresher Pay: ₹280,000.00 - ₹400,000.00 per year Benefits: Cell phone reimbursement Health insurance Paid sick time Provident Fund Compensation Package: Performance bonus Schedule: Day shift Application Question(s): When are you available to start working with us? Education: Master's (Preferred) Work Location: In person

Role Overview: This role focuses on technical support, system maintenance, and cross-disciplinary collaboration in product development. It involves working with mechanical, electrical, and microbiology teams to build, test, and deploy bioreactors and other systems. Key Responsibilities: Reactor Maintenance – Ensure proper functioning of bioreactors through regular cleaning, and troubleshooting. Operating Reactors – Assist in setting up, monitoring, and adjusting reactor conditions as per experimental requirements. Data Management – Record and maintain experimental data, reactor performance logs, and process parameters accurately. Wastewater Management – Handle wastewater samples, ensure proper disposal. Safety Compliance – Adhere to lab safety protocols, handle equipment responsibly, and ensure a clean work environment. Performing regular electrical and mechanical system checks. Involved in the building of bioreactors. Working on deployment activities to install and run systems on different sites. Testing and evaluating new technologies. Provide technical assistance to the team. Supporting Mechanical, Electronics and Microbiology department in product development, testing fabrication. Required Qualifications: Bachelor's degree in Mechanical Engineering, Engineering, or any relevant discipline. Candidates from other educational backgrounds with a strong interest in operations are also encouraged to apply. General Competency Strong problem-solving skills and a proactive approach to tasks. Excellent communication and interpersonal abilities. Ability to follow instructions and work collaboratively with cross-functional teams. Flexible, reliable, and eager to learn on the job. Physical & Logistical Requirements: Willingness and ability to travel to different sites as needed. Comfortable with physical tasks, including lifting and moving equipment or materials (within reasonable limits). Ability to work in outdoor or industrial environments for extended periods. Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹30,000.00 per month Work Location: In person

We are seeking a candidate who has experience in embryology and IVF procedures, skilled in gamete handling and cryopreservation and Retrieve and prepare gametes, perform IVF and ICSI, monitor embryo development, and manage lab quality control Responsibilities: 1. Gamete handling and fertilization: Embryologists are responsible for retrieving, preparing, and manipulating eggs and sperm for fertilization. 2. In vitro fertilization (IVF) procedures: They perform the actual IVF process, including egg retrieval, fertilization, and embryo culture. 3. Embryo development and monitoring: Embryologists closely monitor embryo development, selecting healthy embryos for transfer. 4. Cryopreservation: They freeze and store embryos for future use, ensuring their long-term viability. 5. Quality control and data management: Embryologists maintain laboratory records, perform quality control assays, and manage data related to IVF cycles KRA : 1. Lab Upkeep and Management: Maintaining a controlled environment (temperature, humidity, air quality) within the lab to foster healthy embryo development. Managing and organizing laboratory supplies and equipment. Ensuring adherence to quality control standards and standard operating procedures. 2. Gamete Handling: Retrieving and preparing eggs (oocytes) from the ovaries. Collecting, washing, and preparing sperm samples. 3. Fertilization and Embryo Development: Performing insemination (IVF) or intracytoplasmic sperm injection (ICSI). Monitoring and evaluating fertilization rates. Culturing and observing embryos as they develop. Assessing embryo quality and selecting suitable embryos for transfer. 4. Genetic Analysis and Assisted Technologies: Performing embryo biopsies for genetic testing (PGT-A,PGT-M,PGT-SR). Assisting with assisted hatching procedures. 5. Embryo Transfer and Cryopreservation: Preparing embryos for transfer using specialized catheters. Cryopreserving (freezing) embryos for future Education UG: B.Sc in Bio-Chemistry, Microbiology, General PG: MS/M.Sc(Science) in Bio-Chemistry Work experience: 5-7 years Job Type: Full-time Pay: ₹15,000.00 - ₹30,000.00 per month Benefits: Cell phone reimbursement Flexible schedule Food provided Schedule: Day shift Rotational shift Work Location: In person

Position: Medical Coder Ct: HR Shanmugapriya 8072891550 Medical Coding is the process of converting patient health information into alpha numeric codes. Coders take medial reports from doctors, which may include a patients condition, the doctors diagnosis, a prescription, and whatever procedures the doctor or healthcare provider performed on the patient, and turn that into a set of codes, which make up a crucial part of the medical claim. Eligibility: All (UG/PG) Life Science& Paramedical Graduates BDS BPT BHMS BAMS Siddha,Unani,Naturopathy {Dip Bsc Msc} Nursing/GNM {B.E M.E} Biomedical Engineering {B.tech,M.tech}Biotechnology Biochemistry Bioinformatics Microbiology Zoology and Advanced zoology Biology Botany Medical Lab Tech Plant biotechnology Pharmacy(B.Pharm M.pharm) Paramedical Physiotherapy Physician assistant Critical Care Technology Medical Biochemistry Medical Record Science Operation Theatre & Anaesthesia Technology {Bsc Msc Dip} Clinical Nutrition Human Genetics Medical Laboratory Technology Medical Sociology Epidemiology Molecular Virology Biostatistics Blood Banking Technology Regenerative Medicine Optom. Genetic Counseling Radiology & Imaging Technology Medical Biochemistry Medical Microbiology Clinical Care Technology Clinical Care Technology Medical Physics {Bsc Msc Dip} Accident & Emergency Care Technology Audiology & speech Language Pathology Cardiac Technology Cardio Pulmonary Perfusion Care Technology Critical Care Technology Dialysis Technology Neuro Electrophysiology Medical Sociology Nuclear Medicine Technology Operation Theatre & Anaesthesia Technology Optometry Physician Assistant Radiology Imaging Technology Radiotherapy Technology Medical Record Science Respiratory Therapy Fitness and Lifestyle Modifications Accident & Emergency Care Technology Critical Care Technology Nursing Aide Operation Theatre & Anaesthesia Technology Ophthalmic Nursing Assistant Medical Record Science Optometry Technology Radiology & Imaging Technology Medical Lab Technology Cardiac Non Invasive Technology Dialysis Technology Dentist Requirement: Knowledge in Anatomy and Physiology Good communication and interpersonal skills Basic Computer Skills Benefits System based job Weekly 5 days duty Day shift with Sat and Sun off Food and Cab provided by company Incentives based on performance Starting salary 12k to 25k with increment in 6 months for experienced. Abroad opportunities available Bonus for referring friends Medical expenses covered by company Provident Fund will be provided Gratuity after 5 yrs of work experience. Job Location: Chennai, Coimbatore, Vellore, Trichy, Cuddalore, Pondi Salem, Erode, Namakkal, Thanjavur, Nagercoil, Theni,Dindokal Thiruvannamalai, Villupuram, Karur, Tirunelveli,Kanniyakumari Tirupati, Kerala, AP,Tamilnadu,Telangana Reach Us: HR Shanmugapriya 8072891550 Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology GNM DGNM Physician assistant Anesthesia technician Perfusion Technology Medical coder Freshers Medical coding Freshers jobs in chennai Medical coding openings in chennai Wanted Medical coder Freshers jobs Medical coding Medical coder Medical coding Freshers Jobs in chennai Freshers jobs in chennai Jobs for freshers Nursing jobs for freshers Pharma jobs for Freshers Biotechology Jobs Microbiology jobs Biomedical jobs Bioinformatics jobs Bsc/Msc Jobs Biochemistry jobs Life science jobs in chennai Paramedical jobs in chennai Jobs in Tamilnadu Jobs in Pharmacy Jobs in Hospital GNM STAFF NURSE ANM STAFF NURSE GNM FEMALE STAFF NURSE DGNM FEMALE STAFF NURSE GNM MALE NURSE MALE STAFF NURSE NURSING JOBS IN CHENNAI Perks and Benefits Incentives 3000

Medical Coding is the process of converting Medical Records into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. Hr Priya 9600450980 Designation - Medical Coder Trainee Profile UG / PG in Life Science, Paramedical, Bio Medical, Bio Tech Required Candidate profile Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology DGNM B.Pharm M.Pharm Perks and benefits Incentive Up to 5k Healthcare Insurance PF

We are looking for an Associate Content Editor to join our Clinical Studies team in Hyderabad . This is an amazing opportunity to work on Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence. The team consists of 20 people. We have a great skill set in Clinical and we would love to speak with you if you have skills in Clinical/Drugs As an Associate Content Editor in Clinical team, you will be responsible for actively seeking out information about Clinical Studies, analyze, cross reference, and update all new or previously updated information in the clinical records from various sources, which includes scientific meetings, conferences, trial registries, press releases and other possible internet sources. About You Education (BPharma/M Pharma/MSc in Biotechnology, Microbiology) Work experience (0-1 year of experience in analyzing and updating clinical reports) Knowledge, skills, or abilities (In-depth knowledge of clinical trials, pharmaceutical drug pipelines, drug development and clinical phases) Excellent English written and verbal communication skills. It would be great if you also had . . . Experience in secondary research related to clinical information What will you be doing in this role? Maintain Clarivate database with up-to-date and accurate Clinical trials information from a range of information sources Accountable for the delivery of weekly targets Ensure quality standards are observed Ability to understand and interpret complex and detailed Trials & Drugs related information from source material An inquisitive, analytical mind with strong problem-identification and solving skills Hours of Work Working days Monday to Friday, working hours 9AM to 6PM IST, Hybrid working mode.

What We Want You To Do Maintain accurate and up-to-date data records in databases or spreadsheets.Enter and update data in systems or reporting software.Prepare and generate reports based on collected data.Ensure the accuracy and integrity of all data and documentation.Assist in managing technical inventory and keeping track of supplies.Collaborate with team members to ensure smooth workflow and data sharing.Perform general administrative duties such as filing, organizing, and maintaining documents.Provide timely support to management or other departments as needed. What We Are Looking For In You Master's degree in Biotechnology, Biology, Microbiology, Life Sciences, or a related field.Strong proficiency in Microsoft Office (Excel, Word, PowerPoint) or similar software.Previous experience in data entry, record-keeping, or administrative roles (preferred).Ability to work independently with minimal supervision.Strong attention to detail and excellent organizational skills.Good communication skills (both verbal and written).Ability to handle confidential information appropriately. What You Will Gain Exposure to working in a leading company in the field of GenomicsExperience in data management within a high-tech, innovative environment. Opportunity to be part of a dynamic and fast-growing team. Skills: rna isolation,dna extraction,biotechnology,data entry,microsoft office,powerpoint,ngs,excel,rtpcr,record-keeping,data management,word,organizational skills,communication skills

Job Summary: We are looking for a dedicated and detail-oriented Microbiologist with 1 year of hands-on experience in laboratory work for our fisheries company. The ideal candidate will be responsible for conducting microbiological testing, analyzing samples, and ensuring compliance with safety and quality standards. Key Responsibilities: Perform microbiological testing of raw materials, finished products, and environmental samples. Maintain proper documentation of test results. Conduct microbial limit tests, sterility tests, and identification of microorganisms. Ensure all testing complies with standard operating procedures (SOPs) and regulatory guidelines. Maintain and calibrate laboratory equipment. Prepare reports and communicate findings to relevant teams. Follow safety protocols and maintain a clean and sterile laboratory environment. Job Type: Full-time Pay: ₹10,000.00 - ₹18,000.00 per month Schedule: Day shift Ability to commute/relocate: Medinipur, West Bengal: Reliably commute or planning to relocate before starting work (Required) Experience: Microbiology: 1 year (Required) Work Location: In person

Job Description: Quality Control (Q.C.) Officer Company: Flourish Pharma Location: Daman Experience: Entry level to 1 year of experience Salary: ₹20,000 per month Work Schedule: 6 days a week Key Responsibilities: Sample Analysis: Analyze raw materials, in-process samples, and finished products using instruments like HPLC, GC, UV-Vis, and FTIR. Stability Testing: Perform and document stability studies as per ICH guidelines. Instrument Calibration & Maintenance: Ensure timely calibration and maintenance of lab instruments. Documentation: Prepare and review analytical reports, test records, and logbooks as per GMP. Specification Compliance: Verify that products meet predefined specifications and regulatory standards. OOS & OOT Investigation: Handle Out-of-Specification (OOS) and Out-of-Trend (OOT) results with proper documentation and root cause analysis. Microbiological Testing (if applicable): Conduct microbiological testing for sterile and non-sterile products (for microbiology QC roles). Key Skills Required: Hands-on experience with analytical instruments. Knowledge of pharmacopeias (USP, BP, IP). Understanding of GLP (Good Laboratory Practices) and GMP. Strong analytical and observation skills. Good documentation and communication abilities. Qualifications: B.Sc / M.Sc / B.Pharm / M.Pharm in Chemistry, Pharmaceutical Sciences, or related field. Experience required: Entry level: 1 years Job Type: Full-time Pay: ₹20,000.00 per month Schedule: Day shift Application Question(s): Are you comfortable with a salary of INR 20,000/- per month? Are you located near daman? Work Location: In person

Position: Laboratory Technician and Phlebotomy Location: Ahmedabad, GujaratDepartment: Clinical Pathology / Laboratory ServicesReporting To: Lab Manager / Principal Investigator🔹 Job Summary:We are seeking a detail-oriented and skilled Laboratory Technician to join S3 Clinical Research. The ideal candidate will be responsible for conducting laboratory tests, analyzing results, and ensuring the accuracy and quality of clinical trial samples. The role requires strict adherence to Good Laboratory Practices (GLP) and clinical trial protocols.🔹 Key Responsibilities:✅ Sample Collection & Handling:Collect, label, and store blood, urine, and other biological samples as per protocol.Ensure proper centrifugation, separation, and storage of samples in compliance with GLP and GCP guidelines.Maintain accurate records of sample collection, processing, and storage.✅ Laboratory Testing & Analysis:Perform routine pathological and biochemical tests accurately.Conduct hematology, serology, and microbiology tests, ensuring quality control.Operate and maintain lab equipment such as centrifuges, microscopes, and analyzers.✅ Documentation & Compliance:Maintain detailed records of test results and document findings accurately.Ensure adherence to SOPs, protocols, and regulatory guidelines.Assist in the preparation of lab reports for clinical trial documentation.Ensure proper archival and retrieval of lab data.✅ Equipment Maintenance & Calibration:Regularly calibrate and maintain lab equipment to ensure accuracy.Perform quality control checks and troubleshoot equipment issues.Maintain logs of maintenance activities and report any discrepancies.✅ Safety & Quality Control:Follow lab safety protocols, including proper handling of biohazard materials.Ensure compliance with infection control policies and laboratory hygiene standards.Dispose of biohazardous waste properly.🔹 Required Skills & Qualifications:Education: Diploma or Bachelor's degree in Medical Laboratory Technology (DMLT/BMLT).Experience: Minimum 1-3 years of experience in a clinical laboratory, preferably in clinical trials or pathology labs.Technical Skills: Proficiency in sample processing and testing.Familiarity with lab instruments and software.Knowledge of GCP and GLP guidelines.Strong attention to detail and organizational skills.Ability to work efficiently under tight timelines.🔹 Preferred Competencies:Experience in clinical research labs or SMOs.Familiarity with ICMR and NABL standards.Ability to collaborate with clinical trial teams and investigators.🔹 Benefits:Competitive salary based on experience.Opportunity to work in clinical trials with reputed investigators.Continuous training and development opportunities.Exposure to cutting-edge clinical research.✅ How to Apply:Interested candidates can share their CV with:📧 Email: s3clinicalresearch@gmail.com📞 Contact: +91 9662790725

We are hiring enthusiastic Call Handling Agents to join our team! If you have a background in biology, nursing, dietetics, or a related field and enjoy communicating with people, this is a great opportunity to apply your knowledge in a dynamic environment. Key Responsibilities: Handle incoming and outgoing calls efficiently and professionally Provide accurate information and guidance related to health, nutrition, or related topics Record and update call details in the system Coordinate with internal teams to resolve queries Ensure the regular follow-ups Skills: Good communication skills Empathy and patience in handling health-related queries Basic computer literacy Knowledge of medical terminology Minimum educational background: Graduate degree in a health or life sciences field such as: BSc Nursing BSc Biology / Zoology / Microbiology / Biotechnology BSc Dietetics / Nutrition BPharm (Bachelor of Pharmacy) BPT (Physiotherapy) BHMS, BAMS or other paramedical degrees Prior experience in hospitals, clinics, healthcare BPOs, or call centers is preferred

# Hiring #Marketing Coordinator # Location : Indore, Madhya Pradesh POSITION PURPOSE/OBJECTIVES · The Marketing Coordinator plays a key role in supporting the marketing team by planning, executing, and monitoring marketing campaigns and activities. This position ensures smooth coordination between various departments, vendors, and stakeholders to enhance brand visibility and drive business growth. KEY ACCOUNTABILITIES/ RESPONSIBILITIES: 1. Strategy Development: Develop and implement marketing strategies aligned with business goals and objectives. Analyze market trends, customer needs, and competitor activities to identify opportunities for growth. 2. Campaign Management: Plan, execute, and manage marketing campaigns across multiple channels, including digital, social media, email, and traditional media. Ensure campaigns are delivered on time and within budget. 3. Content Creation: Oversee the creation of high-quality, engaging content for various platforms, including website, blog, social media, and marketing collateral. Collaborate with internal teams and external agencies to produce compelling content. 4. Digital Marketing: Lead digital marketing efforts, including SEO, SEM, email marketing, and social media. Utilize data analytics to measure campaign effectiveness and optimize performance. 5. Brand Management: Maintain and enhance the company’s brand identity. Ensure all marketing materials and communications are consistent with brand guidelines and messaging. 6. Market Research: Conduct market research to identify target audiences, assess market conditions, and understand customer behavior. Use insights to inform marketing strategies and tactics. 7. Budget Management: Develop and manage the marketing budget. Allocate resources effectively to maximize ROI and achieve marketing objectives. 8. Performance Tracking: Monitor and report on the performance of marketing campaigns and initiatives. Use metrics and KPIs to assess effectiveness and identify areas for improvement. Other Duties may include · Actively pursue opportunities to increase knowledge of business processes and systems. · Provide feedback and assistance to the departments for the continued support. · Some travel may be required. · Other tasks that may be delegated by the reporting Manager from time to time. QUALIFICATIONS, SKILLS & EXPERIENCE Educational Requirements: · Bachelor’s degree in Marketing, Business Administration, or degree in food science Microbiology, Biotechnology, Veterinary, Agriculture is highly desirable. · Minimum of 5 years of experience in marketing. · Proven track record of developing and executing successful marketing strategies and campaigns. · Strong understanding of digital marketing, including SEO, SEM, PPC, social media, and email marketing. · Excellent written and verbal communication skills. · Proficient in marketing analytics tools and software. · Ability to manage multiple projects and meet deadlines in a fast-paced environment. · Strong leadership and team management skills. · Creative thinker with a strategic mindset. Preferred & Skills: · Familiarity with marketing automation tools · Knowledge of graphic design and video production · Proficiency in data analysis and reporting Job Types: Full-time, Permanent, Fresher Pay: ₹25,000.00 - ₹50,000.00 per month Benefits: Cell phone reimbursement Health insurance Paid sick time Paid time off Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person Application Deadline: 30/04/2025 Expected Start Date: 05/05/2025

Required a scientific sales officer for a hygiene solutions company. The company is into novel Enzyme based cleaning solutions. The ideal candidate should be a graduate in lifesciences, chemistry with or without experience. Candidate should be willing to travel inside Kerala and develop business. Institutional sales to be done, in places like airport, leading hotels, corporates, hospitals etc. Job Type: Full-time Pay: ₹25,000.00 - ₹35,000.00 per month Benefits: Commuter assistance Compensation Package: Performance bonus Schedule: Morning shift Application Question(s): Are you a graduate in Microbiology or Life sciences? Are you willing to work in sales? Education: Bachelor's (Preferred) Language: English (Required) Work Location: In person Expected Start Date: 15/06/2025

Position: Optometrist Location: MGM Eye Institute, Raipur, Chhattisgarh Reports to: Clinical Lead/Head of Department About MGM Eye Institute MGM Eye Institute (MGMEI) is a premier NABH-accredited eye hospital in Raipur, Chhattisgarh, with a legacy of serving over 8,00,000 patients and performing more than 100,000 surgeries. We are committed to providing state-of-the-art eye care services and fostering a compassionate and inclusive work environment. MGM Eye Institute boasts world-class infrastructure, including modular operation theaters, cutting-edge diagnostic tools, and an advanced microbiology lab. Key Responsibilities Clinical Responsibilities ● Comprehensive Eye Examinations: Perform detailed eye examinations to assess vision and identify refractive errors, ocular diseases, and other visual disorders. ● Diagnosis and Management: Diagnose and manage common eye conditions, providing appropriate treatment and referring complex cases to ophthalmologists as needed. ● Pre- and Post-Operative Care: Assist in the care of patients undergoing cataract, glaucoma, and other ocular surgeries. Patient Education ● Educate patients on maintaining optimal eye health, including preventive measures, lifestyle modifications, and regular follow-ups. ● Counsel patients about their eye conditions, treatment plans, and the importance of compliance with prescribed regimens. Collaboration and Teamwork ● Work closely with ophthalmologists, opticians, and support staff to deliver seamless, patient-centered care. ● Participate in multidisciplinary team meetings to discuss complex cases and develop integrated care plans. Community Engagement ● Participate in community outreach programs, including eye screening camps and public awareness campaigns, as part of MGMEI’s mission to enhance access to quality eye care. Administrative Responsibilities ● Maintain accurate and detailed patient records in compliance with hospital policies and regulatory standards. ● Ensure proper use and maintenance of optometric equipment and instruments. ● Contribute to continuous quality improvement initiatives, ensuring excellence in service delivery. Training and Development ● Mentor and train junior optometrists, interns, and allied healthcare professionals as required. ● Stay updated with advancements in optometry by attending workshops, conferences, and pursuing continuing education opportunities. Qualifications and Skills Educational Qualifications ● Bachelor’s or Master’s degree in Optometry from a recognized institution. ● Certification in specialized areas of optometry (preferred). Experience ● Minimum 3-5 years of experience in a clinical or hospital-based optometry role (preferred). ● Experience in low-vision care, pediatric optometry, or specialized contact lenses will be an added advantage. Key Skills ● Strong diagnostic and analytical skills. ● Excellent interpersonal and communication abilities. ● Ability to build rapport with patients from diverse backgrounds. ● Proficiency in using modern optometric equipment and technology. ● Commitment to ethical and professional standards in healthcare. Why Join MGM Eye Institute? ● Opportunity to work in a NABH-accredited institution committed to quality and innovation. ● Exposure to a wide range of clinical cases and advanced technologies. ● Inclusive and collaborative work culture promoting growth and learning. ● Engagement in community-centered programs delivering impactful eye care. Salary will be commensurate with qualifications, experience, and industry standards, offering a competitive package aligned with organizational policies. Application Process Interested candidates are invited to email their resume and a cover letter to info@mgmeye.org with the subject line “Application for Optometrist – MGM Eye Institute.” For more information, visit our website: www.mgmeye.org MGM Eye Institute is an equal opportunity employer. We encourage applications from qualified candidates, irrespective of gender, caste, or background. Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Schedule: Day shift Ability to commute/relocate: Raipur, Chhattisgarh: Reliably commute or planning to relocate before starting work (Required) Experience: total work: 1 year (Preferred) Work Location: In person

Hiring Senior Resident Radiologist Location – Gaya (Bihar) Hospital Name- Medical College & Hospital Number of Bedded- 650 Number of Year- New Setup CTC- 1.5-2 Lacs (Negotiable) Qualification- MD About Hospital: About: New Hospital and medical college, started in january 2025. Going for LOP. Applying For 150 MBBS Seats New Departments: Anatomy, Physiology, Biochemistry, Pharmacology, Pathalogy, Microbiology, FMT, Community Medicine, General Medicine, Pediatrics, Derma, Psychiatry, General surgery, Ortho, ENT, Opthal, Gyne & Obs, Anasthesia, Radiology, Dentistry Nearest Airport: Gaya International Airport- 27 km Nearest Railway Station: Gaya Junction- 36 km Specialist Requirments: Vacancy of Radiologist as Senior Resident , - 1.5-2 Lacs , Associate Professor & 1 as Professor Assoc- 3.5 to 4 LacsProf- 4-5 lacs-*Male/Female Both can do-*Duty Hours: Mon to Fri- 9 AM to 4 PM (OPD timings)Sat- Half Day- 9 AM to 2 PMIf living in campus 24/7 doctor required as emergencies are there-*Sundays Off-*Accomodation provided in campus*For AP, ASP & professor hospital is okay to buy out the Notice period of candidate Job Type: Full-time Pay: ₹150,000.00 - ₹200,000.00 per month Work Location: In person

Apply now » Sr Dir, Site Quality Head, Goa and Asia Cluster Date: Jun 6, 2025 Location: Goa, India, 403722 Company: Teva Pharmaceuticals Job Id: 61480 Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with. The opportunity Position responsibilities include Quality oversight for Manufacturing, Packaging and Laboratory Operations to ensure a mature culture of quality, compliance with regulatory requirements and quality of products. This oversight includes but is not limited to the establishment and execution of procedure; Establishment Licensing, Quality on the Floor activities including audit and release; handling of laboratory, deviation and complaint investigations; CAPA Creation and implementation; trending and metrics, compliance with validation requirements; verification that equipment, facility and utility systems are maintained in accordance with established requirements. Lead the development, standardization, implementation, monitor effectiveness and continuous improvement of Quality Systems, global and local compliance programs, industry practices, and corporate quality initiatives. Influence quality and compliance initiatives to implement robust and proactive process improvement programs within a strong quality culture to align and demonstrate compliance to Good Manufacturing Practices How you’ll spend your day Leads the Quality organization on site including Quality Control, Microbiology, Quality Compliance, Quality Systems and Quality Assurance Operations. Ensure a current Quality Management System is in place and continuously improved Ensure products are manufactured, released and distributed in accordance to cGMP requirements and registered specifications. Most senior professional and independent decision maker authority on product quality and potential market actions Assess and Mitigate Risks - Identify quality risks and define proactive mitigations, to ensure the products are safe and effective before they reach the market. Work with the business to assure compliant and reliable supply Design and Implement the Site Quality Program—Collaborate with the Site GM and Corporate Quality to create, implement, monitor and update the site quality program. Manage Quality Data -Oversee the delivery of necessary data to site managers and supervisors, Corporate Quality and other internal and external stakeholders, to support the achievement of Quality objectives and ensure compliance Direct Quality Control - Oversee the laboratory activity, including analytical site transfers, testing and approval or rejection of raw materials, packaging materials, in process materials and finished products for the site Promote a Sustainable Culture of Quality -Create, develop and maintain a culture of enhancing quality throughout the entire site operation. Create a space where people can speak openly and are encouraged to present new ideas to improve quality Maintain strong partnership with site leadership team Strategic partner in the site leadership team, with Supply Chain, Project Management, R&D, MS&T and Commercial to ensure project timelines and objectives are met Provide effective Quality leadership during internal, customer and Health Authority inspections Ensure that Quality KPIs are meeting pre-defined targets, Ensures CAPA commitments are implemented in a timely manner and its effectiveness is monitored periodically Plans, manages and monitors the annual Quality Operations budget and all its resources and employees. Ensure the performance and utilization of resources to provide maximum efficiency to the organization. Your experience and qualifications Required – bachelor’s degree in chemistry, Biology, Pharmacy Preferred - Master or equivalent degree in Chemistry, Biology or Pharmacy Key Requirements: Minimum of 10 years pharmaceutical manufacturing site quality operations and leadership experience, including: Deep knowledge of cGMP requirements of local and major international authorities like EMA and US FDA for products and process, High level of understanding of manufacturing, packaging, technology transfer, cGMPs, EU, ICH guidelines as well as CMC content of regulatory submissions, Deep knowledge of chemical/pharmaceutical production operations/ lifecycle, production equipment/ validation and relevant technologies and product types, Experience preparing and/ or leading regulatory authority GMP Deep knowledge of Quality Systems Proven successful track record of leading organizational change to improve efficiency Experience leading, inspiring and coaching large teams Experience developing and implementing and continuously improve existing and new, efficient, and effective business processes Must have adequate knowledge of Quality best practices Must have adequate practical knowledge of pharmaceuticals manufacturing and/ or control Must have adequate practical knowledge of analytical techniques and microbiological principles Must have practical knowledge of pharmaceutical cross functional operations (e.g., Supply Chain, Engineering), product and tech transfer Must have practical knowledge on lean manufacturing/ lean QC and OPEX tools Good knowledge of environmental, health and safety requirements for laboratories and quality operations. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Apply now »

Responsibilities and Duties Pharma QA / QC / Manufacturing Chemist junior / SeniorRoorkee, UttarakhandKLINTOZ Pharmaceuticals Pvt. Ltd Job Description Job Description : 1. Production In-charge: M.Pharm./B.Pharm/M.Sc/ B.Sc with 1-2 yrs exp. in Tablets., Capsules, Oral Liquid and Ointment section, Approved mfg. chemist. preferred. 2. Quality control in-charge: M.Pharm./B.Pharm/ M.Sc/ B.Sc with 1-2yrs exp. in quality control.Q.C.chemist approval in Chemical, Instrumental and microbiology Lab. Work exp. of HPLC, Disso, U.V spectrometer and other Q.C instrument is must. 3.Quality Assurance In-charge: M.Pharm./B.Pharm/M.Sc/ B.Sc with1-2 yrs exp. in quality Assurance & preparation of SOP, BPR, BMR, Validation knowledge is must. 4. Microbiologist : M.Pharm./B.Pharm/ M.Sc ( Micro) with 1-2 yrs exp. in micro lab.& Q.C Chemist approval in Micro lab. 5. Maintenance In-charge : Electrical working experience of 3-4 yrs in maintenance of Pharmaceuticals Machines and Equipments 6. Store in-charge: B. Pharm./B.Sc with 2-3 yrs work exp. in store of a pharmaceutical manufacturing unit. 7. Machine Operators /Technician: ITI/10 th pass with 3-4 years working experience over Tablets., Capsules, Oral Liquid and Ointment section and Packing machine operations in a pharmaceutical manufacturing unit. 8. Accountant: B.Com with 3-4 years working experience in a Pharmaceutical units. Having knowledge of sales tax, income tax, excise, Pf and ESI. 9. Receptionist : fluent in English, 10. Exports/Marketing Executive : having exp. In relevant field. 11. Graphic Designer : knowledge of DTP, Work Experience of 2-3 years in a WHO-GMP certified Pharmaceutical plant will be preferred for all the post. Interested candidate may submit their resume with photograph and relevant documents . Job Type: Full-time Pay: ₹14,000.00 - ₹50,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Ability to commute/relocate: Bhagwanpur, Uttarakhand: Reliably commute or planning to relocate before starting work (Preferred) Work Location: In person

Relocation Assistance Offered Within Country Job Number #165987 - Sricity, Andhra Pradesh, India Who We Are Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specialising in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Our products are trusted in more households than any other brand in the world, making us a household name! Join Colgate-Palmolive, a caring, innovative growth company reimagining a healthier future for people, their pets, and our planet. Guided by our core values—Caring, Inclusive, and Courageous—we foster a culture that inspires our people to achieve common goals. Together, let's build a brighter, healthier future for all. Core Responsibilities Responsible for production KPIs (AU,UPDT&AML) Responsible for EHS & Quality standard expectation related activity implementation Managing resources (Man, Machine, Materials) efficiently, guiding the line teams in minimizing downtime through direct personal involvement & active presence on the shop floor Leading Line Teams to solve quality problems. To maintain the crewing norms, shift rotation, leave planning etc Communication, Coaching & Feedback, Active presence on the shop floor, Participating in the 5S, AM, PM & Small Group meetings with Line Teams. Manage repairing and maintenance to equipment and control spare parts management. Training to Technicians & Team Members on Technical Trainings Key Competencies: Managing Materials and Services: Managing the flow of direct materials in the supply chain—from the acquisition of raw and packaging materials to the production of finished goods—and the indirect materials and services for all functions Involves suppliers on the front end of the innovation cycle Integrates Supply Chain processes for optimum material replenishment and inventory levels (e.g. Supplier Manager Inventory, Vendor Managed Inventory) Understands pull systems relating to material and service replenishment Involve Cost Savings through the identification of activities in the shop floor Drives standardization and simplification initiatives for materials, services, and finished goods Has knowledge of market conditions that influence material and service prices Understands supplier capabilities to meet cost, Quality, and EHS targets Customer Service and Logistics: Grasps the business processes and SAP systems that optimize finished goods replenishment Applies the fundamentals of pull systems, inventory control, and cycle time reduction Managing Production: Managing the process of converting raw materials to finished goods. Develops and executes strategies to consistently manufacture and ensure the quality of finished goods Develops a team-based organization to drive business performance Motivates the workforce to achieve business objectives Understands technical processes in the factory Identifies and communicates equipment capabilities and constraints Knows the handling and storage requirements of raw materials, finished goods, and waste streams Ensures that equipment and processes are capable of meeting production schedules, customer demands, and Quality and Microbiology targets Communicates the need for and impact of Quality, EHS standards while ensuring implementation Promotes safety awareness and models safe behavior Uses SAP data to set the production plan and schedule requirements Executes strategies that deal effectively with operating issues related to labor relations Continuous Improvement: Using continuous improvement (CI) tools to drive growth, profitability, and people development Integrates and applies CI tools such as FP&R Stds and factory modeling tools to drive KPI improvements and reduce cost Exploits data and information to identify and measure potential improvements Applies the Asset Effectiveness Model to identify performance improvement opportunities Uses modeling and statistical tools to better target savings and improvement opportunities Understands the linkages among supply/demand KPIs and the impact of CI tools on those KPIs Conducts Continuous Improvement Reviews (CIR’s) to identify best practices and opportunities for improvement Facilitates sharing of ideas, knowledge, and best practices to improve processes and solve problems Works to standardize best practices Ensures CI processes support Quality and Safety goals Engineering and Capital Project Management: Managing factory and office construction, equipment installation, and relocation projects Support optimal plant layouts and material flows to Engineering function Delivers projects on time and within budget, meeting agreed-upon criteria Uses a systematic approach to track, communicate, and manage the cost and schedule of projects Engages stakeholders in design decisions to ensure projects satisfy quality, cost, service and safety criteria Understands the basic concepts of process control and can direct experts in systems implementation EHS and Quality: Developing, interpreting and applying regulations, standards, and guidelines to ensure the integrity of operations and products Understands the technical requirements of EHS, Quality, in factories Develops and drives strategies to ensure conformance to Quality and EHS requirements Understands and interprets governmental policies and regulations to ensure CP compliance with them Provides support for improving safety, environmental and quality conscious behavior in factories Leads by example and demands safe behaviors and awareness, sound environmental practices and commitment to Quality Understands own role and responsibility as well as that of others in implementing EHS and Quality standards and guidelines Communicates the need for and impact of Quality and EHS standards Establishes effective strategies for implementation of EHS and Quality standards and regulatory conformance Recognizes and acknowledges EHS and Quality performance in sites and individuals Takes corrective actions in a timely manner to mitigate potential Quality or EHS incidents Abides by facility safety and GMP requirements and sets the example Proactive in self- assessing against corporate EHS and Quality standards and governmental regulations Provides appropriate resources to achieve expected levels of EHS and Quality performance Supply Chain Systems & Analysis : Leveraging analytical tools and business data to improve total performance of the Supply Chain. Sees the Supply Chain as a total system Understands the interrelationships of the five supply chain processes: plan, source, make, deliver and product commercialization, with respect to overall performance Applies data and information to balance the various KPIs Uses Supply Chain data and analytical tools effectively including SAP, Business Warehouse, MRS/PGSS, and OPERA Data Exploits modeling tools and techniques to optimize plant flow, sourcing, and distribution systems Leverages data from business tools and information systems to maximize Return on Capital, Total Delivered Cost, Cash Generation and Customer Service Anticipates problems—operational, technical, business, and workforce—and takes action Maintains integrity of the business and operational data processes to deliver accurate assessments of the operation Education: B.E. /B. Tech./Diploma (EC/EI/Mechatronics) or any stream relevant with 3 years of proven experience. Experience: Working experience in production function of large FMCG/Manufacturing organization and experience of handling large teams in rotational shifts. PLC programming knowledge will be an advantage #CPIL #LI-AP1 Our Commitment to Diversity, Equity & Inclusion Achieving our purpose starts with our people — ensuring our workforce represents the people and communities we serve —and creating an environment where our people feel they belong; where we can be our authentic selves, feel treated with respect and have the support of leadership to impact the business in a meaningful way. Equal Opportunity Employer Colgate is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, gender identity, sexual orientation, national origin, ethnicity, age, disability, marital status, veteran status (United States positions), or any other characteristic protected by law. Reasonable accommodation during the application process is available for persons with disabilities. Please complete this request form should you require accommodation. #LI-On-site

Job Overview: Applications are invited from highly motivated and eligible candidates for the position of Junior Research Fellow (JRF) under the Anusandhan National Research Foundation (ANRF)-funded research project titled: "Exploring Diversity and Functional Dynamics of Microbial Communities Inhabiting Sulfur Spring at Sahastradhara, Dehradun, Uttarakhand.” [PI: Dr. Nirjara Singhvi, Assistant Professor, DBUU The selected candidate will be involved in field sampling, microbial isolation, culturing, and molecular characterization of microbial communities. No. of Post: 1 Age: (*Age Limit- 26 years) Qualifications Required: M.Sc. in Microbiology, Zoology, or Biotechnology from a recognized university with a strong academic background. Desirable Skills & Experience: Hands-on experience in microbiological techniques, including microbial handling and culturing. Experience in molecular techniques (DNA/RNA extraction, PCR, sequencing, etc.) will be an added advantage. Fieldwork experience related to environmental or microbial research is desirable. Candidates with a valid NET/GATE qualification will be given preference. Position Details: Location: Dev Bhoomi Uttarakhand University (DBUU), Dehradun The salary will be provided as per Government of India norms. Project Duration: 3 Years The position is temporary and co-terminus with the project. Additionally, the service of JRF will be liable to termination at any time without any notice and without assigning any reason. Application Procedure: Interested and eligible candidates are requested to send their updated CV along with a cover letter detailing their research interests and relevant experience to: dean.research@dbuu.ac.in and (CC to) soas.nirjara@dbuu.ac.in with Subject: Application for ‘JRF Position – ANRF Project’. Selection Process: Shortlisted candidates will be notified via email and invited for an interview (online/offline as applicable). The final selection will be based on academic credentials, research experience, and performance in the interview. No TA/DA will be provided for attending the interview. Deadline for Application Submission: 31/03/2025 Contact Us Dev Bhoomi Campus, Chakrata Road, Navgaon, Manduwala, Dehradun- 248007, Uttarakhand, INDIA Email - hr@dbuu.ac.in Mobile No. - 9258126948

Profile- Associate Professor Radiologist Location – Gaya (Bihar) Hospital Name- Medical College & Hospital Number of Bedded- 650 Number of Year- New Setup CTC- 3.5-4 Lacs Qualification- MD About Hospital: About: New Hospital and medical college, started in january 2025. Going for LOP. Applying For 150 MBBS Seats New Departments: Anatomy, Physiology, Biochemistry, Pharmacology, Pathalogy, Microbiology, FMT, Community Medicine, General Medicine, Pediatrics, Derma, Psychiatry, General surgery, Ortho, ENT, Opthal, Gyne & Obs, Anasthesia, Radiology, Dentistry Nearest Airport: Gaya International Airport- 27 km Nearest Railway Station: Gaya Junction- 36 km Specialist Requirments: Vacancy of Radiologist as Associate Professor & 1 as Professor Assoc- 3.5 to 4 LacsProf- 4-5 lacs-*Male/Female Both can do-*Duty Hours: Mon to Fri- 9 AM to 4 PM (OPD timings)Sat- Half Day- 9 AM to 2 PMIf living in campus 24/7 doctor required as emergencies are there-*Sundays Off-*Accomodation provided in campus*For AP, ASP & professor hospital is okay to buy out the Notice period of candidate Job Type: Full-time Pay: ₹350,000.00 - ₹400,000.00 per month Work Location: In person

Required Radiologist Location – Gaya (Bihar) Hospital Name- Medical College & Hospital Number of Bedded- 650 Number of Year- New Setup CTC- 1.3- 4 Lacs Qualification- MD About Hospital: About: New Hospital and medical college, started in january 2025. Going for LOP. Applying For 150 MBBS Seats New Departments: Anatomy, Physiology, Biochemistry, Pharmacology, Pathalogy, Microbiology, FMT, Community Medicine, General Medicine, Pediatrics, Derma, Psychiatry, General surgery, Ortho, ENT, Opthal, Gyne & Obs, Anasthesia, Radiology, Dentistry Nearest Airport: Gaya International Airport- 27 km Nearest Railway Station: Gaya Junction- 36 km Specialist Requirments: Vacancy of 1 Radiologist as SR, 1 as Associate Professor & 1 as Professor Salary: SR- 1.30 to 1.50 LPMAP- 1.40 to 1.70 LPMAssoc- 1.70 to 2.80 LPMProf- 3 to 4 LPM-*Male/Female Both can do-*Duty Hours: Mon to Fri- 9 AM to 4 PM (OPD timings)Sat- Half Day- 9 AM to 2 PMIf living in campus 24/7 doctor required as emergencies are there Job Type: Full-time Pay: ₹130,000.00 - ₹150,000.00 per month Work Location: In person

Job Overview Apollo Hospitals Jabalpur is looking for a dedicated and detail-oriented Infection Control Nurse (ICN) to strengthen our infection prevention and patient safety protocols. The selected candidate will be responsible for implementing hospital-wide infection control programs, conducting surveillance of healthcare-associated infections (HAIs), and ensuring compliance with NABH and international infection control guidelines. Key Responsibilities Develop and implement infection prevention and control (IPC) protocols across all hospital departments. Conduct infection surveillance, monitoring, and reporting of hospital-acquired infections (HAIs). Train nurses, doctors, and hospital staff on infection control best practices, including hand hygiene, sterilization, and PPE usage. Investigate infection outbreaks, assess root causes, and recommend corrective actions. Ensure strict adherence to NABH, JCI, and WHO infection control standards. Oversee the proper sterilization and disinfection of hospital equipment, operation theaters, and patient care areas. Conduct regular infection control audits, risk assessments, and quality checks to prevent cross-contamination. Develop and implement hospital-wide vaccination programs for patients and healthcare workers. Work closely with hospital microbiologists and quality control teams to minimize infection risks. Educate patients and their families on infection prevention measures during hospital stays and post-discharge. Required Skills & Qualifications GNM / B.Sc. Nursing with a specialization or certification in Infection Control Nursing (ICN). Registered with the Madhya Pradesh Nursing Council. Strong knowledge of infection control policies, microbiology, and epidemiology. Familiarity with hospital infection control software and surveillance tools. Ability to work collaboratively with healthcare professionals, microbiologists, and hospital management. Excellent communication, training, and leadership skills. Strong analytical and problem-solving abilities to manage infection outbreaks. Up-to-date knowledge of national and international infection control guidelines (NABH, JCI, WHO, CDC). Why Join Apollo Hospitals Jabalpur? Work with one of India’s top multi-specialty hospitals. Competitive salary with growth opportunities in hospital infection control management. Exposure to cutting-edge infection control technologies and hospital hygiene practices. Be part of a dynamic team dedicated to patient safety and quality healthcare. Opportunity to train and educate healthcare professionals on infection prevention. Job Category: Clinicalnursing Job Type: Full Time Qualification: GNM / B.Sc. Nursing / ICN Certification Experience (Years): 0-8 years Experience (work area): Hospital Positions: 03 Locations: Jabalpur

Department GOA QC Job posted on Feb 12, 2025 Employment type P-P8-Probationer-HO Executive Please enter job description : The review includes verifications and approved of test reports of Raw materials, In-process Samples, finished, Stability, Calibration & Validation, Environmental monitoring reports of production & microbiology lab, Identification of microorganism (Vitek 2 compact), Biological indicator, BET, sterility, water reports etc. Review of analytical documents and approval through LIMS. Protocol and summary report preparation of method validation of MLT, BET, STERILITY and other miscellaneous study protocols, summary reports etc. Qualification and validation documents reviewed. Handling & Investigation of Microbiological Non-conformances like OOAC, OOAL, OOS and other errors related to microbiological incidences, transcription errors etc. Software handlings like LIMS, SAP, Ample logic, DMS etc. Ensure adherence of cGMP & cGLP regulatory requirement as per standard operating procedure & assurance of the same by means of regular monitoring.

YEAR OF EXPERIENCE : Minimum of 3 Years QUALIFICATION : B.Sc./B.E./B.Tech. (Biotech/Microbiology) or similar LOCATION : Mumbai / Pune / Ahmedabad / Uttarakhand KEY RESPONSIBILITIES : Responsible for Domestic / Institutional sales for all product line in Biotechnology division which includes, Microbiological Media Culture, Lab Chemicals, Lab Consumables, reagents, etc.  To identify & develop new business opportunities in B2B channel by gathering and updating customer intelligence  Manage new and existing clients by providing service, explore and identify all their needs.  Manage and maintain sales / clients database.  Establish & maintain efficient relationship with new and existing clients  Generate new business opportunities in assigned territory / zone / channel  Work closely with marketing and promotion team to design required promotion and awareness campaigns for target market / clients.  Develop Annual and quarterly budgets by product, geography and channel partner, and draw up network and market coverage plans to meet the agreed targets.  Ensure that sales are made strictly within the credit and cash discount parameters.  Performs other duties as assigned or required. COMPETENCIES :  Ability to build and maintain relationship with B2B clients & Knowledge of product line  Must have strong communication skill & experience in techno-commercial interactions  Team player and ability to work with and through others  Very good strategic, analytical & communication skills  Possess Passion, Integrity, attitude & loyalty traits & is available readily.