Summary: Home Health Coder is responsible for coding using ICD-10 all diagnoses and applicable procedures of outpatient service visits. The position is also responsible for reviewing OASIS, Plan of Care and abstracting visit data for billing and data collection purposes. Job Description: Accurately assign ICD-10-CM codes to diagnoses from the care plans and documentation submitted by the client. Prospectively reviews OASIS assessments and Plan of Care to ensure appropriateness, completeness and compliance with federal and state regulations and organization policy. Probe clients’ clinicians when code assignments are unclear or when documentation is inadequate or ambiguous. Act as a subject matter expert regarding Coding and OASIS questions by clients and key stakeholders Review and identify errors and report them to supervisor or department manager for follow-up. Identifies trends in clinical documentation and/or potential problems and works with quality team to develop action plans to address opportunities for improvement. Maintains daily productivity and turnaround times. Assists with initial orientation and education/training of staff. Reads and reviews coding guidelines, Medicare updates, professional journals, etc. to maintain an up-to-date working knowledge of coding and reimbursement principles. Requirements /Qualification: Graduates / Post-Graduates in Life Science (MBBS, BDS, BHMS, BAMS, BUMS, Nursing, Pharmacy, Biotechnology, Microbiology, Biochemistry Pharmacy, Physiotherapy, Zoology, Microbiology, BAMS, BHMS, BUMS Exceptional knowledge of Anatomy, Physiology, Pharmacology and Medical Terminologies. BCHH-C certification is mandatory. Proficient Computing and Logical Reasoning skills. Excellent communication skills, both verbal and written. Who should not apply? If you want to work from home, Please do not apply. If you don't have BCCHH-C certification, Please do not apply. Freshers kindly do not apply (This position is only for experienced Home Health Coders) If you don't have more than 2 years of experience in Home Health Coding, Please do not apply. Salary/Compensation: This is purely based on your experience and your performance in the Interview. Job Type: Full-time Pay: ₹25,000.00 - ₹60,000.00 per month Show more Show less

Dear Doctors, Greetings from Masadir! We have urgent job opening for Pathology (Microbiology) in well-established hospital in Jamshedpur location. JOB DETAILS: Position: Pathology (Microbiology) Location: Jamshedpur, Jharkhand Salary : Industry Standards Qualification: DNB/MD Microbiology Experience : 0-10 years Job description Stay up to date with developments in the fields of pathology and medical practice Study blood samples for transfusion use including the blood type, blood group, cell morphology, and compatibility with other blood types Use medical equipment and computerized systems to perform various lab tests Operate laboratory equipment such as cell counters and microscopes Log data from lab tests and enter results in patient’s record Skills Proven work experience as a Pathologist or similar role Valid and active medical license Experience using lab testing equipment, such as microscopes and flow cytometers Exceptional analytical and research skills Strong oral and written communication skills Other details The doctor should have completed MBBS, MD/DNB Microbiology from a recognized institute. The institute should be NMC/MCI recognized. Show more Show less

Overview Bruker is enabling scientists to make breakthrough discoveries and develop new applications that improve the quality of human life. Bruker’s high-performance scientific instruments and high-value analytical and diagnostic solutions enable scientists to explore life and materials at molecular, cellular and microscopic levels. In close cooperation with our customers, Bruker is enabling innovation, improved productivity and customer success in life science molecular research, in applied and pharma applications, in microscopy and nanoanalysis, and in industrial applications, as well as in cell biology, preclinical imaging, clinical phenomics and proteomics research and clinical microbiology. Today, worldwide more than 9700 employees are working on this permanent challenge at over 90 locations on all continents. Bruker continues to build upon its extensive range of products and solutions, its broad base of installed systems and a strong reputation among its customers. Being one of the world's leading analytical instrumentation companies, Bruker is strongly committed to further fully meet its customers’ needs as well as to continue to develop state-of-the-art technologies and innovative solutions for today's analytical questions. Job Summary: For RSM, South & West Bruker India Scientific Pvt. Ltd is seeking a dynamic and results-oriented Regional Sales Manager to lead the sales efforts for its Microbiology & Infection Diagnostics (M&ID) business across South & West India . The role will involve driving sales targets, expanding market presence, managing channel partners, and building lasting relationships with key decision-makers in hospitals, laboratories, pharmaceutical companies, and research organizations . Job Summary: For RSM, North & East Bruker India Scientific Pvt. Ltd is seeking a dynamic and results-oriented Regional Sales Manager to lead the sales efforts for its Microbiology & Infection Diagnostics (M&ID) business across North & East India . The role will involve driving sales targets, expanding market presence, managing channel partners, and building lasting relationships with key decision-makers in hospitals, laboratories, pharmaceutical companies, and research organizations . This position can be based in Mumbai, Chennai or Bengaluru. Responsibilities Key Responsibilities: Sales & Business Development Drive and achieve annual and quarterly sales targets in the assigned territory as per the M&ID business plan. Identify, qualify, and close business opportunities in segments including clinical microbiology labs, infectious disease departments, infection control, QA in pharmaceuticals & Bio Pharma and research organizations. Generating and converting leads through direct customer engagement and outbound activities. Sales Funnel & CRM Management Manage sales pipeline through Salesforce (SFDC), ensuring timely updates, accurate forecasting, new order booking, and tracking of opportunities. Maintain disciplined funnel management to ensure strong conversion rates and healthy pipeline progression. Channel Partner Support & Control Support, manage, and evaluate existing distribution partners in the region. Conduct regular business reviews, performance tracking, and provide strategic and operational support to drive indirect sales. Ensure proper execution of Bruker sales strategy and compliance by all channel partners. Customer & Market Engagement Conduct market development activities, including product demonstrations, customer education sessions, and roadshows. Attend and represent the company at conferences, seminars, trade fairs, and scientific forums to generate leads and raise brand awareness. Develop relationships with KOLs, decision-makers, and influencers across microbiology, infectious disease, and quality assurance functions. Cross-Functional Collaboration Work closely with application specialists, service teams, and marketing to deliver seamless customer experience. Provide inputs on regional trends, competitor intelligence, and customer feedback for strategic planning. Qualifications Bachelor’s degree or equivalent in Life Sciences, Microbiology, Biotechnology, or Biomedical Sciences. 5+ years of relevant sales experience in clinical diagnostics, microbiology, or life sciences instrumentation. Experience working with or selling to hospitals, pharmaceutical companies, laboratories, and academic/research institutions. Knowledge of microbial identification technologies and infection control workflows. Proven track record in managing sales pipelines and reporting via SFDC or similar CRM platforms. Demonstrated ability in lead generation through market development and scientific events. Strong analytical, communication, and negotiation skills. Willingness to travel extensively (at least 50%) across South & West India -RSM South & West and North & East India - RSM North & East. Bruker is an equal-opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, national origin, disability, veteran status, and other protected characteristics. Show more Show less

Who are we HaystackAnalytics is a HealthTech company creating clinical genomics products, which enable diagnostic labs and hospitals to offer accurate and personalized diagnostics. Supported by India's most respected science agencies (DST, BIRAC, DBT), we created and launched a portfolio of products to offer genomics in infectious diseases. Our genomics based diagnostic solution for Tuberculosis was recognized as one of top innovations supported by BIRAC in the past 10 years, and was launched by the Prime Minister of India in the BIRAC Showcase event in Delhi, 2022. Job Summary We are looking for a fresher MD/PhD with a specialization in Microbiology to join our team as a Clinical Outreach / Scientific Outreach professional. This position requires active field engagement in collaboration with the sales team, including visits to hospitals and clinical institutions to interact with physicians and other healthcare professionals. The candidate will be responsible for effectively communicating the scientific, microbiological, and clinical aspects of our products, ensuring a clear and thorough understanding of their clinical relevance, applications, and value. The candidate will be participating in Continuing Medical Education (CME) programs and Round Table meetings (RTMs). What we want you to do Work closely with the sales team during client visits, primarily engaging with doctors and healthcare providers. Explain the microbiological and clinical aspects of our products in a clear and professional manner. Bridge the gap between scientific knowledge and clinical application to support the adoption of our products. Provide technical support and medical guidance during client meetings and product demonstrations. Help doctors understand how the product integrates into patient care, infection control, and diagnostic workflows. Share relevant case studies, clinical experiences, or infection trends to highlight product effectiveness. Maintain a strong understanding of emerging microbiological trends and technologies, including Next-Generation Sequencing (NGS). Collaborate with internal teams such as R&D, sales, and Operto ensure accurate communication and feedback. Actively participate in Continuing Medical Education (CME) programs and Round Table Meetings (RTMs) What are we looking in you Freshers - Fresher MD/PhD with a specialization in Microbiology Proven track record of effective communication and collaboration with interdisciplinary healthcare teams. Demonstrated understanding of infection control protocols and antimicrobial stewardship principles. Familiarity with molecular and sequencing (NGS) technologies and their applications in clinical microbiology is advantageous. Strong knowledge of clinical microbiology, infectious diseases, and diagnostic methods Excellent verbal communication and presentation skills. Ability to explain complex technical and medical concepts in a simple, clinician-friendly language. Comfortable with on-field client interactions. Must be willing to travel to PAN India for CME programs and RTMs. What you will gain Dynamic and collaborative work environment dedicated to making a meaningful impact in healthcare Experience in working with advanced sequencing technology in the diagnostic industry i.e. NGS, WGS, Nanopore, and Illumina. Opportunities for professional development and continued education Competitive salary commensurate with experience Comprehensive health benefits package Skills: infection control protocols,regulatory compliance,genomics,medical guidance,presentation skills,technical support,next-generation sequencing (ngs),effective communication,outreach,training and development,clinical microbiology,ngs,collaboration,communication,molecular biology,clinical support,scientific communication,microbiology,antimicrobial stewardship,medical genetics Show more Show less

Total Experience - 0-6 Months What we want you to do Work with diagnostic lab partners for smooth functioning of infectious disease test Work with partners to ensure timely upgrades to the test are done Liaison with partners for technical support as needed Document activities What are we looking in you MSc in Microbiology or Biotechnology Experience in DNA Extraction & RT PCR Ability to quickly prioritize and execute tasks Good oral and written communication skills. Strong analytical skills and attention to detail Strong documentation skills Compulsory rotation shift (i.e day shift, mid shift, night shift) 6 days working with rotational week off What you will gain Exposure of working with one of the leading companies in genomics Experience in working with advanced sequencing technology in diagnostic industry i.e NGS, WGS, Nanopore, and Illumina Gain skills in troubleshooting during sequencing. Skills: data management,biotechnology,word,dna extraction,communication skills,data entry,ngs,organizational skills,rna isolation,microsoft office,analytical skills,powerpoint,rtpcr,excel,troubleshooting,record-keeping,documentation,rt pcr Show more Show less

University: French National Research Institute for Agriculture, Food, and the Environment (INRAE) Country: France Deadline: June 13, 2025 The French National Research Institute for Agriculture, Food, and the Environment (INRAE) invites applications for a postdoctoral position in synthetic biology and microbiology, as part of the TARGET Project at the UMR INRAE BFP unit in Villenave d’Ornon, France. This interdisciplinary research initiative aims to advance the cultivation of noncultivable bacteria, focusing on the plant-pathogenic Flavescence Dorée phytoplasma, and integrates approaches from microbiology, culturomics, genetic engineering, systems biology, and computational modeling. Requirements PhD in microbiology, metabolomics, systems biology, molecular biology, biochemistry, or a related discipline Experience with transcriptomics and/or LC-MS-based metabolomics Knowledge of metabolic modeling or biochemical pathway analysis is advantageous Background in microbiology, molecular biology, or bioinformatics Desirable skills include RT-qPCR, metabolic imaging, or protein expression/purification Strong analytical, organizational, and communication skills, with a collaborative approach Role And Responsibilities Develop and validate methods to distinguish phytoplasma metabolic responses from those of host organisms using transcriptomics and metabolomics Conduct targeted and untargeted metabolomics (LC-MS) to identify metabolites in infected and healthy host tissues Utilize metabolic imaging techniques (e.g., MALDI, DESI-MS) to map metabolite distributions Integrate multi-omics data to infer host-pathogen metabolic interactions Support metabolic modeling and culture medium formulation Perform biochemical analyses such as RT-qPCR, enzyme characterization, and protein expression Collaborate with bioinformaticians and contribute to scientific publications and presentations Benefits Gross monthly salary between €3,135 and €4,544, depending on experience and profile Up to 30 days of annual leave plus 15 days of reduced working time (full-time) Parenting support, skills development opportunities, social support, and leisure benefits Access to sports, cultural activities, and collective catering Application Procedure Interested candidates should submit a detailed CV, cover letter outlining research interests and motivation, and contact details for two references to Dr. Pierre Pétriacq (pierre.petriacq@inrae.fr) and Dr. Bessem Chouaia (bessem.chouaia@inrae.fr). Applications will be reviewed on a rolling basis until the position is filled. For further inquiries, please contact the supervisors at the provided email addresses. Start Date: October 1, 2025 Contract Duration: 23 months (with possible renewal for an additional 24 months) Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: phdfinder.com/register Show more Show less

Who are we HaystackAnalytics is a HealthTech company creating clinical genomics products, which enable diagnostic labs and hospitals to offer accurate and personalized diagnostics. Supported by India's most respected science agencies (DST, BIRAC, DBT), we created and launched a portfolio of products to offer genomics in infectious diseases. Our genomics based diagnostic solution for Tuberculosis was recognized as one of top innovations supported by BIRAC in the past 10 years, and was launched by the Prime Minister of India in the BIRAC Showcase event in Delhi, 2022. Job Summary We are looking for a fresher MD/PhD with a specialization in Microbiology to join our team as a Clinical Outreach / Scientific Outreach professional. This position requires active field engagement in collaboration with the sales team, including visits to hospitals and clinical institutions to interact with physicians and other healthcare professionals. The candidate will be responsible for effectively communicating the scientific, microbiological, and clinical aspects of our products, ensuring a clear and thorough understanding of their clinical relevance, applications, and value. The candidate will be participating in Continuing Medical Education (CME) programs and Round Table meetings (RTMs). What we want you to do Work closely with the sales team during client visits, primarily engaging with doctors and healthcare providers. Explain the microbiological and clinical aspects of our products in a clear and professional manner. Bridge the gap between scientific knowledge and clinical application to support the adoption of our products. Provide technical support and medical guidance during client meetings and product demonstrations. Help doctors understand how the product integrates into patient care, infection control, and diagnostic workflows. Share relevant case studies, clinical experiences, or infection trends to highlight product effectiveness. Maintain a strong understanding of emerging microbiological trends and technologies, including Next-Generation Sequencing (NGS). Collaborate with internal teams such as R&D, sales, and Operto ensure accurate communication and feedback. Actively participate in Continuing Medical Education (CME) programs and Round Table Meetings (RTMs) What are we looking in you Freshers - Fresher MD/PhD with a specialization in Microbiology Proven track record of effective communication and collaboration with interdisciplinary healthcare teams. Demonstrated understanding of infection control protocols and antimicrobial stewardship principles. Familiarity with molecular and sequencing (NGS) technologies and their applications in clinical microbiology is advantageous. Strong knowledge of clinical microbiology, infectious diseases, and diagnostic methods Excellent verbal communication and presentation skills. Ability to explain complex technical and medical concepts in a simple, clinician-friendly language. Comfortable with on-field client interactions. Must be willing to travel to PAN India for CME programs and RTMs. What you will gain Dynamic and collaborative work environment dedicated to making a meaningful impact in healthcare Experience in working with advanced sequencing technology in the diagnostic industry i.e. NGS, WGS, Nanopore, and Illumina. Opportunities for professional development and continued education Competitive salary commensurate with experience Comprehensive health benefits package Skills: infection control protocols,regulatory compliance,genomics,medical guidance,presentation skills,technical support,next-generation sequencing (ngs),effective communication,outreach,training and development,clinical microbiology,ngs,collaboration,communication,molecular biology,clinical support,scientific communication,microbiology,antimicrobial stewardship,medical genetics Show more Show less

Job Title: Executive / Senior Executive – QA (Validation & Qualification) Location: Indore Plant Department: Quality Assurance (QA) Reports to: QA Manager – Validation / Head QA Role Summary We are looking for dedicated and experienced professionals to join our Quality Assurance (QA) Department as Executive / Senior Executive . The role involves supporting Validation & Qualification activities in any of the following areas: Process Validation Cleaning Validation Facility & Equipment Qualification Computer System Validation (CSV) Candidates with hands-on experience in one or more of these areas are encouraged to apply. Process Validation Key Responsibilities (based on area of expertise): Prepare and review Process Validation Protocols and Reports (PV). Coordinate validation batches with cross-functional teams. Monitor critical process parameters and ensure adherence to approved specifications. Perform risk assessments and gap analysis as required. Cleaning Validation Develop and execute cleaning validation protocols and sampling plans. Perform visual inspection and swab/rinse sampling for various equipment. Review analytical data and calculate MACO/Residue Limits. Maintain cleaning validation matrix and revalidation schedules. Facility & Equipment Qualification Support IQ, OQ, PQ of equipment, systems, and utilities as per validation master plan. Participate in installation, commissioning, and qualification activities. Ensure periodic qualification and requalification as per schedule. Maintain GMP-compliant records and reports for audits and inspections. Computer System Validation (CSV) Prepare and review URS, RA, IQ/OQ/PQ protocols for GxP systems. Ensure compliance with 21 CFR Part 11, GAMP 5, and data integrity principles. Coordinate with IT, QA, and software vendors during validation life cycle. Maintain validation documentation and change control records. Candidate Profile Qualification: B.Pharm / M.Pharm / M.Sc. (Life Sciences / Chemistry / Microbiology) Experience: 2–6 years in regulated pharmaceutical / API / sterile manufacturing environments Exposure to GMP, ICH, WHO, USFDA, and other regulatory guidelines is essential Experience in one or more of the following: Process Validation, Cleaning Validation, Equipment Qualification, or CSV Desired Skills Strong understanding of validation life cycle and risk-based approach Good documentation and data review skills Ability to coordinate with cross-functional teams (Production, QA, QC, Engineering, IT) Audit readiness and familiarity with regulatory expectations Proficiency in MS Office and documentation systems Employment Type: Full-Time CTC: As per industry norms and candidate’s experience Show more Show less

Job Title: Manager – Section Head (Validation / Qualification / CSV) Location: Indore Plant Department: Quality Assurance (QA) Reports to: Head – Quality Assurance / Site Quality Head Role Summary We are seeking a highly experienced and self-driven professional to lead the Validation & Qualification section within the QA department. The incumbent will be responsible for overseeing end-to-end activities related to Process Validation, Cleaning Validation, Equipment & Facility Qualification , and Computer System Validation (CSV) . This is a managerial role requiring strong cross-functional collaboration, team leadership, and audit readiness for domestic and international regulatory inspections. Key Responsibilities Strategic Planning & Oversight: Lead the development and implementation of the site Validation Master Plan (VMP). Oversee all validation and qualification activities (Process, Cleaning, Equipment, Facility, CSV) to ensure compliance with cGMP and regulatory expectations. Allocate resources and manage workload for validation team to ensure timely execution. Process & Cleaning Validation Review and approve process validation protocols and reports in line with lifecycle approach. Ensure cleaning validation activities meet regulatory expectations and site-specific risk assessments. Support risk-based re-validation and continued process verification programs. Equipment / Facility / Utility Qualification Oversee IQ, OQ, PQ of new and existing equipment, HVAC systems, and utilities. Ensure periodic requalification and deviation handling. Review and approve all qualification documents and summary reports. Computer System Validation (CSV) Ensure GxP software and computer systems are validated as per GAMP 5 and 21 CFR Part 11 requirements. Collaborate with IT, Engineering, and external vendors for new system qualification, periodic reviews, and change management. Review and approve CSV documentation (URS, RA, IQ/OQ/PQ). Compliance & Audit Readiness Ensure all validation activities are audit-ready and compliant with USFDA, MHRA, EU-GMP, WHO, and other regulatory guidelines. Lead responses to regulatory queries and participate in audits and inspections. Maintain robust document control and support data integrity compliance across systems. Team Leadership & Development Lead a team of executives and senior executives in the validation function. Provide technical guidance, training, and performance feedback. Foster a culture of continuous improvement and compliance. Candidate Profile Qualification: B.Pharm / M.Pharm / M.Sc. (Life Sciences, Chemistry, Microbiology) Experience: 10–15 years in Pharmaceutical Quality Assurance, with minimum 5 years in handling validation/qualification/CSV independently Sound knowledge of GMP guidelines, ICH Q8–Q10, GAMP 5, and regulatory requirements Prior experience in handling regulatory audits (USFDA / MHRA / EU-GMP / WHO / ANVISA, etc.) Desired Skills Strong leadership and decision-making capabilities Excellent documentation, communication, and cross-functional coordination skills Proficiency in QMS systems, validation documentation tools, and MS Office Problem-solving mindset with a focus on risk-based, data-driven validation Employment Type: Full-Time Position Level: Manager – Section Head CTC: As per industry standards and candidate profile Show more Show less

Description Regulatory Consultant (Sterile Experience) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Job Responsibilities Primary Experience in regulatory submissions for sterile drug products, including aseptic and terminal sterilization processes. Preparation and review of Module 3.2.P sections related to sterile manufacturing, microbial control, and container closure systems. Post approval variation experience is mandatory for EU market. Familiarity with EU Annex 1 requirements and its application in variation, renewal submissions. Supports in preparation and peer review of regulatory submissions including variations, renewals, and responses to queries. Handling post-approval changes related to sterile facilities, cleanroom classification, sterilization methods, and equipment upgrades. Preparation of regulatory assessments and submission strategies specific to sterile dosage forms. Reviews of media fill protocols, filter validation data, sterility assurance, and cleaning validation documentation for submission readiness. Provides regulatory support during inspections and audits related to sterile manufacturing. Change control assessments and preparation of regulatory impact summaries. Day-to-day execution of tasks in accordance with client SOPs and regulatory standards for high-quality global CMC dossiers. Collaboration with cross-functional teams including QA, QC (microbiology), validation, technical, analytical, and site functions for data collection and dossier preparation. Secondary: Acts as a point of contact for coordination of documentation across functional teams to meet submission timelines. Effective communication through email and calls with internal and client stakeholders for updates and clarifications. Supports and mentors junior team members depending on project needs. Hands-on experience with RIMS/Veeva Vault. Open to working in cross-cultural and virtual team settings. Qualifications Minimum 6 years of experience required for regulatory submissions for sterile drug products with Master’s degree in pharmaceutical sciences (preferred) or Master’s degree in other life sciences. Demonstrated experience in contributing to the preparation of regulatory submissions including, for example IND, PMA, NDA, MAA, and CTD, including electronic submissions. Excellent interpersonal / communication skills including excellent written and verbal communication skills. Excellent customer service skills, with the ability to work both as a team member and independently. Good quality management skills. Advanced skills in Microsoft Office Applications. Ability to interact with staff from multiple departments and offices to establish project standards. Good initiative, adaptability, and pro-activity. Strong analytical skills, good attention to detail. Ability to work concurrently on projects, each with specific instructions that may differ from project to project. Fluent in speaking, writing, and reading English. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

We are seeking a qualified and experienced Consultant Microbiologist to oversee and manage microbiology laboratory services in our hospital/laboratory in Kurnool . The role includes ensuring quality assurance, accurate diagnostics, and adherence to infection control protocols. Key Responsibilities: Supervise daily operations of the microbiology lab Interpret and validate microbiological test results Ensure compliance with NABL/NABH standards and biosafety protocols Collaborate with clinicians for infection control and antimicrobial stewardship Maintain quality control documentation and lab reports Qualifications: MD in Microbiology or DNB (Microbiology) from a recognized institution Valid medical registration with NMC/State Medical Council Minimum 1–2 years of relevant experience preferred Schedule: Timing: 9:00 AM to 1:00 PM (Part-Time – 4 hours) Days: 6 days a week Salary: Attractive and negotiable based on experience Job Types: Full-time, Fresher Pay: ₹100,000.00 - ₹150,000.00 per month Benefits: Cell phone reimbursement Health insurance Leave encashment Paid sick time Provident Fund Schedule: Day shift Work Location: In person

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Self Supportive Training ll be provided for Fresher Required Candidate profile UG / PG in Life Science, Medical, Paramedical Dental, Pharmacy, Physio, Nursing, Microbiology, Biochemistry, Biotechnology, Biology, Bio-Medical, Zoology, Bioinformatics, Botony, Nutrition & Dietetics Perks and benefits 12700/- to 14600/- PM Excluding Special Allowances

We are looking for a skilled and experienced Microbiologist with 2–5 years of hands-on experience in microbiological processes, media optimization, and bioreactor handling. The ideal candidate will support R&D or QC functions in fermentation, strain maintenance, microbial analysis, and yield optimization for industrial and cosmetic applications. Key Responsibilities: Design and optimize culture media for microbial growth and product yield enhancement. Operate and monitor bench-top/lab-scale bioreactors for fermentation processes. Perform sub-culturing, strain preservation, and microbial storage (slant, glycerol stock, etc.). Calibrate lab instruments (e.g., pH meter, autoclave, incubator, spectrophotometer). Conduct biomass/yield analysis through gravimetric or spectrophotometric methods. Perform MLT for raw materials, in-process samples, and final products. Analyze purified water, RO water, and microbiological quality of water samples. Maintain detailed records of test procedures, observations, and results. Ensure proper aseptic handling, sterilization, and biosafety measures. Qualifications: Education: M.Sc. in Microbiology (mandatory) Experience: 2–5 years of relevant lab experience in fermentation, cosmetics, pharmaceuticals, or food industries. Key Skills: Strong knowledge of microbiological techniques and strain maintenance. Experience in handling fermentation processes and yield analysis. Expertise in lab equipment calibration and troubleshooting. Familiarity with water analysis, MLT, and standard microbiological testing. Good documentation and observation skills; ability to follow SOPs. Basic understanding of GLP/GMP and laboratory safety norms. Preferred Experience: Exposure to downstream processing (e.g., centrifugation, filtration). Experience in cosmetic ingredient fermentation or biopolymer production. Knowledge of microbial screening and strain improvement techniques. Salary & Benefits: Salary: As per industry standards Joining: Immediate or within 30 days preferred Show more Show less

Description Regulatory Consultant (Sterile Experience) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Primary Job Responsibilities Experience in regulatory submissions for sterile drug products, including aseptic and terminal sterilization processes. Preparation and review of Module 3.2.P sections related to sterile manufacturing, microbial control, and container closure systems. Post approval variation experience is mandatory for EU market. Familiarity with EU Annex 1 requirements and its application in variation, renewal submissions. Supports in preparation and peer review of regulatory submissions including variations, renewals, and responses to queries. Handling post-approval changes related to sterile facilities, cleanroom classification, sterilization methods, and equipment upgrades. Preparation of regulatory assessments and submission strategies specific to sterile dosage forms. Reviews of media fill protocols, filter validation data, sterility assurance, and cleaning validation documentation for submission readiness. Provides regulatory support during inspections and audits related to sterile manufacturing. Change control assessments and preparation of regulatory impact summaries. Day-to-day execution of tasks in accordance with client SOPs and regulatory standards for high-quality global CMC dossiers. Collaboration with cross-functional teams including QA, QC (microbiology), validation, technical, analytical, and site functions for data collection and dossier preparation. Secondary Acts as a point of contact for coordination of documentation across functional teams to meet submission timelines. Effective communication through email and calls with internal and client stakeholders for updates and clarifications. Supports and mentors junior team members depending on project needs. Hands-on experience with RIMS/Veeva Vault. Open to working in cross-cultural and virtual team settings. Qualifications Minimum 6 years of experience required for regulatory submissions for sterile drug products with Master’s degree in pharmaceutical sciences (preferred) or Master’s degree in other life sciences. Demonstrated experience in contributing to the preparation of regulatory submissions including, for example IND, PMA, NDA, MAA, and CTD, including electronic submissions. Excellent interpersonal / communication skills including excellent written and verbal communication skills. Excellent customer service skills, with the ability to work both as a team member and independently. Good quality management skills. Advanced skills in Microsoft Office Applications. Ability to interact with staff from multiple departments and offices to establish project standards. Good initiative, adaptability, and pro-activity. Strong analytical skills, good attention to detail. Ability to work concurrently on projects, each with specific instructions that may differ from project to project. Fluent in speaking, writing, and reading English. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Show more Show less

Overview Overview : Bruker is enabling scientists to make breakthrough discoveries and develop new applications that improve the quality of human life. Bruker’s high-performance scientific instruments and high-value analytical and diagnostic solutions enable scientists to explore life and materials at molecular, cellular and microscopic levels. In close cooperation with our customers, Bruker is enabling innovation, improved productivity and customer success in life science molecular research, in applied and pharma applications, in microscopy and nanoanalysis, and in industrial applications, as well as in cell biology, preclinical imaging, clinical phenomics and proteomics research and clinical microbiology. Today, worldwide more than 8500 employees are working on this permanent challenge at over 90 locations on all continents. Bruker continues to build upon its extensive range of products and solutions, its broad base of installed systems and a strong reputation among its customers. Being one of the world's leading analytical instrumentation companies, Bruker is strongly committed to further fully meet its customers’ needs as well as to continue to develop state-of-the-art technologies and innovative solutions for today's analytical questions. Bruker India is looking for an experienced Remote Support Engineer (Analytical Instruments) to be based in based in Bengaluru, India . Responsibilities Essential Functions : Work Remotely With Customers To Diagnose BAXS Instruments Like Xray Diffractometers, Fluorescence Spectrometers, Single Crystal Diffractometers, Optical Emission Spectrophotometers Including But Not Limited To Diagnose, test, develop, optimize, communicate, and execute the most efficient solution plan for complex electromechanical hardware/software instrument issues, operations and training related issues. Optimize instrument and/or accessory performance to meet specification. Create and maintain record of activity in support database Provide a great customer experience through the entire support process Ask customers targeted questions to quickly understand the root cause of their instrument issues. Effectively communicate with end-users to understand the technical issues or concerns via various channels (phone, email, Chat etc.) to identify and resolve them within short time. If the first level customer support is unsuccessful, using ticket management and transferring call will be pushed to second level remote support team If job demands for onsite support, engineer should travel and support customers within short notice. Experience in dealing with analytical instruments like spectrophotometers, X-ray based instruments or optical measuring systems is a must Leverage internal technical expertise, including peers, mentors, knowledge base, community forums and other internal tools, to provide the most effective solutions to customer issues. Build knowledge base to reduce reliance over time on other internal resources. Contribute to internal technical knowledge base and publish Frequently Asked Questions to enable customer self-support. Accurately document and update tickets in the tracking systems. Ability to maintain a personal queue of open requests. Maintain communication with the customers on the status of all open tickets. All responses should be professional, complete, well formatted, and consistent with prior communications and Corporate Identity. Future outbound activities as follow up possible (updates, surveys) Properly escalate unresolved issues to appropriate technical support teams Provide necessary information/observations/logs - all the required data to next level support or R&D team to diagnose a reported/escalated problem. Ability to describe incident and requests as part of a ticket management. Ability to create and update operational procedures and proposal of decision trees. (issues resolution, requests, and administration procedures) Perform other tasks as assigned by manager. The job demands to work in rotational shifts (Monday through Friday). 20% on field and 80% on office Excellent customer relation skills and the ability to make timely and effective decisions is a plus. Other duties as assigned Qualifications Knowledge, Skills and Abilities : Customer focused, passionate about science and technology, and eager to enable customers with Bruker technology. Demonstrated Excellent analytical capabilities and theoretical understanding of physics. Customer service-oriented working experience in technology-based instruments like XRD, XRF, OES to support various technical issues Working knowledge of electronics, mechanics, control systems, computers, networking. Able to use common electrical testing tooling like oscilloscopes, multimeters, etc. to be an effective problem solver of complex system, product user, and/or application issues. Demonstrated ability to provide clear, logical, and effective communication in English. Ability to communicate effectively in a professional and friendly manner with both internal and external customers. Experienced in use of Salesforce (CRM) and SAP preferred is a plus Should have worked on remote support tools, e.g., TeamViewers, Webex, any desk. The personality of a natural team player, willing and able to build confidence and to establish strong co-operative relationships with personnel throughout the company, customer base and with key individuals within the industry. A flexible attitude to working hours which are sometimes influenced by factors such as the need to complete the job or the availability of the client. For further development, engineer should be willing in general to travel up to 20% Students of Engineering & Science background are welcome. Start your service career with first step in making our clients happy. Language skills in addition to English are welcome. Education BE/BTech in Electronics/ Electrical/ Instrumentation, MSc in Physics, Chemistry and Material Science Should have a technical education and / or worked already as a technician. Experiences At least 1 year of previous service experience or hotline activity within electronic systems Technical expertise in electronics and mechanics Confident in handling all common PC operating systems and networks Bruker is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, national origin, disability, veteran status, and other protected characteristics. Show more Show less

Job Title: QC Executive – (RM / FG / Stability / AMV & PV / Microbiology) Location: Indore – Regulated Pharma Manufacturing Plant Department: Quality Control Reporting To: QC Manager / Head – Quality Control Job Type: Full-Time | Executive Level Job Purpose To perform quality control testing and analysis of raw materials, finished products, stability samples, and microbiological parameters as per current Good Manufacturing Practices (cGMP), standard operating procedures (SOPs), pharmacopeial standards, and regulatory requirements to ensure product quality and compliance. Key Responsibilities Testing and Analysis Perform chemical and instrumental testing of Raw Materials (RM) and Finished Goods (FG) as per pharmacopeial and in-house specifications. Conduct Stability Studies in line with ICH guidelines and maintain records of stability trends. Execute Analytical Method Validations (AMV) and support Process Validation (PV) testing. Carry out Microbiological analysis of samples, including environmental monitoring, water testing, and microbial limit tests. Documentation and Compliance Maintain accurate, complete, and timely documentation (analytical reports, logbooks, LIMS/ERP entries). Ensure compliance with cGMP, GLP, and regulatory standards (USFDA, EU-GMP, WHO, etc.) . Participate in internal audits, external regulatory inspections , and implement CAPAs. Prepare and review standard operating procedures (SOPs), specifications, and testing protocols. Equipment Operation & Calibration Operate and calibrate instruments like HPLC, GC, UV, IR, Dissolution Apparatus, FTIR, etc. Ensure timely preventive maintenance and validation of QC instruments. Cross-functional Coordination Coordinate with Production, QA, Regulatory Affairs, and other relevant departments to resolve testing issues and support product release timelines. Participate in investigations of OOS/OOT results, deviations, and change controls. Key Skills & Competencies Sound knowledge of cGMP/GLP and ICH guidelines. Hands-on experience with analytical instruments and microbiology techniques. Strong documentation and data integrity practices. Good communication and team collaboration skills. Eye for detail and high level of integrity. Educational Qualifications B.Pharm / M.Pharm / M.Sc. (Chemistry / Microbiology / Pharmaceutical Sciences) Experience 2–5 years of relevant experience in a regulated pharmaceutical manufacturing environment. Preferred Certifications Training in Data Integrity, cGMP, QMS, or Instrument Handling is an advantage. Show more Show less

Vacancy for Associate Professor Microbiology Qualification- MD/DNB Microbiology Salary- Best in industry Accommodation- Available Eligibility- As Per NMC Norms Job Type: Full-time Schedule: Day shift Work Location: In person

Work Location: Salem Number of Vacancies: 2 Gender Preference: Male Age Requirement: Candidates must be below 30 years of age Work Experience: Open to both recent graduates and experienced individuals Qualifications: Bachelor of Science (B.Sc) in Physics, Microbiology, Biochemistry, Chemistry or Biotechnology. Other science graduates may also apply, excluding those with a degree in Computer Science. Nature of work: Field Sales Salary: Competitive, starting from 15000, subject to finalization based on the candidate’s experience and qualifications Benefits: Yearly Bonus, Allowenses, Provident Fund and ESI Key Responbilities: Exploring new sales opportunities is essential for business growth, and this can be achieved through various methods such as networking, cold calling, and thorough research. It's important to clearly understand and communicate the benefits of the products being sold. A structured approach should be followed for qualifying leads, delivering presentations, and successfully closing sales. Additionally, providing accurate sales forecasts and reports to management helps in strategic decision-making. Staying informed about industry trends and competitors allows for a competitive edge. Lastly, delivering engaging presentations and ensuring effective communication enhances the overall sales process. Company Profile: We specialize in the trading of laboratory chemicals, educational furniture, lab glassware, and laboratory instruments. Website: www.psccbe.com Job Types: Full-time, Permanent, Fresher Pay: From ₹15,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person

Position : Medical Coder (Nutrition And Dietetics, Food Microbiology) Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Eligibility: UG / PG in Nutrition & Dietetics, Neuro Science, Food Microbiology, Industrial, Medical, Applied Microbiology, Genomics, Plant Biology, Advance Zoology, Radiology, Emergency Care, Anesthesia, Cardiac Perfusion, Physician Assistant Job Types: Full-time, Fresher Pay: ₹175,000.00 - ₹250,000.00 per year Benefits: Health insurance Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person

Position Overview We are seeking an accomplished and visionary Scientist to lead advanced research and development efforts in algae-based systems for carbon dioxide (CO₂) conversion and protein production . The successful candidate will be responsible for designing and developing scalable, closed-loop culture systems that support climate mitigation strategies and contribute to a circular economy. This leadership role requires deep domain expertise in algal biotechnology and bioprocess engineering , along with a demonstrated ability to manage multidisciplinary teams, oversee laboratory operations, and collaborate with both national and international research institutions. The selected candidate will be expected to drive high-impact research initiatives, mentor scientific staff, and support the translation of innovation into practical application. Key Responsibilities Scientific Leadership and Innovation ● Lead the design, prototyping, and optimization of algae-based systems for CO₂ absorption, oxygen generation, and biomass production. ● Develop methods to enhance photosynthetic efficiency and algal growth rates while ensuring minimal energy consumption. ● Integrate principles from biology, material science, and process engineering to design compact, closed-loop systems. ● Support the development and refinement of gas-liquid exchange, nutrient delivery, waste removal, and long-term system stability. Research and Development ● Conduct bench-scale and pilot-scale experiments to assess system performance under controlled conditions. ● Record, analyze, and report key performance metrics including CO₂ conversion efficiency, oxygen output, biomass yield, and energy utilization. ● Investigate mass transfer dynamics and optimize gas diffusion and mixing within algal bioreactors. ● Explore methodologies for algal strain isolation, cultivation, harvesting, dewatering, drying, and bio-compound extraction. Laboratory Operations ● Oversee day-to-day operations of the algal laboratory, including inoculum development, media preparation, and environmental control. ● Supervise the use and maintenance of analytical and biological instrumentation. ● Ensure adherence to standard operating procedures, safety guidelines, and regulatory requirements. ● Lead troubleshooting efforts and provide guidance on system development, maintenance, and repair. Team Management and Collaboration ● Collaborate with a multidisciplinary team comprising scientists, engineers, and technical staff. ● Prepare and present technical reports, experimental schematics, and scientific publications. ● Serve as a liaison with external collaborators, including research institutions and industry partners. ● Contribute to proposal development for research grants and business development opportunities. Required Qualifications ● PhD or Master’s degree in Microbiology, Biotechnology, Biochemistry, Aquaculture, Bioprocess Engineering, or a closely related field. ● Minimum of 2 years of direct experience in algal cultivation systems and their applications. ● Solid understanding of algal physiology, algal biomass application and environmental system control. ● Extensive publication record in peer-reviewed scientific journals. ● Experience with innovation-driven projects, bioeconomy strategies, or technology commercialization is desirable. ● Excellent communication, and project management skills. Preferred Technical Expertise ● Algal inoculum development, media formulation, and optimization of environmental parameters. ● Proficient operation of biological and analytical laboratory instruments. ● Capability to perform data-driven system diagnostics and technical troubleshooting. Compensation and Benefits ● Competitive salary commensurate with experience and qualifications ● Comprehensive medical insurance coverage ● Opportunity to lead high-impact research in sustainable biotechnology and contribute to global climate solutions Job Type: Full-time Pay: ₹380,000.00 - ₹540,000.00 per year Benefits: Health insurance Work Location: In person

West coast pharma is looking for Product design development assistant - Female preferred Qualification: MSC/BSC Experience: 0 to 2 years only (Fresher are also apply) Job Role: Product Designer Development Assistant (Pharma) Assist in designing and developing pharmaceutical products in alignment with regulatory and industry standards. Conduct research on market trends, materials, and innovations to support product development. Collaborate with cross-functional teams, including R&D, quality assurance, and production. Maintain accurate documentation of design processes, formulations, and testing. Support the preparation of prototypes and samples for evaluation. Assist in ensuring compliance with regulatory requirements during the design and development phases. Monitor and report on project progress and provide updates to the design and development lead. Handle administrative tasks related to product design and development. Job Type: Full-time Pay: ₹10,000.00 - ₹50,000.00 per month Work Location: In person

About Food Whisperer: Food Whisperer is a dynamic and rapidly growing food brand committed to delivering exceptional culinary experiences through innovation, quality, and customer focus. About Manager – HSEQ: The Manager - HSEQ will play a critical role in ensuring that our Kitchen Staff and cafeteria operations comply with all food safety regulations and standards. This position involves implementing, monitoring, and improving food safety protocols to maintain the highest levels of hygiene and safety in all food handling processes. Roles & Responsibilities: • Execute Food Safety audit as per FSSAI requirement. • Conduct customized audit across Catering/Base Kitchen Audits/ Live kitchen Audits. • Reports to be submitted within 2 working days. • Follow up of NC closure for both external and internal audits. • Ensure developed corrective action on nonconformities are implemented effectively. • Supporting for the preparation of external audits. • Involved in root cause analysis for the identified non-conformities or complaints. • Verify the corrective action implementation effectiveness. Prerequisites: Educational Qualification – bachelor’s degree in food science and technology or Microbiology or Hotel management or catering technology from recognized university. Preference would be given if acquired Accredited Lead Auditor Course in food safety Management System (ISO22000/FSSC22000). Have sufficient Knowledge of FSS Act and regulation. Must have sector specific knowledge regarding Hygiene, Sanitary practices, process knowledge, Allergen management, etc. Certified internal auditor on ISO 22000 / HACCP. Knowledge in Quality and Food Safety Management System Show more Show less

🚨 We're Hiring! | Sales & Application Engineer 📍 Locations: Madhya Pradesh | Maharashtra | Chennai | Ahmedabad 🏢 iGene Labserve Pvt. Ltd. 🧪 Industry: Life Sciences | Diagnostics | Laboratory Equipment 🛠 Hybrid Role | Mechanical & Electrical Engineering Backgrounds Welcome We’re looking for skilled and motivated professionals with 1–6 years of experience in Mechanical , Electrical and Biotechnology and Microbiology to join our Sales & Technical Support Team. If you're passionate about servicing lab instruments, offering technical support, and contributing to innovation in the biotech and diagnostic field — we want you on our team! 📌 Key Responsibilities ✔ Installation & maintenance of laboratory instruments ✔ On-site and remote technical support ✔ Customer training, demos & documentation ✔ Regional travel for client support and service 💼 Hybrid Work Model 📧 Apply Now: hr@igenels.in 📞 Contact: +91 88510 83349 Let’s build the future of diagnostics — together! #NowHiring #ServiceEngineer #SalesEngineer #TechnicalJobs #iGeneLabserve #LifeSciencesCareers #DiagnosticsJobs #AhmedabadJobs #ChennaiJobs #MaharashtraJobs #MPJobs #MechanicalJobs #ElectricalJobs Show more Show less

This position is part of the Quality Organization and will be in India. Reporting directly to the Quality Control lead or site lead, the Quality Control Analyst is responsible for managing the day today activities quality control function at Cepheid India Private Ltd. Ensure compliance of quality control procedures as per MDR 2017, European regulations, ISO 13485, Cepheid corporate quality system requirements. In this role, you will have the opportunity to: Conducts routine and non-routine analysis of raw materials, in-process and finished formulations under supervision and according to Standard Operating Procedures (SOPs). Competent technical staff for supervision the Testing/ analysis of diagnostic reagents & kits. Perform inspections of incoming, in-process and finished products. Performs and calibration and maintenance of lab equipment as per requirements. May perform special projects on analytical and instrument problem solving. Ensure that lab cleanliness and safety standards are maintained. Qualify test methods as part of new product development activities. Serve as a technical liaison between quality control and other departments Write technical reports or documentation such as deviation reports, testing protocols, and trend analyses & Write or revise standard quality control operating procedures. Perform validations or transfers of analytical methods in accordance with applicable policies or guidelines. Follow documentation procedure (filling out Data History Records (DHRs), reading and understanding instructions from Work Release (WR), Planned Deviation Report (PDR) or Non-Conformance Report (NCR). Read and follow Standard Operating Procedures (SOPs) and Manufacturing Work Instructions. Review records and documents for completeness and compliance with company policies and procedures. Support for internal audit schedule, NC, CAPA for site. Review production batch records, QC test results and release product. Education and Experience: masters degree in Biochemistry, Molecular Biology, Microbiology or related discipline and a minimum of 3+ years related Quality Control experience. 2+ years experience with in Vitro Diagnostics (IVD) is mandate Experience with in Vitro Diagnostics (IVD) is very beneficial and highly desirable Quality competent technical person approved as per D&C act if any Knowledge and skills: Hands on Experience on IVD product testing. Working Knowledge of current GxP regulations for Invitro Medical Devices and ISO 13485 QMS. Must be flexible to work off-shifts and weekends as per production Schedule. Schedule orientated (able to consistently maintains schedules and meet timelines) Strong interpersonal skills, Effective organization and Communication skills are essential. Good skills in English language Knowledge of Microsoft Word and Excel Strong multi-tasking and attention to details skills. It would be a plus if you also possess previous experience in: Experience working with medical device quality systems in compliance with MDR and ISO 13485 Able to interpret quality problem and establish practical solutions within a dynamic business environment. Experience in leading continuous improvement efforts, in both quality systems and products. Knowledge of the process of establishing facility QMS certifications. Cross functional experience with products and manufacturing processes to influence change at all levels within the organization Visio and Project knowledge desirable

This position is part of the Quality Organization and will be in India. Reporting directly to the Quality Control lead or site lead, the Quality Control Analyst is responsible for managing the day today activities quality control function at Cepheid India Private Ltd. Ensure compliance of quality control procedures as per MDR 2017, European regulations, ISO 13485, Cepheid corporate quality system requirements. In this role, you will have the opportunity to: Conducts routine and non-routine analysis of raw materials, in-process and finished formulations under supervision and according to Standard Operating Procedures (SOPs). Competent technical staff for supervision the Testing/ analysis of diagnostic reagents kits. Perform inspections of incoming, in-process and finished products. Performs and calibration and maintenance of lab equipment as per requirements. May perform special projects on analytical and instrument problem solving. Ensure that lab cleanliness and safety standards are maintained. Qualify test methods as part of new product development activities. Serve as a technical liaison between quality control and other departments Write technical reports or documentation such as deviation reports, testing protocols, and trend analyses Write or revise standard quality control operating procedures. Perform validations or transfers of analytical methods in accordance with applicable policies or guidelines. Follow documentation procedure (filling out Data History Records (DHRs), reading and understanding instructions from Work Release (WR), Planned Deviation Report (PDR) or Non-Conformance Report (NCR). Read and follow Standard Operating Procedures (SOPs) and Manufacturing Work Instructions. Review records and documents for completeness and compliance with company policies and procedures. Support for internal audit schedule, NC, CAPA for site. Review production batch records, QC test results and release product. Education and Experience: masters degree in Biochemistry, Molecular Biology, Microbiology or related discipline and a minimum of 3+ years related Quality Control experience. 2+ years experience with in Vitro Diagnostics (IVD) is mandate Experience with in Vitro Diagnostics (IVD) is very beneficial and highly desirable Quality competent technical person approved as per DC act if any Knowledge and skills: Hands on Experience on IVD product testing. Working Knowledge of current GxP regulations for Invitro Medical Devices and ISO 13485 QMS. Must be flexible to work off-shifts and weekends as per production Schedule. Schedule orientated (able to consistently maintains schedules and meet timelines) Strong interpersonal skills, Effective organization and Communication skills are essential. Good skills in English language Knowledge of Microsoft Word and Excel Strong multi-tasking and attention to details skills. It would be a plus if you also possess previous experience in: Experience working with medical device quality systems in compliance with MDR and ISO 13485 Able to interpret quality problem and establish practical solutions within a dynamic business environment. Experience in leading continuous improvement efforts, in both quality systems and products. Knowledge of the process of establishing facility QMS certifications. Cross functional experience with products and manufacturing processes to influence change at all levels within the organization Visio and Project knowledge desirable.