Job title : Global Medical expert Hiring Manager: Head Scientific Communications/ Team lead Location: Hyderabad % of travel expected: Travel required as per business need Job type: Permanent and Full time About The Job Our Team: Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. Main Responsibilities Works with a team of Medical regulatory writers with different levels of expertise, Develops medical expertise within Medical regulatory writing (on contents, methods, and processes). Ensures compliance with regulatory requirements from various regions (FDA, EU others) for activities supported. Coordinates and supports medical activities related to the maintenance of the marketing authorizations of Established and Generic products, in different therapeutic areas. Works in close collaboration with Global Medical Leads, Global Regulatory Affairs, Global Pharmacovigilance, and vendors Essential Job duties and responsibilities: 1) Responsible to provide a medical assessment with relevant and updated clinical evidence and monitoring the execution of strategic documents such as PBRERs, ACOs, DSURs, Clinical Overviews, Benefit-Risk assessments, Expert statements for MDD, Responses to Health Authority Queries, Ad-hoc literature analyses, and labeling documents for the corresponding therapeutic area or products or any other activities which are the core activities of GMLs. 2) Drafting the extended synopsis of studies in collaboration with RWE experts. He/she will be responsible for overseeing the execution of such plans by the respective operational units in compliance with SOP, GCP, and other regulations. 3) Writing of Key medical/clinical parts of Common Technical Documents (CTD) or Briefing packages (BP). 4) Reviewing and approving compassionate use of individual medical requests for use of Sanofi medicinal products for serious or life-threatening diseases for treatment outside of clinical trials. 5) Secure delivery of high-quality medical documents on time and in compliance with internal and external standards. 6) Collaborates effectively with stakeholders: global medical leads/ medical product leads, global regulatory affairs, medical regulatory writing global or local teams, pharmacovigilance teams, managed access program teams. People: 1) Maintain effective relationships with the end stakeholders (Medical, regulatory, pharmacovigilance community) within the allocated Global business unit and product – with an end objective to develop medical regulatory content as per requirement, 2) Interact effectively with stakeholders in medical and pharmacovigilance departments 3) Constantly assist the medical regulatory writing team in developing knowledge and sharing expertise Performance: 1) Secure deliverables (PBRER, ACO, SO, CSR, ID Cards, Investigator brochure, clinical evaluation report, briefing packages, medical section of CTA, CTD, SBRAs, MDD, HAQs or any other activities which are core activities for GMLs) are supported as per agreed timelines and quality Process: 1) Provide medical strategic insights & evaluation related to Sanofi’s portfolio. 2) Contribute to the management of the marketing authorization dossiers of the current related portfolio. 3) Act as an expert in the field of medical regulatory writing and maintain the regulatory requirement for countries, and teams supported. 4) Assist the assigned medical team in conducting comprehensive medical regulatory writing-needs analysis 5) Implement relevant elements of the medical regulatory plan and associated activities for the year identified for the region 6) Work with selected vendors when required within the region to deliver the required deliverables as per the defined process 7) Assist the head of scientific communications in designing an overall plan of action based on end-customers feedback & improving course content and delivery Stakeholders: 1) Work closely with medical teams in regions/areas to identify medical writing needs and assist in developing assigned deliverables 2) Liaise with the Medical department to ensure relevant & customized are delivered per expectation About You Experience: ≥5 years of experience supporting international pharmaceutical companies: medical affairs, clinical development, pharmacovigilance with experience in at least one of the therapeutic areas- cardiovascular, metabolism, diabetes and lipid, CNS, oncology, anti-infectives, internal medicine Soft skills: Stakeholder management; communication skills; and ability to work independently and within a team environment Technical skills: As applicable (Including but not limited to Medical operational excellence, time, and risk management skills, Excellent technical (medical) editing and writing skills) Education: Medical degree MBBS; MD Languages: Excellent knowledge of the English language (spoken and written) Pursue progress, discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! null Show more Show less

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. The Medical Information Specialist (MIS) position is part of the ProPharma Medical Information Contact Center and follows all corresponding regulations, industry standards, and client/internal policies regarding medical information and the collection and documentation of adverse events, special situation events, and product complaints. Essential Functions Include:Medical Information service delivery Responds to unsolicited consumer, health care professional and other external customer requests for medical and safety information received via telephone, website/e-mail, letter, fax, and scientific meetings on behalf of ProPharma’ s pharmaceutical clients. Provides labeled and unlabeled medical/safety information responses in accordance with regulatory requirements, industry standards and client and ProPharma internal policies and practices. Accurately identifies, documents and reports adverse events, pregnancy reports, special situation events and product complaints in a clear and concise manner per government regulations, ProPharma Standard Operating Procedures (SOPs) and client Working Practices (WPs). Ensures tasks are completed within the deadlines documented in the agreed ProPharma SOPs and WPs. Formulates and provides accurate responses utilizing approved labeling and company standard responses, published literature and other data. Assists with writing custom medical information responses utilizing this data. Logging all enquiries handled in an accurate, comprehensive, and timely fashion into Inquiry Handling Systems. Quality Assurance Maintains quality in all areas of the job, including performing quality checks on Adverse Events, Product Quality Complaints, correspondence, and enquiries logged into the Inquiry Handling Systems General Provides after-hours coverage on a rotated basis subject to business requirements. Adheres to company and country-specific privacy policies, ensuring any confidential information or personal data related to ProPharma and its clients is managed in accordance with Data Privacy regulations described in ProPharma SOPs and the Confidentiality Statement within the Contract of Employment. Complies with the Company’s health and safety policies. Other activities as assigned as delegated by the Manager. Qualified Candidates Must Have Life science degree OR Nursing degree (RN/BS/BA/MS) OR Pharmacy degree Excellent verbal and written communication skills, including proofreading, professional telephone etiquette and empathetic customer service skills. Ability to write in a fluent and grammatically correct manner in the target language for the role English language proficiency. Japan-based roles only: TOEIC 800= Working knowledge of medical terminology, pathophysiology, pharmacology, regulations and industry standards. Strong cognitive abilities, including verbal reasoning, critical thinking and analytical ability. Ability to multitask with attention to detail within restrictive timeframes, including sound planning, prioritizing and organizational skills. Proactive with demonstrative ability to independently identify problems and suggest effective solutions. Ability to learn, take instruction and apply to daily operations/tasks. Receptive to constructive feedback and able to take responsibility for work allocated. Self-motivating. Ability to demonstrate initiative and internal drive. Willingness to seek out additional workload projects. Effectively work independently and as part of a team. Highly proficient in computer applications, including Microsoft Office software platforms and Adobe Acrobat, and experience using a document management system. Aptitude to learn other computer systems including inquiry handling database. We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.*** Show more Show less

Job Title: Regulatory Affairs Director Introduction to role The International Regulatory Affairs Director Markets (IRAD) is responsible for developing and implementing the international regulatory strategy for a group of products. This role ensures that the strategy is designed to achieve rapid approval with advantageous labeling, aligning with the product properties and the needs identified by the business, markets, and patients. The IRAD possesses strategic leadership skills, understands regional regulatory science, and has extensive knowledge of drug/biologic development processes and strategies. Understanding of the disease area is crucial for crafting cross-functional discussions with regional and/or Global Product Teams (GPT) and relevant team members. Familiarity with regulatory systems across international markets and a thorough understanding of commercial factors are critical to success in this role. Accountabilities Project Regulatory Strategy Develop and implement innovative international regulatory strategies for a product/group of products, ensuring rapid approval with advantageous labeling. Lead the development, communication, and updates of the International section of the Regulatory Strategy Document (RSD) for assigned products/projects. Ensure appropriate cross-functional coordination, particularly with International Commercial, peer review, and senior team member endorsement from ILT and GPT. Attain regulatory breakthroughs, including evaluating the likelihood of regulatory success and implementing risk mitigation measures. Objectively assess emerging data against aspirations and update senior management on project risks/mitigation activities. Leadership Serve as the single point of contact and Regional Regulatory Affairs representative on Regional Product Teams. Lead the planning and construction of the International dossier. Develop and implement an optimal regional (International) regulatory strategy for a product/group of products, ensuring rapid market access with advantageous labeling. Ensure effective regulatory representation at all health authority meetings and clear documentation of discussions and agreements. Lead regulatory staff working on a product/project to ensure prioritized objectives are delivered on time and with quality. Participate in skill development, coaching, and performance feedback of other regulatory staff. Provide regulatory leadership in product in-license/due diligence review, product divestment, and product withdrawal. Contribute proactively across RAD community and/or Regulatory Excellence objectives and activities. Regulatory Environment Partner with marketing company staff to monitor changes in the regulatory environment and support regional and/or Global Product Teams (GPT) or ILT accordingly. Influence developing views/guidance within leading Health Authorities on specific topics relevant to their project or regulatory more generally. Essential Skills/Experience Bachelor’s degree in a science-related field or equivalent experience. Previous experience in attending and/or helping a team prepare for Major Health Authority interactions. Extensive experience or equivalent in regulatory drug development, including product approval/launch. Broad background of experience working in the pharmaceutical business and prior experience in several areas within regulatory affairs. Proven leadership and program management experience. Ability to think strategically and critically evaluate risks to regulatory activities. Ability to work strategically within a complex, business-critical, and high-profile development program. Successful leadership of major regulatory approval in the International Region. Strong cross-cultural awareness and ability to work independently with Commercial and Marketing Company colleagues from across the globe. Must demonstrate proficiencies in critical thinking, critical influencing, innovation, initiative, leadership, and excellent oral and written communication skills. Desirable Skills/Experience Strong commercial awareness. Subject Matter Expert in International strategy and tactical delivery. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace, and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. AstraZeneca empowers employees with unprecedented local ownership. We encourage unity and ownership at a local level while fostering collaboration across our global organization. Our diverse community values every voice, promoting open communication that leads to powerful innovation. Join us to be part of a team that is bold in setting new directions for patient care, bringing transformative drugs to those who need them most. Ready to make a difference? Apply now to join our dynamic team! Show more Show less

Job Summary: We are seeking a skilled and compassionate Lab Technician for diagnostic center who is responsible for performing routine laboratory functions, ensuring accurate test results, and maintaining a safe and organized work environment. This includes receiving, labeling, and storing samples, preparing solutions and reagents, conducting tests, and recording results. Additionally, they may be involved in equipment maintenance, quality control, and safety procedures. Male / Female both can apply Minimum 1 year of experience required salary : 15K to 18K in hand Travelling Expenses are given Looking for Immediate joiners Interested candidate can call or msg on 90044 94071 Shraddha Job Type: Full-time Pay: ₹12,000.00 - ₹15,000.00 per month Schedule: Day shift Ability to commute/relocate: Airoli, Navi Mumbai, Maharashtra: Reliably commute or planning to relocate before starting work (Preferred) Education: Higher Secondary(12th Pass) (Preferred) Experience: Clinical laboratory: 1 year (Required) Diagnostic evaluation: 1 year (Required) Language: Marathi (Required) English (Required) Hindi (Required) Location: Airoli, Navi Mumbai, Maharashtra (Required) Shift availability: Day Shift (Required) Night Shift (Required) Overnight Shift (Required) Willingness to travel: 25% (Required) Work Location: In person

Job Title: Office Staff – Operations & Inventory Executive Location: South Ex part 2, New Delhi Job Type: Full-Time Salary: As per industry standards Reporting To: Operations Manager Job Overview: We are seeking a reliable and detail-oriented Office Staff – Operations & Inventory Executive who will be responsible for handling multiple backend tasks, including inventory management, product packaging, labeling, and ensuring timely dispatch of orders. This role requires strong organizational skills and the ability to work comfortably on a PC or laptop. Key Responsibilities: Inventory Management Maintain accurate stock records and perform regular stock audits Monitor inventory levels and notify the team for reordering Update product availability in the system Product Packaging & Labeling Ensure all orders are packed securely and correctly as per brand guidelines Generate and affix shipping labels using e-commerce platforms or courier partner tools Maintain packaging material stock Order Processing & Dispatch Coordinate with courier partners for timely pick-ups and dispatch Prepare daily dispatch reports and update order tracking status Maintain records of dispatched orders and returns Multi-tasking Office Support Assist in preparing basic documentation, reports, or data entries as required Provide support to other departments when needed (e.g., customer support or admin) Required Skills: Proficiency in using computers (PC/Laptop) and basic software like MS Excel, Word, and web browsers Ability to quickly learn and navigate inventory/order management software Attention to detail with a high degree of accuracy Strong organisational and time management skills Team player with a proactive attitude Eligibility Criteria: Minimum qualification: 12th Pass or Graduate Prior experience in inventory or order fulfilment is preferred Basic understanding of e-commerce operations is a plus Working Hours: Monday to Saturday, 10:00 AM to 7:00 PM (timing may vary as per dispatch load) How to Apply: Please email your updated resume to Support@dhwaniastro.com or contact us at 9319490826. Job Type: Full-time Pay: ₹12,000.00 - ₹15,000.00 per month Benefits: Food provided Paid sick time Schedule: Day shift Work Location: In person

Job Description Job Summary - You will be responsible for Packaging design for Industrial & Retail products. In This Role, Your Responsibilities Will Be: Candidate will be responsible for designing Primary / Secondary & Tertiary packaging for Existing / New products & their Accessories Develop new packaging systems and/or improve existing packaging systems to meet standards of quality, function, cost and merchandising using established and well-defined engineering procedures using CAD software Solicit quotes from suppliers and consult with purchasing and production departments to determine the costs and feasibility of producing the proposed packaging Collaborate with various functions in the organization like Product Management / Sourcing along with outside suppliers to determine cost & feasibility of proposed packaging Provide Innovative, Creative & Sustainable packaging solutions for Sustaining & NPD projects Remain abreast of trends in industrial / retail packaging & initiate projects related to packaging improvements to response to changing global sustainability objectives. Manage Engineering Change Requests (ECR) & Engineering Change Notices (ECN) for packaging designs Identify & lead the cost reduction activities related to product packaging Build & maintain relations with various suppliers for packaging, prototyping & production Participate in Emerson sustainability efforts to identify and implement packaging alternatives to reduce the use of single use plastics and other environmentally related packaging. Develop packaging procedures / work instruction for new & existing packaging designs Place request to lab for packaging testing & further analyze the test results Develop & maintain product engineering operating standards relating to packaging & labeling of products Work closely with Graphics design group as & when necessary for developing packaging artwork / to provide necessary die-lines Who You Are: Packaging Engineer 1 For This Role, You Will Need: Qualification - Engineering Graduate (Preferred – Mechanical or Packaging Engineering) Masters in packaging technology or Post Graduate Diploma in Packaging will be an added advantage Candidate should have experience of 5 to 7 years in design and development of packaging for Industrial products and retail displays after Graduation (Include Carton boxes & inserts / wooden pallets / retail packaging like Clamshell & Blister) Require hands on packaging CAD tool like ArtiosCAD / PICADOR ( Preferred ArtiosCAD) Good understanding of Engineering drawings / Standards & Specifications (Knowledge on Engineering CAD tool will be added advantage) Knowledge of Sustainable Packaging Regulations & Best Practices / Packaging test standards Must be able to communicate effectively both orally and in writing Exposure to work in a global work environment with efficient oral & written communication Preferred Qualifications That Set You Apart: Qualification - Engineering Graduate (Preferred – Mechanical or Packaging Engineering) Masters in packaging technology or Post Graduate Diploma in Packaging will be an added advantage Our Culture & Commitment to You At Emerson, we prioritize a workplace where every employee is valued, respected, and empowered to grow. We foster an environment that encourages innovation, collaboration, and diverse perspectives—because we know that great ideas come from great teams. Our commitment to ongoing career development and growing an inclusive culture ensures you have the support to thrive. Whether through mentorship, training, or leadership opportunities, we invest in your success so you can make a lasting impact. We believe diverse teams, working together are key to driving growth and delivering business results. We recognize the importance of employee wellbeing. We prioritize providing competitive benefits plans, a variety of medical insurance plans, Employee Assistance Program, employee resource groups, recognition, and much more. Our culture offers flexible time off plans, including paid parental leave (maternal and paternal), vacation and holiday leave. About Us WHY EMERSON Our Commitment to Our People At Emerson, we are motivated by a spirit of collaboration that helps our diverse, multicultural teams across the world drive innovation that makes the world healthier, safer, smarter, and more sustainable. And we want you to join us in our bold aspiration. We have built an engaged community of inquisitive, dedicated people who thrive knowing they are welcomed, trusted, celebrated, and empowered to solve the world’s most complex problems — for our customers, our communities, and the planet. You’ll contribute to this vital work while further developing your skills through our award-winning employee development programs. We are a proud corporate citizen in every city where we operate and are committed to our people, our communities, and the world at large. We take this responsibility seriously and strive to make a positive impact through every endeavor. At Emerson, you’ll see firsthand that our people are at the center of everything we do. So, let’s go. Let’s think differently. Learn, collaborate, and grow. Seek opportunity. Push boundaries. Be empowered to make things better. Speed up to break through. Let’s go, together. Accessibility Assistance or Accommodation If you have a disability and are having difficulty accessing or using this website to apply for a position, please contact: idisability.administrator@emerson.com . About Emerson Emerson is a global leader in automation technology and software. Through our deep domain expertise and legacy of flawless execution, Emerson helps customers in critical industries like life sciences, energy, power and renewables, chemical and advanced factory automation operate more sustainably while improving productivity, energy security and reliability. With global operations and a comprehensive portfolio of software and technology, we are helping companies implement digital transformation to measurably improve their operations, conserve valuable resources and enhance their safety. We offer equitable opportunities, celebrate diversity, and embrace challenges with confidence that, together, we can make an impact across a broad spectrum of countries and industries. Whether you’re an established professional looking for a career change, an undergraduate student exploring possibilities, or a recent graduate with an advanced degree, you’ll find your chance to make a difference with Emerson. Join our team – let’s go! No calls or agencies please. Show more Show less

We're Hiring: Store Incharge Location: Bharuwa Sumerpur, Uttar Pradesh | Job Type: Full-Time Experience: 1–3 Years Salary: ₹15,000 – ₹22,000 / Month (based on experience) Position: Store Incharge Key Responsibilities: Maintain accurate records of material inward and outward movements. Monitor and manage daily stock levels of raw materials, tools, and finished goods. Issue materials to the production team as per requirements. Update stock registers in Excel regularly. Conduct physical stock verification and reconcile with records. Coordinate with the purchase and accounts departments for timely procurement and documentation. Ensure proper storage, labeling, and safety of all materials in the store area. Requirements: 1–3 years of experience in storekeeping or inventory management. Knowledge of stock management processes and tools. Familiarity with MS Excel and inventory software is a plus. Good organizational and record-keeping skills. Ability to work independently and handle responsibilities with accuracy. Apply Now: Send your resume to digital@saitecnomec.in or call 70094 94752 Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹22,000.00 per month Schedule: Day shift Work Location: In person

We're Hiring: Store Incharge Location: Bharuwa Sumerpur, Uttar Pradesh | Job Type: Full-Time Experience: 1–3 Years Salary: ₹15,000 – ₹22,000 / Month (based on experience) Position: Store Incharge Key Responsibilities: Maintain accurate records of material inward and outward movements. Monitor and manage daily stock levels of raw materials, tools, and finished goods. Issue materials to the production team as per requirements. Update stock registers in Excel regularly. Conduct physical stock verification and reconcile with records. Coordinate with the purchase and accounts departments for timely procurement and documentation. Ensure proper storage, labeling, and safety of all materials in the store area. Requirements: 1–3 years of experience in storekeeping or inventory management. Knowledge of stock management processes and tools. Familiarity with MS Excel and inventory software is a plus. Good organizational and record-keeping skills. Ability to work independently and handle responsibilities with accuracy. Apply Now: Send your resume to digital@saitecnomec.in or call 70094 94752 Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹22,000.00 per month Schedule: Day shift Work Location: In person

Mobile: 93459 12525 Email: hr@vaighaiagro.com Company: Vaighai Agro Products Limited Website: https://vaighai.com/ Location: 350/1, Sholavandan Rd, Nagari, Tamil Nadu 625221 Job Title: Retail Packing Manager Industry: FMCG – Edible Oil / Consumer Goods Job Summary: To manage and oversee the entire retail packing operations for edible oils or FMCG products, ensuring timely, cost-effective, and quality-driven packaging output in line with company standards and regulatory compliance. Key Responsibilities: Production Planning & Control: Plan daily and weekly packing schedules based on sales forecasts and inventory levels. Allocate manpower, machinery, and materials efficiently to meet targets. Operations Management: Oversee day-to-day activities in the retail packing line, including filling, labeling, sealing, and secondary packing. Monitor OEE (Overall Equipment Efficiency) and minimize downtime. Quality Assurance: Ensure packaging quality meets product standards and complies with FSSAI/BIS norms. Coordinate with the QA/QC team for timely sample checks and validations. Inventory & Material Handling: Maintain optimum stock levels of packing materials such as pouches, bottles, cartons, and labels. Coordinate with procurement and stores for timely material availability. Team Management: Lead and train a team of line supervisors, operators, and laborers. Monitor team performance, ensure discipline, and promote a safety-first culture. Process Improvement: Drive continuous improvement initiatives (Kaizen, 5S, Lean) in the packing section. Identify areas of cost reduction and process optimization. Compliance & Documentation: Ensure compliance with GMP, HACCP, and safety standards. Maintain production records, packing logs, material consumption reports, and statutory documentation. Coordination & Reporting: Coordinate with maintenance, production, quality, and logistics teams. Prepare and submit daily, weekly, and monthly packing performance reports. Key Skills & Competencies: Strong knowledge of packaging machinery and operations. Familiarity with edible oil/FMCG packaging materials and processes. Proficiency in SAP/ERP systems for production and inventory tracking. Good leadership and communication skills. Knowledge of safety, hygiene, and food-grade packing compliance. Qualifications & Experience: Bachelor’s degree/Diploma in Mechanical, Production, or Food Technology. 7–10 years of relevant experience in a retail packing role within the FMCG/Oil sector. Experience in handling high-speed automated packing lines preferred. Job Type: Full-time Pay: ₹25,000.00 - ₹30,000.00 per month Work Location: In person

About Us We are a global climate technologies company engineered for sustainability. We create sustainable and efficient residential, commercial and industrial spaces through HVACR technologies. We protect temperature-sensitive goods throughout the cold chain. And we bring comfort to people globally. Best-in-class engineering, design and manufacturing combined with category-leading brands in compression, controls, software and monitoring solutions result in next-generation climate technology that is built for the needs of the world ahead. Whether you are a professional looking for a career change, an undergraduate student exploring your first opportunity, or recent graduate with an advanced degree, we have opportunities that will allow you to innovate, be challenged and make an impact. Join our team and start your journey today! Key Responsibilities - Description Of Duties & Activities 1 Technical Training & Customer Enablement – India Conduct technical training sessions for India-based OEMs, channel partners, SSI OEMs, cold chain integrators, heat pump developers, and transport sector customers. Collaborate with Sales Managers to plan product promotions and new business opportunities (NBOs). Identify key OEM customers and their service/R&D networks for targeted engagement. Design and deliver customized training programs at customer-preferred locations. Provide ongoing support for customer technical and service inquiries. Identify high-priority customers based on business potential. Develop and manage quarterly and annual training calendars. Create tailored training content and deliver sessions aimed at improving field performance and reducing warranty costs. 2 Application Development Support – Cold Chain, Heating, and Integrated Solutions Work closely with Sales, Marketing, and Application Engineering (AE) teams to identify application development and product promotion needs. Develop and maintain annual and quarterly plans for new application development. Support customers in heat load calculations and system configuration for cold chain, heating, and integrated solutions. Collaborate with customers and engineering teams to validate new applications and convert them into viable business opportunities. Work With Customers / Engineering to qualify New Application & Convert to Business Opportunities 3 Standards & Regulatory Engagement Actively participate in technical committee meetings of BIS, RAMA, BEE, MOEF, and other relevant regulatory bodies. Contribute to the development and refinement of standards, regulations, and labeling programs. Advocate for sustainable and compliant solutions that align with business growth objectives. Profile Education And Professional Qualifications B.E. / M.Tech with a specialization in Thermal Engineering, combined with 6–8 years of experience in Engineering, Quality, and Service functions within reputed HVAC OEMs. Demonstrated expertise in managing technical processes along with hands-on experience in technical training and capability development. Requirements And Attributes Strong technical acumen and domain knowledge Excellent communication and presentation skills Proactive learner with a continuous improvement mindset Effective stakeholder management and interpersonal skills Our Commitment to Our People Across the globe, we are united by a singular Purpose: Sustainability is no small ambition. That’s why everything we do is geared toward a sustainable future—for our generation and all those to come. Through groundbreaking innovations, HVACR technology and cold chain solutions, we are reducing carbon emissions and improving energy efficiency in spaces of all sizes, from residential to commercial to industrial. Our employees are our greatest strength. We believe that our culture of passion, openness, and collaboration empowers us to work toward the same goal - to make the world a better place. We invest in the end-to-end development of our people, beginning at onboarding and through senior leadership, so they can thrive personally and professionally. Flexible and competitive benefits plans offer the right options to meet your individual/family needs. We provide employees with flexible time off plans, including paid parental leave (maternal and paternal), vacation and holiday leave. Together, we have the opportunity – and the power – to continue to revolutionize the technology behind air conditioning, heating and refrigeration, and cultivate a better future. Learn more about us and how you can join our team! Our Commitment to Inclusion & Belonging At Copeland, we cultivate a strong sense of inclusion and belonging where individuals of all backgrounds, and with diverse perspectives, are embraced and treated fairly to enable a stronger workforce. Our employee resource groups play an important role in culture and community building at Copeland. Equal Opportunity Employer Copeland is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, marital status, political affiliation, sexual orientation, gender identity, genetic information, disability or protected veteran status. We are committed to providing a workplace free of any discrimination or harassment. Show more Show less

. Job Title: Store cum Purchase Manager Industry: Electrical / Control Panel Manufacturing Location: Turbhe Navi Mumbai Experience: 5+ years (preferred in control panel or electrical manufacturing industry) Job Summary: We are seeking a highly organized and experienced Store cum Purchase Manager to oversee procurement activities and manage inventory and materials for our control panel manufacturing operations. The ideal candidate will ensure timely procurement, optimize inventory levels, and maintain accurate store records while coordinating closely with production and quality teams. Key Responsibilities: Purchase Management: Source and procure electrical components, panels, wiring materials, and other industrial supplies. Identify and negotiate with reliable vendors and suppliers for quality materials at competitive prices. Issue purchase orders and track deliveries to ensure timely availability of materials. Maintain vendor database, evaluate vendor performance, and develop strong supplier relationships. Manage procurement budgets and ensure cost-effective purchases without compromising quality. Store & Inventory Management: Receive, inspect, and store incoming materials and equipment. Maintain accurate stock records using ERP or inventory management software. Conduct regular stock audits and reconcile physical stock with system records. Manage issuance of materials to production as per Bill of Materials (BOM). Ensure proper storage and labeling of materials to maintain quality and avoid damage/loss. Coordination & Compliance: Coordinate with production, quality control, and design departments to ensure materials align with project specifications. Ensure compliance with safety, statutory, and internal standards related to material handling and storage. Prepare and present periodic reports on purchase activities, inventory status, and cost analysis. Key Skills & Qualifications: Bachelor's degree or diploma in Electrical Engineering, Supply Chain, or related field. Minimum 5 years of experience in purchase/store roles in electrical/control panel manufacturing. Strong knowledge of electrical components, control panel parts, and sourcing strategies. Proficiency in ERP/inventory management systems and MS Office. Excellent negotiation, communication, and organizational skills. Ability to multitask and work under pressure in a deadline-driven environment. Preferred: Experience with ISO documentation and compliance. Familiarity with local and international sourcing regulations. Show more Show less

Job Description Compilation & Review of quality ANDAs for General and Complex Injectable Products within timeline. Compilation and review of Amendments (DRL/IR/CR) within stipulated timeline for Amneal Injectable products. Review of technical documents of PD, ARD, QA, QC, Production and CRO to include as a part of Dossier. Follow up with cross-functional team for completion of assigned technical and regulatory task. Preparation of regulatory strategy/white papers and to include any critical/important missing points and finalization in consultation with superior. Primary review of DMFs of General and Complex Injectable API and follow up with purchase team for vendor documentation. Preparation and review of Controlled Correspondences for General and Complex Injectable products. Communication and discussion with CMOs for outside development projects. Co-ordination with R&D, ARD, QC, QA, Clinical, Labeling team for any outstanding technical task and escalation with superiors for resolution. Monitoring the change in regulations, regulatory procedures & guidances and to evaluate impact on product life cycle. Preparation and archival of global regulatory database. Qualifications Master's Degree About Us Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion. About The Team The Human Resources team partners with all aspects of the organization, driving success through the effective and innovative management of people for both current and future business needs. Key Roles That The Human Resources Team Performs Executive Role: Specialists in all aspects of people management. High-level input at strategic level into all key business decisions. Audit Role: Ensures all areas of the organization are compliant with legal requirements AND best practice employment policies and procedures. Facilitator Role: Close partnership to support, advise and extend the ability of all areas of the organization to meet their objectives through implementation of highly effective employment practices in areas such as Talent Acquisition, Learning and Development, Reward systems, Performance Management, Health and Wellbeing. Consultancy Role: Provide expert advice to the organization and it’s managers on any aspect of workforce management and employee relations and performance. Service Role: Ensure the organization is fully aware of and is equipped to deal with developments impacting employment matters, such as changes in legislation, changes in the characteristics of the labor market. Show more Show less

Job Title: Store Keeper – Food Industry Location: Calicut, Kerala Experience Required: Minimum 1 year (specifically in the food industry) Gender Preference: Male Salary Range: ₹15,000 – ₹22,000 per month Industry: Food & Beverage / Food Processing / Hospitality Key Responsibilities: Receive, inspect, and store food items and supplies in compliance with hygiene and safety standards. Maintain accurate inventory records and update stock levels regularly. Follow FIFO (First-In, First-Out) and FEFO (First-Expired, First-Out) principles in stock rotation. Ensure proper labeling, packaging, and storage of perishable and non-perishable items. Monitor temperature and storage conditions as per food safety norms. Coordinate with procurement and kitchen/production teams for timely stock issuance and replenishment. Conduct daily/weekly stock audits and report discrepancies. Maintain cleanliness and orderliness of the storage area as per food safety regulations. Candidate Requirements: Minimum 1 year of experience as a Store Keeper in the food industry . Knowledge of inventory and stock management practices specific to food items. Familiarity with basic food safety and hygiene standards (FSSAI guidelines preferred). Good organizational and communication skills. Physically fit and capable of handling stock movement. Education: SSLC / Plus Two / Diploma. Preference for candidates based in or around Calicut . Interested candidates are requested to share your updated resumes to mdjinitha@gmail.com Job Type: Full-time Pay: ₹15,000.00 - ₹22,000.00 per month Schedule: Day shift Experience: Store: 1 year (Preferred) Work Location: On the road

🎯 Role OverviewThe Godown Incharge is responsible for overseeing the daily operations of the warehouse, ensuring efficient receipt, storage, and dispatch of goods. This role involves managing inventory, supervising staff, maintaining safety standards, and coordinating logistics to meet organizational objectives. 🔑 Key Responsibilities Inventory Management: Maintain accurate records of all incoming and outgoing stock. Conduct regular stock audits and reconcile physical inventory with system records. Warehouse Operations: Supervise the receipt, storage, and dispatch of goods. Ensure proper labeling, organization, and cleanliness of the warehouse. Staff Supervision: Lead, train, and evaluate warehouse staff. Organize shifts to meet operational requirements and ensure productivity. Safety Compliance: Implement and enforce safety guidelines and compliance standards within the warehouse, ensuring a secure working environment. Logistics Coordination: Coordinate with vendors and suppliers to ensure timely receipt of goods. Oversee the accurate picking and packing of orders, minimizing errors and ensuring on-time delivery. Equipment Maintenance: Ensure the proper maintenance and functionality of warehouse equipment, such as forklifts and pallet jacks. Arrange for repairs and maintenance as needed. Documentation: Maintain detailed records of incoming and outgoing goods, as well as stock movements. Prepare and complete orders for delivery or pickup according to schedul ✅ QualificationsEducation: Minimum of a high school diploma; a degree in Business, Logistics, or a related field is advantageous. Experience: Prior experience in warehouse management or a similar role is preferred. Skills: Strong organizational and leadership abilities. Proficiency in inventory management software and systems. Excellent communication and interpersonal skills. Ability to operate warehouse equipment safely.

Job Summary:The Store Executive is responsible for managing and overseeing the day-to-day operations of the store or warehouse. This includes receiving and issuing materials, maintaining proper inventory records, ensuring accurate stock levels, and following inventory control procedures. The role requires close coordination with various departments to ensure timely supply of materials. Key Responsibilities:Receive, inspect, and record incoming materials and supplies. Issue materials as per requisitions and maintain proper documentation. Maintain accurate inventory levels and perform regular stock audits. Update stock records in the ERP or inventory management system. Ensure proper storage, labeling, and handling of materials. Monitor and report stock discrepancies or damages to the supervisor. Maintain cleanliness and organization of the store area. Coordinate with the purchase and accounts departments for material reconciliation. Track and manage slow-moving and obsolete stock. Ensure compliance with company policies, safety standards, and procedures. Requirements:Education: Graduate in any discipline (preferably with a diploma/certificate in Store Management or Inventory Control). Experience: 2–4 years of experience in store or warehouse management. Skills: Good knowledge of inventory control procedures. Familiarity with ERP systems or inventory software. Basic knowledge of MS Office (Excel, Word). Good organizational and communication skills. Attention to detail and problem-solving ability.

Job Title: Store Manager Location: Near Wadala RTO, Wadala Truck Terminal, Sion, Mumbai, Maharashtra 400037 Job Type: Full-time Company: Protomont Technologies LLP About Us:Protomont Technologies LLP is a leading innovator in the 3D printing industry, providing advanced solutions for a range of applications, from rapid prototyping to full-scale production. Our commitment to quality and innovation drives us to continually push the boundaries of what's possible with 3D printing technology. We are seeking a detail-oriented and proactive Store Manager to oversee our inventory and ensure efficient operations of our warehouse and logistics. Job Summary:As a Store Manager at Protomont Technologies LLP, you will be responsible for managing inventory, handling procurement, ensuring accurate stock levels, and maintaining a streamlined supply chain. You will play a vital role in the organization’s operational efficiency and timely delivery of products to clients. Key Responsibilities:• Inventory Management: Monitor and maintain optimal inventory levels of 3D printers, filaments, resins, and accessories. Conduct regular stock audits and reconcile discrepancies. Ensure proper storage, labeling, and handling of products. • Procurement and Reordering: Track stock movement and forecast inventory requirements. Coordinate with suppliers for timely procurement of stock and materials. Negotiate prices and manage vendor relationships. • Store Operations: Maintain cleanliness and organization of the warehouse/store area. Implement standard operating procedures for inventory control. Ensure timely dispatch and receipt of goods. • Record Keeping and Reporting: Maintain accurate records of inward/outward stock and returns. Prepare and submit inventory reports to management regularly. Use inventory management software to track and log all transactions. • Team Collaboration: Coordinate with the sales, service, and logistics teams for seamless operations. Train and supervise store assistants or helpers, if any. Qualifications:• Education: Bachelor’s degree or diploma in Logistics, Supply Chain Management, or a related field. • Experience: Minimum of 1 year of experience in inventory management, warehouse operations, or a similar role. • Skills: Proficiency in inventory or ERP software and Microsoft Excel. Strong organizational and time-management abilities. Good communication skills and problem-solving aptitude. Attention to detail and a proactive work attitude. Compensation:• CTC (Cost to Company): ₹15,000 – ₹25,000 How to Apply:Interested candidates should submit their resume and a cover letter detailing their qualifications and experience to info@protomont.com with the subject line “Store Manager Application.”

Current Employees, Consultants, And Agency Partners If you currently work for Brown-Forman, please apply by clicking the Careers icon on the Workday portal. For best results, use Google Chrome to view this page. Quote from Hiring Manager Brown-Forman, a longstanding leader in promoting the responsible enjoyment of premium beverage alcohol products, seeks to retain a Public Affairs professional to assist in implementing its strategies to enhance and protect Brown-Forman’s commercial and and marketing freedoms, and promote alcohol responsibility in India. Meaningful Work From Day One Assessing the cultural and political environment affecting the distilled spirits industry in India and providing sound strategic and tactical advice to the company. Serving as an advocate for Brown-Forman’s interests with State and Central Governments and regulatory departments within India. Furthering Brown-Forman’s policies as one of its representatives on local industry trade associations and social aspects organizations. Cultivate strong partnerships with key stakeholders in Excise, Government and industry on an ongoing basis to maintain the required/desired Public Affairs goals and objectives. Collaborate regularly with relevant authorities on policies in line with B-F’s organization and business strategy. Spearhead initiatives to implement recommended policies/amendments. What You Can Expect Strategically inform, identify and advise Brown-Forman on public policy initiatives to promote industry self-regulation, alcohol education, and alcohol responsibility throughout India. Contribute to the development of a comprehensive strategy and consistent practice for Brown-Forman government relations for India. Work closely with B-F local management to develop and implement a proactive agenda to advance Brown-Forman’s commercial interests in India. This Will Involve Working to protect Brown-Forman’s interests from threats that would worsen the commercial environment for the responsible sale and marketing of distilled spirits Identifying and working (most often collectively with others in the beverage alcohol industry) to reform existing laws, policies and regulations that unreasonably impede Brown-Forman’s business in India Spokesperson for Brown-Forman on political and alcohol responsibility matters with governments, politicians and regulators. Advise and provide support on strategic and policy matters in the areas of alcohol responsibility and Public Affairs in India. Collaborate with the General Manager, India and South Asia and the leadership team to ensure the commercial imperatives for the India business are reflected in India public policy and regulation. Serve as Brown-Forman’s primary representative on day-to-day matters involving trade associations of which Brown-Forman is a member in India, including ISWAI working groups (International Spirits and Wine Association of India). Work closely with and under the guidance and direction of the VP, Director of Public Affairs EAA in determining policy and involvement in all these and other discussion forums. Support the General Manager, India and South Asia in their capacity as Brown-Forman’s representative on the board of ISWAI. Coordinate lobbying on behalf of Brown-Forman, including ensuring compliance with the highest ethical standards and all applicable laws and governmental regulations. Collaborate with internal colleagues in India and abroad (including the General Manager, India and South Asia, legal, supply chain, marketing, commercial and finance) regarding regulatory issues in India. Coordinate the Responsibility agenda within Brown Forman India. Drive and monitor policy and program interventions with government & industry bodies across the states, monitoring their progress and follow-up in furtherance of the company's growth plans and business objectives. Provide timely information on any policy change with its implications to all regions. Working with the Legal Manager, India, ensures the company’s policy positions are designed and implemented in compliance with relevant laws and company policies. Keep a watching brief and communicate regularly on competitor positions and policy approaches with government. Ensure all issues related to State Excise, Licensing, land matters and environment are timely anticipated and resolved. Establishing, maintaining and developing healthy relationships with the central and state government authorities, Embassy contacts and apex trade bodies (example FICCI, CII, CCPA, ASCI, AmCham) for strategic engagement. Overseeing all applications for permission / approvals/License / registration Working closely with the functional heads and managers, and keeping them. well informed on relevant public policy issues, debates and trends; extend guidance and advice on issues involving clearance from Central/State government and statutory/regulatory authorities. What You Bring To The Table Public Affairs professional with a graduate degree and at least 5 years of applicable experience Experience sitting on or working for an industry trade association Familiarity with navigating the state and central government political systems in India Excellent oral and written communication skills. The successful candidate will be an organized thinker, a good planner and a strong advocate. The candidate must be able to communicate, even on highly complex matters, in short, readable memos Ability to influence and lobby successfully for company and industry positions. Brown-Forman places great emphasis on the ability to strategize and persuade; these qualities are fundamental to this position Dealing with Ambiguity - handles risk and uncertainty comfortably and has good judgment on how new ideas will play out in the market Multicultural mindset, team player Highest reputation for integrity Good judgment. Brown-Forman recognizes that public policy, particularly in the beverage alcohol area, can be sensitive and controversial. The successful candidate will recognize these sensitivities and have demonstrated the ability to use common sense and exhibit balanced thinking Ability to set priorities, identify opportunities, and see matters through to successful completion. The successful applicant will be a self-starter capable of managing a variety of projects efficiently with minimal supervision What Makes You Unique Experience working in a heavily regulated industry within the region Understanding of: ○ the operation of excise, tax and customs laws and regulations in India ○ Food Safety Standards Association of India (FSSAI) labeling requirements ○ ASCI marketing guidelines and operation of the CCPA Who We Are We believe great people build great brands. And we know there is Nothing Better in the Market than a career at Brown-Forman. Being a part of Brown-Forman means you will grow both personally and professionally. You will have the opportunity to solve problems, seize opportunities, and generate bold ideas. You will belong to a place where teamwork matters and where you are encouraged to bring your best self to work. What We Offer Total Rewards at Brown-Forman is designed to engage our people to ensure sustainable and profitable growth for generations to come. As a premium spirits company, we offer equitable pay structures for individual and company performance alongside a premium employee experience. We offer a range of premium benefits that reflect our company values and meet the needs of our diverse workforce. #jackdaniels Requisition Type Employee Management Level Leader Global Job Level L3 Number Of Openings Available 1 Show more Show less

A Packer prepares items for shipment by locating, packaging, and labeling products according to customer orders or company standards. They ensure products are securely packaged, accurately labeled, and ready for transport, often assisting with warehouse duties like unloading, storing, and maintaining order. Show more Show less

Ventra is hiring a Chief R&D Technologist for a major international confectionery company at its production facilities in Russia. Responsibilities: Lead the research and development of innovative chocolate products, including new recipes, textures, formats, and technologies. Benchmark global chocolate trends and raw materials to identify new opportunities for the brand. Define and optimize formulations for taste, texture, shelf life, nutritional value, and production efficiency. Manage and mentor R&D technologists, creating a high-performing, innovation-driven team. Develop and implement pilot testing protocols, including equipment selection and process validation. Ensure compliance with all food safety, labeling, and regulatory requirements. Partner with equipment manufacturers and suppliers to evaluate new technologies and raw materials. Requirements: Relevant degree in Food Technology or related field. Experience in chocolate R&D or innovation roles, preferably in an international FMCG or confectionery company. Understanding of food safety standards (HACCP, ISO, etc.). Willingness to relocate to Russia . Fluency in English. Conditions: Competitive salary (based on interview results). Relocation package is provided by the company (includes relocation assistance, accommodation, and document support). Opportunities for professional growth and involvement in the development of unique products. Work in a modern production facility. Medical insurance. Benefits package. Show more Show less

Ventra is hiring a R&D Technologist for a major international confectionery company at its production facilities in Russia. Responsibilities: Research and development of innovative chocolate products, including new recipes, textures, formats, and technologies. Benchmark global chocolate trends and raw materials to identify new opportunities for the brand. Define and optimize formulations for taste, texture, shelf life, nutritional value, and production efficiency. Ensure compliance with all food safety, labeling, and regulatory requirements. Requirements: Relevant degree in Food Technology or related field. Experience in chocolate R&D or innovation roles, preferably in an international FMCG or confectionery company. Understanding of food safety standards (HACCP, ISO, etc.). Willingness to relocate to Russia . Fluency in English. Conditions: Competitive salary (based on interview results). Relocation package is provided by the company (includes relocation assistance, accommodation, and document support). Opportunities for professional growth and involvement in the development of unique products. Work in a modern production facility. Medical insurance. Benefits package. Show more Show less

Description Amazon is looking for an AI Content Expert II to help with annotations, content generation, and data analysis. As part of the Data Team, you will be responsible for delivering high-quality training data to improve and expand AGI's Large Language Models' (LLMs) capabilities. Key job responsibilities As an AI Content Expert, you will be responsible for creating training data that are complex in nature and will require you to make informed and high judgement decisions in each case. You will be working closely with scientists and engineers to review and update guidelines, identify tooling improvement opportunities, and engage in conversations regarding the quality of data. Creating and annotating high-quality complex training data in multiple modalities (text, image, video) on various topics, including technical or science-related content Writing grammatically correct texts in different styles with various degrees of creativity, stricly adhering to provided guidelines Performing audits and quality checks of tasks completed by other specialists, if required Making sound judgments and logical decisions when faced with ambiguous or incomplete information while performing tasks Diving deep into issues and implementing solutions independently Identifying and reporting tooling bugs and suggesting improvements A day in the life We are looking for a ML Data Associate (MLDA) to undertake the task of foundational labeling functions, such as dialogue evaluation on speech, text, audio, video data. Your ability to concentrate, multi-task and your high attention to detail helps you deliver high-quality work as well as maintaining strict confidentiality and follow all applicable Amazon policies for securing confidential information. You will be a part of a diverse team with the shared vision of improving customers’ lives with practical, useful generative AI innovations. An inner drive, individuality, and a creative mind are extremely beneficial. Basic Qualifications Bachelor’s degree in a relevant field or equivalent professional experience 2+ years of experience working with written language data, including experience with annotation, and other forms of data markup. Strong proficiency in English. Candidate must demonstrate excellent writing, reading, and comprehension skills (C2 level in the Common European Framework CEFR scale). Strong understanding of U.S.-based culture, society, and norms. Strong research skills to gather relevant information, understand complex topics, and synthesize multiple resources; understanding of basic academic integrity, i.e. plagiarism. Excellent attention to details and ability to focus for a long period of time Comfortable with high-school level STEM* Ability to effectively write and evaluate diverse subject matter across various domains* Ability to adapt writing style to suit various style guidelines and customers. Ability to adapt well to fast-paced environments with changing circumstances, direction, and strategy Preferred Qualifications Experience with creating complex data for LLM training and evaluation 1+ year(s) of experience working with command line interfaces and basic UNIX commands Familiarity with common markup languages such as HTML, XML, Markdown Familiarity with common standard text formats such as JSON, CSV, RTF Working knowledge of Python or another scripting language Familiarity with regular expressions syntax Familiarity with Large Language Models Comfort in annotation work that may include sensitive content Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit https://amazon.jobs/content/en/how-we-hire/accommodations for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner. Company - ADCI MAA 12 SEZ Job ID: A2973293 Show more Show less

Review and submission of Product License application for the new product / renewal well in time as per the scheduled commercial product manufacturing plan. Effective dossier compilation, review and submission plan followed by regulatory queries evaluation and timely response to obtain expedited product registration; drafting company's response towards government notifications. Facilitate and co-ordinate plant audits conducted by regulatory/certification bodies/customer audits. Liaise with stakeholders - R&D, Quality, marketing, legal in obtaining necessary product, process and plant related technical information for submission ; certifying bodies and regulatory authorities Facilitate regulatory inputs/reviews during the product development and audit preparation within the scope of quality & regulatory compliance. Regulatory review of supplier quality agreement, Labeling information, Claim grid, ingredients INCI names, country specific caution etc. Evaluate and submit the application for post approval changes in product permission as per the variation regulation of respective country and as directed by the Global head. Liaise with stakeholders on changing regulatory landscape in countries like India/Latam/US/EU/Middle East/GCC/Russia-CIS/Africa regions. Regular updated database of site wise - product wise licenses with validity period; and regulatory compliance. Stay updated on changes in regulatory requirements and communicate these changes to relevant stakeholders. Educate staff on regulatory requirements and updates. Customer / regulatory queries and complaint evaluation with timely closure response ensuring regulatory compliance. Should be well versed in Product Stewardship Expert, REACH, TSCA, GHS Regulations &CLP. Please share your resume on kailas.avhad@vvfltd.com Show more Show less

Are you looking for a new challenge? For our location Amtala we are looking for a Production Operator at Wacker Metroark Chemicals Pvt Ltd. Job Description Contributes directly in the manufacturing activities including packing to ensure production and quality of product meets required specifications as per production plan / target Monitors products and processes from online control system Performs safety checks prior to working on designated equipment Updates required production records such as SOP (work instruction), Log sheet, Yield, internal rejection, breakdown analysis data of plant, WIP, RM balancing etc Involves himself in small maintenance work for the smooth operation of plant Should work with the ERP system Faces audits from time to time Follows all job instructions as communicated. Guides a team of workmen. Observes subordinates to ensure compliance with company standards in production, hygiene and safety Maintains strict guidelines about labeling of goods. Other duties may be assigned as and when required Meeting requirement of all IMS standards (ISO 9001, ISO 14001, ISO 22716, SMETA, HALAL etc) Contact Person: Anupam Nath We are looking forward to your online application! Reference Code: 27927 Show more Show less

Job title : Pharmacovigilance Case MR Oversight Specialist Location: Hyderabad Opella is the self-care challenger with the purest and third-largest portfolio in the Over-The-Counter (OTC) & Vitamins, Minerals & Supplements (VMS) market globally . Our mission is to bring health in people’s hands by making self-care as simple as it should be . For half a billion consumers worldwide – and counting. At the core of this mission is our 100 loved brands , our 11,000-strong global team, our 13 best-in-class manufacturing sites and 4 specialized science and innovation development centers. Headquartered in France, Opella is the proud maker of many of the world’s most loved brands, including Allegra, Buscopan, Doliprane, Dulcolax, Enterogermina, Essentiale and Mucosolvan. B Corp certified in multiple markets , we are active players in the journey towards healthier people and planet. Find out more about our mission at www.opella.com. Main Responsibilities The primary function of the Case Medical Review (MR) Oversight specialist is to perform the medical and regulatory evaluation of all ICSRs. Oversee the Medical Review of ICSRs as per predefined activity and job-role in PV safety database (DB), with special focus on case medical accuracy and documentation. Maintain overall accountability for the timeliness and quality of medical Case Management activities outsourced to service providers. Be the product medical expert from Medical Review Standpoint for all High priority Products and provide training & guidance to MR teams Lead or participate in cross-functional projects or initiatives within global PV collaborates with the Global Safety Officer (GSO) in the review of clinical trial and post-marketing program documentation and on labeling activities. Establish strong collaboration with cross-functional groups within and outside the company (i.e. Business Partners, CRO). Provide or receive training on Customer-specific processes, systems, or products. Perform daily quality review for ICSRs to allow analysis of data entry/ quality. Reconcile SAEs between the Clinical and Safety DBs to meet joint accountabilities and enable locking of Clinical DB. Provide support for the preparation of response to ad hoc HA queries, provide input into responses to inquiries from health care professionals on safety issues. Assist in study configurations of clinicals trials in the safety database Responsible for performing oversight of non-serious line listing as applicable. Creates and maintains relevant SOPs, job aids for medical review activity. Other PV tasks as required Experience About you Experience in PV Databases like ARGUS, Aris-G (LSMV) VAULT Safety, etc. Minimum 4 years of pharmaceutical industry experience with a focus on pharmacovigilance Strong Experience in medical review of ICSRs Experience in labelling and causality assessments is must. Experience in overseeing vendors responsible for case processing. Experience with SDEA agreements Experience review in signal activities, RMP, PBRERS, and PADERS etc. Strong experience review of non-serious line listings. Experience and understanding of the safety/pharmacovigilance process and regulations, ICH GVP and GxP regarding systems validation and documentation Good knowledge of MS Office Strong experience in ICSR quality review and submissions Incumbent should have experience in Process Improvement practices Soft Skills Stakeholder management, Strong negotiation and communication skills, and ability to operate effectively in a global environment and across-line functions. Attention to details, Analytic, pro-active and effective problem-solving skills. Excellent organizational and project management abilities. Strong communication and interpersonal skills. Ability to work effectively in a cross-functional, multicultural environment. Think strategically and lead teams. Excellent team-work and interpersonal skills Ability to work in cross-functional teams Excellent oral and written communication skills Strong communication and interpersonal skills. Ability to work effectively in a cross-functional, multicultural environment. Think strategically and lead teams. Technical Skills Regulatory Standards: In-depth knowledge of global pharmacovigilance regulations and guidelines, such as those from the FDA, EMA, ICH, and other health authorities. Knowledge of how adverse events are reported and classified (e.g., by severity, outcome) and the regulatory requirements surrounding these reports Safety Reporting Requirements: Knowledge of regulatory requirements for safety reporting (e.g., CIOMS forms, EudraVigilance, FDA REMS, etc.) and experience in ensuring compliance with these standards. Good Pharmacovigilance Practices (GxP): Familiarity with GxP guidelines, ensuring that all pharmacovigilance processes adhere to industry standards. Database Management: Familiarity with safety databases and systems (e.g., Aris-G / LSMV, Argus Safety, VigiBase, or similar systems) used for collecting, analyzing, and reporting adverse event data. Microsoft Office Suite: Advanced skills in Excel (for data analysis and reporting), Word (for report writing), and PowerPoint (for presenting findings) Education MD (Pharmacology) degree with 2 years' experience required / or MBBS/Pharm D equivalent Academic qualification is desirable with 4 years’ experience in Global PV/Clinical environments. Languages : Fluent in English (verbal and written) Why us? At Opella, you will enjoy doing challenging, purposeful work, empowered to develop consumer brands with passion and creativity. This is your chance to grow new skills and be part of a bold, collaborative, and inclusive culture where people can thrive and be at their best every day. We Are Challengers: We are dedicated to making self-care as simple as it should be. That starts with our culture. We are challengers by nature, and this is how we do things: All In Together: We keep each other honest and have each other's backs. Courageous: We break boundaries and take thoughtful risks with creativity. Outcome-Obsessed: We are personally accountable, driving sustainable impact and results with integrity. Radically Simple: We strive to make things simple for us and simple for consumers, as it should be. Join us on our mission. Health. In your hands. www.opella.com/en/careers Show more Show less

Having experience in a warehouse can be highly beneficial, and if you’ve worked in a similar role before, it can help you understand the day-to-day tasks and challenges involved in warehouse operations. Here's an example of what warehouse experience might look like: Warehouse Experience: Inventory Management: Handled daily stock counts, ensuring accurate records of both incoming and outgoing items. Regularly updated inventory systems and generated reports for management. Receiving and Shipping: Unloaded and checked incoming shipments, confirming the accuracy of items received. Prepared outgoing orders for shipment, ensuring proper packaging, labeling, and documentation. Coordinated with shipping carriers to ensure timely deliveries. Organization and Maintenance: Ensured all products were stored correctly and in designated areas to maximize space and improve operational efficiency. Maintained cleanliness and orderliness in the warehouse, following safety and health protocols. Team Collaboration and Safety: Worked closely with team members to meet daily goals and improve warehouse workflow. Followed safety procedures to prevent accidents and injuries in the warehouse. Documentation and Billing: Managed and processed paperwork related to shipments, including invoices and shipping documents. Ensured that the accounts department received accurate billing for inbound and outbound goods. Maintained records of all warehouse transactions and communicated any discrepancies to supervisors. Skills Developed: Strong organizational skills and attention to detail Ability to operate warehouse equipment Time management and the ability to handle multiple tasks simultaneously Effective communication and team collaboration skills Good communication skills Proficiency in using computers, including Excel Report preparation and basic English proficiency Attention to detail, physical stamina, and the ability to collaborate in a team environment Education: A diploma, graduation, or any equivalent degree is preferred. Additional Tasks: Handling inward part entries, maintaining outward/inward part reports, and other store-related duties. Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Schedule: Day shift Ability to commute/relocate: Science City, Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Education: Diploma (Preferred) Experience: Warehouse management: 1 year (Preferred) License/Certification: Driving Licence (Preferred) Location: Science City, Ahmedabad, Gujarat (Preferred) Willingness to travel: 75% (Preferred) Work Location: In person Application Deadline: 20/06/2025 Expected Start Date: 10/06/2025