123 Tablets Jobs

As a member of the Lenovo team, you will be part of a global technology powerhouse committed to delivering exceptional products and services. With a revenue of US$57 billion and a strong presence in 180 markets worldwide, Lenovo is dedicated to providing Smarter Technology for All. Lenovo's extensive portfolio includes a range of AI-enabled devices such as PCs, workstations, smartphones, and tablets, as well as infrastructure solutions like servers, storage, edge computing, high-performance computing, and software-defined infrastructure. By investing in world-changing innovation, Lenovo aims to create a more equitable, trustworthy, and smarter future for individuals across the globe. Join us in shaping a more inclusive and innovative world. To learn more about Lenovo and our groundbreaking initiatives, please visit www.lenovo.com and explore the latest updates on our StoryHub platform.,

DKSH's purpose is to enrich people's lives. For 160 years, DKSH has been marketing, selling, and distributing high-quality products and brands for multinational and Fortune 500 companies. Through Business Units Consumer Goods, Healthcare, Performance Materials, and Technology, DKSH delivers sustainable growth for partners, contributing to improving the quality of life for employees and people in the local communities where operations are conducted. Headquartered in Switzerland, DKSH is publicly listed and operates in 36 markets across Asia Pacific, Europe, and North America. With over 28,000 specialists employed, DKSH achieved net sales of CHF 11.1 billion in 2024. The strength of DKSH lies in the diversity of services, industries, clients, products, regions, and employees from various nationalities. DKSH is proud of its people, who are the key to its success. The employees are passionate about their career growth and business success, working as part of an energetic and committed team that positively impacts millions of lives through the products and services provided. Join DKSH today if you are ready to drive growth, be the difference, experience a world of learning and development, own your career, take business responsibility, and have a positive impact that touches people's lives. Job Summary: The Assistant Manager, Business Development, Pharmaceutical Excipients (Raw Materials) is responsible for technical business development for pharmaceutical excipients and nutraceutical actives. Job Responsibilities: - Promote and aggressively develop Pharma business in assigned geographical regions/customers. - Identify and introduce products of clients (existing and new) in the specified regions/customers. - Undergo technical training and support the Pharma sales team and customers with technical know-how and product application. - Ensure that targets set by Senior Manager-Pharma and Head, Pharma Business Line are met to achieve performance bonuses. - Analyze the potential of the pharma market and build the customer base. - Identify prospective customers, generate leads, and support new business development with the reporting manager. - Conduct market mapping and promote new segments while maintaining strong relationships with various functions at customers (R&D, QA, Technology Transfer, Procurement, etc.). - Send monthly and specified reports on business development to the Senior Manager Pharma and principals/suppliers. - Coordinate and organize supplier visits at customer R&D. - Provide technical solutions to customers and support them in shop floor trials. - Align with internal business processes like Salesforce and proactively fulfill digital updation requirements. - Be prepared for new responsibilities assigned by Senior Manager - Pharma based on industry clusters or product groups and the development of other regions. Work Experience: 3-4 years in pharma excipient business development, techno-marketing technical development, formulation research development. Functional Skills and Knowledge: - Knowledge of formulation development activities of solid orals like Tablets, Capsules, Liquid oral, and Topical formulations. - Experience with novel drug delivery systems, regulatory filing of products for US, EU, ROW, and domestic markets. - Problem-solving capabilities in terms of pharma product development and scale-up trials troubleshooting. Education: B.Pharm/M.Pharma,

Walk-in Drive @ Hyderabad on 3rd Aug 2025 (Sunday) Strides Pharma is hosting a Walk-In Drive for multiple roles. Venue: Hotel Ravila Grand, Plot No 9, Mumbai Highway Road, Opposite Pranaam Hospital Lane, Sri Durga Colony, Madeenaguda, Hyderabad, Telangana 500049 Open Positions Department: Production (OSD) Experience: 2-5 years Qualification: B.Pharm/M.Pharm Job Location: Chennai Key Skills: Granulation, Compression, Coating, Capsule Filling, OSD Production, BMR, Production QMS, Change Control, Deviation, CAPA. Department: Packing (OSD) Experience: 2-5 years Qualification: B.Pharm/M.Pharm Job Location: Bangalore Key Skills: OSD Packing, Bottle Packing, Blister Packing, BQS, CVC, BPR Department: Quality Control Experience: 2-5 years Qualification: B.Pharm/M.Pharm/M.Sc. Job Location: Pondicherry Key Skills: HPLC, GC, UV, IR, KF, FTIR, Dissolution, LIMS, GLP Department: Quality Assurance-IPQA (OSD) Experience: 2-5 years Qualification: B.Pharm/M.Pharm Job Location: Chennai Key Skills: IPQA, BMR Review, BPR Review, Line Clearance, In process & process validation sampling. Department: Formulation & Development (OSD) Experience: 2-7 years Qualification: M.Pharm Job Location: Bangalore Key Skills: Planning & Execution of Lab scale experiments. DOE, Quality by Design, Product Development, Stability Protocol, Regulatory Market. Best Regards, Talent Acquisition Team, STRIDES PHARMA SCIENCE LTD

please share your CV on renu.kumari@adecco.com or watsapp on 8758695449 Role & responsibilities 1. Compression (OSD MFG) Technician / Operator 3 to 8 yrs ITI, Diploma 2. Compression (OSD MFG) Staff / Officer 3 to 7 yrs B.Pharma, M.Pharma Preferred candidate profile

Role & responsibilities Lead formulation and development projects from concept through commercialization Design and optimize formulations to meet product specifications and regulatory requirements Manage and mentor a team of formulation scientists and technicians Collaborate with cross-functional teams including QA, QC, regulatory, and manufacturing Ensure timely completion of project milestones and deliverables Prepare technical reports, presentations, and documentation Stay updated on industry trends, regulatory changes, and best practices Qualifications Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or related field Minimum of 2-3 years of experience in formulation and development Proven track record of successful product formulations Strong understanding of regulatory requirements and guidelines Excellent project management and leadership skills Strong analytical and problem-solving abilities Fluent English International Travelling - Targeted Country - Ghana, Africa, Nigeria, Ethiopia, Uganda, Kenya, Myanmar, Thailand etc. Skills Formulation development Project management Analytical techniques Regulatory compliance Team leadership Technical writing Problem-solving Benefits Yearly Bonus Provide PF, ESIC, PT Benefits Medical Insurance Travelling Allowances Yearly Increment

We are conducting Walk-in Interview at Indore for our OSD manufacturing Facility based out of our Ahmedabad (SEZ-II), please find the below details. Date : 27th May 2025 (Sunday) Interview Location: Ahmedabad Timings: 9:00 am 5:00 pm Interview Venue: PTC-Sigma Block No. 2, 3, 4, 5, Sigma Commerce Zone,Nr Iskon Mandir BRTS Bus Stand, Ambli Bopal Road, Ahmedabad – 380015 ? Job Location: Ahmedabad Education Qualification: ITI/Diploma/BSC/ /B.Pharma Departments are as follows : Production- OSD : Plant Operator/ Technical Assistant : ITI / Diploma having 3 - 8 years of experience in operating machines like Granulation (ACG, Glatt, Tapasya, GEA), Fitzpatrick Roll Compactor, Compression machines (Fette), Wurster Coater (ACG, Glatt, Anish), imprinting, Visual Inspection. Perform line clearance, operation and cleaning of equipment / instrument / auxiliary items Executive/ Sr Executive: B. Pharma with 3 - 8 years of experience in Tablet/ Capsule department with experience in Granulation, Compression, Coating, Inspection . Responsible to plan for the manufacturing of batches in coordination with PPMC. To monitor line clearance, cleaning of equipment, instrument, auxiliary items. To carry out qualification activities. To initiate QMS activities (Change control, deviation, CAPA, investigation) and E-BMR. To handle manpower and allocate daily activities.. Engineering: Technician : Diploma / ITI with 3- 8 years of experience in plant maintenance & Process Equipment (Electrical/ Instrumentation) and Instrumentation . Candidates should have experience in Plant maintenance, preventive maintenance and breakdown maintenance of OSD plant equipment. Troubleshooting of mechanical and electrical equipment . Instrument and calibration of OSD plant equipment. They should have knowledge and experience in instruments sensors, PLC, HML, SCADA, and experience in calibration activities. Quality Assurance (Qualification) Assistant Manager / Deputy Manager / Associate Manager: B.Pharm with 10-20 years QA & MFG – Qualification. Candidates should have experience in Qualification, Validation. They would have to prepare, execute and review of equipment/ instrument/ system /utility /area qualification program. Review of data backup activity, data restoration and its compliance. QMS documentation exposure is required. completion of CAPAs and to perform change control/CAPA effectiveness. Associate Manager: CSV B.Pharm with 15-20 years with experience in Issuance and retrieval of documents. Candidate should have experience in Review of various Qualification and CSV Documents. Review of system audit trail, system security user privileges and ensure the compliance. Review of data backup activity, data restoration and its compliance. To ensure timely completion of CAPAs and to perform change control/CAPA effectiveness. For all the positions, candidate should have exposure in pharmaceutical company and exposure to regulatory requirements of documentation and cGMP will be added advantage. Interested candidates Please Walk-in for an interview along-with their Aadhar Card, Passport size Photograph, updated CVs, Salary Structure, Salary Slip and relevant documents(original as well as Photocopies) as per the schedule.

We are looking for a dynamic and experienced Sales Engineer to join our team at Xtragen Technologies Pvt. Ltd. in J. P. Nagar, 8th Phase Bengaluru. If you have a passion for selling rugged tech devices, smart industrial solutions, and mobility hardware, this opportunity is for you! As a Sales Engineer or Sales Executive with 3-4 years of experience in B2B Tech Sales, you will be responsible for promoting products in domains such as Rugged Tablets, IT Devices, and Enterprise Mobility. Your role will be crucial in understanding client needs, offering custom tech solutions, and delivering excellent client service. Key Requirements: - B.E/B.Tech in Computer Science, IT, or Electronics - Strong background in B2B Sales of tech hardware - Excellent pitching, communication, and client-handling skills - Knowledge of rugged devices, tablets, and smart solutions - Ability to provide tailored tech solutions based on client requirements Please Note: We are specifically seeking Sales Engineers or Sales Executives with experience in tech sales. Developers, freshers, or unrelated applicants are kindly requested not to apply for this position. If you are interested in this exciting opportunity, please send your updated resume to hr@xtragen.in. For further inquiries, you can reach out to us at +91 97314 96302 or visit our website at www.xtragen.in.,

Role & responsibilities Granulation Supervisor Responsibilities: Supervise the granulation process, ensuring compliance with Batch Manufacturing Records (BMR) and adherence to Good Manufacturing Practices (GMP) . Ensure effective process adherence, timely production, and achievement of department goals. Focus on yield improvement , identifying and implementing strategies to optimize production efficiency and minimize waste. Monitor and maintain granulation equipment, ensuring smooth operation and troubleshooting as needed. Collaborate with cross-functional teams to address any production or quality-related issues. Provide training and mentorship to junior staff, ensuring operational efficiency and safety. Analyze production data and report on key performance indicators (KPIs) to senior management for continuous improvement. Granulation Pharmacist Responsibilities: Responsible for operating and overseeing more than two granulation machines during production, ensuring quality and quantity targets are met. Perform regular quality checks at various stages of production to maintain high-quality standards. Ensure proper machine performance, identify potential issues, and support troubleshooting and preventive maintenance activities. Ensure compliance with GMP and regulatory standards throughout the production process. Collaborate with Quality Control and Maintenance teams to resolve operational challenges and maintain machine performance. Maintain accurate production records, monitoring machine performance and production metrics. Pellets Supervisor Responsibilities: experience in pellets manufacturing in a regulated OSD pharmaceutical environment. Strong understanding of GMP, GDP, regulatory (USFDA/EU/WHO) guidelines. Good documentation, team management, and communication skills.

Role & responsibilities 1. Drive product robustness for all products in area of responsibility and lead the third party operation team. 2. Lead and manage all TPO Process activities and process validation for products developed and manufactured at outside contract facilities. 3. This includes, providing product stewardship by ensuring the performance of all products are monitored and maintained in a validated state, supporting root cause investigations by providing Technical intelligence to deviations, technical complaints, OOS & CAPAs. 4. Identifying and executing continuous improvement opportunities, leading New Product Launch third party teams and leading technical activities related to transfers of Drug Product Manufacture and Packaging. 5. Be familiar with statistical tools to analyze data. 6. Provide third party and techno-commercial leadership in the areas of production and packaging process and process optimization using pharmaceutical processes. 7. Knowledge of all pertinent technical information related to an assigned product. Detailed knowledge of the operation, maintenance, and utility of all manufacturing and/or packaging equipment for assigned projects. Thorough familiarity with cGMPs, SOP's, relevant government regulations, and current industry standards. 8. Responsible for Techno-commercial activities for all dosage form. 9. Responsible for Sourcing / coordinate with LL/TP manufacturers for product related documents. 10. Supplier Identification: • Identifying potential suppliers capable of meeting the quality, regulatory, and supply requirements for markets. 11. Supplier Qualification and Onboarding: • Developing and implementing a robust supplier qualification process to ensure that selected suppliers meet the necessary standards and regulations in coordination with quality team. Preferred candidate profile PHARMA THANKS YOU REGARDS MILAP RATHOD (7486829377) call or whtup HR DEPARTMENT OPES HEALTHCARE PRIVATE LIMITED

RESPONSIBILITIES Ensure achievement of budgeted targets on a monthly and yearly basis. Ensure site is in state of compliance for multiple authorities inspections and guide / coordinate during inspections and local statutory authorities. Work out areas of improvement in product cost, engineering cost and implement the same. Create and maintain an environment of mutual trust, respect, and customer centricity. Build and maintain a high performing team and culture. Ensure manpower management and engagement. Brand ambassador of Unichem for any internal and external stakeholders at the plant. DESIRED SKILLS Excellent Experience in manufacturing formulations (Tablets & Capsules). Exposure in Managing and working with International Regulatory Authorities like MHRA, EU etc. is a must. Should have strategic, operational excellence, collaboration, and customer-centric mindset. Excellent experience in general management, team management, and networking Should have experience in budgeting and cost optimization. Should have functional knowledge of LEAN Aptitude for automation and use of technology. Should have experience of working in a matrix environment. Should be ready to work in a dynamic environment. Excellent negotiation skills and interpersonal skills Experience in Site Transfer, New Product Launch & Green field Project will be appreciable.

Role & responsibilities Manage technology transfer activities from development to commercial manufacturing for OSD tablets. Oversee and execute process scale-up, process optimization, and validation to ensure smooth transition into commercial production. Maintain an in-depth knowledge of USFDA regulations for OSD products and ensure compliance with all regulatory requirements during tech transfer activities. Work closely with R&D, manufacturing, and quality teams to address any technical challenges during tech transfer. Preferred candidate profile Prefered candidates from OSD (manufacture Tablets , capsules,)background . USFDA experince is must Its a plant based role.

1. To study and understand the project quality and documentation requirements from the project brief with the help of the project design team. 2. To prepare the project and quality plan for all the ongoing projects. 3. To prepare the document list based on the project scope, project timeline, and quality plan, including internal and vendor-provided documents. 4. To inform all relevant departments about the documentation and quality requirements. 5. To collect, prepare, review, modify, and approve documents related to procurement, installation, commissioning, qualification, validation, and handover using standard tools and software. 6. To track all documents for availability, correctness, and approvals from the project team, concerned departments, and clients. 7. To prepare critical qualification and validation document requirement specifications (URS), validation master plan (VMP), project and quality plan, impact analysis, corrective action and preventive action (CAPA), standard operating procedures (SOPs), risk analysis, etc. 8. To prepare and update standard templates for design qualification (DQ), installation qualification (IQ), operational qualification (OQ), performance qualification (PQ), handover forms, installation protocols, commissioning protocols, etc. 9. To maintain the document history and change logs throughout the project life. 10.To verify the documents and drawings for numbering, formats, signature panels, approvals, etc. 11.To coordinate with the client for document approvals, maintain records, and confirm receipt and version control. 12.To follow up on all site activities documentation related to installation, commissioning, qualification, validation, and handover. To perform the site as required If needed, visit the. 13.To track and send protocols to the site as per testing and reporting needs. Supervisory Role: 1. To prepare a work plan and work hour list for all new projects within the heating, ventilation, and air conditioning (HVAC) department. 2. To regularly update the plan and work hour list and get the same approved by the project team and superiors. 3. To allocate workload to team members as per project needs and deadlines. 4. To coordinate with the project management department team on client queries and documentation timelines. 5. To review and approve the workload and deliverables of subordinates for accurate submission of documents required for purchases, client approvals, construction at sites, etc. 6. To ensure that all the department reports are updated on a timely basis. 7. To ensure that all the documents, internal and external, are accurately organized in the data management system (DMS) as per the project requirements and plan. Requirements Skills and Competencies: 1. Good understanding of the basic concepts of HVAC, clean room construction, clean room flooring, piping, utilities, production equipment, and electrical systems. 2. Fluent in written and spoken English and Hindi. 3. Self-motivated and target-oriented. 4. Capable of drafting SOPs and templates aligned with GMP and regulatory requirements. 5. Strong analytical and logical reasoning skills. 6. Competent with spreadsheets and document tracking tools. 7. Ability to perform under pressure and meet strict deadlines. 8. High accuracy in documentation and effective time management. Knowledge: 1. Knowledge of the pharmaceutical industry in general, dosage forms in the formulation industry, and various equipment and systems that go into the operation and construction of a facility. 2. Knowledge of the latest Food and Drug Administration (FDA) and international good manufacturing practice (GMP) documentation standards. 3. Good knowledge of qualification and validation documentation for a pharmaceutical facility. 4. Attending and representing the company in GMP audits, inspections by FDA agencies, and practical validation on the production floor would be an added advantage.

Role & responsibilities Review and approve Finished Goods and corresponding Certificates of Analysis (COA). Maintain detailed records of received samples in an organized manner. Ensure proper allocation and storage of approved COAS in the shared drive. Verify and confirm drug product permissions as per regulatory requirements. Oversee the finalization of packing materials in coordination with relevant departments. Conduct audits of new vendors, ensuring compliance with quality standards. Ensure proper implementation of Corrective and Preventive Actions (CAPA) for any deviations or complaints. Visit manufacturing sites to address and investigate market complaints effectively. Coordinate with manufacturing partners for handling market and sample-related complaints. Perform joint analysis of complaint samples in collaboration with manufacturers to identify root causes. Maintain strict adherence to Good Documentation Practices (GDP). Possess sound knowledge of Schedule M, USFDA, MHRA and ensure compliance in relevant activities. Sound knowledge of IPQA (In-Process Quality Assurance) activities across different dosage forms (e.g., tablets, capsules, syrups, ointments, etc.) Sound knowledge of different types of SOPS (Standard Operating Procedures), including preparation, review, implementation, and compliance monitoring. Basic understanding of QMS (Quality Management System), including its elements and relevance in pharmaceutical operations.

Technology transfer, scale-up at external/Third-party manufacturing/CMO sites. Coordinate with CMOs/internal teams for trials, validation and commercial production. Documents preparation for scale-up, validation and timely execution at CMOs. Food allowance Provident fund Health insurance

Job Location : Ahmedabad Role - Blister Machine Operators (Secondary/ Primary) Qualification ITI/Diploma Exp 2-5 Years Role - Blister Machine Officer (Secondary/ Primary) Qualification B. Pharma / Bsc Exp 3-10 Years Renu Kumari Senior Recruitment Consultant Adecco [ India] Watsapp +91, 6364920532 Email ID : renu.kumari@adecco.com

As a skilled technician, you will be responsible for diagnosing, troubleshooting, and repairing a variety of electronic and mechanical equipment, including computers, in an office setting. Your passion for technology and gadgets will drive you to excel in a clean and positive work environment. Your tasks will involve performing high-quality repairs and refurbishment on gadgets such as smartwatches, drone cameras, tablets, and computers. Routine maintenance activities will also be part of your responsibilities to ensure equipment functionality and longevity. Utilizing diagnostic tools, manuals, and schematics will aid you in the repair process, including replacing faulty components, parts, or modules as needed to ensure compatibility and functionality. Testing the repaired equipment to verify proper functionality and performance is crucial, along with documenting all repairs accurately and comprehensively. Adherence to safety protocols and collaboration with colleagues and supervisors to optimize repair processes are essential for preventing accidents and improving efficiency. To qualify for this role, you must possess a high school diploma or ITI, technical certification, or relevant vocational training. Excellent knowledge of technical management, information analysis, and computer hardware/software systems is required. Hands-on experience with computer networks, network administration, and network installation is a plus. Proficiency in using diagnostic tools, equipment, and software for troubleshooting and repair, along with excellent problem-solving skills and attention to detail, are essential. You should be able to work independently with minimal supervision and collaboratively in a team environment, demonstrating strong communication skills, both verbal and written. Flexibility to adapt to changing priorities and work schedules, along with a commitment to upholding quality standards and delivering exceptional service to clients, are key attributes for success in this role. In return for your expertise, we offer professional growth opportunities in the serene setting of the City of Lakes - Bhopal. You will enjoy generous paid time off, including vacation days, sick leave, and holidays, as well as clear career progression paths and regular performance reviews to support your personal and professional development. Outstanding performance and contributions will be acknowledged and rewarded to motivate and inspire you further. This is a full-time position with benefits such as paid sick time. The work schedule is during the day shift. As part of the application process, we would like to know your current/expected CTC and if you are an immediate joiner. A bachelor's degree is preferred for this role, and at least 1 year of experience with drones is required. The work location is in person to ensure effective collaboration and communication among the team members.,

The position of Manager, IT - End User Computing at Exela in Pune, IN-MH requires a Bachelor's degree in Computer/Information Technology or a related field. It is preferred for candidates to have relevant certifications such as MCSE/MCP, CCNA along with at least 3+ years of experience in IT infrastructure design, implementation, and management. The ideal candidate should have a proven track record of managing complex IT environments in a fast-paced setting. The primary responsibilities of the EUC Specialist include the maintenance of IT equipment and troubleshooting of all IT-related devices such as PCs, laptops, tablets, wireless handheld devices, thin clients, Virtual Desktop environment (e.g. AVD, Citrix), network printers, and other end-user devices. The candidate should possess strong technical skills including a deep knowledge of hardware and operating systems, workstation virtualization, experience with monitoring tools, and automation frameworks. In addition to technical skills, the candidate should also demonstrate excellent problem-solving and analytical abilities. Effective communication and interpersonal skills are essential for collaborating with various teams. The ability to manage multiple tasks and projects simultaneously is crucial for success in this role. If you meet the qualifications and have a passion for IT infrastructure management, this role at Exela's Global Operation Center could be the next step in your career. Join a team of over 17,500 employees operating in 23 countries and be part of a leading business process automation company dedicated to digital transformation solutions.,

Wipro Limited is a leading technology services and consulting company dedicated to developing innovative solutions to meet clients" complex digital transformation needs. With a worldwide presence and a diverse team of over 230,000 employees, we are committed to helping our customers, colleagues, and communities thrive in a constantly evolving world. **About the Role:** As a Desktop Support Engineer at Wipro Technologies-Ireland, you will be instrumental in ensuring the smooth and efficient operation of our technology environment. This role provides an excellent opportunity to utilize your advanced technical skills within a dynamic and collaborative team. Your primary responsibility will be to deliver exceptional support to our clients and promptly resolve any technical issues that may arise. **Roles & Responsibilities:** - Demonstrate advanced technical expertise in troubleshooting and fault resolution to minimize user downtime. - Maintain a high level of proficiency in standard technology practices and tools to contribute to an effective IT environment. - Communicate complex technical solutions in a clear and friendly manner to non-technical audiences. - Possess in-depth technical knowledge of various devices including PCs, desktop hardware, laptops, Cisco phones, mobile devices, MAC devices, and tablets. - Provide exceptional software support for tools such as O365, Zoom, and Teams. - Utilize Microsoft toolsets for effective problem-solving and troubleshooting. - Regularly update and enhance desktops and laptops to improve user experience and productivity. - Engage in daily huddles with the Team Leader to discuss objectives and progress. - Proactively address 2nd and 3rd line issues, maintain the issues log, and assist users in raising incident tickets for unresolved problems. - Undertake any other reasonable tasks as assigned to promote flexibility and adaptability in the role. This position requires a combination of technical expertise, effective communication, and problem-solving skills to uphold our commitment to client satisfaction. **Benefits:** In addition to a competitive salary, you will receive a comprehensive benefits package, training, and development opportunities for a rewarding career in a fast-paced and dynamic environment. The benefits include: - Contributory pension - Extra holiday purchase - Life insurance policy - Private medical insurance **Equal Opportunities:** Wipro advocates for positive change and conscious inclusion, striving to build a diverse Wipro family by fostering a culture of diversity, equality, and inclusion in the workplace. All applicants are welcome to apply.,

Role & responsibilities Good experience in HPLC Formulation background Male candidate only Location - Mahad, Raigad Preferred candidate profile M.Sc candidate only

In-Process as per BMR. Monitoring of environmental condition in cubicles under operation. line clearance without any observation . Identifying and resolving production-related issues, implementing corrective and preventive actions (CAPA), and conducting root cause analysis. Maintaining accurate and up-to-date manufacturing documentation, including batch records, logbooks, and SOPs. Maintaining a strong understanding and adherence to Current Good Manufacturing Practices (cGMP) within the production facility. Maintaining a strong understanding and adherence to Current Good Manufacturing Practices (cGMP) within the production facility. Preferred candidate profile Preferred Candidate from pharma formulation background only .

Job Summary: Walter Bushnell is seeking a Research Scientist - Formulations with experience in Solid Oral Products to join our R&D team . The candidate will be responsible for formulation development, process optimization, and ensuring regulatory compliance for solid dosage forms. Key Responsibilities: Develop and optimize formulations for solid oral dosage forms (tablets, capsules, granules, etc.). Conduct pre-formulation studies, excipient compatibility tests, and stability studies . Perform process development, scale-up, and technology transfer for new formulations. Prepare and maintain technical documentation, protocols, and reports as per regulatory guidelines. Ensure compliance with cGMP, ICH, and regulatory standards for formulation development. Collaborate with analytical, regulatory, and manufacturing teams for successful product development. Troubleshoot formulation and process-related challenges to improve product stability and quality. Qualifications & Skills: Education: M. Pharm / B. Pharm in Pharmaceutics or related field. Experience: 4-5 years in formulation development of solid oral products . Strong knowledge of cGMP, ICH guidelines, and regulatory requirements . Hands-on experience in process optimization, scale-up, and tech transfer . Proficiency in documentation and regulatory compliance . How to Apply: Interested candidates can share their resumes at akanksha.jaiswal@walterbushnell.com . For further details, you can directly reach out at 7042636289 .

1. Oversee & execute production batches for OSD formulation 2.Maintaining Good housekeeping in workplace as per cGMP 3.Documentation of batch records, raw material usage & production log 4. Standard operating procedure and standard cleaning procedure Required Candidate profile 1. Minimum 5 years experience in Pharma Formulations (OSD) 2. Willing to work in Chennai/Chengalpet 3. Candidates having regulatory plant experience would be preferred

Tablet section 2 persons Liquid section 2 persons one approved Stripping alu alu section 1person Capsule section 1 person

Job Location Wada, Palghar Approval Tablets, Capsule, Liquid and Ointment Experience 10 Yrs and Above Role & responsibilities : Thorough Knowledge of formulation manufacturing. The role involves managing production teams Optimizing processes, and ensuring efficient and safe production workflows Manage day-to-day production operations, ensuring timely and efficient manufacturing. Ensure compliance with GMP, safety, and environmental regulations. Timely getting work done as per planning Troub le shooting and managing all aspect of production. Reporting to Plant Head.

Job Location Wada, Palghar Age Below 50yrs Role & responsibilities : Operate the organization as per plan & profitable through strategy planning and execution of a Tablet Capsules Ointment & Liquid section. To meet the manufacturing target within the norms and budget. To motivate all functional department to achieve management goal. To ensure all functional heads are executing their responsibilities are effectively. Review weekly, monthly, quarterly and year planning and budgeting. Operate the plant as per regulatory and Government norms. Handling of production documents and review. Preliminary and first hand knowledge and handling all types of equipment which are used in Tablet/ Capsules/ Ointment/ Liquid manufacturing. Process trouble shooting, new product batches monitoring, RM + PM Planning. Maintaining and updating batch production record online Keeping all documents as required by cGMP, WHO GMP, GLP norms. Handle all production activities including co-ordination with QA / QC / RA / FDA / Store & Maintenance Department. Execution & Monitoring of process validation & Cleaning Validation Batches. Ensuring that all products are manufactured and stored as per WHO-GMP norms. Ensuring product quality is maintained. Others as added and or required in the course & duty.