2560 Microbiology Jobs - Page 42

Perform basic microbiological tests on raw materials, finished products, and environmental samples.Conduct environmental monitoring in production areas. Perform water ) as per pharmacopoeia standards.Carry out sterility tests under supervision. Required Candidate profile Maintain proper records and documentation in line with cGMP requirements.Assist in microbial limit tests for non-sterile formulations.Support investigations of microbiological

Responsible for lab related activities for a large NABL accredited lab. must have exposure & Experience as a microbiologist. Required Candidate profile MSc - Microbiology with 7+ Yrs of experience in NABL accredited lab.

*Pediatrician / Neonatologist Vacancies* Bathinda Punjab DM Neonatologist Required Salary Rs 5 Lakhs Ludhiana Punjab NNF Fellowship Course Stipend 2 to 2.5 Lakhs + Accommodation Panipat Haryana DM Neonatologist Required Salary 5 Lakhs + Required Candidate profile Hodal Haryana Salary 3 Lakhs + Accommodation Roorkee Uttarakhand DM Neonatologist Req. Salary 6 Lakhs + Accommodation Gadchiroli Maharashtra Salary 3 to 3.5 Lakhs + Accommodation + Food

The Food Technology Intern will assist the R&D, production, and quality control teams in projects related to product development, food safety, and process optimization. This role offers hands-on experience in the food technology industry, providing exposure to the latest trends and innovations. Key Responsibilities: Support R&D in product formulation, testing, and analysis. Assist in quality control processes to ensure compliance with food safety standards. Conduct research on industry trends, ingredients, and regulatory requirements. Help optimize production processes for efficiency and quality improvement. Document findings and prepare reports for internal review. Collaborate with cross-functional teams to drive innovation and process enhancements. Requirements: Currently pursuing or recently completed a degree in Food Technology, Food Science, or a related field. Basic understanding of food safety regulations and quality standards. Strong analytical and problem-solving skills. Effective communication and teamwork abilities. Passion for the food industry and eagerness to learn. This internship is an excellent opportunity for individuals looking to gain practical experience in the food technology sector while working alongside industry professionals.

Job Description To report and log OOS, OOT and EM Excursion To perform Environment monitoring of Laboratory. To Perform analytical validation, culture maintenance and GPT of media, recording observation and report generation. Perform microbiology laboratory tests such as Bioburden Analysis, MLT, Sterility, BET etc. in compliance with approved procedures. To maintain the media stock and its reconciliation record of media used in Analysis. To perform Water Sampling and analysis as per defined SOP/protocol and related documentation. Qualifications Educational Qualification: M.Sc. (Microbiology) Min. Exp. Required: 1 Year Note: Candidates who want to apply for internal jobs, must have completed at least 2 years within existing role.

Job Description Maintain media stock and reconcile records of media used in analysis. Perform water sampling and analysis following defined SOPs/protocols and ensure proper documentation. Report and log OOS (Out of Specification), OOT (Out of Trend), and EM (Environmental Monitoring) excursions. Conduct environmental monitoring of the laboratory. Perform analytical validation, culture maintenance, and growth promotion testing (GPT) of media; record observations and generate reports. Carry out microbiology laboratory tests such as Bioburden Analysis, MLT (Microbial Limit Test), Sterility Testing, BET (Bacterial Endotoxin Test), etc., in compliance with approved procedures.

Are you a dynamic and driven individual looking to kickstart your career in recruitment? Novonesis is seeking a recruitment intern with excellent English proficiency, both written and spoken, along with solid MS Office and MS Excel skills. As a Recruitment Intern at Novonesis, you will have the opportunity to gain hands-on experience in the fast-paced world of talent acquisition. Selected Intern's Day-to-day Responsibilities Include Assisting with the recruitment process by sourcing candidates, conducting interviews, and scheduling appointments. Maintaining candidate databases and ensuring all information is up to date and accurate. Assisting with the coordination of recruitment events and job fairs. Providing administrative support to the recruitment team, such as preparing documents and reports. Contributing to the development of recruitment strategies and initiatives. Learning and applying best practices in recruitment and talent acquisition. If you are a proactive and enthusiastic individual with a passion for people and a desire to learn, then we want to hear from you! Join us at Novonesis and take the first step towards a rewarding career in recruitment. Apply now! About Company: At Novonesis, we are leading the era of biosolutions. By leveraging the power of microbiology with science, we transform the way the world produces, consumes and lives.

Job Title: Quality Control Officer Department: Quality Assurance Location: 123/ 1A1 Mambakkam Medavakkam Road, Mambakkam Village, Chennai 600 127 Reports to: Quality Assurance Manager / Plant Manager About Convenio Foods Convenio Foods is a leading provider of high-quality ready-to-eat and frozen food products. We are committed to excellence in taste, safety, and nutrition. Our mission is to deliver convenience without compromising on quality. Job Summary: The Quality Control Officer is responsible for monitoring, inspecting, and ensuring that all food products meet regulatory, company, and customer standards. This role is key to maintaining the integrity of Convenio Foods’ production process and brand reputation. Key Responsibilities: Conduct in-process and final product inspections to ensure compliance with internal standards and food safety regulations (e.g., FSSAI, HACCP, ISO 22000). Monitor raw materials, packaging materials, and finished goods for quality and safety. Perform routine microbiological, chemical, and physical tests as required. Ensure proper hygiene and sanitation practices are followed across the production facility. Maintain accurate and detailed records of inspections, tests, and corrective actions. Identify non-conformities and work with relevant departments to implement corrective and preventive actions (CAPA). Assist in internal and external audits and regulatory inspections. Calibrate and maintain quality control instruments and equipment. Train production staff on quality standards and food safety practices. Contribute to continuous improvement initiatives and quality control process enhancements. Requirements: Master’s degree in Food Technology, Microbiology, Chemistry, or related field. 1–3 years of experience in quality control or quality assurance in the food industry. Knowledge of HACCP, GMP, ISO 22000, FSSAI regulations. Strong attention to detail and analytical skills. Excellent communication and documentation skills. Ability to work in a fast-paced manufacturing environment. Proficient in MS Office and QC-related software tools. Preferred Qualifications: Certification in HACCP or Food Safety Management Systems. Experience with audits (internal, FSSAI, customer). Work Environment: Work is performed in a production facility with cold storage and warm kitchen areas. Must wear appropriate PPE (Personal Protective Equipment). Shift work may be required depending on production schedules.

Company : ICHOR biologics Qualification : MSc in Microbiology Experience :Freshers Position : QC Microbiology Interview : Face to Face 2 way transport facility available & food provided 2 years bond and you need to submit any one original document

Sterility, bioburden, endotoxin, AET/PET testing Method validation for medical & polymer products Lab setup, media prep, equipment handling Water (WFI/CS) & environmental monitoring Data review as per cGMP & compliance norms and Maintain lab records

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. Position Summary Do you want to spend your working time making a difference in the world around you? Are you motivated by impactful work? Do you have a passion for cleanroom environments, microbiology, and possess strong stakeholder communication and service delivery skills? If so, then a career with STERIS in our Life Sciences team could be a great fit for you. The Account Manager, creative thinkers and curious, will be primarily responsible for sales, technical consultation, and lead generation in their assigned territory for STERIS products to the Life Sciences industry. [pharmaceutical, biotech, vaccine, cell gene, medical device, neutraceutical and related industries]. Responsible for achieving all revenue, gross margin, and product sales objectives established by the Business Unit. Participates in the design and implementation of sales strategies, identifies prospects and opportunities presents new concepts and products, calls on Customers, and ensures optimal STERIS experience. Ensures high customer satisfaction, effectively establishes multi-level relationships with customers, and possesses excellent listening skills. Effectively manages and utilizes company provided sales resources to maximize sales outcomes while providing best solutions to the customer. Duties Business Development (60%) Achieves assigned sales quota for territory through the consultative sales process. Identifies and proactively seeks qualified sales opportunities with new and existing Customers within but not limited to, Pharmaceutical, Biotech, Medical Device, Vaccine and Cell Gene Therapy markets. Develops strategic growth plans for new and existing Customers. Creates and manages a multi-faceted execution plan with key stakeholders and decision makers leveraging all available resources Provides high level of service to Customers, including timely and accurate responses to inquiries, and to maintain/build STERIS reputation in the marketplace. Collaborates and maintains strategic partnerships with internal resources and designated channel partners to achieve high levels of Customer satisfaction Utilize CRM to capture detailed Customer notes, manage sales funnel, forecast business, maintain and build pipeline Duties - cont'd Technical (30%) Generates and presents STERIS Life Sciences products and innovative solutions using a compelling value based approach to ensure Customer satisfaction. Use question based selling approach to gain knowledge regarding Customer environment, regulatory requirements and specific needs to provide tailored Customer solution. Maintains current knowledge of regulated industry and market trends as well as technical knowledge and understanding of products and services. Attends educational workshops, reviewing professional publications and participating in professional affiliations. Educates Customers in the area of cleaning, contamination control and sterility maintenance and the features and benefits of using STERIS consumable products. Business/Administrative (10%) Communicates regularly with STERIS management, Customers, and local channel partners in order to support their needs and obtain market intelligence. Plans sales calls/travel itineraries to maximize effectiveness of sales strategies while providing timely follow-up and managing operating expenses Maintains CRM required data, updates sales funnel and top accounts as required in order to measure progress against goals. Provides accurate and on time reports as required by leadership Education Degree Bachelor's Degree in Biological Science or Other Needed Experience ↵ Bachelor's Degree in a Science Related field, Engineering (both strongly preferred) Several years of sales experience to pharma manufacturer or cGMP industry related experience required Experience in consultative selling technical products/services. Knowledge of regulated industries (cGMP, GLP, or similar) Involvement with PDA, ISPE or similar industry organization Strong understanding of Customer and market dynamics and requirements, with demonstrated ability to expand existing Customer relationships as well as develop new ones Experience using current CRMs Skills Client-focused problem-solving. Persuasion and negotiation skills. Active listening and technical aptitude. Perseverance and follow-through. Strong communications skills at all levels of the organization Self-directed, good ability to adapt and set priorities Strong business acumen, with ability to understand and monitor trends Proficiency in Microsoft Office. Must have/maintain a valid driver’s license and the ability to be granted clearance to travel globally. Valid driver's licence and ability to work a flexible schedule and travel as territory requires up to 60% STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare, life sciences and dental products and services. STERIS is a $5 billion, publicly traded (NYSE: STE) company with approximately 17,000 associates and Customers in more than 100 countries. STERIS strives to be an Equal Opportunity Employer.

University: Helmholtz Centre for Infection Research (HZI) Country: Germany Deadline: 2025-07-30 Fields: Chemistry, Biochemistry, Pharmacology, Molecular Biology, Microbiology The Chemical Biology Department at the Helmholtz Centre for Infection Research (HZI), under the leadership of Prof. Brönstrup, is seeking applications for a PhD researcher in the field of Bioanalytical Chemistry / Metabolomics. HZI is a member of the Helmholtz Association of German Research Centres, the largest scientific organization in Germany, and is dedicated to advancing strategies for the prevention, diagnosis, and treatment of infectious diseases. Research at HZI focuses on both bacterial and viral pathogens, their interactions with the immune system, and the discovery of novel therapeutic compounds. The Chemical Biology Department is committed to the discovery and characterization of new anti-infective agents through screening, mode of action studies, and chemical synthesis. Requirements For Application – Cover letter outlining your motivation and suitability for the position – Curriculum vitae (resume) – Employment references and certificates – Work samples or reference projects (if available) – Please do not include a photograph Application Procedure Applicants should submit all required documents, quoting the reference number 076/2025, to the Human Resources Department, Helmholtz Centre for Infection Research GmbH, Inhoffenstr. 7, 38124 Braunschweig, Germany. Applications may also be submitted by email as a single PDF document to jobshzi@helmholtz-hzi.de. Further information about the position can be found at: https://www.helmholtz-hzi.de/en/career/job-portal/job/076-2025-phd-researcher-f-m-d-in-bioanalytical-chemistry-metabolomics/ Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/position-alert-service/ We’re an independent team helping students find opportunities. Found this opportunity helpful? Support us with a coffee!

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. Position Summary Do you want to spend your working time making a difference in the world around you? Are you motivated by impactful work? Do you have a passion for cleanroom environments, microbiology, and possess strong stakeholder communication and service delivery skills? If so, then a career with STERIS in our Life Sciences team could be a great fit for you. The Account Manager, creative thinkers and curious, will be primarily responsible for sales, technical consultation, and lead generation in their assigned territory for STERIS products to the Life Sciences industry. [pharmaceutical, biotech, vaccine, cell gene, medical device, neutraceutical and related industries]. Responsible for achieving all revenue, gross margin, and product sales objectives established by the Business Unit. Participates in the design and implementation of sales strategies, identifies prospects and opportunities presents new concepts and products, calls on Customers, and ensures optimal STERIS experience. Ensures high customer satisfaction, effectively establishes multi-level relationships with customers, and possesses excellent listening skills. Effectively manages and utilizes company provided sales resources to maximize sales outcomes while providing best solutions to the customer. Duties Business Development (60%) Achieves assigned sales quota for territory through the consultative sales process. Identifies and proactively seeks qualified sales opportunities with new and existing Customers within but not limited to, Pharmaceutical, Biotech, Medical Device, Vaccine and Cell Gene Therapy markets. Develops strategic growth plans for new and existing Customers. Creates and manages a multi-faceted execution plan with key stakeholders and decision makers leveraging all available resources Provides high level of service to Customers, including timely and accurate responses to inquiries, and to maintain/build STERIS reputation in the marketplace. Collaborates and maintains strategic partnerships with internal resources and designated channel partners to achieve high levels of Customer satisfaction Utilize CRM to capture detailed Customer notes, manage sales funnel, forecast business, maintain and build pipeline Duties - cont'd Technical (30%) Generates and presents STERIS Life Sciences products and innovative solutions using a compelling value based approach to ensure Customer satisfaction. Use question based selling approach to gain knowledge regarding Customer environment, regulatory requirements and specific needs to provide tailored Customer solution. Maintains current knowledge of regulated industry and market trends as well as technical knowledge and understanding of products and services. Attends educational workshops, reviewing professional publications and participating in professional affiliations. Educates Customers in the area of cleaning, contamination control and sterility maintenance and the features and benefits of using STERIS consumable products. Business/Administrative (10%) Communicates regularly with STERIS management, Customers, and local channel partners in order to support their needs and obtain market intelligence. Plans sales calls/travel itineraries to maximize effectiveness of sales strategies while providing timely follow-up and managing operating expenses Maintains CRM required data, updates sales funnel and top accounts as required in order to measure progress against goals. Provides accurate and on time reports as required by leadership Education Degree Bachelor's Degree in Biological Science or Other Needed Experience ↵ Bachelor's Degree in a Science Related field, Engineering (both strongly preferred) Several years of sales experience to pharma manufacturer or cGMP industry related experience required Experience in consultative selling technical products/services. Knowledge of regulated industries (cGMP, GLP, or similar) Involvement with PDA, ISPE or similar industry organization Strong understanding of Customer and market dynamics and requirements, with demonstrated ability to expand existing Customer relationships as well as develop new ones Experience using current CRMs Skills Client-focused problem-solving. Persuasion and negotiation skills. Active listening and technical aptitude. Perseverance and follow-through. Strong communications skills at all levels of the organization Self-directed, good ability to adapt and set priorities Strong business acumen, with ability to understand and monitor trends Proficiency in Microsoft Office. Must have/maintain a valid driver’s license and the ability to be granted clearance to travel globally. Valid driver's licence and ability to work a flexible schedule and travel as territory requires up to 60% STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare, life sciences and dental products and services. STERIS is a $5 billion, publicly traded (NYSE: STE) company with approximately 17,000 associates and Customers in more than 100 countries. STERIS strives to be an Equal Opportunity Employer.

As discussed, please find the below Company details Position – Technical Application Specialist Location - Kolkata Work Time -9.00am to 6.00pm Work Days - Monday to Saturday Salary – Best in Industry Other benefits- PF, Mediclaim, bonus, paid leaves Minimum Skill, Education, Experience Bachelors degree or equivalent qualification or experience required. Bachelors / Engineering degree in medical / electrical / mechanical or medical technology is preferred ? Preferably 2 Years of experience in Relevant field Job Description – Major Responsibilities: Deliver Customer Operator training in Abbott facilities or on-site Perform new instrument and assay implementations through to Test Of Record On-site assay investigation, troubleshooting and operator training and coaching

Job Summary We are looking for an individual for the SIT Team to oversee the investigation of major and critical deviations, working closely with Cross-Functional Team (CFT) members to identify root causes and implement corrective and preventive actions. The role involves active participation in investigating Out of Specification (OOS) cases, ensuring accurate classification in the DCMS deviations log, and providing support during regulatory inspections. Roles & Responsibilities • You will be responsible for overseeing the investigation of major and critical deviations from the outset, collaborating closely with Cross-Functional Team (CFT) members to identify root causes, corrective actions (CA), preventive actions (PA), and preparing comprehensive reports. Your will also be working on the trending of the deviations and identification of adequate action items for reduction of the same. • Your role involves active participation in investigating OOS (Out of Specification) and other relevant cases, working closely with CFT members to determine root causes, CA, PA, and report writing. • You will review minor and critical , providing constructive feedback for improvement. • Your responsibilities include periodically assessing the trending of minor deviations, highlighting or escalating key observations, regularly reviewing the deviations log to ensure accurate classification, and utilizing the Rubrics template for crafting investigation reports. • You will offer necessary support to the site in readiness for or during regulatory inspections related to investigations. Qualification Educational qualification: A Bachelor's or Master's degree in a relevant scientific field, such as Chemistry, Biochemistry, Pharmacy, or related discipline Minimum work experience : 7 to 10 years of experience in a pharmaceutical or related industry with a focus on investigations and quality assurance Skills & attributes: Technical Skills • In-depth knowledge and experience in overseeing investigations, and familiarity with root cause analysis, corrective actions (CA), and preventive actions (PA). • Expertise in investigating valid OOS and other relevant cases. • Familiarity with reviewing deviations / OOS log and ability to perform classification of data. • Ability to craft comprehensive investigation reports. • Experience in providing necessary support for regulatory inspections related to investigations. • Knowledge of regulatory requirements pertaining to deviations investigations. Behavioural Skills • Ability to collaborate closely with CFT members. • Analytical mind set for identifying root causes and developing effective solutions. • Strong problem-solving skills and attention to detail in reviewing deviations, reports, and trending data and implementing corrective actions. • Effective communication skills for report writing and escalation of key observations. • Commitment to ensuring compliance with regulatory requirements in investigations. • Ability to offer necessary support to the site in readiness for or during regulatory inspections. Additional Information looking someone with strong QC Microbiological investigation background. Should have exp in Microbiological compliance. Education :M.Sc. Microbiology Exp : 8-10 Years Industry : Injectable preferred/ OSD will be second preference Person will be responsible to manage 3 sites Microbiological compliance at Baddi

Interview patients whose blood is to be drawn with regard to the pre-conditions mandatory for particular tests & note significant findings on requisition Draw blood samples in the correct manner Care of the patients after phlebotomy Ensure that specimen is transported to lab in reasonable time Visit patient homes for phlebotomy when advised

About the Role: Risk Assessment: Utilize your expertise to make prudent case assessments and offer recommendation, even in situations that fall outside standard guidelines. Operational Efficiency: Assist the team in identifying inefficiencies and recommend solutions to enhance operational excellence and service delivery. Team Collaboration: Work effectively within a team environment, sharing responsibilities and supporting mutual dependencies through clear communication and collaboration. Value Creation: Actively contribute to the teams value by simplifying processes, identifying opportunities for improvement, and implementing efficiency gains. Training & Development: Develop and deliver training modules for underwriters and clients. Mentor junior team members by identifying skill gaps and providing constructive feedback. Market Intelligence: Demonstrate competence in Life and Health insurance products available in the local market. Hands on experience in conduct trainings/audits and other cross functional initiatives. About the team: The Life & Health Underwriting Services team provides comprehensive support across Asia, including India, Southeast Asia (SEA), Hong Kong/Taiwan, and the Australia-New Zealand (ANZ) region. We are responsible for delivering 100% case assessments for India, SEA, and Hong Kong/Taiwan, including High Net Worth business. Our team is also expanding its expertise in disability income products for the ANZ region. With a decade of experience, we are dedicated to developing proficient underwriters by crafting a roadmap for competency enhancement and offering growth opportunities through rotations and stretched learning assignments. In addition to core responsibilities, experienced underwriters have the opportunity to participate in in-house Life Guide projects, product development, client trainings, and audits. We embrace a One Team culture, fostering positive working relationships with our on-shore business partners and sharing in our collective success. About You: Educational Background: A degree in science (Biology, Microbiology) or a paramedical qualification (Nurse, Pharmacist), or experience as a Junior Dentist. Underwriting Experience: 8 to 10 years of experience in Life and Health underwriting is preferred. Industry Knowledge: Comprehensive understanding of the insurance value chain, with awareness of the legal, regulatory, tax, and consumer protection frameworks in the market. Reinsurance Expertise: Advanced knowledge of reinsurance principles and operations. Team Work: Proven ability to work collaboratively across teams, functions, and regions. Communication Skills: Strong communication skills, approachable demeanor, and the willingness to make difficult decisions and resolve team conflicts. Adaptability: Demonstrated agility and multi-tasking capabilities to meet core expectations and adapt to change as necessary. Results-Oriented: Strong focus on achieving results, with the ability to provide solutions to KPI challenges and meet performance targets. Product Competence: Proficient in Life Underwriting and familiar with all other products available in the local market. About Swiss Re Swiss Re is one of the world s leading providers of reinsurance, insurance and other forms of insurance-based risk transfer, working to make the world more resilient. We anticipate and manage a wide variety of risks, from natural catastrophes and climate change to cybercrime. We cover both Property & Casualty and Life & Health. Combining experience with creative thinking and cutting-edge expertise, we create new opportunities and solutions for our clients. This is possible thanks to the collaboration of more than 14,000 employees across the world. If you are an experienced professional returning to the workforce after a career break, we encourage you to apply for open positions that match your skills and experience. Keywords: Reference Code: 134465

SPL Infrastructure is looking for Lab Technician to join our dynamic team and embark on a rewarding career journeyAssist with testing and calibrating lab equipment in preparation for specific tasksAnalyze retrieved data and prepare reports for laboratory managementExperience in data collection and interpretation as well as the storage and retrieval of samples in a laboratory setting

Qualifications: MBBS, MD (Paediatrics) and Fellowship in Haematology-oncology or Immunology and relevant Bone Marrow Transplant experience Experience: The applicant must have relevant haematology-oncology or immunology and bone marrow transplant experience. The successful applicant will work with bone marrow transplant consultants (1:3 rota) and BMT nursing team leaders. The unit provides comprehensive pre-transplant care for patients with leukaemia and immunodeficiencies, including the use of advanced immunotherapies. Transplants are performed for immunodeficiencies, malignant haematology, non-malignant haematology, and metabolic disorders. As an academic unit, there are ample opportunities for involvement in transplant-related research projects, with support for publication. Please email your application, including all required documents to info@wadiahospitals.org by 7th July 2025. For further information or to arrange an informal visit please contact Dr Prashant Hiwarkar or Dr Ambreen Pandrowala in the Bone marrow transplant unit at BJWHC. Shortlisted candidates will be invited for an interview.

A) Job description:- 1. Execution and monitoring of production batches in the Upstream process area as per approved BPR and timely documentation of the same. 2. Operating of Upstream equipment for process and CPI/ SIP as per SOP e. g. 100 L & 200 L fermenter, Centrifuge, High pressure homogenizer, spectrophotometer, Autoclave. DHS, Cold room, Integrity Machine etc. 3. Preparations of process and equipments related SOPs. 4. Raising change control and deviations in the QA approved format and working with concern departments for closer of the same. 5. Timely instructions to engineering team in case of facility or equipment breakdown. 6. Coordinate for PM/AMC of manufacturing equipment. 7. To Assist in technology transfer from R&D to Manufacturing. 8. To attend on Job cGMP and safety training 9. To ensure safety at workplace. B) Relevant work experience - 5 to 12 Years. C) Education Qualification - M. Sc (Microbiology/ Biotechnology)

We are seeking a Quality Control (QC) Manager to oversee product testing, quality analysis, and compliance with regulatory standards. The QC Manager will be responsible for ensuring the integrity of raw materials, in-process materials, and finished products. Designation: QC Manager Department: Quality Control Experience: Minimum 7 years in Medical Device/Pharma/Life Sciences Industry Regulatory Experience: Minimum 3-5 years in GMP, US FDA, ISO 13485, and Analytical Testing Industry/Background: Medical Device / Pharma / Lifesciences Industry Qualification: B. Pharm / M. Pharm / M.Sc. Life Science / B.Tech Biotechnology / Related Field Employment Status: Permanent Workplace Type: On-site Minimum Requirements: Strong knowledge of analytical techniques, stability studies, and microbiology testing. Experience in handling QC documentation, test reports, and specifications. Proficiency in GMP, ISO 13485, US FDA, and MDSAP compliance. Expertise in using HPLC, GC, UV, and other analytical instruments. Experience in raw material, in-process, and finished product testing. Strong knowledge of deviation handling, OOS investigations, and CAPA. Ability to lead a QC laboratory and ensure smooth functioning of testing operations. Roles and Responsibilities: Oversee quality control operations and ensure compliance with regulatory standards. Ensure proper testing and validation of raw materials, in-process, and finished products. Review and approve test reports, analytical data, and quality records. Monitor and maintain stability studies and analytical testing procedures. Conduct investigations for out-of-specification (OOS) results and deviations. Ensure the calibration and maintenance of laboratory instruments. Coordinate with cross-functional teams to ensure product quality. Support regulatory submissions and participate in regulatory inspections.

Job Summary Provide excellent customer service and delight customers by exceeding their expectations. Ensure logical and meaningful extraction of url content along with 100% SLA adherence. Prepare and implement action plans to drive process improvements. Deliver high quality of extraction consistently wt fail and ensure process compliance. Develop domain expertise and work like an SME. Challenge what seems not right! Perform high quality RCAs to identify the root causes of repeating high severity issues Responsibilities Preferable-Customer support or technical support experience in online industry 2 to 3 years preferably with processes related to data curation extraction Good knowledge of websites and how to navigate to obtain desired information Excellent Communication Skills both written & oral Decision making skills Basic knowledge of excel sheets Strong Logical Analytical skills cognitive ability Focus on accuracy eye for details Excellent time management skills most workload involves fluctuation Extremely proactive and organized with a track record of success in a team environment

Applications are invited for the faculty positions Senior Resident, Assistant Professor, Associate Professor, and Professor. JOB LOCATION -TAMIL NADU 1. Anatomy – Senior Resident /Assistant professor /Associate professor/Professor 2. Physiology – Senior Resident /Assistant professor /Associate professor/Professor 3. BioChemistry – Senior Resident /Assistant professor /Associate professor/Professor 4. Pathology – Assistant professor /Associate professor/Professor 5. Microbiology – Senior Resident /Assistant professor /Associate professor 6. Pharmacology – Senior Resident /Assistant professor /Associate professor/Prof 7. Forensic Medicine– Senior Resident /Assistant professor /Associate professor/Professor 8. Community Medicine– Senior Resident /Assistant professor /Associate professor/Professor 9. General Medicine – Senior Resident /Assistant professor /Associate professor/Professor 10. Paediatrics – Senior Resident /Assistant professor /Associate professor/Professor 11. Dermatology –Associate professor/Professor 12. Psychiatry –Senior Resident/Associate professor/Professor 13. Respiratory-medicine– Senior Resident /Assistant professor /Professor 14. General Surgery– Senior Resident /Assistant professor /Associate professor/Professor 15. Orthopaedics –Senior Resident /Assistant professor /Associate professor//Professor 16. Ophthalmology– Senior Resident /Assistant professor /Professor 17. Obstertics & Gynaecology –SR/Assistant professor /Associate professor/Professor 18. Anaesthesiology –SR /Assistant professor /Associate professor/Professor 19. Radiology– Senior Resident /Assistant professor /Associate professor/Professor 20. Emergency-Medicine –Assistant professor /Associate professor/Professor 21.ENT-Associate professor/Professor Eligibility: As per NMC Norms. Remuneration: As per qualification & Experience JOB LOCATION -TAMIL NADU Job Type: Full-time Pay: ₹90,000.00 - ₹250,000.00 per month

Join the PSC family and connect with accomplished and diverse colleagues who inspire and innovate students and transform lives and futures. Along with helping our students reach their goals, Pensacola State makes career fulfillment a reality. Job Description The Natural Sciences Department offers college-level Microbiology courses in the following formats: face-to- face, live online via Zoom, and asynchronous online. Adjunct instructors instruct students, develop curricula, assess student learning, participate in program evaluation, and maintain College and department standards. This position reports to the Department Head, Natural Sciences. Minimum Qualifications: To teach college-level courses, graduation from an accredited institution with a master’s degree in field or a master’s degree and 18 graduate hours are required. Successful results of a criminal background check are also required. Instructors must be able to use and demonstrate the use of technology required for assigned course(s). SUPPLEMENTAL MATERIALS: All supplemental materials must be submitted electronically via the Workday applicant portal. For questions or to obtain assistance uploading the supplemental materials, contact HR Recruiting at HRrecruiting@pensacolastate.edu. Salary Range: Adjunct Faculty shall be paid on an hourly basis according to degree level as follows: Master’s Degree: $34.00 Doctorate: $37.00 NOTE: This is an open applicant pool. Positions are filled by the department on an as needed basis. Pursuant to College policy, it is an employment eligibility requirement for an applicant to meet the requirements of 435.04(2), Florida Statutes, related to background investigations. Any person failing to meet the requirements of the statute will be deemed not qualified to hold employment in this position. A Florida Department of Law Enforcement (FDLE) approved background check will be conducted on every successful candidate as a condition of employment, and any person who fails to disclose any adverse information contained in the background investigation at the time of submitting the employment application will be disqualified from employment. Pensacola State College does not discriminate against any person on the basis of race, ethnicity, national origin, color, sex, age, religion, marital status, pregnancy, disability, sexual orientation, gender identity, or genetic information in its educational programs, activities, or employment. For inquiries regarding Title IX and the College’s nondiscrimination policies, contact the Executive Director of Equal Opportunity Compliance at (850) 484-1759, Pensacola State College, 1000 College Blvd., Pensacola, Florida 32504.

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