Job Description Job Title: Maturation & Lab Process Senior Executive About Us With over 200 brands sold in nearly 180 countries, we’re the world’s leading premium drinks company. Bring your passion and use your curiosity as you explore, collaborate, and innovate to build brands consumers love. Together with passionate people from all over the world, you’ll test new ideas, learn and grow, and unlock a brighter, more exciting future. Join us to create a career worth celebrating. About The Function Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo’s 30,000+ people work in Supply Chain and Manufacturing. It’s an intricate and sophisticated operation that’s the product of logistical, manufacturing, and technical collaborations. Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We’re committed to realising our ‘Society 2030: Spirit of Progress’ goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience, we’ll help you to thrive in our inclusive culture. Role Responsibilities Report if quality variation found in RM/chemicals/ enzymes during operation Report if the quality of product deviated from specification and take corrective action Analyse treated & untreated effluent To control quality defects in incoming and finished goods so as to get customer satisfaction by applying high quality standards in the product and the process. Responsible for delivery of production as per shift/day target Accountable for operation of plant as per SOP and ensure production as per defend quality parameters of product. Monitor and maintain record of all process parameters, Production and plant efficiency, raw material, utilizes consumption on daily basis and explore methods for improvements. Analyse process / quality parameter as per SOP and record in log book, take decision in changing plant operating parameters to deliver production Troubleshoot plant breakdown, report plant breakdown/ report maintenance requirements of the plant. Support maintenance team during planned long shutdown Analyse and record online quality parameters as per SOP Verify the FF, FE & DE as per budget. Maintain hygiene and safety in area of plant, cooling tower & ETP Ensure proper gas generation takes place at ETP & as per norms of RSPCB Coordinate with utilities and maintenance team to ensure upkeep of plant equipment Co-ordinate with internal departments to ensure smooth operations Engage with external government bodies as required (Pollution Board officials) Capability to build and promote food safety and quality culture in unit. Responsible for end-to-end Quality monitoring in incoming and online checks. Responsible for Quality Control and other control activities in the factories and material. Responsible for checking raw material used in production, packaging material and in process material and finished goods- accept or reject as per set quality standards. Responsible for record maintaining and SAP records updation. Undertake training and development of shop floor workmen. To conduct internal quality audits for GMP, GRMS and SQIP. Deal with the Government authorities like FSSAI , LMR and Excise for audit and compliance. Ensuring that samples of all products are sent to external laboratory and calibration of equipment’s done as per requirement. To conduct analysis of raw materials and packaging materials and report in time. To visit market whenever new product / product quality survey / complaint samples collection is required. Implement GMP/ GLP, GSP and GHP in premises at all times and 5S. Good oral and written communication skills and to maintain MIS data. Vendor communication for rejection and its handling on time and development in co-ordination with site QA team. Quick learning and initiative attitude in working. Experience / Skills Required Candidate shall be Graduate/Postgraduate in Science, Food technology/ Microbiology/DIFAT, Shall have min. 2-4 years of experience in FMCG i.e. distilleries/Breweries /Beverages/Food industries. Hands on experience in analysis techniques, lab instruments calibration and maintenance Knowledge on QMS and FSMS Knowledge on word, Excel and power point. Ensure sufficient inventory of RM in day tanks / warehouse required for production Monitor and record the consumption of RM in the shift/day Monitor the sensory quality of FMS produced as per required norm Flexible Working Statement Flexibility is key to our success. Talk to us about what flexibility means to you so that you’re supported to manage your wellbeing and balance your priorities from day one. Diversity Statement Our purpose is to celebrate life, every day, everywhere. And creating an inclusive culture, where everyone feels valued and that they can belong, is a crucial part of this. We embrace diversity in the broadest possible sense. This means that you’ll be welcomed and celebrated for who you are just by being you. You’ll be part of and help build and champion an inclusive culture that celebrates people of different gender, ethnicity, ability, age, sexual orientation, social class, educational backgrounds, experiences, mindsets, and more. Our ambition is to create the best performing, most trusted and respected consumer products companies in the world. Join us and help transform our business as we take our brands to the next level and build new ones as part of shaping the next generation of celebrations for consumers around the world. Feel inspired? Then this may be the opportunity for you. If you require a reasonable adjustment, please ensure that you capture this information when you submit your application. Worker Type Regular Primary Location: Nasik Unit III (Nass) Additional Locations : Job Posting Start Date 2025-05-19 Show more Show less

Job Description: The Phlebotomist in Home Care will be responsible for performing blood collection and related procedures in a home setting, ensuring patient comfort and safety at all times. The role involves traveling to patients' homes to conduct blood draws, as well as maintaining accurate records of patient information and samples collected. The Phlebotomist will work closely with other healthcare professionals to facilitate effective patient care and ensure timely delivery of laboratory results. Roles and Responsibilities Key Responsibilities: - Perform venipunctures and blood draws in a variety of settings, primarily in patients' homes. - Ensure proper preparation of patients for blood collection and provide education regarding the procedure. - Maintain strict adherence to safety and infection control protocols while handling specimens. - Accurately label and document specimens collected for laboratory analysis. - Communicate effectively with patients, caregivers, and healthcare providers regarding procedures and results. - Keep up-to-date with best practices and attend training sessions as required. - Maintain equipment and supplies in accordance with safety standards. - Ensure timely reporting and follow-up on any issues that arise during home visits.

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

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

Urgent Requirement SR, AP, Associate Professor and Professor for Qualified MS/MD Doctors .

Key Responsibilities JOB DESCRIPTION Water sampling and analysis Microbial Limit Test Sterility test Bioburden test Preservative efficacy test Bacterial endotoxin test. Qualifications Qualification: M.Sc. (Microbiology) Experience: 4-9 years Person should have an experience to perform Microbial analysis Show more Show less

Job Description Manager, Regulatory Affairs - CMC This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance’s and defined regulatory strategies. He would even be responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. Your role at our organization is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. Regulatory Responsibilities Primary responsibilities include, but are not limited to Provide input to global product and project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements and critically evaluating supporting documentation to assess acceptability and identify potential risks. Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements/variations, annual reports, registration renewals and responses to health authority questions per established business processes and systems. Liaise with global CMC, Our Manufacturing Division and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. Assess and communicate potential regulatory risks and propose mitigation strategies. Deliver all regulatory milestones for assigned products across the product lifecycle Identify and communicate potential regulatory issues to GRACS CMC management, as needed Technical Skills Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills. Demonstrated understanding of related fields (e.g., pharmaceutical manufacturing, analytical testing, and quality assurance). Proficient computer skills and previously demonstrated ability to operate in electronic document based GMP systems Leadership Skills Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders. Demonstrated flexibility in responding to changing priorities or dealing with unexpected events. Capability to handle multiple priorities and balance work to achieve business goals. Demonstrated effective leadership, communication, and interpersonal skills Qualifications & Skills Bachelor’s in Science, Engineering, or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry Minimum 5 – 7 yrs of Industry Pharmaceutical industry experience out of 4 years’ experience in managing CMC Regulatory submissions for small molecules/vaccines/biologics The candidate may be required to travel to other CMO sites on a need basis. We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively for the common good. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status Regular Relocation VISA Sponsorship Travel Requirements Flexible Work Arrangements Hybrid Shift Valid Driving License Hazardous Material(s) Required Skills Preferred Skills Job Posting End Date 06/30/2025 A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID R339386 Show more Show less

About GRG Health: GRG Health (A Growman Group Company) is an awarded, global healthcare knowledge services and market research company headquartered in Pune (India) with offices in Gurgaon, Bangalore, Boston (USA), and Singapore. GRG Health is working on developing machine learning models that can be implemented in traditional insights gathering and analytics approaches. Our dedicated team of data scientists is working with a few clients on a pilot run of our AI engine. Experience: Fresher Qualifications: • (Biotech, Microbiology, and any life science or healthcare stream) and above graduates (in healthcare) Roles & Responsibilities: • You will be responsible for conducting online market/business. • Support in research and analysis of market topics. • Generate market reports/information database. • Create leads across EU and APAC countries and recruit them for interviews via email and phone. • Assisting moderate qualitative and quantitative interviews with professionals across the globe via phone. • Candidate is expected to conduct in-depth interviews (both face-to-face and telephonic) of target respondents. • Candidate is expected to interpret the data and liaise with the team to generate insights and develop reports. Skill set required: • Strong communication and presentation skills • Ability to interpret data and do multitask • Knowledge of Market Research • Strong analytical and critical skills Job type: Full Time (Work from Office) Location: Pune Probation – 3 Months Bond – 1 Year Selection process: There will be two rounds of the selection process: • PI - 1st Round – HR Interview • PI - 2nd Round – Management Interview Show more Show less

Job Description Manager, Regulatory Affairs - CMC This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance’s and defined regulatory strategies. He would even be responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. Your role at our organization is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. Regulatory Responsibilities Primary responsibilities include, but are not limited to Provide input to global product and project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements and critically evaluating supporting documentation to assess acceptability and identify potential risks. Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements/variations, annual reports, registration renewals and responses to health authority questions per established business processes and systems. Liaise with global CMC, Our Manufacturing Division and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. Assess and communicate potential regulatory risks and propose mitigation strategies. Deliver all regulatory milestones for assigned products across the product lifecycle Identify and communicate potential regulatory issues to GRACS CMC management, as needed Technical Skills Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills. Demonstrated understanding of related fields (e.g., pharmaceutical manufacturing, analytical testing, and quality assurance). Proficient computer skills and previously demonstrated ability to operate in electronic document based GMP systems Leadership Skills Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders. Demonstrated flexibility in responding to changing priorities or dealing with unexpected events. Capability to handle multiple priorities and balance work to achieve business goals. Demonstrated effective leadership, communication, and interpersonal skills Qualifications & Skills Bachelor’s in Science, Engineering, or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry Minimum 5 – 7 yrs of Industry Pharmaceutical industry experience out of 4 years’ experience in managing CMC Regulatory submissions for small molecules/vaccines/biologics The candidate may be required to travel to other CMO sites on a need basis. We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively for the common good. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status Regular Relocation VISA Sponsorship Travel Requirements Flexible Work Arrangements Hybrid Shift Valid Driving License Hazardous Material(s) Required Skills Preferred Skills Job Posting End Date 06/30/2025 A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID R339386 Show more Show less

Job Description Summary The Senior Manager, Quality Control Microbiology is responsible for overseeing the day-to-day operations of the Microbiology laboratory operations. Supervision and enforcing cGMP’s, GLP’s, conducting investigations, verification of compendia methods and training of new employees. Additional responsibility includes building the data integrity aspects in the tasks performed at the lab and responsible to comply to 21 CFR part 11 of lab instruments. Job Description The Senior Manager, Quality Control Microbiology is responsible for overseeing the day-to-day operations of the Microbiology laboratory operations. Show more Show less

Company Description: Established in 1951, Fermenta Biotech Limited (FBL) is a global Vitamin D3 manufacturer with state-of-the-art R&D and manufacturing facilities in Thane, Kullu, and Dahej. FBL also offers niche APIs, enzymes for antibiotic synthesis, and environmental solutions for wastewater management. www.fermentabiotech.com Summary: Fermenta Biotech Limited is looking for an experienced and highly motivated Jr. Executive / Executive to join our Biotech Division. The ideal candidate will have hands-on experience in both upstream and downstream processes, with specific expertise in fermentation and critical shift process handling. This role is integral to the production of high-quality pharmaceutical APIs, and the candidate must possess knowledge of cGMP standards, documentation practices, and sterilization processes. The successful candidate will play a key role in supporting the production team and ensuring the smooth operation of biotech manufacturing processes. Roles & Responsibilities: Upstream and Downstream Process Handling: Manage and monitor both upstream (fermentation) and downstream (purification, recovery, etc.) processes to ensure the smooth production of biotechnological products. Operate and maintain equipment involved in these processes. Fermentation Expertise: Operate fermentation systems, monitor fermentation parameters, and ensure optimal conditions for microbial growth and product yield. Handle fermentation media, inoculation, and harvest processes. Dry Heat Sterilization: Perform dry heat sterilization for equipment, media, and related items as per SOPs to ensure sterile conditions are maintained in the production environment. Critical Shift Process Management: Oversee critical shift operations during fermentation and other biotechnological processes. Ensure processes are running according to predefined protocols and handle any process deviations or issues during shifts. Compliance with cGMP & Documentation: Ensure all activities are conducted in compliance with current Good Manufacturing Practices (cGMP). Maintain and update necessary documentation, including batch records, process logs, and compliance reports. Troubleshooting & Process Optimization: Troubleshoot any issues or deviations in the production processes and provide solutions. Assist in process improvements and optimization activities to enhance production efficiency and yield. Safety & SOP Adherence: Ensure all safety protocols and standard operating procedures (SOPs) are strictly followed during biotech production activities. Participate in training sessions to stay updated on safety, regulatory, and technical advancements. Cross-functional Collaboration: Collaborate with other departments such as Quality Control (QC), Quality Assurance (QA), and Maintenance to ensure the production process runs smoothly and meets the required standards. Qualification & Skill Requirements: Graduate in Science (e.g., Biotechnology, Microbiology, Biochemistry, or related field). Minimum 3 years of proven experience in biotech production, specifically in fermentation and downstream/upstream processing within the pharmaceutical/API industry. Extensive experience in fermentation processes. Hands-on experience with downstream and upstream processing techniques. Thorough understanding of cGMP regulations and documentation requirements. Proficiency in dry heat sterilization and handling critical shift processes. Knowledge of relevant equipment and instrumentation. Strong analytical and problem-solving skills. Excellent communication and interpersonal skills. Ability to work effectively in a team environment. Strong attention to detail and accuracy. Ability to work under pressure and meet deadlines. Adaptability to changing priorities and tasks. Show more Show less

Established in 1806 as a small soap and candle business in New York City, Colgate-Palmolive is now a truly global company with products sold in over 200 countries and territories under such internationally recognized brand names as Colgate, Palmolive, Softsoap, Irish Spring, Protex, Sorriso, Kolynos, elmex, Tom's of Maine, Sanex, Ajax, Axion, Soupline, Haci Sakir, Suavitel, PCA SKIN, EltaMD, Filorga and Hello as well as Hill's Science Diet and Hill's Prescription Diet. Colgate-Palmolive is a leading consumer products company that serves hundreds of millions of consumers worldwide with brands and products across four core businesses – Oral Care, Personal Care, Home Care and Pet Nutrition. We are committed to offering products that make lives healthier and more enjoyable, and programs that enrich communities around the world. Every day millions of people trust our products to care for themselves and the ones they love. Our goal is to use our technology to create products that will continue to improve the quality of life for our consumers wherever they live. A career at Colgate-Palmolive is an excellent opportunity if you seek a global experience, constant challenge, and development opportunities in an environment that respects work/life effectiveness. Job Title: Research Trainee - GS&S Travel Required?: No Travel Date: Jun 10, 2025 No Relocation Assistance Offered Job Number #167436 - Mumbai, Maharashtra, India Who We Are Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Our products are trusted in more households than any other brand in the world, making us a household name! Join Colgate-Palmolive, a caring, innovative growth company reimagining a healthier future for people, their pets, and our planet. Guided by our core values—Caring, Inclusive, and Courageous—we foster a culture that inspires our people to achieve common goals. Together, let's build a brighter, healthier future for all. What are we looking for: We are looking for smart, dynamic candidates to join us as trainees who will work in our India Global technology center (GTC) based in Mumbai. It will be a learning & growth opportunity for them to learn about many aspects of Product Lifecycle Management. We are the guardians of Colgate’s Proprietary data in the form of its raw materials and recipes. Data governance of master data of Colgate raw materials and recipes is our primary responsibility. All activity related to assigning correct master data to raw materials and recipes post proper review, assigning access after due diligence of each user’s background and supporting allied functions of the group like PDM data Cleansing and System testing would be a part of the regular activities. Along with this administrative role, every Scientist in India GTech is expected to be an integral part of EHS & Quality standards that ensures Safety & Quality of our products and working environment. This team works on strong partnerships with cross categories within India GTech & other GTechs & plants. The tenure for a trainee is proposed to 2 years from the date of joining. What you’ll need Post graduate in Pure sciences (Chemistry ,Biology)/ Pharmacy/ Technology (Cosmetics) with strong fundamental knowledge in basic chemistry and fair to good exposure to SAP database management / system administration activities and concepts Working knowledge of Microsoft Office or Google Suite proficiency (i.e, Sheets, Slides, Docs) Strong aptitude for computer systems What you will do: 1.Data governance of first level review of CP Raw materials and Recipes within a turnaround time of 72 hours 2. Provide Security Access roles to PDP/DMS /PPM/LIMS system with due diligence 3. Route Human Use Protocols (HUP) through SAP-DMS to the correct reviewers; support the process in Veeva as Admin. Route Adverse Event (AE) for all HUP studies to Pharmacovigilance team who will then perform an evaluation 4. Provide technical support and procedural guidance to 2000+ English-speaking PDM end-users via phone calls, emails and instant messages 5. Support Team in PDM Cleansing / Ancillary activities like Obsoleting recipes and Searches What you will learn: Core expertise on principles that govern data regarding our raw materials and recipes Elements of due diligence while providing access to SAP system users Functional Linkages - you will get an overview of how different departments are integrated into overall R&D eg: Analytical, R&I, Microbiology and implementation & support teams. Operational Excellence - Build on technical expertise, expanding it in complementary directions. Use technical expertise and creativity to proactively identify potential problems and address them using appropriate resources in discussion with team leads. You will also learn to integrate yourself into a high-performing team focused on balancing both execution and innovation. You will be coached for success on technical and soft skills. We will evaluate your progress periodically and ensure scheduled training sessions for your continued success during your traineeship at Colgate. Quality and Safety principles: At Colgate we strive for excellence in everything we do, Quality and safety is not far away. These principles are not only important for our trusted brands but also to our workplaces. You will be exposed to specific training on Q & S, to assure your trust while working in a safe environment where quality is paramount. Compensation and Benefits Salary Range $ - $ USD Pay is determined based on experience, qualifications, and location. Salaried employees may also be eligible for discretionary bonuses, profit-sharing, and long-term incentives for Executive-level roles. Benefits: Salaried employees enjoy a comprehensive benefits package, including medical, dental, vision, basic life insurance, paid parental leave, disability coverage, and participation in the 401(k) retirement plan with company matching contributions subject to eligibility requirements. Additional benefits include a minimum of 15 vacation/PTO days (hourly employees receive a minimum of 120 hours) and 13 paid holidays (vacation days are prorated based on the employee's hire date within the calendar year). Paid sick leave is adjusted based on role and location in accordance with local laws. Detailed information regarding paid sick leave entitlements will be provided to employees upon hiring and may be subject to adjustments based on changes in legislation or company policies. Our Commitment to Inclusion Our journey begins with our people—developing strong talent with diverse backgrounds and perspectives to best serve our consumers around the world and fostering an inclusive environment where everyone feels a true sense of belonging. We are dedicated to ensuring that each individual can be their authentic self, is treated with respect, and is empowered by leadership to contribute meaningfully to our business. Equal Opportunity Employer Colgate is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, ethnicity, age, disability, marital status, veteran status (United States positions), or any other characteristic protected by law. Reasonable accommodation during the application process is available for persons with disabilities. Please complete this request form should you require accommodation. For additional Colgate terms and conditions #LI-[[filter12]]

No Relocation Assistance Offered Job Number #167436 - Mumbai, Maharashtra, India Who We Are Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Our products are trusted in more households than any other brand in the world, making us a household name! Join Colgate-Palmolive, a caring, innovative growth company reimagining a healthier future for people, their pets, and our planet. Guided by our core values—Caring, Inclusive, and Courageous—we foster a culture that inspires our people to achieve common goals. Together, let's build a brighter, healthier future for all. What are we looking for: We are looking for smart, dynamic candidates to join us as trainees who will work in our India Global technology center (GTC) based in Mumbai. It will be a learning & growth opportunity for them to learn about many aspects of Product Lifecycle Management. We are the guardians of Colgate’s Proprietary data in the form of its raw materials and recipes. Data governance of master data of Colgate raw materials and recipes is our primary responsibility. All activity related to assigning correct master data to raw materials and recipes post proper review, assigning access after due diligence of each user’s background and supporting allied functions of the group like PDM data Cleansing and System testing would be a part of the regular activities. Along with this administrative role, every Scientist in India GTech is expected to be an integral part of EHS & Quality standards that ensures Safety & Quality of our products and working environment. This team works on strong partnerships with cross categories within India GTech & other GTechs & plants. The tenure for a trainee is proposed to 2 years from the date of joining. What you’ll need Post graduate in Pure sciences (Chemistry ,Biology)/ Pharmacy/ Technology (Cosmetics) with strong fundamental knowledge in basic chemistry and fair to good exposure to SAP database management / system administration activities and concepts Working knowledge of Microsoft Office or Google Suite proficiency (i.e, Sheets, Slides, Docs) Strong aptitude for computer systems What you will do: 1.Data governance of first level review of CP Raw materials and Recipes within a turnaround time of 72 hours 2. Provide Security Access roles to PDP/DMS /PPM/LIMS system with due diligence 3. Route Human Use Protocols (HUP) through SAP-DMS to the correct reviewers; support the process in Veeva as Admin. Route Adverse Event (AE) for all HUP studies to Pharmacovigilance team who will then perform an evaluation 4. Provide technical support and procedural guidance to 2000+ English-speaking PDM end-users via phone calls, emails and instant messages 5. Support Team in PDM Cleansing / Ancillary activities like Obsoleting recipes and Searches What you will learn: Core expertise on principles that govern data regarding our raw materials and recipes Elements of due diligence while providing access to SAP system users Functional Linkages - you will get an overview of how different departments are integrated into overall R&D eg: Analytical, R&I, Microbiology and implementation & support teams. Operational Excellence - Build on technical expertise, expanding it in complementary directions. Use technical expertise and creativity to proactively identify potential problems and address them using appropriate resources in discussion with team leads. You will also learn to integrate yourself into a high-performing team focused on balancing both execution and innovation. You will be coached for success on technical and soft skills. We will evaluate your progress periodically and ensure scheduled training sessions for your continued success during your traineeship at Colgate. Quality and Safety principles: At Colgate we strive for excellence in everything we do, Quality and safety is not far away. These principles are not only important for our trusted brands but also to our workplaces. You will be exposed to specific training on Q & S, to assure your trust while working in a safe environment where quality is paramount. Compensation and Benefits Salary Range $ - $ USD Pay is determined based on experience, qualifications, and location. Salaried employees may also be eligible for discretionary bonuses, profit-sharing, and long-term incentives for Executive-level roles. Benefits: Salaried employees enjoy a comprehensive benefits package, including medical, dental, vision, basic life insurance, paid parental leave, disability coverage, and participation in the 401(k) retirement plan with company matching contributions subject to eligibility requirements. Additional benefits include a minimum of 15 vacation/PTO days (hourly employees receive a minimum of 120 hours) and 13 paid holidays (vacation days are prorated based on the employee's hire date within the calendar year). Paid sick leave is adjusted based on role and location in accordance with local laws. Detailed information regarding paid sick leave entitlements will be provided to employees upon hiring and may be subject to adjustments based on changes in legislation or company policies. Our Commitment to Inclusion Our journey begins with our people—developing strong talent with diverse backgrounds and perspectives to best serve our consumers around the world and fostering an inclusive environment where everyone feels a true sense of belonging. We are dedicated to ensuring that each individual can be their authentic self, is treated with respect, and is empowered by leadership to contribute meaningfully to our business. Equal Opportunity Employer Colgate is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, ethnicity, age, disability, marital status, veteran status (United States positions), or any other characteristic protected by law. Reasonable accommodation during the application process is available for persons with disabilities. Please complete this request form should you require accommodation. For additional Colgate terms and conditions, please click here. #LI-[[filter12]]

We are seeking a highly skilled Microbiologist to conduct microbiological tests and experiments, prepare samples and reagents for analysis, maintain laboratory equipment, and ensure compliance with safety standards.

JOB TITLE: CTI Sensory Panel Leader FUNCTION: R&D REPORTS TO: CTI Manager, Foods and Beverages SCOPE: Beverages WORK LOCATION: Unilever R&D Bangalore About Unilever Be part of the world’s most successful, purpose-led business. Work with brands that are well-loved around the world, that strive to improve the lives of our consumers and the communities around us every day. Every day, nine out of ten Indian households use our products to feel good, look good and get more out of life – giving us a unique opportunity to build a brighter future. We promote innovation, big and small, to make our business win and grow; and we believe in business as a force for good. Our brilliant business leaders and colleagues provide mentorship and inspiration, so you can be at your best. At HUL, we believe that every individual irrespective of their race, colour, religion, gender, sexual orientation, gender identity or expression, age, nationality, caste, disability or marital status can bring their purpose to life. So apply to us, to unleash your curiosity, challenge ideas and disrupt processes; use your energy to make the world a better place. As you work to make a real impact on the business and the world, we’ll work to help you become a better you! Business Context And Main Purpose Of The Job Consumer technical Insight (CTI) is a strategic capability for Unilever Research & Development (R&D). Its main remit is to generate and translate product insights into innovation and growth opportunities for the business across several expertise areas (product qualitative research, product testing/quantitative research, claims and demonstrations, sensory evaluation, laboratory testing). CTI is one of the core functions within R&D which represents the voice of consumers to the business and translates consumer insights and language into actionable technical understanding to help in decision making. The Sensory Panel is one of the core capabilities that we have within the CTI function. The Sensory Panel is used for evaluations of products for shortlisting options, and also for providing guidance for future product development. Main Accountabilities We are looking for an appropriate candidate who can take up the responsibility of managing the Tea sensory panel in Bangalore. The person will be accountable for the daily operations of the panel, necessary training, quality control and delivery of results. The person needs to have sensory acuity and be passionate about pursuing a career in sensory science. While the key responsibility would be to manage, maintain and train the sensory panel, the candidate is also expected to help out the CTI Manager in the management of consumer insights workstream within Foods and Beverages (consumer research qualitative and quantitative) as needed. The Specific Responsibilities Are Listed Below Manage the sensory panel to enable the delivery of sensory insights Guide the team on product development based on the correlation of consumer and sensory insights. Build the sensory capability and expertise on site. Understand and interpret sensory panel data to help the team make the right choices. Ongoing maintenance and training of the sensory panel to improve the quality of the QDA panel. Have an in depth understanding of the consumers, category, brands and market to generate, develop and support insights from a sensory perspective. Represent the voice of CTI in product development forums, to bring in the sensory perspective. Support the CTI Manager in the management of F&B consumer insights workstream; for all key projects and activities. Independently manage and co-ordinate consumer studies from end to end to support project networks. Engage with key stakeholders for communication of insights and results of sensory studies on a regular basis. Engage with cross functional teams to understand requirements and suggest suitable actions, appropriate for the problem, in the sensory space. Cataloguing of information to ensure access to information by all in a transparent manner. Work with a cross cultural team with ease. Key R&D Interfaces India F&B CTI team India Beverages R&D team Project team network (Marketing project leader, Technical PL, CMI) Global CTI community External agencies/service providers Key Skills Sensory orientation and acuity Effective communication skills (verbal/ written) Excellent influencing skills Good interpersonal skills and a team player Attention to detail and good analytical power, aptitude for problem solving Proven project management skills Drive, energy to make a real contribution Proactive and enthusiastic approach Flexible and adaptive working style Relevant Experience 3+ years of experience in Sensory Science, having worked in management of panels; in the capacity of a panel leader. Candidates with relevant experience in consumer research will be preferred Bachelor qualification in sciences or equivalent (e.g. chemistry, microbiology, biology, pharma). Our commitment to Equality, Diversity & Inclusion Unilever embraces diversity and encourages applicants from all walks of life! This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity. Show more Show less

Roles and Responsibilities Required doctors for Anatomy, Physiology, pharmacology, microbiology, forensic medicine, general medicine, Obg, Radiology, General Surgery, Dermatology, Pulmonary medicine, Opthal including Professors, Associate professors, assistant professor, Teach undergraduate and postgraduate students in various medical specialties Participate in departmental meetings and contribute to medical college development initiatives.

URGENTLY REQUIRED CANDIDATES IN ANATOMY, ANAESTHESIA, MEDICINE, TB&CHEST, DERMATOLOGY, ORTHOPAEDICS, GENERAL SURGERY, OBS& GYNAE. POST: ASSISTANT PROFESSOR, SENIOR RESIDENT. BG CONSULTANCY 7909992043(Whatsapp) BGCON.INDORE@YAHOO.COM Perks and benefits Accomodation will be Included in salary.

Candidates urgently needed for Anatomy, Anaesthesia, Medicine, TB & Chest, Dermatology, Orthopedics, General Surgery, and Obstetrics & Gynecology. Salary commensurate with experience. BG CONSULTANCY 9893026830,7909992043 BGCON.INDORE@YAHOO.COM

Candidates urgently needed for Anatomy, Anaesthesia, Medicine, TB & Chest, Dermatology, Orthopedics, General Surgery, and Obstetrics & Gynecology. Salary commensurate with experience. BG CONSULTANCY 9893026830,7909992043 BGCON.INDORE@YAHOO.COM

Division Department Sub Department 1 Job Purpose Overseeing all aspects of Microbiology (Sterile and Non-sterile) at site. Responsibility for maintaining & monitoring cGMP Compliance by ensuring applicable systems, processes and procedures are in place. Keeps informed of existing and proposed FDA regulation relating to assigned responsibility, appraised their effect on company operation and sees that appropriated action is taken to assure compliance with FDA regulator and compliances for various regulatory agencies. Ensuring closure, investigation for investigation of out of specification / out of trend (OOAC &OOAL), complaints, deviation and batch failures (including stability) are appropriately performed and documented, taking appropriate corrective and preventive action based on the results of the investigation. To approve all appropriate microbiology related documents pertaining to stability, QMS, Validations e.g procedures, SOPs, layouts, plans, Specifications impacting product quality which include but not limited to Protocols, reports, master document etc, to assure the completeness, consistency and accuracy of cGMP data. Collaborate with cross-functional teams including production, stores, engineering, CDC, regulatory affairs, IPD to address microbiology concerns and ensure smooth operations. Identification of training needs and imparting training with respect to cGMP, GLP, Safety, Hygiene, application and principles of Quality function. Ensure the review of annual product quality report of all drug products and its relevant data / records to assure that products are meeting consistently quality standards. To participate in Quality management review. Key Accountabilities (1/6) Ensure on time completion/closure of microbiology analysis as per defined SOP s. To make all resources available at site for analysing all samples as per defined SOP. To make sure testing are carried out as per Specification and within SOP timeline. To investigation/conclude any non-conformance occurred during analysis/process To implement/take adequate CAPA against non-conformance and monitoring of the same for effectiveness Key Accountabilities (2/6) Ensuring monitoring and on time completion of complaints / deviation / CAPA / regulatory compliances/FMECA/Audits and remaining activity pertaining to QMS. Monitoring of given KPI within QMS function and ensure complaince stated in respective SOP. Facilitate internal/external audits and ensure on time closure submission of response. Provide support to individual team member to complete activity as per SOP. Key Accountabilities (3/6) Ensure validation, Qualification and technology transfer activities executed as per schedule/SOP Monitoring of given KPI pertaining to stated function. Collaborating within CFT for on time validation, qualification of process/equipment s/area etc and on time closure/execution of technology/product transfer. Investigation, conclusion and on time closure of non-conformance like OOAC, OOAL, OOS, deviation and incidences Detailed investigation of non-conformance through RCA tools by taking personnel interview, 5why analysis, conducting cross functional meetings to find out the root cause within specified timeline. Based on root cause analysis implementation of CAPA. Ensure on time closure of non-conformances and CAPA Key Accountabilities (4/6) Ensure to perform / make availability of analytical method validation / verification Ensure to perform analytical method validation and verification by verifying analytical method validation/verification protocols and reports. Ensure on time launch of new product or tech transfer To be involved in product transfer/launch meetings/discussion. Arrange all relevant documents like method validation, material/product codes. To make availability of resources. To perform method transfer / validation / verification. To perform analysis of validation batches. Key Accountabilities (5/6) Ensure to achieve all assigned KPI To monitor and ensure to meet the RM, PM and FP productivity and SLA. To monitor and providing trainings on precautionary measures and techniques to analysts to reduce the manual error. To identify and robust the analytical methos of analysis. To provide decision and technical assistant to analysts and section heads. Provide decision on technical matters or any kind of relevant information and analysis or any situations. Provide technical assistant on any kind of troubleshooting depending upon the situations/field and to train others on technical tools. Key Accountabilities (6/6) Major Challenges Ensuring smooth function of respective functions by optimising/managing resources. Ensuring on time delivery/analysis of products complying with all established SOP/guidelines. Ensuring all time audit readiness and comply all the laid down process wrt functioning of lab. Coordination with internal/external stakeholders to ensure functioning of laboratory. Key Interactions (1/2) Address quality issues identified during analysis and during production/process and implementation of CAPA. Work closely with unit stakeholders to ensure new product meet quality specifications before launch and completion of validation/qualification. Resolve quality related issues and ensure timely resolution. Report on quality performance, compliance and improvement initiatives. Participate in recruitment and performance evaluation of staff. Ensure compliance with internal and external audit observations Key Interactions (2/2) Collaborate with IPD/service providers to resolve quality issues. Interact with internal and external agencies during audit and inspection. Collaborate with peers to benchmark quality standards and processes. Dimensions (1/2) Sound knowledge of quality standards, tools and methodologies Good leadership and team management skill. Good communication skill and interpersonal skill Dimensions (2/2) Key Decisions (1/2) Resource Allocation Compliance Training Deliveries Quality Standards Process Improvement CAPA Key Decisions (2/2) Allocate resources for activities Ensure adherence to quality/regulatory standards. To provide the methodology to find out root cause during investigation of non conformance Approve training programs for microbiologists Completion of all microbiology related activities on time at site as per SOP Implement quality policies and procedures Approve initiatives to enhance quality and efficiency Implement corrective and preventive actions for quality issues Education Qualification M.Sc. (Microbiology) Relevant Work Experience 15-20 Years Technical Skill, leadership skills, communication skills, Analytical Skills and should have CLE prospects.

Bhagwan Mahaveer Cancer Hospital & Research Centre is looking for Senior Resident Radiation Oncology to join our dynamic team and embark on a rewarding career journey. Patient Care: Provide comprehensive medical care to patients under the supervision of attending physicians Perform physical examinations, diagnose medical conditions, develop treatment plans, and monitor patient progress Clinical Supervision: Supervise and provide guidance to junior residents, interns, and medical students in their clinical duties Assist in their training, evaluation, and professional development Hospital Rounds: Conduct regular hospital rounds to assess patients, review test results, and discuss treatment plans with the healthcare team Coordinate and communicate patient care plans with nurses, specialists, and other healthcare professionals Medical Procedures: Perform or assist in various medical procedures, such as venipuncture, wound care, suturing, and bedside procedures Ensure adherence to sterile techniques, safety protocols, and best practices Medical Documentation: Maintain accurate and up-to-date medical records, including patient history, physical examination findings, treatment plans, and progress notes Ensure compliance with legal and regulatory requirements Patient Education: Educate patients and their families about their medical conditions, treatment options, and preventive measures Provide counseling on lifestyle modifications, medication management, and post-discharge care instructions Interdisciplinary Collaboration: Collaborate with other healthcare professionals, including nurses, pharmacists, therapists, and social workers, to ensure coordinated and holistic patient care Participate in interdisciplinary team meetings and contribute to care planning Continuity of Care: Facilitate smooth transitions of care between inpatient and outpatient settings Coordinate follow-up appointments, referrals, and discharge planning to ensure continuity of care and optimal patient outcomes Medical Research and Education: Stay updated with the latest medical advancements, evidence-based practices, and clinical guidelines Engage in research activities, present at conferences, and contribute to medical education and scholarly activities Quality Improvement: Participate in quality improvement initiatives to enhance patient safety, clinical outcomes, and healthcare delivery Identify areas for improvement, implement evidence-based practices, and contribute to quality assurance programs Professional Development: Engage in continuing medical education (CME) activities, attend conferences, and pursue opportunities for professional growth Maintain licensure and board certification requirements

About the role Originated in 1864, DNV operates globally in more than 100 countries with our 16,000 professionals dedicated to helping our customers make the world safer, smarter and greener. As a world-leading certification body, we work with companies to assure the performance of their organizations, products, people, facilities and supply chains through certification, verification, assessment and training. As part of the larger DNV Group, our 2,000 Business Assurance employees worldwide help our customers build sustainable business performance and create stakeholder trust. We promise to be focused on your future. With more than 70,000 certificates issued worldwide, our name evokes a strong commitment to safety, quality, and concern for the environment. For years, we have been the preferred certification partner for many Fortune 500 companies, as well as for medium and smaller businesses. With our extensive local presence, consolidated global experience across industries and acknowledged technical competence, we are an ideal partner for companies in all sectors. We partner with our customers to help them create value while meeting the world s economic, social and environmental needs. Through our certification, verification, assessment and training services, we assure the performance of our customers organizations, products, people, facilities, and supply chains. Working with companies in most industries, and some of the world s leading brands, in practice, we are virtually everywhere. Major Duties as ISCC and IMS Lead Auditor: Perform ISCC/Food Safety / IMS / other management system audits according to specific client requirements or international recognized GFSI / ISO schemes and perform value added training. Technical knowledge and a good understanding of the audited activities of the System User relevant to ISCC, sufficient for identifying, assessing and managing the risks during each audit the auditor performs. Reporting audit results accurately and timely manner in compliance to the scheme / Organizational requirements. Cooperation with sales and planning team for smooth delivery of projects. Demonstrated experience in managing key accounts and client relationships in business development situations Market input to regional tactical plans Developing new and large project opportunities Member of Key account team for relevant Key customers Opportunity portfolio management; ensure good processes that keep track on BA activities toward customers, prospects and order backlog. What we offer Flexible work arrangements for better work-life balance Generous Paid Leaves (Annual, Sick, Compassionate, Local Public, Marriage, Maternity, Paternity, Medical leave) Medical benefits ( Insurance and Annual Health Check-up) Pension and Insurance Policies (Group Term Life Insurance, Group Personal Accident Insurance, Travel Insurance) Training and Development Assistance (Training Sponsorship, On-The-Job Training, Training Programme) Additional Benefits (Long Service Awards, Mobile Phone Reimbursement) Company bonus/Profit share. *Benefits may vary based on position, tenure/contract/grade level* About you Position Qualifications: Master.s or Graduate in Science/ Chemistry / Food Technology/ Food Science / Bio-Technology / Microbiology / Dairy Technology / Agriculture / Science / Fisheries Science / Aquaculture or Equivalent discipline from a reputed institute. At least 2 years of work experience in the relevant work area; all in all, at least 3 years of work experience. At least 40 hours of audit training (e.g. according to ISO 19011). To be approved as an MSC Lead Auditor. Knowledge in the handling, evaluation and assessment of plausibility of data sources. Knowledge in traceability verification and relevant databases, chain of custody options, supply chain logistics, especially mass balance calculation and verification, bookkeeping, and similar. Competence in group certification and sampling principles (if applicable during an audit). Participation in the ISCC EU and PLUS Basic Training before the first ISCC audit can be conducted. Participation in the ISCC EU and PLUS Basics Training must be repeated at least every five years. Participation in the ISCC Waste and Residues Training before the first ISCC audit covering waste/residues can be conducted Participation in this training must be repeated at least every five years.

About Us At bioMrieux, we have been dedicated to making the world a healthier place for nearly 60 years Throughout our global presence, we have continuously imagined and developed innovative diagnostic solutions to enhance the health of patients and consumers As a family-owned company, bioMrieux has evolved into a world leader in the field of in vitro diagnostics Our entrepreneurial journey, which began over a century ago, is fueled by an unwavering commitment to improve public health on a global scale and contribute to a healthier world bioMerieux India We are proud to be a 100% subsidiary of bioMrieux SA, based in Marcy L'Etoile, France, and have been serving the Indian market for over 25 years With our comprehensive diagnostic solutions in clinical microbiology, immunology, molecular biology, and industrial microbiology, we cater to over 5000+ customers Our offerings provide essential information to healthcare professionals and industry players, addressing critical areas such as antimicrobial resistance, sepsis, acute care syndromic approaches, and food safety Through these efforts, we aim to protect the health of patients and consumers By joining bioMrieux, you become a part of an innovative company with a long-term vision, deeply committed to serving public health Our corporate culture emphasizes a humanistic approach, and we are driven by a pioneering spirit We seek candidates who are motivated to invest in themselves, contribute to future projects, and be part of a collective adventure led by a pioneering spirit Join us as we work towards a healthier future for all Location: Pune Position: Application Specialist BACT Education & Experience Desirable: Graduate / Postgraduate in Microbiology preferably clinical microbiology Experience: Minimum 1-3 years field applications Experience Familiarity with laboratory techniques, practises and requirements Familiarity with high medical value diagnostic markers Must have excellent written and oral communication and presentation skills Listening carefully/patiently and acting upon the same Key Responsibilities Coordinate and provide consulting, technical training and on-going support on bioMrieux solutions Answer internal & external customer inquiries and ensure compliance with regulatory through timely and accurate documentation in ERP system (CRM) Provide consistent follow up to ensure customer satisfaction and meet KPI Develop & retain business, strengthen customer relationship Make organizational recommendations around the equipment in order to optimize the workflow, addressthree dimensions: technical, quality and productivity (SOP) Ability to perform routine training Promote bioMrieux solutions demonstration, evaluations, onsite visits on both pre and post sales Enable bioMrieux customer in fully utilizing the technical potential of the solutions (interpretation of results, specimen management, workflow optimization) Demonstrate a technical expertise which allows to easily take in charge new products and new technologies Key Deliverables Provide field scientific support & services, including sales support, training, qualification, field actions deployment at all stages of BMX solutions life cycle management, guarantee added value, assess patient result impact Achievement of Objectives for the year in the relevant SBS Awareness within the regions healthcare community about bioMerieux and partner company solutions and their relevance to patient care Developing KOL network and proactive/taking initiatives in conducting workshops/activities This also includes 70-80% travelling Show more Show less

Click here to download form From The Head Department of Climate Change & Agricultural Meteorology Punjab Agriculture University Ludhiana To All Deans/Directors/ Officers/Head of the Departments PAU, Ludhiana & All Directors of Outstations/ Incharges of KVKs of the PAU Ludhiana Memo No AM/2025/ Dated Subject: Filling up the one position of Junior Field/ Lab Helper on contract basis at a fixed salary of @Rs 11390/(additional Rs 800/p m ) One post of Junior Field/Lab Helper at the fixed salary of Rs 11390/p m (additional Rs 800/p m ) is to be filled up on contractual basis in the scheme, ?All India Coordinated Research Project on Agrometeorology? ICAR-029 (PC-2038) in the Department of Climate Change & Agricultural Meteorology at PAU, Ludhiana for six months or till the termination of the scheme fixed with the following qualifications: - Middle with Punjabi Age 18-63 Desirable: Preference will be given to the candidates who have been working as DPLs in the respective field in PAU for 10 years Note: 25% and 12% posts are reserved for candidates belonging to schedule caste/tribes and backward classes belonging to Punjab State respectively: 13% posts are reserved for Ex-serviceman and 3% posts are for physical handicapped persons The desirous candidates fulfilling the required qualifications/experience for the above mentioned post may apply in the attached application form along with copies of testimonials and a bank draft of Rs 100/drawn in the favour of the Comptroller, PAU, Ludhiana in this office on before 09 06 2025 Applicant must mention his/her name in capital letters on the back side of the Bank Draft They should appear before the selection committee for the Interview on 24 06 2025 in the office of the undersigned at 11:00 AM No separate letter for the interview will be issued The original copies of the testimonials should be brought at the time of interview No TA/DA will be given for attending the interview Applications received after the due date/without the application fee shall not be considered This department shall not be responsible for any postal delay or loss in transits The services of the incumbent are liable to be terminated at any time without any notice Head Department of Climate Change & Agricultural Meteorology Show more Show less

Gujarat Biotechnology University is looking for Junior Research Fellow to join our dynamic team and embark on a rewarding career journey Research Support: JRFs work under the guidance of senior researchers or principal investigators on research projects They assist in conducting experiments, data collection, literature reviews, and data analysis Data Collection and Analysis: Collecting and recording data from experiments or research studies and using appropriate software or statistical tools for data analysis Literature Review: Conducting comprehensive literature reviews to understand the current state of research in the field and to inform the research design and methodology Experimental Work: Depending on the field, JRFs may perform laboratory experiments, fieldwork, surveys, or other research activities specific to their project Documentation: Keeping detailed records of research procedures, findings, and outcomes This documentation is critical for the research process and for publishing research results Research Proposal Writing: Assisting in the preparation of research proposals and grant applications to secure funding for research projects