58 Labelling Jobs

You will be joining EY to work as a SAP Product Life Cycle Management (PLM) Senior Level professional. In this role, you will be expected to have at least 3-5 years of experience in SAP PLM and have completed a minimum of 2 end-to-end implementations in PLM. It is important to note that support candidates are not required for this position. Good communication skills and a positive attitude are essential for this role. Key Responsibilities: - Possess skills in SAP PLM Discrete Manufacturing modules such as SAP ECTR, Change Records, Document Management System, and Bill of Materials. - Demonstrate proficiency in SAP PLM Process Manufacturing modules including SAP Recipe Management, Engineering Change Master, Specification Management, Labelling, Formulation Management, Product Compliance, Product Data Integration, and Enterprise Product Structure. - Be willing to travel as part of the job requirements. Qualifications Required: - At least 3-5 years of experience in SAP PLM. - Minimum of 2 end-to-end implementations in PLM. - Good communication skills and a positive attitude. EY is focused on building a better working world by creating new value for clients, people, society, and the planet, all while fostering trust in capital markets. Leveraging data, AI, and advanced technology, EY teams assist clients in shaping the future confidently and addressing the most critical issues of today and tomorrow. With a wide range of services in assurance, consulting, tax, strategy, and transactions, EY operates across more than 150 countries and territories, supported by sector insights, a globally connected network, and diverse ecosystem partners.,

Interview for SVP Formulation Plant in Bharuch on Permanent Payroll on 21-09 Experience: 2 to 6 Yrs Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch Venue: SDP HR SOLUTION 611 Golden Square Bs Dmart Bholav Bharuch Required Candidate profile Autoclave Operator Granulation Operator Manufacturing Operator Grinding Operator Washing Tunnel Operator Ampoule Filling Operator Vial Filling & Sealing Operator Lyo Operator Labelling Operator

Interview for SVP Formulation Plant in Bharuch on Permanent Payroll on 21-09 Experience: 2 to 6 Yrs Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch Venue: SDP HR SOLUTION 611 Golden Square Bs Dmart Bholav Bharuch Required Candidate profile Autoclave Operator Granulation Operator Manufacturing Operator Grinding Operator Washing Tunnel Operator Ampoule Filling Operator Vial Filling & Sealing Operator Lyo Operator Labelling Operator

Azurity Pharmaceuticals is a specialty pharmaceutical company dedicated to providing innovative products for underserved patients. With a focus on unique, accessible, and high-quality medications, Azurity continuously expands its commercial product portfolio and late-stage pipeline through integrated capabilities and a vast partner network. The company's patient-centric products cover various markets including cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan, benefiting millions of patients globally. As an inclusive workplace and Equal Opportunity Employer, Azurity attributes its success to a talented and dedicated team committed to improving patients" lives with a strong emphasis on science and quality. We are looking for individuals who are highly motivated, possess integrity, dedication, and a creative spirit to excel in our organization. **Job Responsibilities:** - Design, supervise, and conduct formulation development, process optimization, scale-up, and manufacturing of products. - Prepare and review essential documents including batch records, SOPs, stability protocols, specifications, and reports. - Analyze test results, identify variances, and recommend solutions to achieve project goals. - Schedule experiments, prioritize assignments, and meet project objectives and deadlines. - Maintain laboratory equipment and adhere to company safety standards. - Conduct laboratory experiments, prepare detailed reports with conclusions, and recommendations. - Develop and follow laboratory procedures to meet project objectives efficiently. - Identify and manage potential risks within complex projects promptly. - Maintain accurate documentation of experimental methods and results as per good documentation practices. - Serve as the primary scientific contact for external collaborators. - Manage inventories of supplies and raw materials. - Ensure completion of all required training on time. **Qualifications And Education Requirements:** - M. Pharm or Ph.D. in Pharmacy with a minimum of 3 to 6 years of industrial experience in pharmaceutical development and product scale-up. - Expertise in oral dosage forms, particularly in Modified Release, Extended Release, Targeted Release, Immediate Release solid/suspensions/solutions. - Experience in Global Product Development across markets like US, EU, China, and ROW. - Experience in developing branded and differentiated products, preferably in the 505(b)(2) category. - Familiarity with working with CROs/CDMOs is preferred. - Proficiency in Microsoft Office applications. By applying for this role, you confirm your ability to fulfill the job responsibilities outlined in the job description without any restrictions. If you have any concerns or disabilities that may affect your performance, please inform HR in advance.,

Walk-in interview For Sun Pharmaceutical Industries Limited, Dadra Date: 14th Sept 25 (Sunday) We are recruiting for our OSD manufacturing facility located at Dadra Time: 10 AM to 4 PM Interview Venue: Sun Pharmaceutical Industries Ltd, Survey No. 694, Dadra - 396193, (U.T. of D & N. H.), India, Following are the requirements for our manufacturing facility at Dadra Location. 1) Designation: Operator / Sr. Officer / Executive / Sr. Executive Engineering Education: ITI / Diploma / B. E (Elect. / E.C /Inst./ Mech) Department: Engineering Experience : 6 8 years of Experience of handling Engineering QMS, OSD Process Maintenance, Engineering Projects, Utility and Water System in OSD manufacturing plant. 2) Designation Operator / Officer / Executive Manufacturing & Packing Education: ITI / Diploma/ B. Sc/ B. Pharm / M. Pharm Department: OSD Manufacturing & Packing Experience: 6 - 8 years of work experience in pharmaceutical company, handling Granulation, and Primary & Secondary Bottle Packing activities in a regulated OSD manufacturing plant. 3) Designation: Technician Warehouse Education: ITI / Diploma Department: OSD Warehouse Experience: 4 - 8 years of work experience in pharmaceutical company handling Raw Material & Packing Material Dispensing in Warehouse in a regulated OSD manufacturing plant. For all the positions, we are looking for candidates with experience in regulated plants like USFDA, MHRA, ANVISA, TGA etc. Interested candidates meeting with criteria should carry their updated resume along with photograph, Photocopy of Salary Supporting/Appointment/latest Increment letters giving salary breakups of Monthly & Annual Salary is must.

We are seeking a diligent Regulatory Affairs specialist to support our compliance efforts, ensuring adherence to FSSAI, Legal Metrology, and AYUSH regulations. The successful candidate will play a key role in preparing and submitting statements for new product endorsements, license renewals, and quarterly/annual returns, maintaining strict regulatory compliance. Key Responsibilities: FSSAI Compliance: Review formulations and packaging to ensure alignment with FSSAI guidelines, manage product endorsements via the FOSCOS Portal, and provide recommendations for necessary modifications to meet compliance requirements. Artwork & Labeling Compliance: Validate and coordinate changes in product formulas, artwork, and packaging to ensure they meet regulatory standards set by FSSAI, ICMR-RDA, and AYUSH. License Management: Prepare and submit documents for new product endorsements and license renewals/modifications across FSSAI and AYUSH authorities, ensuring timely and accurate filings. Client Support: Address and resolve client queries related to product and artwork compliance. Regulatory Filings: Timely submission of required forms and returns, including Schedule TA, Form D-II, and Form V, to relevant authorities. Candidate Profile: Bachelors degree in Food Technology, B.Pharm, or a related field. 5-7 years of experience in Regulatory Affairs, particularly in food and nutritional products. Strong understanding of FSSAI, ICMR-RDA, AYUSH, and Legal Metrology regulations. Excellent communication skills, attention to detail, and a research-oriented mindset.

Role & responsibilities Department - Packing (FP) Assistant Manager Job Discription: Labelling & packing, SAP compliance, Visual inspection, QMS, SOP, MPR and BPR, cGMP Regulatory and non-regulatory audits Qualification: B.Sc/ B.Pharm/ M.Sc/ M.Pharmacy Experience: 8 - 15 years Job Description: Labeling & Packing activities, Equipment operation, SOP cGMP, Operator / Sr.Operator / Jr. Executive / Executive Qualification ITI/Diploma/B.Sc /B.Pharm /M.Sc /M.Pharmacy Experience: 2 - 8 years Preferred candidate profile

As a Lab Assistant in this role, your primary responsibilities will include housekeeping tasks such as maintaining the cleanliness and order of lab items, tools, glassware, accessories, and workbench. You will be assisting with Metallographic sample preparation by cutting, mounting, and polishing samples according to instructions. Additionally, you will support Light microscopy activities as directed. Ensuring the availability of lab consumables like gloves, lab wipes, and tissues will be part of your routine. You will also be responsible for collecting and transporting materials or chemicals for the lab from various sources as instructed. Proper labelling and storage of samples will be essential tasks that you will need to carry out diligently. Monitoring gas and compressed air pressure gauges, changing oil in FESEM vacuum pumps, and ensuring the water level in the FESEM cooler are maintained at appropriate levels are crucial aspects of this role. You will be required to monitor control panels in the lab for normal operation and promptly address any issues that may arise. Your duties will also involve escorting contractors and service personnel as needed to ensure a safe and secure working environment. This position is contractual/temporary for a period of 12 months, with the benefits of health insurance and Provident Fund provided. The work schedule is during the day shift from Monday to Friday. The ideal candidate will have a Diploma qualification, with at least 1 year of prior experience preferred. The work location is in Bangalore, Karnataka, and the role requires in-person presence. The application deadline is 28/02/2025, with an expected start date of 01/03/2025.,

The Stock Keeper position at Deva Steels in the manufacturing industry involves managing and overseeing the inventory of raw materials and finished goods. Your responsibilities will include receiving, inspecting, and storing incoming materials, maintaining accurate stock records, issuing materials based on requisitions, and ensuring adherence to safety and inventory control procedures. You will be expected to conduct regular stock checks, cycle counts, and physical inventory to guarantee stock accuracy, monitor inventory levels, and report any shortages or discrepancies to your supervisor. Additionally, you will be responsible for proper labelling, handling, and storage of goods to prevent damage or loss. This is a full-time, permanent position with benefits such as cell phone reimbursement, leave encashment, and Provident Fund. The work schedule includes day shift, fixed shift, and morning shift. In addition to the base salary, there are opportunities for quarterly and yearly bonuses. The work location for this role is in person.,

As a Legal Associate-Intake, you will play a crucial role in the legal team by managing various responsibilities to ensure efficient case management and client satisfaction. To qualify for this position, you must be a Law graduate with excellent English communication skills, both oral and written. Your main responsibilities will include drafting professional emails to clients, organizing and uploading case files into Cloud Storage/Case Management Systems, and maintaining client confidentiality. You will also be required to coordinate with attorneys, manage the attorney's professional diary, and communicate effectively with clients by providing case updates and maintaining a high level of professionalism. In addition, you will be responsible for calendar court hearings, deadlines, meetings, and depositions, as well as working closely with clients on the case management systems they use. You will independently handle tasks such as receiving case instructions, drafting legal correspondences, conducting legal research, and assisting with trial preparations. As part of your role, you will also perform various administrative duties, manage email communications, and coordinate with other staff members to ensure smooth operations. Your computer skills, including proficiency in Internet software and MS Office, will be essential for success in this position. This full-time, permanent position offers benefits such as medical insurance, provided food, health insurance, leave encashment, paid sick time, and Provident Fund. The work schedule is fixed from Monday to Friday with morning shifts and weekend availability as required. If you have a Bachelor's degree in Law and preferably 1 year of experience in Personal Injury cases, we encourage you to apply for this opportunity. The work location is in-person, and we are looking for a dedicated individual to join our team and contribute to our legal operations effectively.,

Genpact (NYSE: G) is a global professional services and solutions firm dedicated to shaping the future through the delivery of outcomes. With a workforce of over 125,000 employees spanning across 30+ countries, we are fueled by curiosity, entrepreneurial agility, and a commitment to creating lasting value for our clients. Our purpose, driven by the relentless pursuit of a world that works better for people, enables us to serve and transform leading enterprises, including the Fortune Global 500, leveraging our profound business and industry expertise, digital operations services, and proficiency in data, technology, and AI. We are currently seeking applications for the position of Manager- Labelling. As a Manager, you will thrive in a fast-paced business environment, working towards meeting deadlines and collaborating effectively as a team player. The ideal candidate for this role should exhibit the ability to excel within cross-functional teams, demonstrating active listening skills and the confidence to influence decision-making related to document content strategy. **Responsibilities:** - Oversee the content management of core data sheet (CDS) and local product documents (LPDs) - Update documents in accordance with local safety signals - Stay informed about regional labeling regulations - Develop labelling submission packages - Coordinate and facilitate translations in local languages - Conduct gap analyses of local labels, citing supportive literature and publications for updated text - Proofread documents crafted by the team **Qualifications we seek in you:** - Master's in Lifesciences or equivalent with experience in regulatory affairs/labelling or related field - Proficiency in the principles and concepts of Labelling, generics, authorized generics, private labels, device/combination products, and interpreting HA regulations and guidance - Ability to identify discrepancies in local implementation of corporate labels and take remediation actions - Capable of constructing a Company Response (MAH response) for health authority inquiries **Preferred Qualifications:** - Excellent communication and PC skills **Job Details:** - Job Title: Manager - Location: India-Hyderabad - Schedule: Full-time - Education Level: Bachelor's / Graduation / Equivalent - Job Posting Date: Feb 28, 2025, 8:00:32 AM - Unposting Date: Ongoing - Master Skills List: Operations - Job Category: Full Time,

The primary responsibilities of this role include ensuring the quality of all incoming PM, RM, in-process materials, stability samples, and finished products. You will be responsible for sampling and testing all PM, RM, in-process materials, and finished products within the specified lead time. Additionally, you will be expected to prepare testing reports in a timely manner and ensure correct labeling on materials such as sampled, approved, and rejected. You will also be responsible for sampling and testing raw water and purified water as per specifications. Other responsibilities include checking the dye strength of stock color solutions, verifying preservative traces in equipment used for preservative-free materials preparation, and monitoring various quality systems such as GLP, GDP, c-GMP, ISO, FDA, 5S, internal audits, and others effectively. You will need to ensure the effective implementation of in-process and final quality control checks, as well as the verification, calibration, and validation of all Q.C. instruments on time. Ensuring EHS compliance in the workplace is also a key part of this role. The qualification required for this position is a BSC/MSC degree.,

The role involves providing support and legal assistance specifically in areas of Labelling and Packaging across diverse product categories. You will be responsible for overseeing and managing the detailed review and approval process for all artworks and labels, ensuring legal compliance and proper substantiation of claims made on labels and artworks. You will work closely with Internal Stakeholders to ensure compliance across all labelling and packaging activities. In terms of Litigation and Notice Management, you will support in handling regulatory matters related to food laws for Amway India, including food litigation and representing the organization in court matters. You will also be responsible for drafting responses to legal notices. Additionally, you will support in Business Partnering by evaluating and reviewing offers and schemes for new and existing products, providing feedback on marketing content, advertisements, and promotional activities to ensure consistency, effectiveness, and brand integrity. You will advise on the wordings of terms and conditions for promotions and contests to ensure compliance with relevant regulations. Furthermore, you will offer guidance on various legal issues such as DS rules, Labor laws, Factory and environment laws, consumers, Food Laws, Legal Metrology, ASCI, advertising and marketing-related issues, and other developments impacting Amway India's business. The ideal candidate should possess knowledge in relevant laws and regulations, including advertising, marketing, and consumer laws. Strong understanding of Drugs & Cosmetic laws, Legal Metrology laws, Civil & criminal laws, Consumer laws, food laws, and Labor laws is required. Basic knowledge of Regulatory Compliance under FSSAI and Legal Metrology, as well as the India legal environment, is also necessary for this role.,

As a UPS team member, your primary responsibilities will include receiving, sorting, and accurately putting away inbound shipments. You will be tasked with picking, packing, and releasing goods with precision while ensuring proper labeling and stocking of kits. Your role will also involve verifying physical stock against documentation and releasing cargo to forwarders or carriers. Additionally, you will handle manifests, conduct cycle counts, and receive indirect materials on behalf of end users. In this position, you will be responsible for maintaining warehouse or production store facilities through housekeeping activities. You will also be required to upkeep and maintain materials handling equipment while adhering to standard operating procedures and warehouse safety and health rules. Furthermore, you will inspect all outbound orders information, including serial numbers, CoO, HS Code, ECCN, Export License Category, and Strategic Good Indicator, against physical items, invoices, and factory labels. To qualify for this role, you should have a minimum of Secondary 2 education with a certificate. Possessing a forklift license will be advantageous, and you should demonstrate reliability and commitment to your job. Proficiency in operating warehouse equipment such as reach trucks and hand pallet jacks is essential for successful job performance. Join the UPS team and contribute to our efficient and organized warehouse operations.,

You will be responsible for the monthly and daily calibrations of weighing balances and maintaining their records. You will update cleaning records and packing records regularly. Additionally, labeling all equipment in the Packing Department and filling BPR are crucial tasks that you will handle. Ensuring that packing materials received from Stores are as per BPR requirements will be part of your responsibilities. Monitoring yield losses during the packing process, overseeing the production process to ensure timely packing and shipping of all products, and maintaining the quality standards of the products will be essential duties. You will also be required to maintain accurate records of the production process and troubleshoot any issues that may arise. Your role will involve monitoring inventory levels and ordering supplies as needed. Coordination with other departments such as QA, QC, Production, and Stores will be necessary to ensure smooth operations. Apart from the mentioned responsibilities, you may be assigned other tasks by Senior Management. It is imperative to follow all safety protocols diligently in the workplace. To be considered for this role, you should have 3-5 years of relevant experience in the Packing Department of a Pharmaceutical Manufacturing Company.,

As a Phlebotomy (Blood Collection) Executive at our organization in Trivandrum, you will play a crucial role in our advanced medical diagnostics services. Your primary responsibility will involve performing blood sample collection from patients, both at the lab and in various settings including field and home visits. It is imperative that you ensure accurate labeling, proper documentation, and safe transportation of the collected samples. Maintaining a hygienic and sterile environment during sample collection is paramount to uphold our standards of professionalism. To be considered for this position, you must have a DMLT under DME (Diploma in Medical Laboratory Technology) or a +2 Science background with relevant experience. Freshers who have completed DMLT under DME can also apply. Additionally, for candidates with a +2 Science qualification, a minimum of 1 year of experience in blood collection is required. Your role will involve adhering to all phlebotomy protocols and safety guidelines to guarantee the well-being of both patients and staff. You will be expected to coordinate effectively with laboratory personnel and support staff to ensure the timely processing of samples for accurate diagnosis. The ideal candidate should possess a valid two-wheeler driving license and own a two-wheeler for commuting purposes. The role will require you to work in rotational shift duties between 6:00 AM and 8:00 PM. Strong communication and patient-handling skills are essential, along with a basic understanding of phlebotomy procedures and equipment handling. We value attributes such as punctuality, attention to detail, and reliability in our team members. A friendly and respectful approach towards patients is highly appreciated, as it contributes to our commitment to providing top-notch medical services. This is a full-time position based in Thiruvananthapuram with a monthly salary of 8,000 INR. The age limit for applicants is below 35 years. If you meet the eligibility criteria and are enthusiastic about contributing to our reputable organization, we encourage you to apply before the deadline on 07/06/2025. The expected start date for this role is 11/06/2025. Thank you for considering this opportunity to join our team of dedicated healthcare professionals.,

Description We are looking for an experienced SAP Product Compliance (EH&S) professional to join our team in India. The ideal candidate will have a robust background in implementing and managing SAP EH&S solutions, ensuring compliance with environmental, health, and safety regulations. This role requires a strategic thinker who can collaborate with various departments to enhance our compliance processes. Mandatory Skills Sap Product Compliance,Business Process Management,EH&S module,Loftware Labelling Optional Skills Javascript Additional Comments Work closely with Product Compliance Business and IT resources to establish robust processes and design to support business needs and initiatives. Align with Business Process Owner on requirements and long-term direction of Business Process Design and maintenance of business processes and data (business architecture) Business Process Management and continuous improvement of process landscape Prioritizing and managing change for processes and data in alignment with the business Discovering useful data insights, suggesting conclusions, and supporting decision making Closely aligns with technical subject matter expert for related IT systems to ensure seamless alignment of process, data and IT solution. Works independently. Skills and Qualifications 7-15 years of experience in SAP EH&S module implementation and support. Strong knowledge of environmental, health, and safety regulations in India. Experience with SAP S/4HANA and related compliance tools. Proficiency in configuring SAP EH&S solutions and enhancing existing functionalities. Ability to analyze complex data and generate compliance reports. Excellent communication and collaboration skills to work with cross-functional teams. Strong problem-solving skills and attention to detail.

You should have a strong hold on the Software Development Life Cycle (SDLC), Python Scripting, and AI packages. Your conceptual knowledge should include GenAI techniques such as Prompt engineering (Template, Curation, modification) and various foundation models related to text, image, video, and other data. Experience in DNN module training & Integration, CNN, Transformer/RNN is essential. You should also possess GenAI knowledge in LLM, Multimodal Models (Stable diffusion/Autoregression/Diffusion Transformer) to utilize World Foundation model and peripheral development effectively. Additionally, familiarity with Finetuning (Transfer learning) techniques for Multimodal Foundation models and Multi-modal Data pipeline (Cleaning, augmentation, embedding creation) is required. Data pruning/Curation and labeling with respect to AI training and validation is also part of the responsibilities. Knowledge of AD domain including domain stack components, Features, Sensor configuration, Format, and types of Annotations required for various components in the stack for development/testing, Validation is necessary. Proficiency in Python, GENAI, DNN, CNN, LLM is a must. Experience in Automotive, ADAS, and AD Domain will be beneficial for this role.,

Interested candidates please share your CV's to: pavanrai@mytechglobal.in NOTE: Looking for candidate who can join below 60 days Role & responsibilities We are currently seeking a resource with expertise in SAP Product Lifecycle Management (PLM) to support our ongoing SAP ECC to S/4 HANA migration initiatives. Please help share profiles of candidates who have relevant experience in PLM. Were particularly looking for someone with hands-on experience in PLM configuration and a strong understanding of end-to-end business process flows. Familiarity with S/4HANA PLM would be a significant advantage. Key focus areas include: Recipe Management / Development PLM Workflow Management Specification Management Labelling Document Management (within PLM scope) PLM Report Management Classes & Characteristics (within PLM scope)

Develop SOPs for production, filling, packaging & QA/QC; ensure FDA, EU, BIS & Drug Act compliance; conduct audits; review BMR, BPR & MFR; implement QMS; train staff on GMP/GLP; manage labelling, claims & documentation for regulatory compliance.

The Production Packing Assistant Manager/Manager is responsible for overseeing day-to-day production planning and execution to ensure requirements are met. You will be in charge of supervising and evaluating the performance of production personnel, organizing workflow to meet specifications and deadlines, and distributing staff/workers according to production planning. Additionally, you will review, approve, and implement departmental SOPs in accordance with current guidelines. You will also be responsible for monitoring online documentation such as BMRs, BPRs, log books, and other relevant documents. Monitoring the stage-wise process for product yield, reviewing QMS documents, qualification protocols, and other online documents for CAPA implementation will also be part of your duties. The ideal candidate should have knowledge of aseptic area practices, vial/ampoule filling and sealing, LYO products, regulatory audits, and packing and visual activities to ensure targets are achieved for packing, labeling, and visuals. Experience with cartridge printing, specifically Track & Trace, is also required for this role.,

As an ideal candidate, you should have a strong grasp of the Software Development Life Cycle (SDLC), Python Scripting, and Artificial Intelligence (AI) packages. Your conceptual knowledge should extend to General Artificial Intelligence (GenAI) techniques, including Prompt engineering such as Template, Curation, and modification. You should be well-versed in various foundation models related to text, image, video, and other data. Experience in training and integrating Deep Neural Network (DNN) modules, Convolutional Neural Network (CNN), and Transformer/Recurrent Neural Network (RNN) is essential for this role. Additionally, you should possess GenAI knowledge concerning Large Language Models (LLM) and Multimodal Models like Stable diffusion, Autoregression, and Diffusion Transformer for utilizing World Foundation models and peripheral development. Your expertise should also include fine-tuning (Transfer learning) techniques for Multimodal Foundation models, as well as managing Multi-modal Data pipelines involving tasks like cleaning, augmentation, and creating embeddings. You should be familiar with Data pruning/Curation and labeling in the context of AI training and validation. Furthermore, a good understanding of the Autonomous Driving (AD) domain is required, encompassing knowledge of domain stack components, features, sensor configuration, and the format and types of annotations necessary for various components in the stack for development and testing. Your comprehensive skill set in these areas will be crucial for excelling in this position.,

As a Crane Operator, your main responsibilities will include operating cranes by controlling crane levers, buttons, and pedals to lift and position heavy loads. Safety is a top priority, so you must ensure safe crane operation by adhering to safety protocols, inspecting equipment, and wearing appropriate personal protective equipment (PPE). Routine maintenance tasks such as cleaning, lubricating, and reporting any issues to supervisors are also part of your role. You will need to follow blueprints, schedules, and instructions to accurately lift and move materials, while keeping records of materials moved and completing necessary paperwork. Collaboration with other team members, such as signalers, is essential to ensure safe and efficient operations. For Packing roles, you will be responsible for packaging products according to company guidelines, ensuring correct labeling and documentation. Maintaining accurate inventory records, monitoring stock levels, and ensuring stock accuracy are key tasks in inventory management. You will also play a crucial role in order processing by ensuring accurate picking, packing, and loading of products for timely dispatch. Contributing to the overall efficiency of warehouse operations, including storage and handling of materials, is part of your daily responsibilities. Tracking and reporting on warehouse performance metrics like order accuracy, packing speed, and inventory turnover will be crucial. Ensuring the quality and accuracy of packaging materials and processes, maintaining a safe and clean working environment, and adhering to company safety regulations are also important aspects of the role. Collaboration with cross-functional teams to support seamless product distribution is essential, along with coordinating equipment troubleshooting and potentially assisting with packing machine challenges and fill weight verifications. As a Forklift Operator, you will be responsible for operating forklifts to move pallets, crates, and other materials within the warehouse or to/from loading docks and trucks. Loading and unloading materials from trucks, trailers, and other vehicles, as well as stacking, locating, and moving materials efficiently and safely, are part of your daily tasks. Performing routine checks, reporting malfunctions, and ensuring the forklift is in good working order are essential for equipment maintenance. Tracking inventory, verifying shipments, and ensuring the accuracy of stock will also be part of your responsibilities. Following all safety regulations and procedures to ensure a safe work environment, collaborating with other team members and supervisors to coordinate operations and maintain a clean work area are crucial aspects of the role. Qualifications required for these positions include holding any diploma.,

As a Pharma Package Component Development Engineer, you will be responsible for leading and executing packaging development initiatives across primary, secondary, and tertiary packaging systems. With 4 to 6 years of relevant experience, you will utilize your expertise in component design, specification creation, SAP BOM management, and cGMP documentation to work effectively in a regulated environment. You will be required to plan and execute packaging engineering assignments related to lifecycle management and new product development. Your key responsibilities will include developing material and structural designs for packaging systems, creating and approving component drawings and specifications, collaborating with R&D on product changes, authoring packaging documentation, leading physical testing and validation, troubleshooting packaging issues, and ensuring compliance with cGMP and regulatory standards. To excel in this role, you must possess a strong understanding of Package Component Development and Specification Creation, proficiency in cGMP documentation practices, experience with SAP especially in BOM creation, and familiarity with copy, graphics, pallet pattern design, and finished goods specs. Strong cross-functional collaboration skills, project and program management abilities, proficiency in Microsoft Office, effective communication, negotiation, and analytical skills are essential for success in this position. Preferred qualifications for this role include a degree in Packaging Engineering, Pharmaceutical Sciences, Mechanical Engineering, or a related field, prior experience in the pharmaceutical or healthcare industry, and familiarity with regulatory packaging requirements in FDA, EMA, or ICH regulated environments. Our hiring process for the Pharma Package Component Development Engineer position includes screening, followed by technical rounds and final HR round. If you meet the screening questions, possess the required skills, and are looking to take on a challenging role in packaging development within the pharmaceutical industry, we encourage you to apply and be part of our dynamic team.,

Position Name: Chief Manager Legal Department: Legal Department Reporting Position: AGM Legal Qualification: Basic Graduation / Law Graduate Qualification: Basic Graduation / Law Graduate Years of Experience: 10 to 14 years Location : Mumbai Purpose of the Position: The position is required to handle product based litigation arising out of claims made by customers against alleged manufacturing defects and servicing of cars. The position also has responsibility of owning the data on product cases and handing customer complaints where escalations are made to Legal Department. Also supporting business in commercial property transactions and issues pertaining to labelling and packaging Authority: 1. To represent Company before various judicial bodies / Local Authorities / Police & Investigation Authorities. 2. To execute documents on behalf of Company based on Authorisation Schedule. Skills Required: Strong background in independently handling voluminous litigations Solutions oriented approach to the business needs with strong inter personal & conceptual skills High level of integrity and compliant behavior Key Responsibilities &Tasks: A) Litigation: 1. Independently handling litigations including conducting analysis, evaluation and defence of any legal dispute on behalf of the company at various courts, forums, tribunals, corporations, commissions and other judicial bodies that may be required from time to time. 2. Ensuring that Company is represented by capable lawyers for legal cases all over India. 3. Independently handling alternate dispute resolution including proceedings under arbitrations and mediations. 4. Briefing advocates on records of the company before different courts, forums, authorities, etc., as required all over India. 5. Independently drafting legal replies, para wise comments for products claims in co-ordination with various brands. 6. Independently developing the monthly reporting system and ensuring dissemination of the same to the brands for inputs on legal cases. 7. Handling legal cases for overseas Group Companies and ensuring that the matter is suitably represented before the various forums. 8. Endeavoring and assisting the brands wherever required in reaching settlements in the cases filed before various Forums or Courts involving dispute(s) and preparing necessary documentation for the same. 9. Handling criminal complaints filed by customers, dealers, vendors, etc before police authorities / criminal courts. 10. Active participation with the police authorities and other investigating officers during inquiry / investigations. 11. Handling employee (including third party) related issues/court cases for sales related functions. Provide assistance in mitigating such legal disputes. 12. Actively supporting all Group Companies including overseas companies in areas of litigations and projects involving these Group Companies in India. 13. MIS on litigations & legal notices. 14. Regular reviews with business teams on active litigations and notices. B) Documentation and Advisory: 1. Independently drafting, vetting and negotiating of various contracts, settlement deeds and other legal documents. 2. Reviewing legal issues on behalf of Company with external advisors and counsel. 3. Independently handling high value and long term property projects including liaising with solicitors towards title due diligence of the property, drafting all property documents like, LOI, Lease Agreements, License Agreements, Bank Guarantees, etc. and conducting advanced level of negotiations with the developers, lessors, licensors, solicitors, etc. 4. Advising senior management on the various risks associated with property matters including developing a risk analysis and presentations to senior management. 5. Defining the strategy and legal stand of the company in so far as the cases under labelling laws are concerned, including streamlining the process of packaging & labelling laws at warehouses, ensure obtaining registrations under packaging & labelling laws for warehouses and Director nomination. 6. On case to case basis, advising brands on critical customer issues and vetting of communications including Non-Disclosure Agreement to/ with such customers 7. Independently handle documentation for lease premises including title verification, drafting, negotiating, finalising Letter of Intents, Agreements and also on termination / separation issues. 8. Giving advice to internal departments as may be required on a day to day basis for quick resolution of legal issues. 9. Discuss status of active litigations with Auditors. C) Compliance: 1. In charge of monitoring the statutory Compliance Tool to ensure legal compliances for the spare parts business at all warehouses. 2. Part of the team that performs test checks for statutory compliances for various departments.