93 Sterility Testing Jobs

TT Ampoule: To Support the EM activities continuously in 3 shifts, Water sampling and Product testing. Good exposure in Microbiology technique

As a Microbiologist at Syngene Unit 3 Bangalore, your role involves being responsible for sterility testing, BET analysis, and ensuring the qualification and requalification of equipment in the Microbiology laboratory. Your core responsibilities also include initiating and closing OOS, Deviation, Change control, CAPA, and microbial data excursions, as well as participating in the preparation of SOPs and relevant documents. Additionally, you will be involved in analyzing raw materials, finished products, stability samples, and conducting various QCM related activities in the laboratory. Key Responsibilities: - Perform sterility testing using isolator - Conduct BET analysis using KTA/PTS - Qualification and requalification of equipment/instruments - Initiate and close OOS, Deviation, Change control, CAPA - Analyze raw materials, finished products, stability samples - Conduct QCM related activities such as sterilization, media preparation, growth promotion, culture maintenance, equipment calibration, etc. - Maintain microbiological trend data for the facility - Plan and schedule analytical activities in the department - Undertake any other tasks allocated by HOD or team leader Qualifications Required: - Experience: 6-10 years - Education: M.Sc in Microbiology or Biotechnology - Skills and Capabilities: Good knowledge of Microbiology skills and techniques, sterility testing, QMS knowledge, teamwork, communication skills About Syngene: Syngene is an innovation-led contract research, development, and manufacturing organization offering integrated scientific services from early discovery to commercial supply. Safety is a top priority at Syngene, with a focus on adherence to safe practices and procedures, driving a corporate culture that promotes environment, health, and safety mindset at the workplace. As an equal opportunity employer, Syngene values excellence, integrity, and professionalism in all its employees. Join Syngene to contribute to cutting-edge research and development in a dynamic and safety-focused work environment.,

Walk In Drive For Microbiology Department In Formulation Division @ Kothur Department :- Microbiology Qualification :- BSC | MSC - (Microbiology| Biotechnology | Biochemistry ) Experience :- 2 to 6 Years Division :- Formulation Interview Date:- 13-09-2025 Interview Time:- 9.00AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location:- MSNF-II, Kothur Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Note:- Candidate should bring Update Resume , Certificates, Aadhaar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

We are hiring for Multiple Position in Microbiology Dept. Please Note: Contact person Mr. Srinivasa M, those who are unable to attend the interview are requested to forward their resumes to email id: naveenkumarp@microlabs.in, jonesnaveenrajp@microlabs.in Candidates are requested to carry their copies of Resume, Mark Sheets, Experience Certificates, Latest salary certificate, pay slips of three months and one photograph Any queries call us on: 080-27839033, 34 & 38 MICROBIOLOGY: 1. Position: Asst. Manager/ Manager (Only for male candidates) Qualification: B.Sc/ M.Sc- Microbiology/ BioTech Experience: 9-14 years experience in Sterile Manufacturing facility. Job Profile: Reviewer and section incharge for QMS, MLT, Sterility and Environmental monitoring in sterile manufacturing facility 2. Position: Sr.Officer/ Executive / Sr. Executive ( Only for male candidates) Qualification: B.Sc/ M.Sc- Microbiology/ BioTech Experience: 2-8 years experience in Sterile Manufacturing facility. Job Profile: Microbiology Analytical Activities (MLT, BET, Sterility), Environmental monitoring, QMS activities in sterile manufacturing facility.

Role & responsibilities -Responsible to follow Good laboratory practice and lab safety practice in Quality Control Laboratory. -Responsible for preparation and standardization of volumetric solution and reagents. - Responsible for sampling of FP Product (Micro Sample) -Testing and release of microbial sample -Testing and release of environment monitoring of powder processing area of plants -Responsible to inform and abnormalities to QC head and responsible for investigation of incidents, system suitability failures, deviation, out of specification and out of trend -Responsible for providing on job training of QC personal, responsible for SOP training as per TNI -Responsible for maintenance & storage microbial cultures. -Responsible for standardization of microbial cultures and growth promotion test of media. -Responsible for calibration of instruments. -Disinfectant, maintenance & storage of microbial cultures. Indent & Procurement of chemicals, media and consumable items related to micro lab -Responsible for review of microbial data. -Review SOP index for SOP revision -Responsible for other activity define by QC head Mail ID: jagpal.dewal@ipca.com

Role & responsibilities 1. Maintain the equipment's and responsible for machines like ultrasonic cleaner & washer disinfector steam, ETO & Plasma sterilizer 2. Responsible for machine working condition , stock of instruments, dressing materials 3. Working knowledge in receive ,clean ,assemble ,pack, sterilize ,store and distributions 4. Washing unsterile instruments both manual and ultrasonic & washer disinfector 5. Arranging the unsterile materials with label and send for sterilization 6. Storage sterile items in proper area. Preferred candidate profile Candidates should be willing to do rotational shifts

You will be responsible for collecting, preparing, and analyzing samples using microbiological techniques. Your duties will include performing culture media preparation, sterilization procedures, microbial limit testing, sterility testing, and environmental monitoring. Operating and maintaining laboratory equipment such as autoclaves, incubators, and microscopes will also be part of your role. It will be essential to record and analyze test results accurately and promptly, while maintaining proper documentation, logs, and laboratory records in compliance with GLP/GMP standards. Additionally, you will assist in troubleshooting laboratory issues, reporting abnormal results, ensuring adherence to safety and quality control procedures, and disposing of hazardous materials and samples according to safety regulations. Supporting research and development projects as assigned will also be required. To qualify for this position, you should hold a Bachelor's degree or diploma in Microbiology, Biotechnology, or a related field. While 2 years of experience in a microbiology laboratory setting is preferred, freshers may be considered for entry-level roles. Experience with aseptic techniques and microbiological testing is also advantageous. You should possess knowledge of microbiological laboratory practices and techniques, along with attention to detail and accuracy in data recording. Good organizational and time-management skills are essential, as well as a basic understanding of lab safety and regulatory requirements (GLP, GMP, ISO). Proficiency with MS Office and laboratory information systems (LIMS) is considered a plus. This is a full-time or part-time position with a schedule that may include day shift, morning shift, and rotational shift. The work location is in person.,

Walk-in Drive @ Sanand, Ahmedabad location for Quality department (EM, Micro Testing & IPQA) for Injectable plant on 7thSep25 (Sunday). We are looking for suitable candidates for injectable/ sterile manufacturing plant for Ahmedabad location. Interview Venue Details: Date: 7thSep25 (Sunday) Time: - 9:00 AM to 2:00 PM Venue : Amneal Pharmaceuticals Pvt. Ltd. Plot No: 161/1, Sanand Bavla Highway Road, Village : Pipan, Sanand, Ahmedabad, Gujarat 382110 JOB LOCATION: Sanand, Ahmedabad 1. Quality Assurance - Environmental Monitoring (Microbiologist) Designation : Trainee/ Officer/ Sr. Officer / Executive Department : EM (Environmental Monitoring) Qualification : B.Sc. (Micro) / M. Sc (Micro) / B. Tech. (Biotech.) / M. Tech (Biotech)/ Total Experience: 1 to 05 years in injectable/ sterile manufacturing plant. Shift Type : Rotational Shift timing Total Positions: 5 Job Description: Environmental monitoring of manufacturing clean room area. Non-viable particle monitoring of manufacturing clean room area. Compressed air /nitrogen gas monitoring and Personnel monitoring. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g. plates, swabs, etc. To perform line clearance activity. 2. Quality Control – Micro Testing Designation : Trainee/ Officer/ Sr. Officer / Executive Department : Micro Testing Qualification : B.Sc. (Micro) / M. Sc (Micro) / B. Tech. (Biotech.) / M. Tech (Biotech)/ Total Experience: 1 to 05 years in injectable/ sterile manufacturing plant. Shift Type : Rotational Shift timing Total Positions: 5 Job Description: Candidate must have hands on experience of Sterility Testing, Bacterial Endotoxin Test (BET), Bioburden testing, water testing. Candidate must have handled OOS, OOT and EM Excursion. 3. Quality Assurance - IPQA (Injectable/Parenteral Unit) Designation : Officer/ Sr. Officer / Executive Department : QA- IPQA Qualification: B. Pharma/ M. Pharma Total Experience: 2 to 07 years in injectable/ sterile manufacturing plant. Shift Type : Rotational Shift timing Job Description: To perform line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labeling and packing. To perform Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP. Candidate with good communication & interpersonal skills, computer knowledge, exposure to cGMP and understanding of regulatory requirement will be preferred. Note : Candidate should relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliant) organization. Kindly carry your updated CV along with copies of CTC proof, Appointment letter, Increment letter, last 3 months salary slips, Bank statement, Education certificates & Marksheets, Aadhar & PAN card and passport size photograph, at the interview venue. Candidates who want to attend this walk IN can register themselves by filling their details on the below given URL: https://forms.office.com/r/qBd13HH2ZG Interested candidates who are unable to attend interview, can share their CV on below mentioned Email Id with subject line “Application for EM/Micro/ IPQA” or can apply online by scanning the QR Code: hitenkumar.patel@amneal.com or ajaykumar.pandey@amneal.com Disclaimer: Beware of fake job offers claiming to be from Amneal Pharmaceuticals Pvt. Ltd. or Companies under Amneal Group (collectively referred to as “AMNEAL”). Amneal neither send job offers from free email services like Gmail, Rediffmail, Yahoo mail, Hotmail, etc. nor charges any fees/security deposit from any job seekers. Amneal will not be responsible to anyone acting on an employment offer not directly made by Amneal. Stay vigilant and report any suspicious activity to Amneal.

Microbiology In-Charge to oversee and manage all microbiological activities within facility. The ideal candidate will be responsible for ensuring compliance with regulatory requirements, performing microbial testing, analyzing data, and maintaining the sterility assurance of products. This role includes leading a team, training staff, documentations related to micro, validation and implementing laboratory best practices.

Role Description We are seeking a detail-oriented and analytical professional to join our team as an AVP responsible for performing balance sheet spreading of corporate clients using the BARS (Balance Sheet Analysis and Reporting System) tool . This role is critical in supporting credit risk assessment and financial analysis processes. Lending Operations team is responsible in managing Lifecycle events on Syndicated Loan Deals, which provides Middle Office and Back Office support to Corporate and Investment banking divisions of the bank. The team is also involved in various aspects of recording and maintaining all Middle and Operational Roles of Loan Life Cycle includes trade support, trade documentation, trade settlements, cash reconciliation, Drawdown, Re-pricing, Payment. Team works closely with stakeholders in the Finance, Credit and technology divisions for multiple business lines such as Distressed Product Group (DPG), Commercial Real Estate (CRE) Global Credit Trading (GCT), Credit Solutions Group (CSG), and Structured Trade & Export Finance (STEF) etc. The role is demanding, complex & critical in nature and requires interaction with Front Office, Business, CRM Finance, Sales, Agent Bank and Clients. Your key responsibilities Background in Accounting and financial statement. Strong organisational skills; ability to identify and prioritise multiple tasks based on criticality, impact and franchise importance. Exceptional communication skills verbal, written and presentation. Independent problem solver who demonstrates accountability as well as execution capability. Ability to independently coordinate and manage work requirements across multiple business areas and functions. Ability to work in a fast-paced, highly regulated environment. Ability to connect with people as well as desire to learn process flows. Dedication to servicing a demanding internal and external client base. Should able to contribute as individual contributor as well. Accurately spread financial statements (balance sheet, and income statement) of corporate clients into the BARS system. Analyze financial data to ensure consistency, accuracy, and completeness. Collaborate with credit officers and relationship managers to clarify financial inputs and resolve discrepancies. Maintain documentation and audit trails for all financial spreads. Ensure compliance with internal policies, regulatory requirements, and data quality standards. Support periodic reporting and data validation exercises. Maintains the highest level of confidentiality with all information obtained. Meets expectations for attendance and punctuality. Manage the daily operations of the department in an efficient and effective manner Establish and maintain an efficient and productive working environment within the department based on continuous and effective staff communication. Participates in the review and recommendations of operational systems and procedures Communicate with management team to coordinate system and control activities Your skills and experience Considering the demanding, complex & critical nature of the role and able to work in fast passed environment with consistent deadlines, candidates should meet the below requirements. Bachelors degree in finance, Accounting, or a related field. German Language proficiency B1 and above Strong understanding of financial statements and accounting principles. Proficiency in Microsoft Excel; experience with BARS or similar financial spreading tools is a plus. 12+ years of experience in financial analysis, credit risk, or a similar role. High attention to detail and accuracy. Strong communication and collaboration skills. Excellent verbal & written communication along with dynamic & confident approach. Flexible with Shift. Ability to implement tasks and projects with minimal supervision. Team player who fosters team spirit in a global setting.

As a Quality Control Testing Technician in a Cell Therapy Lab, your primary responsibility is to ensure the quality and safety of cell therapy products through rigorous testing and analysis. You will work in a highly regulated environment, adhering to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) to support the development and production of cell-based therapies. This role requires a strong attention to detail, analytical skills, and the ability to work collaboratively with cross-functional teams. You will execute a variety of tests to assess the quality, purity, and potency of cell therapy products, including but not limited to viability assays, sterility testing, endotoxin testing, and identity testing. Operate and maintain specialized laboratory equipment and instruments used in cell therapy testing, such as flow cytometers, PCR machines, and automated cell counters. Maintain accurate and detailed records of all testing activities, ensuring compliance with regulatory requirements. Document deviations, investigations, and corrective actions as necessary. You are expected to stay current with industry regulations and standards related to cell therapy and ensure all testing activities align with applicable GMP, GLP, and other regulatory requirements. Participate in the validation and optimization of testing methods, ensuring that methods are robust, accurate, and reproducible. Work closely with Research and Development teams to transfer validated methods into routine quality control testing and collaborate with Production teams to troubleshoot and resolve any issues related to product quality. Conduct environmental monitoring to ensure the cleanliness and sterility of the laboratory environment. Analyze test results and prepare detailed reports for review by senior management. Communicate any deviations or trends that may impact product quality. Participate in continuous improvement initiatives to enhance laboratory processes and procedures, providing input on improving efficiency and reducing testing turnaround times. Train and mentor junior staff members on laboratory techniques, safety protocols, and quality control procedures. Qualifications required for this role include a postgraduate or masters degree in Life Sciences/Biochemistry/Microbiology. Previous experience in a quality control or analytical testing role within the biopharmaceutical or cell therapy industry will be of added value but not compulsory. A strong understanding of GMP, GLP, and other regulatory requirements, excellent communication and teamwork skills, attention to detail, and a commitment to quality are essential for this position. This job description is a general outline of the responsibilities and qualifications typically associated with the position of a Quality Control Testing Technician in a Cell Therapy Lab. Specific duties and qualifications may vary depending on the organization and the stage of development and production of cell therapy products.,

The work involves testing the sterility of rubber products used in pharmaceutical applications, analyzing water, overseeing the sterilization process, and conducting physical and chemical testing of rubber stoppers in the laboratory. The ideal candidate for this position would have a Bachelor's or Master's degree in Microbiology. They should have 2 to 3 years of experience, preferably in pharmaceutical testing. Candidates residing near Vasai will be given preference. This is a full-time position with day shift schedule. Candidates should be able to reliably commute to Vasai - 401208, Maharashtra or be willing to relocate before starting work. Overall, the successful candidate should have at least 2 years of relevant work experience in the field.,

You will be responsible for actively participating in the qualification activities within the manufacturing and Microbiology areas. This includes monitoring Compressed air/nitrogen gas and Personnel monitoring efficiently. Your key tasks will involve planning and executing environmental monitoring of the manufacturing and microbiology lab clean room area as per the defined schedule. Additionally, you will be responsible for planning the monitoring of compressed air/nitrogen gas and personnel. In this role, you will be expected to perform the calibration/qualification of instruments/equipment as per the predefined schedule. Furthermore, your duties will include active involvement in media fill simulation studies. You will also be responsible for handling tasks such as sterility testing, microbial identification, and bacterial endotoxin testing. This role requires a qualification of B.Sc./M.Sc./B. Pharm.,

Role & responsibilities To take care of Sterility Assurance Involved and well aware about Aseptic processing area requirement, personal qualification, Aseptic practices and concept Daily round at shopfloor for review and gap assessment. To do transfer Sterility assurance trending Aseptic area cleaning requirement and practices, on spot cleaning checking CCIT Preferred candidate profile Exposure in PFS, Cartridge, Vial filling line process Knowledge about sterility assurance concept Knowledge of Contamination control strategy and risk assessment Aware of Environment Monitoring concept Acquainted with media fill concept, BMR, Regulatory requirement Acquainted and involved in smoke study concept, execution and review w.r.t sterility practices

Eurofins is the world leading Food Testing laboratory group, deploying a comprehensive range of state-of-the-art analytical techniques in order to support its clients' increasingly stringent quality and safety standards. We are present in India as Eurofins Analytical Services India Pvt Ltd and provide a comprehensive and one-stop testing service to businesses and organizations involved in food and feed processing, Agro products, Export, Hospitality and Retail chains. About The Role Preparation of microbiology media Maintenance and calibration of Balance, Autoclave, water bath, LAF, BSC, Microscope etc. Performs microbiological testing in accordance with standard procedures Collect and analyze data to draw conclusions and recommend actions Apply appropriate methodologies and data interpretation techniques to assist in overcoming technical difficulties and promote continuous improvement. Maintains the laboratory quality assurance systems to assure validity of data Maintain accurate, up to date and concise laboratory records Supports a microbiological sampling and testing program. Understand and use basic laboratory safety equipment and instructions, precautions in handling and disposing of biological materials, in accordance with local environmental regulations. Additional Information Good interpersonal and communication skills. Energetic, flexible and innovative. Able to work independently and to coordinate several activities simultaneously. Good in communication, read and write in English and local language. Acts quickly and decisively. Knowledge in Microsoft Office (such asMicrosoft Word, Excel, Power Point, & etc.),

Eurofins is the world leading Food Testing laboratory group, deploying a comprehensive range of state-of-the-art analytical techniques in order to support its clients' increasingly stringent quality and safety standards. We are present in India as Eurofins Analytical Services India Pvt Ltd and provide a comprehensive and one-stop testing service to businesses and organizations involved in food and feed processing, Agro products, Export, Hospitality and Retail chains. About The Role Preparation of microbiology media Maintenance and calibration of Balance, Autoclave, water bath, LAF, BSC, Microscope etc. Performs microbiological testing in accordance with standard procedures Collect and analyse data to draw conclusions and recommend actions Apply appropriate methodologies and data interpretation techniques to assist in overcoming technical difficulties and promote continuous improvement. Maintenance of standard Reference Materials, Chemicals, Reagents and Glassware used in the laboratory. Maintains the laboratory quality assurance systems to assure validity of data Perform or assist vendor in the installation qualification (IQ), operational qualification (OQ) and performance qualification (PQ) of laboratory instruments and equipment. Maintain accurate, up to date and concise laboratory records Supports a microbiological sampling and testing program. Understand and use basic laboratory safety equipment and instructions, precautions in handling and disposing of biological materials, in accordance with local environmental regulations. Troubleshoot basic instrument or methodology problems. Qualifications 4-6 years experience of working in food testing laboratory. Strong knowledge of Food microbiology analysis. Additional Information Good interpersonal and communication skills. Energetic, flexible and innovative. Able to work independently and to coordinate several activities simultaneously. Good in communication, read and write in English and local language. Acts quickly and decisively. Knowledge in Microsoft Office (such asMicrosoft Word, Excel, Power Point, & etc.),

Eurofins is the world leading Food Testing laboratory group, deploying a comprehensive range of state-of-the-art analytical techniques in order to support its clients' increasingly stringent quality and safety standards. We are present in India as Eurofins Analytical Services India Pvt Ltd and provide a comprehensive and one-stop testing service to businesses and organizations involved in food and feed processing, Agro products, Export, Hospitality and Retail chains. About The Role Preparation of microbiology media Maintenance and calibration of Balance, Autoclave, water bath, LAF, BSC, Microscope etc. Performs microbiological testing in accordance with standard procedures Collect and analyse data to draw conclusions and recommend actions. Apply appropriate methodologies and data interpretation techniques to assist in overcoming technical difficulties and promote continuous improvement. Maintains the laboratory quality assurance systems to assure validity of data Maintain accurate, up to date and concise laboratory records Supports a microbiological sampling and testing program. Understand and use basic laboratory safety equipment and instructions, precautions in handling and disposing of biological materials, in accordance with local environmental regulations. Qualifications 2-3 years experience of working in food testing laboratory. Strong knowledge of Food microbiology analysis. Additional Information Good interpersonal and communication skills. Energetic, flexible and innovative. Able to work independently and to coordinate several activities simultaneously. Good in communication, read and write in English and local language. Acts quickly and decisively. Knowledge in Microsoft Office (such asMicrosoft Word, Excel, Power Point, & etc.),

Roles and Responsibilities Should have Hands on Experience in Handling the Microbiology Tastings/Pathogens Testing's at Quality Control Laboratory. Should have basic knowledge of Media Preparations, Discarding, Environment Monitoring, Swabs Testing's. Should have basic knowledge of CGMP, GLP, GHP. Documentation with Hands on Experience of SAP QA Module. Conduct microbiological testing, including bet, MLT, sterility testing, water analysis, and environmental monitoring. Desired Candidate Profile Proficiency in performing microbiological tests according to established protocols. Strong understanding of microbial culture techniques, microorganism identification methods, and quality control principles. Only Male Candidates required for this position.

Eurofins is a leading provider of assurance and inspection services, covering a broad spectrum of sustainable supply chain practices, including the circular economy. Eurofins helps the customers to identify and mitigate risks in their supply chain and to ensure the benchmarking performance with operations, processes, systems, people, or capabilities. We hold accreditations for various industry standards and memberships, ensuring comprehensive service throughout the supply chain. Whether you are in the food, consumer products, healthcare, or cosmetics industries, we offer a full range of services including product inspection, auditing, certification, training, and consultation. Eurofins Assurance helps you mitigate compliance risks, enhance quality, and prevent safety failures early on, safeguarding your business from brand damage, product recalls, and other potential issues in the future. Sustain your business growth and commitment with Eurofins Assurance, a global network of assurance experts that you can trust. Manage accreditation activities. Oversee certification operations. Handle unannounced, semi-announced, and additional audits. Support the Coordinator for reviewing and accepting applications. Maintain auditor qualifications and plan related activities for all schemes. Provide technical support to the team. Address technical queries from clients. Compile scheme updates for clients. Act as the product owner of IT tools for operation management. Verify and submit all scheme data internally and externally (scheme owner and accreditation body). Ensure readiness and updates for dTrackit, eTrackit, GTB, and the BCI portal. Investigate complaints. Conduct technical reviews of audit reports and documentation. Make certification decisions. Conduct calibration, harmonization, and technical training sessions. Manage accreditation activities. Oversee certification operations. Handle unannounced, semi-announced, and additional audits. Support the Coordinator for reviewing and accepting applications. Maintain auditor qualifications and plan related activities for all schemes. Provide technical support to the team. Address technical queries from clients. Compile scheme updates for clients. Act as the product owner of IT tools for operation management. Verify and submit all scheme data internally and externally (scheme owner and accreditation body). Ensure readiness and updates for dTrackit, eTrackit, GTB, and the BCI portal. Investigate complaints. Conduct technical reviews of audit reports and documentation. Make certification decisions. Conduct calibration, harmonization, and technical training sessions. Qualifications Bachelor's Degree in Textile Engineering from a reputed institute (preference for Postgraduates). 12 years of professional experience in a technical capacity in the textile industry, with at least 6 years in a certification body. ISO 9001 Lead Auditor Training Course. ISO 14001 Lead Auditor Training Course. SA 8000 Auditor Training Course. High level of proficiency with standards, related documents, interpretations, and the latest updates. Detailed knowledge of norm requirements for GOTS, GRS, RCS, OCS, MMS, Better Cotton. Knowledge of production methods and processes applicable to textile, plastic, paper, leather, and metal industries. Ability to produce clear, accurate, and complete written audit reports and technical review reports. Experience conducting shadow audits for auditors. Bachelor's Degree in Textile Engineering from a reputed institute (preference for Postgraduates). 12 years of professional experience in a technical capacity in the textile industry, with at least 6 years in a certification body. ISO 9001 Lead Auditor Training Course. ISO 14001 Lead Auditor Training Course. SA 8000 Auditor Training Course. High level of proficiency with standards, related documents, interpretations, and the latest updates. Detailed knowledge of norm requirements for GOTS, GRS, RCS, OCS, MMS, Better Cotton. Knowledge of production methods and processes applicable to textile, plastic, paper, leather, and metal industries. Ability to produce clear, accurate, and complete written audit reports and technical review reports. Experience conducting shadow audits for auditors. Additional Information Impeccable proficiency in both written and spoken English. Knowledge of a foreign language is an added advantage. Highly organized with the ability to plan and prioritize work. Efficient time management. Working knowledge of Microsoft Office tools (Word, Excel, PowerPoint, SharePoint, Teams). Experience with IT tools used in certification or accreditation bodies.

Bachelor (s)/master(s) degree in microbiology, Biotechnology, Biochemistry, Chemical Engineering or a related field. Min.experience of 8-10 years in industrial fermentation, preferably in bio-fertilizer, agriculture, or biotech manufacturing. Proven expertise in scaling microbial fermentation processes from lab to industrial scale. Strong understanding of microbial cultures, anaerobic/aerobic fermentation processes, and downstream processing techniques. Experience with fermentation equipment, reactors, control systems, and process automation. Knowledge of quality control standards, Good Manufacturing Practices (GMP), and regulatory requirements for bio-fertilizer production. Excellent problem-solving skills and the ability to troubleshoot fermentation processes. Strong leadership, communication, and team management skills. Proficiency in SAP, ERP, Microsoft & Analytical ability for process control and monitoring Skills Required : Sop Preparation, GMP, HACCP, Food Safety, Food Microbiology, Industrial Microbiology, biotechnology,Quality Standards, fermentation, downstream processing, Fermentation Technology, Environmental Monitoring, Sterility Testing Roles and Responsibilities : Oversee fermentation processes to ensure high-quality bio-fertilizer production. Manage daily operations of fermentation systems, including starter cultures, inoculation, scaling, and fermentation controls. Monitor the fermentation process parameters (e.g., temperature, pH, dissolved oxygen) and make necessary adjustments to optimize productivity and yield. Supervise and train the fermentation team, ensuring that the team follows the appropriate standard operating procedures (SOPs), safety guidelines, and quality control measures. Collaborate with R&D and process engineering teams to develop and optimize fermentation protocols and implement process improvements. Troubleshoot and resolve any issues related to fermentation equipment, microbial contamination, and process failures. Ensure that production schedules are met while maintaining quality and efficiency targets. Conduct routine checks, data analysis, and prepare reports on fermentation performance, yields, and deviations. Ensure compliance with environmental and safety regulations related to bio-fertilizer production. Maintain proper documentation of fermentation batches, quality control data, and other critical process information. Work closely with maintenance teams to ensure equipment is properly maintained and calibrated. Stay updated on the latest trends and technologies in fermentation, microbial growth, and bio-fertilizer production. Batch failure Analysis and Trouble shooting. Cost Control w.r.t RM, Process efficiency & Operation

Roles and Responsibility Conduct microbial testing and analysis to ensure product quality and safety. Develop and implement microbiological protocols and procedures. Collaborate with cross-functional teams to achieve project goals. Maintain accurate records of test results and inventory management. Ensure compliance with regulatory requirements and industry standards. Participate in continuous improvement initiatives to enhance laboratory operations. Job Requirements Bachelor's degree in Microbiology or related field. Strong knowledge of microbiological techniques and principles. Excellent analytical and problem-solving skills. Effective communication and teamwork skills. Ability to work in a fast-paced environment and meet deadlines. Familiarity with laboratory information systems and software.

We are looking for a highly motivated and experienced Assistant in Microbiology to join our team at Vijaya Diagnostic Centre Limited. The ideal candidate will have 1-3 years of experience in the field. Roles and Responsibility Conduct microbial testing and analysis to ensure product quality and safety. Develop and implement microbiological protocols and procedures. Collaborate with cross-functional teams to achieve project goals. Maintain accurate records of test results and inventory management. Ensure compliance with regulatory requirements and industry standards. Participate in continuous improvement initiatives to enhance laboratory operations. Job Requirements Bachelor's degree in Microbiology or related field. Strong knowledge of microbiological techniques and principles. Excellent analytical and problem-solving skills. Effective communication and teamwork skills. Ability to work in a fast-paced environment and meet deadlines. Familiarity with laboratory information systems and software.

Job Summary: We are seeking a dedicated and experienced Executive - Microbiologist (Sterility) to join our Quality Control Microbiology team in a sterile injectable manufacturing environment. The candidate will be responsible for performing and supervising sterility testing, monitoring aseptic practices, environmental monitoring, and ensuring microbiological compliance with cGMP and regulatory standards. Key Responsibilities: Perform sterility testing of finished injectable products as per pharmacopoeial and regulatory guidelines (USP, EP, IP, JP). Operate and maintain sterility testing isolators or sterility testing rooms in compliance with aseptic techniques. Conduct environmental monitoring of aseptic manufacturing areas (settle plates, air sampling, surface monitoring, personnel monitoring). Carry out media fill (process simulation) testing and participate in its execution and analysis. Perform bioburden, endotoxin (LAL test), water testing , and microbial limit tests . Ensure proper documentation as per GDP (Good Documentation Practices). Maintain calibration and qualification records of instruments such as incubators, isolators, particle counters , etc. Investigate microbial deviations, sterility failures , and environmental excursions. Assist in the preparation of documents for regulatory inspections (USFDA, MHRA, EU, etc.) and participate in audits. Adhere to EHS (Environmental Health & Safety) guidelines and laboratory safety protocols. Required Qualifications & Skills: Educational Qualification : M.Sc. in Microbiology / Biotechnology or B. Pharm with Microbiology specialization. Experience : 25 years of relevant experience in a sterile injectable pharmaceutical plant. Strong knowledge of cGMP, GLP, aseptic techniques , and sterile area practices . Hands-on experience with sterility testing isolators / sterility test rooms . Familiarity with regulatory guidelines (USFDA, EU GMP, WHO, PIC/S). Good communication and documentation skills. Ability to work in shifts (if required). Preferred candidate profile

About ALS India ALS is a global leader in testing, inspection, certification & verification, present in 65+ countries with 350+ labs. ALS India offers cutting-edge analytical services across Pharmaceutical, Food, Environment & Consumer Products from a 30,000 sq. ft. facility in Bengaluru. Key Responsibilities Responsible for Environmental monitoring, calibration, routine activity, maintain cleanliness of the laboratory, Media Preparation and Growth Promotion Test, Microbial Limit Test, Preservative Efficacy Test, Sterility Testing, Bacterial Endotoxin Test, Antibiotic Assay. Instrumentation Skills Handling of Weighing balance, pH meter, Autoclave, Biosafety Cabinet/Laminar Air Flow cabinet, Micropipette, Incubators etc. Core Competencies Microbial Limit Test and Antibiotic Assay Regulatory Frameworks Should have knowledge of Guidelines like USFDA, MHRA, WHO, schedule M, EU-GMP, ICH, TGA and other regulatory requirements.

Job description Lead the verification and validation of analytical and microbiological methods, ensuring they meet all regulatory and internal quality requirements. Design, execute, and document method validation protocols, including accuracy, precision, specificity, and robustness studies, in compliance with FDA, TGA, ICH, and EMA guidelines. Review and approve validation protocols and reports, ensuring they are scientifically sound and fully compliant with Good Laboratory Practice (GLP) and other relevant regulatory standards. Analytical and Microbiology Methods: Provide expert review and oversight of analytical and microbiological testing protocols, data, and reports, ensuring compliance with regulatory standards and internal quality systems. Oversee the development, validation, and implementation of new analytical and microbiological methods and, including but not limited to chemical analysis, sterility testing, microbial limits testing, and endotoxin testing. Ensure that all methods are validated to provide reproducible and accurate results, adhering to FDA, TGA, ICH, and EMA requirements Data Review and Integrity: Conduct thorough reviews of raw data and final reports related to analytical and microbiology testing and method validation. Ensure that all data generated during analytical and microbiological testing is accurate, complete, and adheres to the approved protocols and SOPs. Identify and resolve any data discrepancies or deviations from established protocols. Regulatory Compliance: Ensure that all analytical and microbiological methods and validations comply with FDA, TGA, ICH, and EMA regulations. Assist in the preparation of documentation for regulatory submissions, providing quality assurance support for analytical and microbiological data and validation reports. Continuous Improvement: Contribute to the development and continuous improvement of quality systems related to analytical and microbiological methods and validation processes. Participate in root cause analysis of quality issues and support the implementation of corrective and preventive actions (CAPAs). Training and Development: Provide guidance and training to R&D staff on best practices in analytical and microbiological testing, method validation, and quality assurance. Act as a mentor and resource for junior staff in the areas of analytical development, microbiology and quality assurance What you d gain: Invaluable hands-on experience working alongside seasoned developers. Opportunity to learn and grow in a supportive environment. Gain exposure to the entire software development lifecycle. Contribute to real-world software projects and make a positive impact. Qualifications: Bachelor s degree in Chemistry, Microbiology, Biology, Pharmaceutical Sciences, or a related scientific discipline is required. Advanced degree (Master s or Ph.D.) in a related field is preferred. Minimum of 5-7 years of experience in quality assurance with a focus on analytical, microbiology, method verification, and validation within the pharmaceutical, biotech, or life sciences industries. Extensive experience with analytical and microbiological testing methods, including method verification, validation, sterility, microbial limits, and endotoxin testing. Strong expertise in analytical and microbiological methods and their application in product development. Excellent attention to detail and analytical skills with a focus on data integrity and accuracy. Strong written and verbal communication skills, with the ability to document and present complex technical information clearly. Ability to work effectively in a team-oriented environment and collaborate across multiple departments. Proficiency with quality management systems and software tools. This position is remote and may require occasional travel to other sites or meetings. The role may involve working in a laboratory environment with exposure to chemicals and biohazardous materials.