2539 Microbiology Jobs - Page 14

Sales & Business Development Relationship Management Presentation & Counseling Skills Negotiation & Target-Driven Attitude Customer Service Orientation Team Collaboration

Sales & Business Development Relationship Management Presentation & Counseling Skills Negotiation & Target-Driven Attitude Customer Service Orientation Team Collaboration

Urgent vacancies for Faculties Senior Residant with good experience in medical college at a medical college in jaipur Salary as per industry Norms,

Teaching & training Undergraduate (MBBS) Medical students including Interns/ Postgraduate Medical students so as to achieve the Educational Objectives i.e. to develop their knowledge, skills & attitude.

Salary & Benefits: Apprentice salary: 17,000 per month 1 paid leave per month Free transportation facility Subsidized canteen food at our facility Please note that candidates will be initially hired as apprentices (For 1 Year). However, based on their performance, they will be considered for permanent roles, subject to the availability of vacancies.

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. What You Will Achieve In this role, you will: Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles. Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials. Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies. Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Here Is What You Need (Minimum Requirements) Masters degree in microbiology with minimum of three years experience Demonstrated technical skills in method validation and testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Bonus Points If You Have (Preferred Requirements) Experience with laboratory work, particularly using microbiological techniques Proven track record in leading continuous improvement projects Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis Strong problem-solving skills and attention to detail Ability to manage multiple priorities and meet deadlines. Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels Adaptability and willingness to learn new techniques and procedures Work Location Assignment: On Premise Quality Assurance and Control #LI-PFE

We are Looking for self-motivated and experienced PGT Biology Teacher to join our qualified team of educators. Teacher responsibilities will include Grading assignments, evaluating students progress and planning educational activities. Teacher should be a competent professional with in-depth knowledge of teaching & Should have excellent written and verbal communication skills. Details: Job Category: Teaching Teaching Subject: Biology, Teaching Class UPTO: Std. 11th-12th, Teaching Degree: B.Ed, Qualification: Post Graduation Experience: 3 Years Facilities: Lodging,Child Education No. of Vacancy: Only 1 Salary: Rs. 2 To Rs. 4 per month

Histopathology Technician (Only Female Candidates) We are seeking a skilled and detail-oriented Histopathology Technician to join our pathology laboratory team. Female candidates only Bachelor s degree in Medical Laboratory Technology. Minimum 1 or 2 years of experience in histopathology. Should be flexible and available for all shift schedules Good communication and teamwork skills.

We are seeking a diligent and meticulous Junior Executive - Laboratory Medicine to oversee the daily operations of our quality control laboratory, with a specific focus on the Microbiology department . This role is crucial in ensuring that all products consistently meet our established standards of quality, safety, and reliability. The ideal candidate will be responsible for supervising lab personnel, managing testing procedures (including microbiology samples), enforcing compliance with internal and external standards (e.g., ISO), and contributing to continuous improvement initiatives to optimize our quality processes. If you have a strong background in laboratory quality control, microbiology, and a commitment to excellence, we encourage you to apply. As a Junior Executive - Laboratory Medicine, your key responsibilities will include: 1. Quality Control & Assurance Supervise and guide the QA/QC team in product sampling, testing, and evaluation processes. Ensure all products consistently meet company and regulatory quality standards. Investigate non-conformities and initiate timely corrective and preventive actions (CAPA). Develop, implement, and maintain robust quality control procedures and essential documentation. Review and approve test results for raw materials, in-process samples, and finished goods. 2. Laboratory Operations & Microbiology Management Oversee the daily operations of the quality control laboratory, including staff scheduling, training, and performance monitoring. Specifically supervise the Microbiology department , ensuring adherence to standard protocols for processing, testing, and managing all microbiology samples. Ensure all lab equipment is properly calibrated, meticulously maintained, and functioning accurately. Develop and validate new testing methods as required to enhance efficiency and accuracy. Maintain an accurate inventory of lab supplies and ensure strict compliance with all safety standards. Prepare and maintain comprehensive SOPs (Standard Operating Procedures), detailed logs, and technical reports. 3. Compliance & Documentation Ensure full compliance with applicable industry standards and stringent regulatory requirements (e.g., ISO 9001, GMP, FDA, HACCP). Maintain accurate and complete quality records, ensuring readiness for all audits and inspections. Assist with both internal and external audits and effectively implement any required corrective actions. 4. Continuous Improvement Identify opportunities for process enhancements and actively lead quality improvement projects. Monitor key quality metrics (e.g., defect rates, test turnaround times) to drive performance. Provide essential training to production and laboratory personnel on critical quality principles and procedures.

Department Responsibilities : Overall supervision of the daily activities of the MicrobiologySerology & Molecular Laboratory section. Evaluatingpreparingand updating documents pertaining to NABLCAPNABH and JCI standards and participation GC meetings. Interacting with the patients / relatives & the referring doctor regarding the MicrobiologySerology & Molecular Laboratory tests & test results Guidingtrainingand motivating the technicians in Laboratory Medicine. Guiding and teaching the Medical Laboratory Technology (MLT) students and other students Monitoring the daily QCEQAS programs Performing all those investigations that the technicians are not qualified to perform. Managing all the equipment & monitoring regularly for the functioning of the same. Monitoring the corrective and preventive actions in coordination with the Quality In-charge of Department of MicrobiologySerology & Molecular Laboratory. Ensure quality laboratory service and turnaround time. Capex planning. Participation in HIC & Antibiotic stewardship program. Administration of laboratory Responsibilities: Effectively evaluate the scopequalityand timeliness of laboratory services to meet the patient care needs of the hospital. Ensures that proficiency testingalternative performance assessmentand QC procedures are sufficient for the extent of testing performed in the laboratory. Ensures that the performance specifications for new testsinstrumentsand methods introduced to the laboratory have been properly validated or verified prior to being used for patient testing &ensures communication of laboratory data and appropriate result reporting. ensures provision of educational programsstrategic planningand research and development appropriate to the needs of the laboratory and institution. ensures enough personnel with appropriate educational qualificationsdocumented training and experienceand adequate competency to meet the needs of the laboratory. ensures implementation of a safe laboratory environment in compliance with good practice and applicable regulations. Interaction with Government or Regulatory Interaction.

Experience: 6 - 8 years of experience in Quality Assurance / Quality control of sterile dosage manufacturing facility. Core Competencies Change Management process Risk assessments principles and tools Validation of lab equipment s Drug Product Process validations Regulatory requirements Compendial Changes Technical Skills Knowledge in validation principles and practices related to the Process validation, cleaning validation, Analytical Method validation, Water system, HVAC system, Equipment & Utility Qualifications. Knowledge of various Quality tools required for investigations Technical Writing- Ability to create documentation that is accurate, complete, unambiguous, and as concise as possible aimed to be understood by any level of organization Knowledge in change control assessment Knowledge on Chemical and Microbiology analysis. Basic idea on manufacturing operations, validation and engineering functions Experience in handling Regulatory agency inspections Behavioral/Any Other Skills Interpersonal Skills: Effective communication with all staff from different levels and builds constructive and effective relationship Managerial Skills: Persistent approach to resolving issues, Effective situation handling capabilities, strong time management skills. Acts Decisively: Makes decision in a timely manner based on available information Grows Self: Identify Individual development needs and create a plan and work towards achieving those objectives Self-accountable & Proactive approach Critical thinking and Compliance mindset Core Responsibilities Partially/fully independent, reviews critical change controls and protocols, trains others. Responsible for review & approval of documents as per current regulatory requirements. Assessment, approval & closure of change control and action items Site change review committee (SCRC) meeting with cross functional team to assess the change before initiation in gqts and present the critical change controls to the leadership team for its adequacy. Coordinating with CFT for addressing & resolving of Review Comments for timely Closure. Review & approval of Sops, Job aids, forms, Quality Risk Assessment (QRA), validation protocols, study protocols & summary reports. Review and approval of STP s and specifications. Review and approval of stability compilation reports. Review and approval of APR s. Review and approval of Environmental monitoring trends, Water monitoring trends, bioburden, BET, sterility trends, isolate trends and summary reports. Ensure manufacturing policies, procedures conform to Pfizer Report any non-compliance to the Manager Experience in handling regulatory, corporate and internal auditors/ inspectors. Work Location Assignment: On Premise Quality Assurance and Control #LI-PFE

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver meets the highest standards of safety and efficacy. What You Will Achieve In this role, you will: Create, review, and approve test method transfer and validation protocols, reports, and equipment qualification records. Maintain compliance with Current Good Manufacturing Practices in Quality Control and Stability laboratories. Support media preparation, Bio ball culture handling, and conduct microbiology-related investigations. Perform testing on various samples, manage Laboratory Information Management System builds, and review laboratory data. Serve on cross-functional teams, conduct safety inspections, participate in investigations, recommend corrective actions, and train junior colleagues. Here Is What You Need (Minimum Requirements) Masters degree in microbiology with minimum of 6 years relevant experience Strong technical skills in method validation and testing Experience in microbiological testing of water Deep understanding of pharmaceutical manufacturing, packaging, and quality assurance operations Detail-oriented with robust knowledge of quality systems Familiarity with research unit clinical and analytical laboratory environments Effective written and verbal communication, as well as interpersonal skills Bonus Points If You Have (Preferred Requirements) Relevant pharmaceutical experience Strong understanding of computer system hardware, infrastructure, and networks Experience with Laboratory Information Management Systems (LIMS) Proficiency in data analysis and interpretation Knowledge of regulatory requirements and guidelines Strong problem-solving abilities Effective time management and organizational skills Ability to mentor and train junior colleagues Work Location Assignment: On Premise Quality Assurance and Control #LI-PFE

Job Description Role : Executive Microbiologist Location : Hyderabad Job Purpose/Overview To ensure the Dry Pet Food products leaving the factory operation confirms to the MARS specifications through the assurance of raw materials quality & compliance to process parameters by demonstrating quality inspections, process monitoring & control through microbiological testing of samples. The Microbiologist shall assist the Quality control lab manager in managing the Laboratory (microbiology) in terms of executing test plans in timely manner, follow GLP, & cost optimization. Shall participate & support effectively in design & implementation of Food Safety Quality Management Systems (HACCP) and essential Pre-requisite programs (PRPs) for Dry Pet food plant. Job Responsibilities Plant Responsibilities: Conduct analysis of incoming raw materials, Finished products as per Microbiological test plan. Conduct routine microbiological tests as per the Mars Micro verification standard. Communicate the status of materials or products for release/hold/ rework/ reject Ensure effective implementation of personal-plant hygiene, cleaning & sanitations programs in line with GMP standard Ensure Calibration the laboratory testing & measuring equipment’s as per calibration plan Conduct microbiological analysis for intermediate products & finished products as per test plan Learn & implement new testing methods, as required. Track & report the microbiological performance using ‘trend charts’, suggest & follow up corrective & preventive actions Maintain Lab testing data and relevant test records. Ensure timely completion of all testing and documentation. Conduct Environmental Monitoring of plant by taking Swabs samples, Air Monitoring and water testing. Suppliers Interface: Track supplier performance basis raw materials quality, microbiological contaminations, handle non-conformities & record Communicate materials/ suppliers related issues to Supply chain and follow up Conduct/ Co-ordinate analysis of Shelf life samples, Market samples & Concerned samples to track product performance and feedback Co-ordinate/ facilitate with external testing laboratories for analysis & records Support Quality & Food Safety Systems: Support effective implementation of HACCP in the plant by ensuring cleaning sanitation. Assist in designing MRAs for raw materials by sharing the analysis outcomes. Support in CCP/OPRP verifications wherever applicable through Microbiological Samples collections, Testing and reports sharing. Support in GMP verifications at site. Other Responsibilities: Demonstrate GLP & support Lab cost optimization initiatives Conduct Associate on-job and classroom training on Food Safety Management. Focus on personal-plant hygiene, cleaning & sanitation plans. Quality- “Associate is responsible to ensure effective implementation of Mars QMP (Quality Management Process), Quality and Food Safety requirements including Personnel Hygiene and GMP stated by the Organization as applicable. Associate shall deliver through Respective Area/Process Standard Operating Procedures. Meet basic competency requirements mentioned in the job Role Skill Matrix to ensure Quality and Food Safety requirements are implemented to satisfactory level.” SES-Overall responsibility to ensure the individual compliance to Mars Global/Asset conservation standards and other relevant local SES legislation. Responsible for implementing and maintaining all relevant SES Management systems in their respective work area. Responsible for understand risks and controls in their area, get appropriate training, report all incidents and ensure that SES objectives are captured as KRA's in TMS The incumbent would work collaboratively with other Executives Microbiology for supporting the deliverables of the Lab He/She would act along with other Executives Microbiology as interface to Suppliers related to Microbiology testing Media procurement, PCR vendors and External microbiology labs. Job Specifications/Qualifications Educational & Professional Qualification MSc- Microbiology or B. Tech with Microbiology Knowledge/Experience 3-4 years’ experience in microbiology Lab Required experience with Food/ Pharma Company

RESPONSIBILITIES: Manage the technical team, guiding them in maintaining high standards of accuracy, reliability, and integrity in laboratory operations. Ensure the microbiological Sampling, Testing, and Approval of Raw Materials/Bulk/FG as per the defined SOP and complete the analysis within the stipulated lead-time. Approve test results, calibration/verification/intermediate checks records, and certificates of analysis before final submission to clients. Conduct Preservative Efficacy Test as per defined protocol and schedule. Conduct Environmental Monitoring/Compressed Air Monitoring as per defined protocol and schedule. Conduct the study of CEHT/DEHT/Water Validation/Swab/Rinse Water & other validation studies from the microbiological perspective as per the requirements. Prepare and share Daily Quality Reports/Monthly Quality Reports/Analysis Trackers within the stipulated period. Ensure timely external calibration and Internal verification of all microbiology lab instruments/equipment as per the defined frequency. Handling & preservation of the cultures as per defined procedure. Ensure proper disposal of Bio-Medical Waste generated from Microbiology lab. Oversee and maintain the inventory of media, chemicals, and glassware, ensuring the smooth and efficient operation of laboratory testing, calibration, and measurement processes in compliance with NABL standards. Conduct training for all concerned members on GMP, GLP, Personnel Hygiene, and MB related specific topics for the microbiologist team. Prepare all required Manuals/Protocols/SOPs/WIs/Formats and conduct training as per NABL Certification requirements/QMS requirements. Initiate Proficiency Testing and Inter Laboratory comparison for NABL certification. Ensure that all laboratory procedures, reports, and results are properly documented, traceable, and easily accessible for audits and inspections. Oversee the regular internal audits and assessments to ensure continuous compliance with QMS/NABL accreditation criteria.

Role & responsibilities Quality Control: Qualification: B. Pharm/ M. Pharm / M. Sc chemistry Experience: 1 to 6 years of experience in Pharmaceutical Quality Control experience. Job Description: Perform HPLC analysis. Familiarity with analytical laboratory equipment's like HPLC, GC, AAS,ICP-MS, UV, IR and etc., Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Demonstrated technical skills in method validation and testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Experience with laboratory work, particularly using analytical HPLC (High Pressure Liquid Chromatography) techniques Create, review, and approve test method transfer and validation protocols, reports, and equipment qualification records. Maintain compliance with Current Good Manufacturing Practices in Quality Control and Stability laboratories. Perform testing on various samples, manage Laboratory Information Management System builds. Detail-oriented with robust knowledge of quality control process Effective written and verbal communication, as well as interpersonal skills Experience with Laboratory Information Management Systems (LIMS) Quality Control - Microbiology Qualification: M. Sc(Microbiology) Experience: 1 to 6 years of experience in Pharmaceutical Quality Control - Microbiology. Demonstrated technical skills in microbiology testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles. Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials. Perform various microbiological tests such as water analysis, Microbial Limit Test, , Bacterial Endotoxin Test, Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Conduct analyses on finished products, raw materials, and components, including data entry, review, Effective written and verbal communication, as well as interpersonal skills

Job Summary: We are seeking a responsible and experienced Lab Incharge to oversee the daily operations of our laboratory. The ideal candidate will ensure that all laboratory functions run smoothly, maintain quality standards, and comply with safety protocols. This role involves supervision of lab staff, inventory management, maintaining records, and ensuring timely reporting of test results. Key Responsibilities: Supervise all laboratory operations and ensure smooth day-to-day functioning. Manage and coordinate the lab staff, assigning duties and ensuring adherence to protocols. Ensure the accuracy, reliability, and timely delivery of all laboratory reports. Monitor laboratory equipment and arrange for routine maintenance and calibration. Maintain inventory of lab supplies, chemicals, and reagents; place orders as needed. Implement and monitor quality control procedures. Ensure all lab practices are in compliance with health and safety regulations. Provide training and guidance to laboratory technicians and assistants. Maintain accurate documentation and records of test results, calibration, and maintenance logs. Collaborate with doctors/medical professionals for interpretation of test results (if applicable). Participate in audits and implement corrective actions when necessary. Stay updated on new testing techniques, equipment, and procedures. Qualifications: Bachelor’s or Master’s degree in Medical Laboratory Technology, Biotechnology, Microbiology, or a related field. Minimum [2-3] years of experience in a laboratory setting, with at least 1 year in a supervisory or incharge role. Strong knowledge of laboratory safety and quality protocols. Familiarity with laboratory information systems (LIS). Excellent organizational and leadership skills. Attention to detail with good analytical and problem-solving abilities. Strong communication and interpersonal skills. Preferred Skills: Experience with NABL or ISO accreditation standards. Basic knowledge of biomedical waste management. Ability to manage team performance and resolve conflicts effectively. Job Type: Full-time Pay: ₹10,000.00 - ₹20,000.00 per month Schedule: Day shift Work Location: In person

Urgently hiring for Senior Executive or Assistant Manager - Micro. Location: Panchkula, Haryana Experience Required: 5+yrs Early joiners Preferred Job Type: Full-time Pay: ₹20,000.00 - ₹35,000.00 per month Schedule: Day shift Morning shift Application Question(s): Notice Period? Current Salary? Expected Salary? Current Location? Relevant experience in Microbiology? Work Location: In person

Responsible for Sales of IVD Diagnostic Products. Product Segment Focus: ELISA, RIA, Hematology, IFA, HPLC, LC/MS, Molecular Diagnostics, Analytical, Autoimmunity, Microbiology, Endocrinology

Key Responsibilities: Perform in-process and final product quality checks as per defined SOPs Test raw materials, packaging materials, and finished goods for compliance Monitor and maintain quality control records and reports Ensure all products meet regulatory standards and internal specifications Conduct stability studies and validation of cosmetic/healthcare products Investigate quality-related issues and implement corrective actions Ensure compliance with GMP, ISO, and other relevant regulatory guidelines Coordinate with production and QA teams to resolve quality issues Assist in preparation and review of batch manufacturing records (BMR) and quality documentation Support audits and inspections (internal/external) Key Requirements: B.Sc. / M.Sc. in Chemistry, Microbiology, Pharmacy, or related field 1–2 years of experience in QC, preferably in cosmetics, personal care, or health products Sound knowledge of analytical techniques, product testing, and cosmetic regulations Familiarity with instruments like HPLC, UV, pH meter, viscometer, etc. Good documentation practices and attention to detail Knowledge of BIS/AYUSH/FDA norms is a plus Preferred Skills: Understanding of skin care, personal care, and wellness product formulations Strong communication and reporting skills Ability to work independently and in a team environment Problem-solving and analytical thinking Employment Type: Full-Time Location: Kothariya, Rajkot, Gujarat (Preferred) Work Location : In person Application Deadline: 30/07/2025 Job Type: Full-time Pay: ₹13,000.00 - ₹15,000.00 per month Schedule: Day shift Work Location: In person

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver meets the highest standards of safety and efficacy. What You Will Achieve In this role, you will: Create, review, and approve test method transfer and validation protocols, reports, and equipment qualification records. Maintain compliance with Current Good Manufacturing Practices in Quality Control and Stability laboratories. Support media preparation, Bio ball culture handling, and conduct microbiology-related investigations. Perform testing on various samples, manage Laboratory Information Management System builds, and review laboratory data. Serve on cross-functional teams, conduct safety inspections, participate in investigations, recommend corrective actions, and train junior colleagues. Here Is What You Need (Minimum Requirements) Master's degree in microbiology with minimum of 6 years relevant experience Strong technical skills in method validation and testing Experience in microbiological testing of water Deep understanding of pharmaceutical manufacturing, packaging, and quality assurance operations Detail-oriented with robust knowledge of quality systems Familiarity with research unit clinical and analytical laboratory environments Effective written and verbal communication, as well as interpersonal skills Bonus Points If You Have (Preferred Requirements) Relevant pharmaceutical experience Strong understanding of computer system hardware, infrastructure, and networks Experience with Laboratory Information Management Systems (LIMS) Proficiency in data analysis and interpretation Knowledge of regulatory requirements and guidelines Strong problem-solving abilities Effective time management and organizational skills Ability to mentor and train junior colleagues Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control #LI-PFE

Experience: 6-8 years of experience in Quality Assurance / Quality control of sterile dosage manufacturing facility. Core Competencies Change Management process Risk assessments principles and tools Validation of lab equipment’s Drug Product Process validations Regulatory requirements Compendial Changes Technical Skills Knowledge in validation principles and practices related to the Process validation, cleaning validation, Analytical Method validation, Water system, HVAC system, Equipment & Utility Qualifications. Knowledge of various Quality tools required for investigations Technical Writing- Ability to create documentation that is accurate, complete, unambiguous, and as concise as possible aimed to be understood by any level of organization Knowledge in change control assessment Knowledge on Chemical and Microbiology analysis. Basic idea on manufacturing operations, validation and engineering functions Experience in handling Regulatory agency inspections Behavioral/Any Other Skills Interpersonal Skills: Effective communication with all staff from different levels and builds constructive and effective relationship Managerial Skills: Persistent approach to resolving issues, Effective situation handling capabilities, strong time management skills. Acts Decisively: Makes decision in a timely manner based on available information Grows Self: Identify Individual development needs and create a plan and work towards achieving those objectives Self-accountable & Proactive approach Critical thinking and Compliance mindset Core Responsibilities Partially/fully independent, reviews critical change controls and protocols, trains others. Responsible for review & approval of documents as per current regulatory requirements. Assessment, approval & closure of change control and action items Site change review committee (SCRC) meeting with cross functional team to assess the change before initiation in gqts and present the critical change controls to the leadership team for its adequacy. Coordinating with CFT for addressing & resolving of Review Comments for timely Closure. Review & approval of Sops, Job aids, forms, Quality Risk Assessment (QRA), validation protocols, study protocols & summary reports. Review and approval of STP’s and specifications. Review and approval of stability compilation reports. Review and approval of APR’s. Review and approval of Environmental monitoring trends, Water monitoring trends, bioburden, BET, sterility trends, isolate trends and summary reports. Ensure manufacturing policies, procedures conform to Pfizer Report any non-compliance to the Manager Experience in handling regulatory, corporate and internal auditors/ inspectors. Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control #LI-PFE

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. What You Will Achieve In this role, you will: Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles. Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials. Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies. Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Here Is What You Need (Minimum Requirements) Master's degree in microbiology with minimum of three years' experience Demonstrated technical skills in method validation and testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Bonus Points If You Have (Preferred Requirements) Experience with laboratory work, particularly using microbiological techniques Proven track record in leading continuous improvement projects Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis Strong problem-solving skills and attention to detail Ability to manage multiple priorities and meet deadlines. Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels Adaptability and willingness to learn new techniques and procedures Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control #LI-PFE

Job Title: Head – Quality Assurance Company Name : Kedia Pavitra LLP Location: Merta & Jaipur Job Type: Full-time on site job. Reports To: Plant Head / Director – Operations Job Summary: We are seeking an 10-12 Years of experienced and detail-oriented Quality Head to lead the Quality Assurance and Quality Control functions for our FMCG operations. The ideal candidate will ensure that all products meet the highest standards of safety, quality, and regulatory compliance, while driving continuous improvement initiatives across production units. Key Responsibilities: Develop and implement quality assurance systems, protocols, and SOPs across all production lines. Lead the QA/QC teams and ensure compliance with FSSAI , ISO , GMP , and other applicable regulatory standards. Oversee in-process quality checks , raw material inspection, finished goods testing, and packaging quality. Monitor and improve product quality parameters based on customer feedback, audits, and market returns . Drive root cause analysis (RCA) and implement corrective and preventive actions (CAPA) for deviations. Lead internal quality audits and manage third-party certifications and inspections . Collaborate with R&D, Production, Procurement, and Supply Chain teams for quality alignment. Maintain and regularly update quality documentation , test records, and regulatory submissions. Train and upskill quality teams on hygiene, food safety, testing techniques, and compliance requirements. Stay updated on evolving FMCG regulations, labelling laws, and food safety trends . Handling of customer complaint. Required Skills & Competencies: In-depth knowledge of FSSAI , GMP , HACCP , ISO 22000 , and BRC standards Strong analytical, documentation, and communication skills Proven leadership in handling quality audits and compliance processes Ability to manage teams across multiple plant locations Skilled in using LIMS, SAP, and quality testing Qualifications & Experience: B.Tech / M.Tech / M.Sc. in Food Technology, Microbiology, Chemistry, or related discipline 10–12 years of experience in quality assurance/control in the FMCG or food manufacturing industry Experience in leading large QA/QC teams and managing external audits Job Types: Full-time, Permanent Pay: ₹120,000.00 - ₹125,000.00 per month Work Location: In person

Job Title: Quality Assurance (QA) Manager – Food Manufacturing Reports to: Directors Job Summary: The QA Manager is responsible for ensuring that all products meet company and regulatory quality and safety standards. This role oversees the implementation, management, and improvement of quality systems within the facility, leads internal and external audits, manages QA staff, and works closely with production, maintenance, and R&D teams to maintain compliance and drive continuous improvement. Key Responsibilities: Quality Systems & Compliance Develop, implement, and maintain QA programs and procedures (HACCP, GMP, FSMS, BRC/SQF/FSSC 22000 etc.). Ensure compliance with all local, state, and federal food safety regulations (FSSAI, FDA, USDA, etc.). Manage document control related to quality and food safety systems. Testing & Inspection Oversee incoming raw material, in-process, and finished product inspections. Ensure lab testing is performed accurately and timely (microbiological, chemical, sensory). Investigate and resolve customer complaints and product non-conformities. Audits & Certifications Lead preparation and execution of internal, third-party, and regulatory audits. Implement corrective and preventive actions (CAPA) based on audit findings. Team Leadership Manage and develop QA team members, providing training and coaching on quality systems, food safety, and regulatory requirements. Foster a culture of quality and continuous improvement across the plant. Process Improvement Drive root cause analysis and continuous improvement initiatives to reduce quality defects and customer complaints. Collaborate with production and maintenance to ensure process controls are effective. Reporting & Documentation Maintain accurate quality records and prepare regular quality performance reports for management. Track key quality KPIs such as customer complaints, first pass yield, and audit scores. Qualifications: Bachelor’s degree in Food Technology, Microbiology, Chemistry, or related field (Master’s preferred). Minimum 5-7 years of QA experience in food manufacturing, with at least 2 years in a managerial role. Strong knowledge of HACCP, GMP, food safety standards, and regulatory requirements. Experience with certifications such as BRC, SQF, FSSC 22000. Familiarity with laboratory testing methods and equipment. Excellent leadership, problem-solving, and communication skills. Key Competencies: Attention to detail and strong analytical skills. Ability to work cross-functionally with production, R&D, and supply chain. Skilled in training and motivating teams. Strong documentation and organizational skills. Proficient in MS Office and quality management software. Work Environment: Manufacturing plant environment with exposure to production equipment, noise, and food allergens. Occasional extended hours or weekend work during audits or production trials. Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus 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 Beckman Coulter Diagnostics, 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. As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory’s role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible. The Mechanical Engineer is responsible for the design and re-design of certain Hardware components and the development of new products, on-market products and support manufacturing activities. This position reports to the Head of Life Cycle Management & Group Manager and is part of the R&D Hardware/Systems Development team located in Bengaluru – BDC and will be an on-site role. In this role, you will have the opportunity to: Design and develop innovative mechanical solutions to improve performance, safety, reliability, throughput and cost-effectiveness (Knowledge of Should costing and estimation), in Design Change Project. Act as a change lead, managing the entire Design change process independently. Handle multiple projects with proper project planning and minimal guidance Conduct root cause analysis and implement corrective actions. Collaborate with cross function teams to resolve manufacturing and field issue, conduct feasibility studies, risk assessments, and design reviews and validate designs through analysis and testing. The essential requirements of the job include: Bachelor’s degree in mechanical engineering or a related field with 5 years of experience in mechanical design principles, materials, manufacturing processes. Proficiency in SolidWorks CAD software and simulation tools. Create and maintain detailed engineering documentation, including CAD models, drawings, specifications and test plans. Knowledge of dFMEA/pFMEA, DFX, Tolerance Stack-up Analysis and GD&T Basic knowledge of metals and materials, its application knowledge on mechanical parts fabrication, Rapid prototyping and testing. It would be a plus if you also possess previous experience in: Experience with medical device regulations (FDA, ISO 13485, ISO 14971, IEC 60601) Experience in IVD instrumentation, such as clinical chemistry, immunoassay, hematology, urinalysis, molecular, microbiology or flow cytometry systems is a plus Advanced certification in CAD tools Familiarity with lean manufacturing and Six Sigma principles. Prior work experience in Electro-Mechanical products, Robotics and Automation 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.