2560 Microbiology Jobs - Page 32

About Us We are the independent expert in assurance and risk management. Driven by our purpose, to safeguard life, property, and the environment, we empower our customers and their stakeholders with facts and reliable insights so that critical decisions can be made with confidence. As a trusted voice for many of the world’s most successful organizations, we use our knowledge to advance safety and performance, set industry benchmarks, and inspire and invent solutions to tackle global transformations. About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About The Role As part of our continued growth, we are looking to recruit technical and experienced In-Vitro Diagnostic Medical Device Assessors and Lead Auditors. The successful candidates will be responsible for planning and conducting audits / assessments against the manufacturing of medical devices, in accordance with ISO 13485, IVDR 2017/746 and MDSAP standards, enabling the delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards. Key Accountabilities: Assessor Conduct assessments (either desk-based or on client’s sites) in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer communication. Conduct Technical File reviews specific for products being authorized. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete specific projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification decisions within target timescales and in line with DNV policies and accreditation/approval requirements. Key Accountabilities: Auditor Responsible to carry out audits of the manufacturer's quality management system (QMS) and of its suppliers and/or subcontractors when appropriate and to draw up records and reports on the corresponding audits. Conduct surveillance audits including follow-up activities in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer relationships. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification recommendations within target timescales and in line with DNV policies and accreditation/approval requirements. Project manage auditing teams, as appropriate, to maximize efficiencies, enhance client satisfaction and ensure compliance with standards. What we offer Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. *Benefits may vary based on position, tenure/contract/grade level* DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity. About You Assessors and Auditors shall have a technical college degree in a relevant product or medical area, as described below. In-Vitro Diagnostic devices: Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology Education In addition to a relevant educational degree, candidates must have a minimum 4 years’ work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the design, manufacturing, testing or use of the device in which they are qualified to Audit or Assessment, and/or experience as an assessor or auditor in a notified body. Specifically: Auditor - Practical experience in the quality management system and specific production process/technologies for the IVD medical devices. Assessor - Practical experience in conducting and/or assessing performance evaluation data or related scientific aspects with in-vitro diagnostic medical devices in one or more of the following areas Microbiology, Immunology, Genetic testing/Cancer Biology and Molecular Biology. A PhD in a relevant area for in-vitro diagnostic medical devices can substitute 3 years of work experience provided it includes 2 years’ experience in design, manufacture or testing. In addition to the above, knowledge of the following would be preferred: An excellent working knowledge of medical device management systems, standards and medical device compliance/auditing techniques. Work experience in positions with significant QA Regulatory or management systems responsibility. Experience with Harmonized medical device standards for In-Vitro diagnostic medical devices. Experience with Risk Management EN ISO 14971. Medical device experience from auditing/work. Experience auditing against recognized standards. Experience of working under own initiative and in planning and prioritizing workloads. Should have a flair for technical writing, essential for exhaustive report writing.

Job Category: Quality Job Family: Plant Quality Assurance Job Description: To ensure microbiology laboratory function operation and full compliance as per company requirement . This position is a combination of a subject matter expertise in Microbiology that requires people leadership and customer facing skills. The successful candidate and will lead (direct & indirect) the efforts of development, implementation, training, troubleshooting, and auditing of microbiological methods and best practices; work with customers on their expectations and ensure we are complaint with them; and work with operations to identify trends, implement action plans, oversee appropriate CAPA development driven by data; and instill Food Safety Quality Culture through words and actions. Duties include ensuring full compliance of the Baramati plant Main micro laboratory function, which includes ensuring the laboratory safe, accurate, and timely functioning. Hiring, retaining, training and coaching partners. Maintaining compliance through internal audits and ensuring all internal, regulatory and customer s requirements are fully compliant. Evaluating partner performance, including partner accountability for adherence to microbiology department functions including but not limited to sampling, analysis, ensuring all monitoring plan are met, data / information trending and communication and Proficiency test participation, ISO 17025 or good laboratory practices management compliances. In addition to microbiology function, this role will provide support and active involvement in leading continuous improvement and expertise related food safety and sanitation related improvement process mainly to Baramati plant and as and when required to other plant of India region. Will be closely collaborating with EQFS SFI microbiologist What you ll do: Serves as laboratory microbiology leader and technical resource to collaborate with operations leaders on expectations, results interpretation, sampling plans (including customer-specific and regulatory requirements), method use, determining process capabilities/troubleshooting, and projects and programs as required. Coordinate and be the primary contact for external labs. Meet with external customers to explain programs and results. Provide input and work with departments on conducting risk assessments for HACCP and quality of products and processes. Be able to explain programs and requirements for customer and regulatory auditors. Lead the microbiology team on microbiology lab management and accreditation requirements. Remove barriers for testing execution and provide direction on methods that should be used. Promote safe working environments for partners. Review and optimize sampling as per risk and review workload of partner. The role is responsible for laboratory information system implementation and assuring adherence of partners to use the system effectively. Ensure all requirements Good Laboratory Practices and customer testing expectations (ex. ISO17025 or equivalent) are being met. Evaluate CAPAs for thoroughness and effectiveness - within operations, sanitation, as well as within the laboratory. Escalate outages and work with corporate Home Office as necessary to resolve issues. Support all India facilities as needed. Develop Food Safety and Quality and Culture - train, coach, evaluate, and reinforce continuous improvement principles with partners as well as personal, people, business, and process leadership. Support all India facilities as needed. Work with corporate Food Safety & Microbiology partners or topics of Pathogen Environmental Monitoring expectations, formula evaluation & process food safety, method validations & changes, etc. Assist with troubleshooting of issues at other plants as needed (may be outside of India). Support new projects to assess food safety evaluation along with key stake holders. Closely with all plants and support India region Food Safety and Sanitation process by working on development /improvement of systems, training partners, implementing and reviewing Food safety systems. Support in trouble shooting of the process when required to overcome the challenges and applying / implementing lessons learned as applicable. Financial - Track and maintain control of department budgets to assure plant goals are met. Plan for capex for laboratory and food safety related. Plan for capex for laboratory and food safety related. What you need to succeed: M. Sc Microbiology 10+ years experience in Quality Assurance, Food Safety or Production Subject-matter expertise Incumbent shall have a sound knowledge of microbiology analysis of food and food products HACCP and Food safety risk assessment preferably in field of microbiology Performance skills (accuracy with detail, planning and organizing, efficiency, business acumen) Good technical communication skills explaining programs and policies to internal and external people and bodies Good documentation skills Comfortable in a food manufacturing environment as well as in a laboratory Leadership Leadership skills in managing and developing team Interpersonal skills (relationship building, teamwork, interpersonal insight, conflict resolution, customer orientation) Communication (verbal communication, persuasive impact, listening, written communication) - English preferred Judgment and thinking (strategic thinking, original thinking, judgment and decision making, problem solving, awareness) Personal characteristics (motivation/commitment, flexibility, assertiveness, development orientation, results orientation resilience, quality orientation) Excellent interpersonal and problem-solving abilities Comfortable escalating situations to leadership as needed Ability to make good business decisions quickly Desire to grow and take on new challenges and opportunities Ability to travel up to 5-10%

Leading pharmaceutical company looking for Microbiologist Position: Microbiologist Designation :Trainee/Jr.Officer package : 1.50 lacs pa No post : 8 nos. location ; Gandhinagar District, Gujarat. email cv : hr@tgigroup.in

Purpose: The Global Patient Safety (GPS) organization is responsible for delivering scientific, medical and pharmacovigilance expertise in support of Lilly s products in development as well as for marketed medicines and devices globally. The Clinical Surveillance Scientist leverages clinical and scientific expertise to lead the detection of safety signals, evaluation of safety data, assessment of safety risks, responses to regulatory inquiries, and regulatory-required periodic reporting. In this role, you will apply effective prioritization, critical thinking, and judgment-based decision making to execute these key deliverables in compliance with global regulations and internal processes. Effective communication and influence with internal and external stakeholders is an important capability for this role. Primary Responsibilities: This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervisor regarding your actual job responsibilities and any related duties that may be required for the position. Signal Detection and Safety Data Evaluation Drive the identification, analysis, and evaluation of safety signals that arise from multiple internal and external data sources to determine signals or risks that could result in changes to labels and/or benefit-risk profile and consult and collaborate with other safety personnel as appropriate. Develop and review label changes and labelling modifications in collaboration with teams, regulatory and legal. Apply effective communication skills to lead and facilitate safety team meetings for compounds in clinical development and marketed products Define data acquisition strategy, methodology, and approach for safety evaluations. Perform analysis of safety data and lead authoring of safety topic reports Collaborate with GPS Medical physicians, scientists, pharmacoepidemiologists, and other personnel as appropriate to ensure thorough evaluation and aggregate analysis of safety data, demonstrating the ability to understand and communicate scientific issues and strategy Communicate relevant safety information to core team, business partners, and key stakeholders in a timely manner. Apply judgment-based decision-making principles to contribute to key scientific/clinical discussions Risk Assessment, Regulatory Inquiries, and Periodic Reporting Lead analysis of safety data and author relevant safety sections of global regulatory inquiries and periodic reports including Development Safety Update Reports (DSURs), Periodic Adverse Drug Experience Report (PADER)/ Periodic Adverse Experience Report (PAER), Periodic Safety Update Reports (PSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs), and Risk Management Plans (RMPs) Provide input to safety communications in the form of labeling, medical information inquiries, and healthcare professional (HCP) letters Promote and Advance the Field of Pharmacovigilance Responsible for effective communication and influence with internal Lilly customers (e.g. medical, regulatory, labeling) and external stakeholders (e.g. FDA, MHRA, EMA, other regulatory agencies) Accelerate the advancement of and contribute to the development and coaching of peers and less experienced employees Identify and develop innovative approaches to continuously improve organizational effectiveness and productivity Effectively function and communicate as part of inclusive cross functional teams (e.g. GPS Medical physicians and scientists, Pharmacoepidemiologists, Research and Business Unit team members, other safety personnel) that foster trust, respect, and accountability Demonstrate and apply pharmacovigilance knowledge, including the role of the QPPV, to ensure compliance with local laws and regulations Adhere to requirements in quality system document and process improvement initiatives to ensure compliance with local laws and regulations Minimum Qualification Requirements: Advanced medical related graduate degree, such as: pharmacy (PharmD), nursing with advanced clinical specialty (Clinical Nurse Specialist/Nurse Practitioner), PhD with 1-3 years experience in related scientific field, e.g. pharmacology, physiology, microbiology or scientifically related field. OR BS degree in a health-related or scientific field with 7-10 years of experience in pharmaceutical industry, directly related clinical trial experience or experience in areas relevant to drug discovery or development, e.g. epidemiology, toxicology, pharmacovigilance, regulatory affairs. OR 3-5 years of clinical experience or 3-5 years of pharmaceutical experience, at least 2 years of which was clinical development experience Other Information/Additional Preferences: Clinical knowledge of various disease states, drug effects, human physiology and pharmacology Experience within Global Patient Safety or demonstrated understanding of Pharmacovigilance is preferred Demonstrated ability to manage multiple deliverables simultaneously Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability, or any other legally protected status. . .

Inspector - Chennai Cotecna is a leading provider of testing, inspection and certification services. Founded in Switzerland in 1974, Cotecna started off as a family business and has now grown to become a world-class international player with over 7000 employees in more than 140 offices across 50 countries. To perform coordination of inspection orders for PSI clients. Key Responsibilities Carry out pre shipment physical inspection (PSI) in line with QMS and specific operating guidelines Undertake physical inspection of goods as per Company guidelines. Submit Inspection reports to department. Maintain accurate, impartial and factual reporting of inspection carried out and in any communication with customers. Provide feedback on any competitor activity or possible commercial inspection opportunities that may be gleaned during an inspection Qualifications, Experience and Technical Skills Science Graduate in Microbiology, Chemistry or Agriculture-MUST Exp - Fresher or 1-2 years of field experience

Inspector - Kandla/Gandhidham/Mundra Cotecna is a leading provider of testing, inspection and certification services. Founded in Switzerland in 1974, Cotecna started off as a family business and has now grown to become a world-class international player with over 7000 employees in more than 140 offices across 50 countries. To perform coordination of inspection orders for PSI clients. Key Responsibilities Carry out pre shipment physical inspection (PSI) in line with QMS and specific operating guidelines Undertake physical inspection of goods as per Company guidelines. Submit Inspection reports to department. Maintain accurate, impartial and factual reporting of inspection carried out and in any communication with customers. Provide feedback on any competitor activity or possible commercial inspection opportunities that may be gleaned during an inspection Qualifications, Experience and Technical Skills Science Graduate in Microbiology, Chemistry or Agriculture-MUST Exp - Fresher or 1-2 years of field experience

Business Development Manager We are seeking a dynamic and experienced Business Development Manager to lead and grow our testing and analytical services across Food, Pharmaceutical, and Environmental sectors . The ideal candidate will have a strong background in sales and business development within the TIC (Testing, Inspection, Certification) industry , specifically in the Food or Pharma division. This is a Pan-India role requiring strategic thinking, client acquisition skills, and market penetration capability. Location: Pan India (Travel Required) Experience: Minimum 7 Years Industry Preference: TIC Industry (Food or Pharma Division) Key Responsibilities: Identify, target, and secure new business opportunities across Food, Pharma, and Environmental Testing domains. Build and nurture client relationships with key decision-makers at manufacturing units, regulatory bodies, exporters, and service providers. Develop and execute Pan-India sales strategies to achieve revenue and market share growth. Monitor market trends, competitor activities, and customer needs to inform business strategies. Collaborate with technical teams to offer tailored testing solutions and ensure customer satisfaction. Drive business growth in both existing and new verticals, including potential expansion into allied industries. Participate in trade shows, industry events, and customer meetings to promote services. Prepare proposals, negotiate contracts, and close deals. Generate regular sales forecasts, pipelines, and performance reports. Ensure full compliance with regulatory requirements and internal quality systems. Requirements: Minimum 7 years of experience in B2B sales and business development in the Food, Pharma, or Environmental Testing sectors. Must be from the TIC (Testing, Inspection, Certification) industry , preferably from Food or Pharma testing divisions. Proven Pan-India exposure and strong client network in the above sectors. Deep understanding of national and international testing standards, FSSAI, FDA, MoEF, etc. Strong communication, negotiation, and presentation skills. Willingness to travel extensively across India. Bachelor’s or Master’s Degree in Chemistry, Microbiology, Pharma, Environmental Science, or related field. MBA is a plus. How to Apply: Interested candidates who meet the above criteria are invited to send their updated resume along with a cover letter to: 📧 [Sangita.sheet@efrac.org/talentacquisition@efrac.org] 📌 Please mention "Application for BDM – Food/Pharma Testing" in the subject line.

About Us We are the independent expert in assurance and risk management. Driven by our purpose, to safeguard life, property, and the environment, we empower our customers and their stakeholders with facts and reliable insights so that critical decisions can be made with confidence. As a trusted voice for many of the world’s most successful organizations, we use our knowledge to advance safety and performance, set industry benchmarks, and inspire and invent solutions to tackle global transformations. About SCPA We help our customers respond to the increased demand for trust and transparency around products, assets, supply chains, and ecosystems, driving the transformation of the assurance industry. Whether certifying products, sharing claims or optimizing and decarbonizing supply chains, DNV helps companies manage risks and realize their long-term strategic goals, improving ESG performance and generating lasting, sustainable results. Drawing on our wide technical and industry expertise, we work with companies worldwide to bridge trust gaps among consumers, producers and suppliers. About The Role As part of our continued growth, we are looking to recruit technical and experienced In-Vitro Diagnostic Medical Device Assessors and Lead Auditors. The successful candidates will be responsible for planning and conducting audits / assessments against the manufacturing of medical devices, in accordance with ISO 13485, IVDR 2017/746 and MDSAP standards, enabling the delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards. Key Accountabilities: Assessor Conduct assessments (either desk-based or on client’s sites) in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer communication. Conduct Technical File reviews specific for products being authorized. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete specific projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification decisions within target timescales and in line with DNV policies and accreditation/approval requirements. Key Accountabilities: Auditor Responsible to carry out audits of the manufacturer's quality management system (QMS) and of its suppliers and/or subcontractors when appropriate and to draw up records and reports on the corresponding audits. Conduct surveillance audits including follow-up activities in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer relationships. Complete all chargeable work within the required timeframes to ensure customer satisfaction and efficiency of the business. Complete projects in relation to IVDR procedures, processes, systems and documentation as requested by the Operations Manager. If required, undertake reviews of files and make certification recommendations within target timescales and in line with DNV policies and accreditation/approval requirements. Project manage auditing teams, as appropriate, to maximize efficiencies, enhance client satisfaction and ensure compliance with standards. What we offer Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. *Benefits may vary based on position, tenure/contract/grade level* DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity. About You Assessors and Auditors shall have a technical college degree in a relevant product or medical area, as described below. In-Vitro Diagnostic devices: Biology or Microbiology Chemistry or Biochemistry Human Physiology Medical Technology or Biotechnology Medicine, Veterinary Medicine Biomedical science - e.g. haematology, virology, molecular diagnostics Nursing Pharmacy, Pharmacology, Toxicology Physiology Education In addition to a relevant educational degree, candidates must have a minimum 4 years’ work experience (full time) in an In-Vitro diagnostic medical device related industry, academia or hospital environment, with at least 2 of these years in the design, manufacturing, testing or use of the device in which they are qualified to Audit or Assessment, and/or experience as an assessor or auditor in a notified body. Specifically: Auditor - Practical experience in the quality management system and specific production process/technologies for the IVD medical devices. Assessor - Practical experience in conducting and/or assessing performance evaluation data or related scientific aspects with in-vitro diagnostic medical devices in one or more of the following areas Microbiology, Immunology, Genetic testing/Cancer Biology and Molecular Biology. A PhD in a relevant area for in-vitro diagnostic medical devices can substitute 3 years of work experience provided it includes 2 years’ experience in design, manufacture or testing. In addition to the above, knowledge of the following would be preferred: An excellent working knowledge of medical device management systems, standards and medical device compliance/auditing techniques. Work experience in positions with significant QA Regulatory or management systems responsibility. Experience with Harmonized medical device standards for In-Vitro diagnostic medical devices. Experience with Risk Management EN ISO 14971. Medical device experience from auditing/work. Experience auditing against recognized standards. Experience of working under own initiative and in planning and prioritizing workloads. Should have a flair for technical writing, essential for exhaustive report writing.

Urgent requirement: Experience: Minimum 5+ years Location: Hyderabad (Work from Office) Immediate requirement Notice period: Immediate or 1 month Job Summary / Overview: Responsible for the execution of batch record reviews and associated product quality issue resolution. Authorizes shipments from Client contract manufacturing organizations (CMO) once all applicable documentation has been reviewed and deemed acceptable. Will provide direct support and guidance to new product launch initiatives and supply chain concerns. Ensure standards and requirements are met for all executed activities. Supports the existing quality systems, including executing SOPs and data management activities in association with the company’s management review process. Can interface with the company’s partners to clarify, assess, and/or approve product quality concerns. Key Duties & Responsibilities:  Review and approve batch records related to cGMP documentation- deviation and investigation reports, QC data, CoA, CoC, product labeling and specification sheets, and all documentation supporting shipment of products prior to shipment, including temperature profiling data. Provide guidance and support in all aspects of cGMP to our CMOs including in particular good documentation practices and root cause analysis during investigations.  Ensure all applicable data is accurate, up to date, and defendable to regulatory authority.  Provide ongoing support to the existing Quality Management System and training programs.  Write, review, or implement new standard operating procedures and policies, as necessary.  Participate on Global Alliance Management project teams to communicate quality concerns and team progress. Knowledge or Experience:  Excellent knowledge of current GMP and GLP as well as FDA trends guidelines.  Must possess exceptional communication and interpersonal skills.  Must have excellent organizational and project management skills to coordinate multiple projects.  Expertise in microbiology, aseptic processing, and terminal sterilization processes.  Possesses strong organizational skills for prioritizing workload and responsibilities.  Strong written communication, interpersonal, negotiations and problem-solving skills are required.  Ability to manage indirect relationships and projects successfully.  Proficient with PC – based word processors, databases and spreadsheets.  Attention to detail.  Elevates issues to management, when appropriate. Minimum Qualifications / Experience:  5+ years of experience in a Quality related position and knowledge of current GMP and GLP as well as FDA trends  5+ years of hands-on experience with Chemistry instrumentation including HPLC  Track Wise software experience preferred 2  Must have excellent organizational and project management skills to coordinate multiple projects  Strong interpersonal communication skills required – verbal, written and presentation.  Ability to work in a cross-functional team environment and a flexible team-oriented perspective  Travel not typically required or can be less than 5% per annum. Education / Certifications:  Bachelor’s degree in a Scientific related field Client is an EEO/AA employer and does not discriminate on the basis of race, colour, religion, sex, age, creed, national origin, veteran status, physical or mental disability and sexual orientation

We require doctors for Medical Colleges & Hospitals PAN India Qual: MD/MS, DNB, (All Dept) Position: Consultant, SR, AP, Associate Professor, Professor Department: Clinical & Non Clinical Vishakha Call/Whatsapp: 9041008939 weps.services17@gmail.com

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait. We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. " Job Description Job Summary We are seeking an individual to test samples and release results within Turnaround Time (TAT) for commercial and stability batches, adhering to GMP (Good Manufacturing Practices). This role involves calibrating and maintaining assigned equipment within departmental and organizational guidelines, processes, and procedures. The primary objective is to ensure accuracy in results provided within timelines. " Roles & Responsibilities Your responsibilities encompass Bioassay testing for assigned samples and releasing data within defined timelines, ensuring absence of executional errors against established procedures. You will be responsible for preparing required reagents and buffers in alignment with the testing plan and ensuring the availability of equipment for analysis. Your role involves documenting activities contemporaneously, adhering to Good Documentation Practices and compliance expectations, and conducting self-checks post-analysis to ensure accuracy. You will promptly inform the supervisor about risk actions, providing necessary data and analysis to support the investigation process. You will adhere to QMS (Quality Management systems) and closure timelines, actively participate in laboratory investigations and discrepancy closures, fulfilling defined roles in audits. Your responsibilities also include ensuring lab cleanliness, proper sample storage, chemical labeling, removal of expired material, usage of calibrated equipment, equipment calibration, maintenance, and qualification. You will address instrument-related issues and conduct root cause analyses (RCAs) for unknown problems, and play a crucial role in training new team members on analytical techniques. " Qualifications Educational Qualification An M.Sc., M.Tech. or B.Tech. in Microbiology, Biochemistry, or Biotechnology or equivalent Minimum Work Experience 2-7 years Skills & Attributes Technical Skills: Basic understanding of the Biologics/Biosimilar industry, including processes, regulations, and trends. Hands-on experience in cell based bioassays, SPR technique, FACS techniques. Basic knowledge and hands-on exposure to cell culture techniques, specifically for working in Bioassay (BA) Labs. Hands-on experience in Biochemical analysis techniques, specifically Electrophoresis, Enzyme-Linked Immunosorbent Assay (ELISA), and Polymerase Chain Reaction (PCR), with a focus on Analytics. Working experience in a cGMP (Current Good Manufacturing Practice) environment, with a special emphasis on Good Documentation Practices (GDP). Basic knowledge in protein chemistry, including an understanding of protein structure, function, and relevant analytical techniques. Basic understanding about bioassay method validations. Behavioural Skills: Prioritizes effective communication and demonstrates a performance-oriented mind-set. Effective verbal and written communication skills. Performance-oriented approach, consistently striving for high standards. Demonstrates flexibility in working shifts and a clear understanding of team dynamics. " Additional Information About the Department Biologics Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon... " Benefits Offered At Dr. Reddy’s, we actively help to catalyze your career growth and professional development through personalized learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards... " Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions... For more details, please visit our career website at https://careers.drreddys.com/#!/ "

JOB Description Job Title : Business Development- Third Party (IVD Industry) Location : Netaji Subhash Place Company : Astam Diagnostics Department : Sales & Marketing Reporting to : Head – Business Development / Director – Sales About Astam Diagnostics Astam Diagnostics is a rapidly growing company specialising in the development, manufacturing, and marketing of high-quality diagnostic solutions, with a focus on enhancing healthcare outcomes. With a strong presence in the IVD sector, we are expanding our footprint and are looking for passionate professionals to join our journey. Key Responsibilities Identify new business opportunities and develop strategies to increase sales in the IVD product segment (e.g., Rapid Tests, ELISA Kits, etc.)through Third party Develop and manage strong relationships with distributors, hospitals, diagnostic labs, and healthcare providers. Achieve revenue targets and market share growth in assigned territories. Conduct market research to stay updated on competitor activities, pricing, and customer needs. Collaborate with the marketing team to plan and execute promotional campaigns. Prepare sales forecasts, reports, and business plans. Ensure customer satisfaction through timely support, training, and communication. Attend industry events, trade shows, and conferences to network and showcase Astam’s offerings. Work closely with internal teams (Regulatory, QA, R&D) to align business development efforts. Requirements Bachelor’s degree in Life Sciences, Biotechnology, Microbiology, or related field. An MBA in Marketing/Sales is an advantage. 3+ years of proven experience in Business Development/Sales in the IVD diagnostics industry .• Strong understanding of IVD products and the diagnostics ecosystem in India. Excellent communication, negotiation, and interpersonal skills. Willingness to travel extensively within assigned regions. Self-motivated, target-driven, and capable of working independently. Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Language: English (Preferred) Work Location: In person

We are looking for a Pharma Content Writer to join our editorial team and enrich our websites with new blog posts, guides and marketing copy. The candidate should be a Graduate of biotechnology, microbiology and any other pharma Related Experience- 6 Month To 1 Year > Research pharma-related topics > Write clear marketing copy to promote our products/services > Proofread and edit blog posts before publication > Submit work to editor for input and approval on time > Coordinate with marketing and design teams to illustrate articles > Promote content on social media > Identify customers’ needs and gaps in our content and recommend new topics > Ensure all-around consistency (style, fonts, images and tone) Job Type: Full-time Pay: ₹11,070.02 - ₹302,156.00 per month Schedule: Day shift Language: Hindi (Preferred) English (Preferred) Work Location: In person

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cepheid, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. At Cepheid, we are passionate about improving health care through fast, accurate, molecular diagnostic systems and tests. As a member of our team, you’ll get to make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Our mission drives us to develop groundbreaking solutions for the world’s most complex health challenges. Together, we bring MORE change to the world. Learn about the Danaher Business System which makes everything possible. The Quality Control Analyst is responsible for ensuring inspection process as per MDR 2017, European regulations, ISO 13485 and Cepheid corporate quality system requirements. This position reports to the quality manager and is part of the quality and regularity compliance department located in Cepheid Manufacturing facility, Bengaluru and will be an on-site role. In this role, you will be responsible for: Perform inspections of incoming, in-process and finished products/stability testing and identify/troubleshoot product if non-conformance. Performs/monitor the laboratory equipment validation/calibration/maintenance and ensure quality control lab as per safety standards/GLP. Write/review SOP/WI, technical reports or documentation such as deviation reports, testing protocols, and trend analyses. Support for internal/external audit schedule, NC, CAPA for site. The essential requirements of the job include: Master’s degree in Biochemistry, Molecular Biology, Microbiology, Biotechnology or related discipline and a minimum of 3+ years related to quality control experience. 2+ years’ experience in Vitro Diagnostics (IVD) is mandate. Need to act as competent technical staff for supervision the testing / analysis of diagnostic reagents & kits Business Schedule Requirement Must be flexible to work in shift-based time schedules (able to consistently maintain schedules and meet timelines). 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 Experience in leading continuous improvement efforts, in both quality systems and IVD products. Required strong interpersonal skills, effective communication skills / micro-soft word and excel knowledge / strong multi-tasking skill. Cepheid, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com. At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Need an Infection Control Nurse for a reputed hospital in Ghaziabad. The Infection Control Nurse is responsible for preventing and controlling healthcare-associated infections by monitoring infection trends, implementing hygiene protocols, training staff, and ensuring compliance with infection control policies and standards. Key Responsibilities: Monitor, investigate, and report hospital-acquired infections (HAIs) Conduct regular infection control audits and surveillance rounds Educate and train healthcare staff on infection prevention practices Ensure adherence to hand hygiene, PPE use, and sterilization protocols Assist in developing and updating infection control policies and SOPs Maintain records for NABH, NABL, and other regulatory bodies Collaborate with microbiology and housekeeping departments for infection control measures Requirements: GNM or B.Sc. Nursing Certification in Infection Control (preferred) 1–3 years of nursing experience, preferably in infection control Strong observation, communication, and documentation skills Registered with State Nursing Council Job Type: Full-time Pay: From ₹22,000.00 per month Work Location: In person

Designation – Senior Research Associate Location: Sahibabad, Ghaziabad Preferred Qualifications (Full time): · M.Sc. (Microbiology/Industrial Microbiology/Biotechnology) Experience Range and Knowledge: 2 – 3 years post qualification Job Responsibilities: Experienced candidate with proven analytical skills and track record of delivery Proficient in all basic microbiology tools and techniques for handling bacteria, yeast an fungi. Hands on experience in microbiology lab techniques like sterilization, aseptic techniques, serial dilution, inoculation, streaking, screening and isolation of microbes, staining techniques, biochemical and morphological tests for microbial identification, microscopy, cell enumeration, MIC studies Experience in handling strictly anaerobic and pathogenic microbes Knowledge of industrial bio-processes like alcoholic fermentation, biogas production, food and beverages industry, wastewater treatment etc. Knowledge of molecular techniques like gel electrophoresis, gel documentation, SDS PAGE, DNA isolation etc Knowledge of industrial enzymes and their applications Fair understanding of ISO 9001, Lab safety & GLP management Microsoft office, Documentation and reports preparation Good communication skills (oral and written) Job Types: Full-time, Permanent Pay: ₹400,000.00 - ₹500,000.00 per year Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Experience: Analytical Skills: 2 years (Required) Microbiology tools & techniques: 2 years (Required) Microbiology lab techniques: 2 years (Required) MIC Studies: 2 years (Required) SDS Page: 2 years (Required) GLPC: 2 years (Required) ISO 9001: 2 years (Required) Work Location: In person

Department FILL AND FINISH QC Job posted on Jul 09, 2025 Employment type P-P8-Probationer-HO Executive 10-14 year of experience in environment monitoring, water sampling and analysis. Knowledge of microbiology functions like, culture handling and media preparation.

Cotecna is a leading provider of testing, inspection and certification services. Founded in Switzerland in 1974, Cotecna started off as a family business and has now grown to become a world-class international player with over 7000 employees in more than 140 offices across 50 countries. To perform coordination of inspection orders for PSI clients. Key Responsibilities Carry out pre shipment physical inspection (PSI) in line with QMS and specific operating guidelines Undertake physical inspection of goods as per Company guidelines. Submit Inspection reports to department. Maintain accurate, impartial and factual reporting of inspection carried out and in any communication with customers. Provide feedback on any competitor activity or possible commercial inspection opportunities that may be gleaned during an inspection Qualifications, Experience and Technical Skills Science Graduate in Microbiology, Chemistry or Agriculture-MUST Exp – Fresher or 1-2 years of field experience GENERAL INFORMATION Geographical Scope Area Function Operations Seniority Entry level Country India City Kandla/Gandhidham/Mundra Contract Full-time limited Subject To Travel Up to 75% Open Until 2025/08/09 Explore our job opportunities. Filter by locations All Locations Argentina Bahrain Bangladesh Belgium Benin Brazil Bulgaria Canada Chile China Cote d'Ivoire Czech Republic Denmark Egypt France Germany Ghana Guatemala Hong Kong India Indonesia Italy Japan Kenya Latvia Malaysia Myanmar Netherlands Nigeria Oman Paraguay Peru Philippines Poland Republic of the Congo Romania Russia Saudi Arabia Singapore South Africa South Korea Spain Sri Lanka Sweden Switzerland Taiwan Thailand Togo Turkey Ukraine United Arab Emirates United Kingdom United States Uruguay Vietnam Zimbabwe Sales Manager Function : Sales / Business Development Country : Hong Kong Contract : Full-time limited Front Office and Admin Executive Function : Operations Country : India Contract : Full-time unlimited Telemarketer Function : Sales / Business Development Country : France Contract : Full-time unlimited Accounts Executive Function : Finance Country : India Contract : Full-time unlimited Assistant Manager – Direct taxation Function : Finance Country : India Contract : Full-time unlimited Field Chemist Function : Operations Country : Malaysia Contract : Full-time limited Admin Executive Function : Operations Country : Malaysia Contract : Full-time unlimited Inspector - Chennai Function : Operations Country : India Contract : Full-time limited Inspector - Kandla/Gandhidham/Mundra Function : Operations Country : India Contract : Full-time limited

IET Bhaddal Technical Campus, Ropar is looking for LAB TECHNICIAN to join our dynamic team and embark on a rewarding career journey Assist with testing and calibrating lab equipment in preparation for specific tasks Analyze retrieved data and prepare reports for laboratory management Experience in data collection and interpretation as well as the storage and retrieval of samples in a laboratory setting.

Alembic Group is looking for Senior Executive - Digi Labs to join our dynamic team and embark on a rewarding career journey Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising junior auditing personnel and implementing their research work into the auditing process. Preparing and reviewing annual audit memorandums. Researching applicable federal and state laws and regulations to ensure the company's books are compliant.

Immediate Hiring !! Designation: Medical Coding Analyst . Salary: Upto 20k PM + Incentives. Shift : General, Day. Skills: Anatomy, Physiology, Pathology. Location: Chennai, Coimbatore, Bangalore. Required Candidate profile Eligibility: UG or PG or Diploma ( 3 Years) Specialization: Life Science, Non - Life science , Para-Medical & Medical Studies. Passout: 2020- 2025

Company Description: Unipath Specialty Laboratory Limited (USLL) is one of India's leading diagnostics companies, with a presence in over 40 cities across 15 states. The multi-speciality pathology laboratory offers a wide range of tests in several segments, including Molecular Biology, Cytopathology, and Microbiology. Unipath is known for its state-of-the-art equipment and quality diagnostic support. The company is NABL accredited and continues to leverage modern equipment and mobility to stay ahead in the healthcare industry. Role Description: This is a full-time on-site role for a Sr. Manager - Talent Acquisition located in Ahmedabad. The Sr. Manager - Talent Acquisition will be responsible for managing full-life cycle recruiting, which includes sourcing, screening, interviewing, and hiring candidates. Additionally, tasks will include developing and maintaining employer branding initiatives to attract top talent. The role requires close collaboration with hiring managers and implementing recruiting strategies to meet organizational staffing goals. Objectives of this role: Create and implement end-to-end hiring processes to ensure a positive experience for hiring managers and candidates Form close relationships with hiring managers to ensure clear expectations for candidates and interviewers Ensure that staffing needs are being met with a long-term strategy in mind Provide input to ensure that teams consist of diverse, qualified individuals Devise and implement sourcing strategies, such as an employer branding initiative, to build pipelines for potential applicants Responsibilities: Vacancy closure within the defined TAT Manage a team of recruiters and deliver on KRA’s of the Talent Acquisition team Coordinate with hiring managers to identify staffing needs and candidate selection criteria Source applicants through online channels, such as Naukri, LinkedIn and other professional networks Create job descriptions and interview questions that reflect the requirements for each position Compile lists of most-suitable candidates by assessing their CVs, portfolios, and references Organize and attend job fairs and recruitment events to build a strong candidate pipeline Maintain records of all materials used for recruitment, including interview notes and related paperwork, to share with key stakeholders Skills and qualifications: Bachelor's degree in Human Resources, Business Administration, or related field 5+ years of experience in the field of talent acquisition Experience in full-cycle recruiting, using various interview techniques and evaluation methods Proficiency with social media, CV databases, and professional networks Experience in using various Job Portals including Naukri & LinkedIn to proactively source candidates Proficiency in documenting processes and keeping up with industry trends Excellent interpersonal and communication skills Strong organizational and analytical skills Capability to work in a fast-paced environment and meet deadlines Experience in the healthcare industry is a plus

Company Description Scholars Scientific Services is a global leader in organizing high-quality conferences, meetings, workshops, symposia, and webinars in various fields, including Pharma, Healthcare, Science, Technology, and Medicine. With teams in the US, UK, Japan, and India, we bring together experts to foster the dissemination of scientific knowledge and research. Our events are renowned for their outstanding scientific quality and informal, interactive settings. Role Description This is a full-time, on-site role for a Program Manager located in Hyderabad. The Program Manager will be responsible for managing and coordinating various programs, including conferences, meetings, and workshops. Day-to-day tasks involve program development, project management, and ensuring excellent customer service. The Program Manager will also be responsible for effective communication within the team and with external stakeholders to ensure the successful execution of all programs. Qualifications Program Management and Program Development skills Project Management skills Excellent Communication and Customer Service skills Ability to work effectively on-site in Hyderabad Bachelor's degree in a related field Experience in the scientific or academic conference industry is a plus Strong organizational and multitasking abilities B. Tech Biotechnology, Msc Microbiology, Pharmacy (B. Pharmacy and M. Pharmacy), Pharm D (Preferably Freshers)

Job Requirement only apply Female candidates Minimum Education: Graduate in Msc Microbiology. Minimum Experience: 1- 2 years in a Microbiology in beverage industry. but have knowledge in chemical testing also in water treatment plant package depending on experience and interview Job Type: Full-time Pay: ₹14,000.00 - ₹20,000.00 per month Schedule: Day shift Supplemental Pay: Overtime pay Ability to commute/relocate: Karjat, Maharashtra: Reliably commute or planning to relocate before starting work (Required) Experience: total work: 1 year (Preferred) Work Location: In person

Company: Pune Instrumentation Pvt. Ltd. (PIPL) Location: Pune About PIPL:Pune Instrumentation Pvt. Ltd. (PIPL) is a pioneering Custom Application Development Lab with over 50 years of experience in designing and developing high-quality, critical solutions. We are an ISO 9001 & ISO 13485 certified, and DSIR (Department of Scientific and Industrial Research, Govt. of India) recognized R&D company. Under the Suraxa brand, PIPL is making strides in Health Care with a focus on Infection Control & Respiratory Technology. PIPL Health Care, a crucial startup segment within the company, is key to driving revenue growth and innovation. Position Overview: We are seeking an experienced, innovative, and driven Senior Executive for our Health Care division. This role is ideal for someone with a deep understanding of R&D and a passion for creating groundbreaking solutions. As a New Product Development Senior Executive, you will be instrumental in managing and driving the development of new healthcare products, ensuring they meet market demands and adhere to the highest standards of quality and innovation. Key Responsibilities: 1. Lead and manage New Product Development (NPD) programs for PIPL Healthcare devices, coordinating across Business Development, R&D, Manufacturing, Procurement/Sourcing, and external regulatory agencies (e.g., DCGI). 2. Develop and monitor Key Performance Indicators (KPIs) to track the progress of various NPD initiatives, ensuring timely and budget-compliant commercialization. 3. Collaborate with the Business Development (BD) team to identify and manage critical validation activities, coordinating both internal and external efforts. 4. Contribute to and refine Go-to-Market strategies with BD and business teams. Develop and implement program timelines, ensuring alignment across all functional areas to meet strategic goals. 5. Ensure the Voice of the Customer is reflected in product attributes and features by working closely with validation customers and translating these into Critical to Quality (CTQ) parameters. 6. Partner with marketing agencies (PR, Ad, Film Production) to strengthen the PIPL Health Care brand and communication strategies. 7. Work closely with the E-marketing and IT teams to enhance the companys digital presence across all web and social media platforms. Qualifications and Skills: 1. A Bachelors Degree, preferably in Microbiology, Chemical Engineering, Application Chemistry, or a related field. 2. At least 10 years of experience in New Product Development within the healthcare sector, specifically in disinfection devices. Experience with startups is highly desirable. 3. Strong written and verbal communication skills, with the ability to represent PIPL Health Care at events, conferences, and other public forums. 4. Proficiency in presentation tools (Word, PowerPoint, Excel) with a creative flair for delivering impactful presentations. 5. Proven leadership capabilities with a track record of managing cross-functional teams. 6. Commitment to the organizations core values: Integrity, Quality, Speed, and Innovation. Why Join Us This is an exciting opportunity to be part of a dynamic, growth-oriented team that is dedicated to pushing the boundaries of healthcare innovation. If you thrive in a challenging environment and are passionate about making a real impact, we invite you to apply and contribute to the future of PIPL Health Care.,