196 Tablets Jobs

Effective operation and maintenance of equipment like autoclave, Garment cubicle, sealing machine, vessels CIP and SIP SKIDS To practice the c GMP activities and to follow the clean room discipline Cleaning and sterilization of the vessels and transfer lines using CIP & SIP equipment Preparation and filtration of disinfectant and cleaning of the area Monitoring of LAFU, AHU, Dynamic pass box, Garment cubicles and cold rooms Maintaining of all cGMP activities and housekeeping activities in the critical operations Maintenance and updating of equipment log books and GCRs Manual recording of the temperature and positive pressures Cleaning of equipment Blending of vaccines Preparation, Sanitization and sterilization of the items to be sent into Grade-B area Destruction of the rejected & unwanted materials and recording of the same Release of vaccine from blending to filling area To follow the usage of personnel protective equipment (PPE) during handing of corrosive liquids, WFI and steam Solution preparation Operation of Filter integrity machine Perform aseptic operations in Grade B area Any other tasks assigned by the supervisor.

Hands-on experience in monitoring manufacturing and packaging processes, line clearance, and in-process checks. Proficiency in DOC-MS systems, SOP preparation, deviation handling, and change control. Involvement in TT activities including protocol review, execution, and coordination between RCD and manufacturing. Familiarity with validated software systems that meet FDA electronic records and signatures requirements. Strong understanding of equipment qualification (D, I, O, P), process validation, and cleaning validation. E-BMR G E-Log: Experience with electronic Batch Manufacturing Records and Logbooks for real-time documentation and traceability. uality Management Systems (MS): Implementation and maintenance of MS aligned with regulatory standards . Risk Assessment: Ability to conduct and document risk assessments for processes, equipment, and product quality.

As a Retail Sales Consultant at our boutique store in HSR Layout, Bengaluru, you will play a crucial role in offering personalized recommendations, building genuine relationships, and creating exceptional shopping experiences for our customers. Your consultative sales approach will require empathy, strong product knowledge, and a focus on customer connection. Key Responsibilities: - Guide customers in selecting jewellery pieces such as engagement rings and fashion wear - Offer a warm and consultative sales experience to every customer - Maintain a strong product knowledge and stay updated on new arrivals and custom options - Capture customer details and preferences using CRM tools - Ensure the store is clean, well-displayed, and always guest-ready - Collaborate with the team to achieve monthly sales goals Qualifications Required: - 1-3 years of retail experience, preferably in jewellery, fashion, or luxury - Strong communication skills in English and Hindi - Demonstrated consultative selling skills with a genuine interest in customer stories and style - Passion for aesthetics, fashion, or design - Tech-savvy and comfortable using POS systems, CRM tools, and tablets - Warm, professional, and service-oriented personality Please note that the work schedule is full-time with a 6-day workweek on a day shift basis. In addition to a competitive salary higher than industry standards, you will have the opportunity to earn performance incentives. If you meet the qualifications and are excited to be part of a dynamic team in a boutique retail environment, we encourage you to apply for this permanent position.,

Key Responsibilities Lead and manage the Quality Assurance department, ensuring compliance with GMP norms and regulatory requirements of WHO, EU GMP, PICS, TGA, MHRA, USFDA, and other global agencies . Develop, implement, and monitor Quality Management Systems (QMS) across all QA functions. Ensure strict adherence to SOPs and continuous improvement practices in line with regulatory expectations. Oversee handling of rejected materials, market complaints, product recalls, deviations, change controls, CAPA, and CCF . Manage end-to-end Validation and Qualification activities (process validation, cleaning validation, equipment qualification, analytical method validation, etc.). Ensure audit readiness at all times and lead regulatory/customer audits and inspections. Review, approve, and monitor the control of documents, records, and quality risk management systems . Provide leadership and guidance to QA teams, including training, mentoring, and performance monitoring. Collaborate with cross-functional teams (Production, QC, R&D, Regulatory Affairs) to maintain high-quality standards. Drive initiatives for continuous quality improvement and compliance to ensure products meet global regulatory expectations. Desired Candidate Profile B.Pharm / M.Pharm with 1520 years of proven experience in Quality Assurance of Pharma Formulation Units . Strong command over WHO GMP, EU GMP, PICS, TGA, MHRA, and USFDA regulatory guidelines . Expertise in handling market complaints, investigations, and product recalls . Thorough knowledge of CAPA, deviations, and change control processes . In-depth experience in validation & qualification activities . Excellent leadership, decision-making, and cross-functional coordination skills. Strong communication skills with the ability to face regulatory and customer audits confidently. Willingness to relocate to Gandhidham . Candidates who can join immediately will be given preference. Compensation & Benefits Competitive salary aligned with industry standards. Relocation support for suitable candidates. Opportunity to head the QA function and drive strategic quality initiatives for a regulated market facility. Role & responsibilities

Develop and execute business development strategies for African markets Identify and build partnerships with distributors, government bodies, and local stakeholders Drive product registration, market entry & tender participation Achieve sales targets Required Candidate profile B.Pharm /B.Sc (MBA) 10+ years in pharmaceutical formulations business development Proven success in sales, partnership & market expansion in Africa Excellent communication, negotiation & leadership

Officer Sr. Officer - Engineering: Qualification - B. E (Mechanical/ Electrical) Experience - 03-06 years experience in pharmaceutical manufacturing machine maintenance Job Responsibility - 1. E xperience in maintenanceof semisolids (Ointment/ cream / gel manufacturing machines, Metal andlaminated tube filling machines) oral liquid manufacturing (mfg. Tanks withbottom entry agitators, volumetric filling machine, ROPP Cap sealing machine). 2. Should be able to draw & edit 2 D drawings with AutoCAD. 3. Mechanicalseal handling, assembly, dismantling and troubleshooting 4. Should haveknowledge about CLIT 5S and Kaizen 5. Maintaindocumentation related to ISO - EMS and OHS standards 6. GMPdocumentation (Preparation of qualification protocols for Productions machines, daily log books updation) 7. To scheduleand execute planned maintenance of machines. 8. Should be ableto operate and maintain utilities like compressor boilers and chillers 2.

We are seeking an experienced in Production Manager to lead the end-to-end lifecycle of pharmaceutical / Nutraceutical .The candidate should possess hands-on experience in the manufacturing of Tablets, Capsules, Softgels, Sachets & Protein Powders. Required Candidate profile 1. Production Planning & Management , Quality Assurance & Compliance, Process Improvement & Cost Control, Equipment & Facility Management, Team Leadership, Compliance with Health & Safety Regulations

Candidate having minimum 3 to 5 year experience in Granulation, Compression & Coating section in pharmaceutical industry. Interested candidate can call on this mobile no-+91-78310 31890, 9816336040 Food allowance Health insurance Annual bonus Provident fund

Role & responsibilities Perform granulation process operations as per SOP and batch requirements. Handle RMG (Rapid Mixer Granulator) machine for mixing and wet granulation. Operate and monitor FBD (Fluidized Bed Dryer) machine for drying granules. Ensure cleaning and maintenance of equipment (RMG, FBD, and associated accessories) as per cGMP and safety guidelines. Record operational parameters, cleaning logs, and maintain proper documentation. Follow SOPs, GMP, and safety protocols during operations. Coordinate with production and quality teams for smooth batch execution. Preferred candidate profile Experience: 14 years in Pharma Production (Granulation). Hands-on experience in RMG & FBD operations . Knowledge of cGMP guidelines, equipment cleaning, and documentation . Ability to work in shifts and follow strict compliance requirements.

Roles and Responsibilities Operate compression machines to produce tablets in OSD manufacturing process. Ensure accurate weight control during compression operations. Monitor machine performance and troubleshoot issues as needed. Maintain cleanliness and organization of production area. Collaborate with team members to achieve production targets. Desired Candidate Profile 1-4 years of experience in pharmaceutical production, preferably in compression operations. Strong understanding of formulation, compression, and manufacturing processes. Ability to work accurately with precision instruments and equipment. Basic knowledge of tablet coating techniques would be an added advantage.

Job Title: HVAC Executive (MNC) Industry: Pharmaceutical Location: Bari Brahmana (Jammu) Experience Required: Minimum 5 Years Salary: Up to 7 LPA 9796871050 Job Description: We are looking for an experienced HVAC Executive to join our team in the pharmaceutical industry. The ideal candidate should have hands-on experience in HVAC system validation, operation, and maintenance along with a strong understanding of Quality Management Systems (QMS). Key Responsibilities: Ensure smooth operation, preventive maintenance, and breakdown maintenance of HVAC systems. Execute and monitor validation activities for HVAC systems as per regulatory guidelines. Maintain proper documentation in compliance with cGMP, regulatory, and company requirements. Prepare and review SOPs related to HVAC operations and maintenance. Coordinate with cross-functional teams to ensure uninterrupted facility operations. Support quality audits and inspections by providing HVAC-related documents and compliance reports. Monitor and control environmental conditions (temperature, humidity, differential pressure, etc.). Implement energy efficiency and cost optimization measures in HVAC operations. Ensure adherence to QMS standards including deviation handling, CAPA, and change control. Desired Candidate Profile: B.Tech in Mechanical related engineering discipline. Minimum 5 years of experience in HVAC operations and maintenance in a pharmaceutical manufacturing environment. Strong knowledge of HVAC validation, QMS practices, and regulatory compliance. Ability to troubleshoot HVAC equipment and systems. Excellent documentation, analytical, and communication skills. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: Facility Management & Administration Executive / Sr. Executive Industry: Pharmaceutical Location: Bari Brahmana (Jammu) Experience Required: 5+ Years (in Pharma Industry) Salary: Up to 7 LPA (Negotiable) 9796871050 Job Description: We are looking for an experienced Facility Management & Administration Executive/Sr. Executive with strong exposure to pharmaceutical industry facility operations. The candidate will be responsible for managing housekeeping, pest control, laundry, security, canteen services, contract labour management, and ensuring compliance with QMS and cGMP requirements. Key Responsibilities: Oversee facility management services including housekeeping, pest control, laundry, security, and canteen operations. Manage and monitor contract labour workforce ensuring compliance with labour laws and company policies. Implement and monitor QMS practices in facility operations with adherence to pharma industry standards. Coordinate with internal departments to ensure seamless support for production and administrative functions. Ensure compliance with cGMP, safety standards, and regulatory requirements in all facility-related operations. Prepare and maintain records, SOPs, and documentation related to facility management. Handle vendor management, service contracts, and negotiations. Support audits and inspections by providing facility and administration compliance documents. Drive continuous improvement initiatives in facility management and cost optimization. Desired Candidate Profile: Graduate / Diploma / MBA preferred with relevant specialization. 5+ years of experience in facility management & administration in a pharmaceutical industry. Strong knowledge of QMS, cGMP, and pharma compliance requirements. Experience in managing contract labour and third-party vendors. Excellent organizational, leadership, and communication skills. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: QMS Production Executive Industry: Pharmaceutical (OSD Plant) Location: Bari Brahmana (Jammu) Experience Required: 5+ Years (OSD Pharma Plant) Salary: Around 6 LPA 9796871050 Job Description: We are seeking an experienced QMS Production Executive to join our Oral Solid Dosage (OSD) pharmaceutical manufacturing plant. The ideal candidate should have in-depth knowledge of Quality Management Systems (QMS) and hands-on experience in managing production activities in compliance with cGMP and regulatory requirements. Key Responsibilities: Ensure compliance with QMS requirements in production operations. Manage and maintain production documentation including BMR, SOPs, deviations, and change controls. Monitor and review CAPA, deviations, OOS, and audit observations related to production. Coordinate with QA, QC, and regulatory teams to ensure smooth operations. Support qualification and validation activities for equipment and processes. Implement best practices to ensure adherence to GMP, safety, and regulatory guidelines. Train production staff on QMS and compliance requirements. Support internal and external audits and regulatory inspections. Desired Candidate Profile: B.Pharm / M.Pharm or equivalent qualification. 5+ years of experience in OSD pharma production with strong QMS exposure. Strong understanding of cGMP, QMS, and regulatory compliance. Good documentation, analytical, and problem-solving skills. Ability to work independently and lead a team effectively. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: Production Supervisor Industry: Pharma (MNC) Location: Bari Brahmana, Jammu Qualification: M.Sc. Chemistry / B.Pharm Experience: 3 to 6 years Salary: Up to 5 LPA Contact: 9796871050 Job Responsibilities Supervise day-to-day production activities in OSD, Capsule, and Tablet manufacturing plant . Ensure adherence to cGMP, SOPs, and regulatory guidelines during production. Monitor production processes to meet daily, weekly, and monthly targets. Maintain accurate documentation and batch records as per pharma compliance. Coordinate with QA, QC, Engineering, and Warehouse teams for smooth operations. Implement continuous improvement practices to enhance productivity and reduce wastage. Ensure proper training and guidance to operators and shop floor staff. Maintain strict compliance with EHS (Environment, Health & Safety) standards. Key Skills & Competencies Strong knowledge of pharma production processes (OSD, Tablets, Capsules). Familiarity with regulatory audits (USFDA, MHRA, WHO, etc.) . Excellent leadership, team handling, and communication skills. Ability to handle deviations, change control, and CAPA. Good problem-solving and decision-making abilities. Desired Candidate Profile 36 years of relevant experience in a reputed Pharmaceutical OSD plant . Hands-on experience in tablet/capsule manufacturing processes. Strong understanding of GMP compliance and documentation practices . Candidates with exposure to multinational pharma setups will be preferred. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: OSD Packaging Supervisor Industry: Pharmaceutical Qualification: B. Pharma Location: Bari Brahmana (Jammu) Experience Required: 2 to 5 Years Salary: Up to 5 LPA (Negotiable) 9796871050 Job Description: We are seeking a skilled and detail-oriented OSD Packaging Supervisor to join our pharmaceutical team. The candidate should have experience in Oral Solid Dosage (OSD) packaging operations, ensuring compliance with GMP standards and regulatory requirements. Key Responsibilities: Supervise daily packaging activities of OSD products as per production schedules. Ensure compliance with cGMP, SOPs, and regulatory guidelines during all packaging operations. Monitor line clearance, in-process checks, and reconciliation of packaging material. Handle and train packaging staff to maintain efficiency and quality standards. Maintain documentation including batch packaging records, deviation reports, and logbooks. Coordinate with quality assurance and production teams for smooth operations. Implement safety measures and maintain housekeeping standards in packaging areas. Support regulatory audits and inspections with packaging-related documentation. Desired Candidate Profile: B. Pharma degree is mandatory. 2 to 5 years of experience in OSD packaging operations in a pharma manufacturing setup. Knowledge of blister, strip, and bottle packaging lines. Familiarity with cGMP, QMS, and documentation practices. Strong leadership, communication, and team management skills. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: Granulation Operator Industry: Pharmaceutical Location: Bari Brahmana (Jammu) Qualification: ITI / Diploma Experience Required: 3 to 6 Years Salary: Up to 4 LPA 9796871050 Job Description: We are looking for an experienced Granulation Operator to join our pharmaceutical manufacturing unit. The candidate will be responsible for operating and monitoring granulation equipment and processes while ensuring compliance with cGMP and safety standards. Key Responsibilities: Operate and monitor granulation machines (RMG, FBD, multi-mill, sifter, etc.). Perform granulation activities as per SOPs, BMR, and regulatory requirements. Ensure proper cleaning, calibration, and maintenance of equipment. Monitor critical process parameters (temperature, pressure, RPM, etc.). Maintain accurate documentation of production processes and equipment logs. Support in process validation and qualification activities. Adhere to safety protocols, GMP standards, and quality guidelines. Coordinate with production, maintenance, and QA teams for smooth operations. Desired Candidate Profile: ITI / Diploma in relevant discipline. 3 to 6 years of experience as a Granulation Operator in the pharmaceutical industry. Hands-on experience in handling RMG, FBD, sifter, multi-mill, and related granulation equipment. Knowledge of cGMP, documentation, and safety compliance. Team player with good communication and problem-solving skills. https://www.linkedin.com/in/satnam-singh-37b9b518/

Job Description: Regional Manager - Sales Location: Bangalore, Mumbai Reporting To: Head of Sales, Primebook Experience Required: Minimum 812 years of experience in the Laptops and Tablets business , with a strong background in managing Enterprise Sales through the Channel Partner Ecosystem. Industry: Laptops and Tablets About Primebook: Primebook is India’s most innovative, education-first laptop brand, rethinking affordable computing for the next billion learners. Our Android-powered laptops are now trusted by over 700 institutions, supporting digital education and skill-building for more than 70,000 students across India. Role Overview: We are seeking an energetic, results-driven Regional Manager to spearhead growth across Enterprise, SMB, and NGO segments through a strong channel partner ecosystem . This role requires a dynamic professional who can individually drive business initially while progressively building and leading a high-performing team. The Regional Manager will play a pivotal role in scaling business to 10 Cr+ in revenue from the assigned geography by driving direct enterprise engagements, structured SMB outreach, and impactful partnerships with NGO organizations. This role demands a strategic, futuristic approach , strong relationship management, and the ability to build scalable business processes in collaboration with partners. Key Responsibilities: Revenue Ownership : Own and achieve the B2B annual revenue target (10 Cr+) for the assigned region. Channel Ecosystem Management : Build, develop, and manage a strong channel partner network focused on enterprise clients. Market Development : Identify market gaps, new vertical opportunities, and emerging sales channels to expand business reach. Enterprise Account Leadership : Drive sales at large and strategic accounts (1000+ users), engaging with CXOs, CTOs, and other key decision-makers . Sales Funnel & Deal Closure : Lead sales funnel development, ensure consistent follow-up, and close high-value, large-ticket deals. Negotiation & Closing : Demonstrate strong negotiation, consultative selling, and sales closing capabilities. CRM & Reporting : Manage leads and sales pipeline using CRM tools; familiarity with applications such as Zoho CRM (or similar) is required. Must-Have Qualifications: Enterprise Sales Experience : Minimum 8–12 years in Enterprise Sales, with mandatory experience in the Laptops and Tablets business . Territory & Channel Expertise : Proven experience in building and managing channel partners dedicated to enterprise clients in dedicated geographies. Channel Ecosystem Knowledge : Excellent understanding of the channel partner ecosystem with demonstrated success in establishing and scaling partner networks. Revenue Track Record : Proven ability to generate 10 Cr+ in annual B2B revenue through strategic partnerships and enterprise sales. Procurement Expertise : Deep knowledge of institutional procurement processes in both Enterprise and SMB segments. CXO-Level Engagement : Experience in working with CTOs, Department Heads, and CXOs, with the ability to influence strategic decision-making. Strategic & Execution Skills : Strong strategic mindset with hands-on execution abilities to build sales pipelines and close high-value deals. Communication & Stakeholder Management : Excellent verbal and written communication skills, with proven stakeholder engagement capability. CRM & Analytical Skills : Strong discipline in CRM usage, pipeline management, and data-driven decision-making, with familiarity in tools like Zoho CRM (or equivalent). What We Offer: Regional Leadership Role : A unique opportunity to lead and grow within an inspiring IT brand that is disrupting established product offerings. High-Growth Environment : Work in a dynamic setup that provides autonomy, resources, and high visibility to drive measurable impact. Purpose-Driven Mission : Be part of a passionate team that is reshaping digital learning in India, creating both business and social impact. Meritocratic Culture : Thrive in a results-oriented, performance-driven environment where talent and outcomes are recognized and rewarded. Work-Life Balance : Enjoy a 5-day work week, with a flat organizational structure and an innovation-first mindset that encourages fresh ideas and creativity.

Formulation Development (OSD) 1 to 5 Years Experience Company Overview Jodas Expoim Pvt. Ltd. JODAS Expoim is a research-driven, specialty biopharmaceutical company based in Hyderabad, Telangana, with EUGMP–certified facilities focused on oncology, contrast media, and cephalosporin injectables Position Summary We’re seeking a motivated Formulation Development Scientist with 1 to 5 years of experience in Injectables or OSD formulations. You'll contribute to pre-formulation, prototype development, stability studies, and support scale-up activities within a cGMP environment. Key Responsibilities Conduct literature and patent reviews to inform formulation strategy . Execute pre-formulation studies, characterize APIs and excipients, and assess compatibility . Develop and refine prototype formulations to match innovator quality profiles Perform lab-scale trials and support stability testing protocols. Assist in scale-up/tech-transfer and oversee pilot manufacturing batches and PDRs Prepare documentation for regulatory and manufacturing use, including pre-product development strategies and specifications Maintain detailed lab records and communicate findings in clear, data-driven reports Required Qualifications Bachelor’s or Master’s in B.Pharm, M.Pharm, 1–5 years of experience in formulation R&D, particularly in OSD . Hands-on experience with pre-formulation characterization, prototype work, stability studies, and lab documentation. Familiarity with cGMP, lab safety, and regulatory documentation standards. Best Regards Team Jodas Expoim

Develop and establish product formulations based on industry trends. Develop and optimize formulations for new and existing nutraceutical products. Conduct thorough research on ingredients and their interactions. Required Candidate profile Qualification: Bachelor's degree (Food Science & Food Technology) Exp: Min 3 year in any Nutraceuticals Industry/Manufacturing or production Required only Male Candidates

Line Clearance for Dispensing, Manufacturing & Packing activities Dispensing of RM/PM for batch Mfg Monitoring of IPQA activities (Granulation, Blending, Capsulation, Compression, Coating, Packing Sampling of IP and FP Samples Batch documents review

Line Clearance for Dispensing, Manufacturing & Packing activities Dispensing of RM/PM for batch Mfg Monitoring of IPQA activities (Granulation, Blending, Capsulation, Compression, Coating, Packing Sampling of IP and FP Samples Batch documents review

You will be responsible for the formulation development of Pharmaceutical and Nutraceutical products including tablets, capsules, effervescent tablets, sachets powders, and liquid formulations. This involves conducting literature search and patent search for the formulation, as well as developing cost-effective and fast production processes along with stable formulations. You will be required to create MFR and relevant specifications, facilitate tech transfer, and maintain documentation. Additionally, you will need to address any ongoing issues in the existing formulations. The ideal candidate should have 7 to 10 years of experience in this field. If you are interested in this opportunity, please reach out to hrd@stravahealthcare.com for further details.,

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.

Responsible for handling raw materials, monitoring critical process parameters, shop floor management and maintaining cleaning & compliance in tablet compression. Company gives free accommodation, Wada Maharashtra Urgent Opening Office cab/shuttle Food allowance Health insurance Annual bonus Provident fund

Job Description Position: Junior research scientist (JRS)/Research scientist (RS) Job Location: - Plot No. 214, Borsad - Tarapur Road, Ta: Petlad, Dist: Anand, Gujarat, India. Department: R&D / Formulation Experience: 3-6 years in Nutraceuticals Formulations. Industry: Nutraceutical / Food / Pharma Manufacturing Reports To: Manager FRD. Job Type: Full-Time Company Profile: - Pharmanza Herbal Pvt. Ltd. is one of the few companies which is focusing on standardizing and proving the efficacy of Herbal products. Our strong supplier base, fully equipped R&D facility, FDA approved manufacturing facility, infrastructure for conducting human trials as well as our formulations unit provides a one stop solution to our valued customers. Pharmanza Herbal Pvt Ltd. is one of the leading research-oriented companies, manufacturing herbal extracts used in the Ayurvedic and nutraceutical segment. Our journey began in 1997 with Pharmanza India, our group company located in Khambhat, India, where we started producing herbal extracts. While Pharmanza India primarily focuses on veterinary allopathic formulations, we leveraged its facilities to manufacture herbal products such as Garcinia cambogia, Commiphora Mukul, and Withania somnifera from 1997 to 2004. As the business expanded, and we began exporting our products to countries like the US, Japan, and Germany. Pharmanza Herbal was established in Dharmaj, India, to continue our commitment to quality and innovation in herbal solutions. The facility is certified by Food safety authority of India (FSSAI), Food and drug Administration, India (Gujarat office) with NSF-GMP International. Current certifications include ISO9001:2015, ISO22000:2018, NSF-GMP, NSF-SPORT,USP-GMP,USP Ashwagandha,Bosewelia with Kosher and Halal and USDA/APEDA organic certifications for products. Additionally, we are also certified SEDEX 4 Pillers and ECOVADIS. Job Overview: - We are seeking a highly motivated and detail-oriented Formulation Scientist with 2-4 years of experience to join our team. The ideal candidate will have expertise in formulation development and optimization, along with a strong understanding of dosage forms, excipients, and manufacturing processes. As a key member of our R&D department, you will be responsible for designing and developing solid, semi-solid, or liquid dosage forms, performing stability studies, and ensuring regulatory compliance throughout the formulation process. Responsibilities and Duties: - 1. Research & development along with optimization of formulations for Nutraceutical and Health Supplement as per the organization requirements. 2. Development of solid, semisolid, and liquid dosage forms for herbal and nutraceutical ingredients for domestic, and regulated markets like US, EU, Brazil, and Canada. 3. Ensure adherence to regulatory requirements and customer expectations during product development. 4. Collaborate with cross-functional teams, including Analytical Development, Quality Control, and Manufacturing, to ensure smooth transition from development to production. 5. Contribute to total product development activity from material procurement to stability studies and technology transfer to the manufacturing units. Troubleshooting as required during these operations. 6. Handling different equipment, performing experiments, and documenting the results in a prescribed format. 7. Pre-formulation and excipient compatibility studies, assist in research activities as instructed. 8. Preparation of literature search, patent search, prepare product development reports, stability protocol, process validation protocol, reports and SOPs. 9. Responsible for inventory management and lab management ensuring GDP during documentation and fulfilment of GLP requirements during routine lab work. 10. Troubleshoot formulation-related issues during clinical trials and commercial production. 11. Data compilations and record maintenance. 12. Any other responsibility, as assigned by management. Qualifications: - Education level: Bachelor's or Masters degree in Pharmaceutical Sciences, Chemistry, or a related field Experience: 3-5 years Personal characteristics: Hands-on experience with various formulation techniques, Strong knowledge of drug delivery systems, excipient selection, and stability studies, Familiarity with regulatory guidelines (USFDA, EMA, ICH) and industry standards. Ability to work collaboratively in a fast-paced, team-oriented environment. Salary Range: - Competitive Computer Competency: -Efficient Skills: - Excellent problem-solving and analytical skills with keen attention to detail, Strong written and verbal communication skills Benefits: Competitive salary package. Subsidized food facility. Free Transportation facility from Vadodara location. Medi-claim facility. Opportunities for professional development and growth. A dynamic and collaborative work environment committed to sustainability. Join our dynamic team and contribute to the success of our mission to provide high-quality nutraceuticals and dietary supplements that positively impact people's health and well-being. If you possess the required qualifications and share our passion for quality, we encourage you to apply for this exciting opportunity as an JRS/RS in our manufacturing unit. Company Website: - www.pharmanzaherbal.com Company Email id: - hrm@pharmanza.com

Role & responsibilities: Perform routine and non-routine analysis using GC and GC-MS as per SOPs and approved test methods. Prepare samples, reagents, and calibration standards accurately. Conduct method validation, system suitability, and performance checks for GC instruments. Maintain proper documentation of all analytical results in accordance with GMP/GLP requirements. Troubleshoot analytical issues and assist in resolving deviations and OOS (Out of Specification) results. Ensure proper calibration, maintenance, and operation of GC instruments. Support development and validation of new methods as required by R&D or Quality Assurance teams. Maintain a clean, organized, and safe laboratory environment.

Job Title: Granulation Operator Work Location: Gagillapur, Hyderabad Department: Production / Manufacturing Experience: 2 to 7 Years Qualification: ITI / Diploma (Mechanical/Electrical) or B.Sc. (Chemistry or related field) Job Description: We are seeking skilled professionals to join our Formulation Manufacturing team as Granulation Operators. The ideal candidate should have practical experience in handling granulation equipment and ensuring smooth execution of batch manufacturing processes in a pharmaceutical setup. Key Responsibilities: Operate and monitor Granulation equipment including RMG (Rapid Mixer Granulator), FBD (Fluid Bed Dryer), Multi Mill, Sifter, and Blenders as per batch manufacturing records. Ensure adherence to manufacturing instructions, SOPs, safety procedures, and cGMP guidelines. Perform in-process checks to maintain quality standards and record observations accurately. Maintain proper cleaning, maintenance, and housekeeping of equipment and work area. Report any equipment malfunction or deviation immediately to the concerned department. Coordinate with cross-functional teams such as Quality Assurance, Quality Control, Engineering, and Maintenance for smooth operations. Candidate Profile: Qualification: ITI / Diploma in Mechanical or Electrical Engineering, or B.Sc. in Chemistry or equivalent. Experience: 2 to 7 years of relevant experience in Granulation operations within pharmaceutical manufacturing. Strong knowledge of cGMP, safety, and regulatory compliance. Good documentation, communication, and team coordination skills. Willingness to work in shifts.

As a Pharma Professional at Angia RX Life Science Pvt. Ltd., you will play a crucial role in overseeing the production process to ensure the quality and compliance of pharmaceutical products. Located in Roorkee, this full-time on-site position requires your expertise in managing manufacturing operations, coordinating with various departments, supervising staff, and maintaining production schedules and documentation. Your responsibilities will include ensuring high-quality standards in the manufacturing of Tablets, Capsules (Beta & Non-beta), Liquid & Dry Syrup, Ointment & lotion, and Nutraceuticals for both domestic and export markets. You will be expected to uphold compliance with international regulations and contribute to the overall success of our facilities. Your daily tasks will involve hands-on involvement in the production process, effective coordination with different departments, and meticulous supervision of staff to streamline operations. Additionally, you will be responsible for maintaining accurate production documentation and schedules to support the efficient functioning of our manufacturing operations. If you are a dedicated Pharma Professional with a passion for maintaining quality standards and ensuring compliance in pharmaceutical production, we invite you to join our team at Angia RX Life Science Pvt. Ltd. and contribute to the success of our organization.,

As India's leading after-sales service provider, Onsitego offers a range of services including Extended Warranty, Damage Protection, AMC Plans, and On-Demand Repair Services for electronic devices and home appliances. With a commitment to delivering exceptional customer experiences, we have achieved the highest Net Promoter Score (NPS) globally in after-sales services. Our hassle-free and reliable services are accessible through retail stores and online marketplaces. Join us on our mission to enhance the lives of device users nationwide by becoming a part of our dynamic team. Role: Technical Support Experts Responsibilities: - Assist customers in resolving common technical issues and provide guidance on optimizing product usage. - Conduct training sessions for customers on newly purchased products. - Utilize persuasive skills to understand customer needs and effectively promote our Warranty plans. - Present our offerings to customers at the store level. - Use our knowledge base (Knowmax) to address customer queries and update the database with new solutions. Desired Candidate Profile: - Prior experience with the latest technologies and Modern Trade Store operations. - Proficient in providing Face-to-Face customer support. - Strong communication skills in English and Hindi. - Sound troubleshooting abilities for various products and familiarity with system and internet usage. For more information, visit our website at www.onsitego.com. Join us in creating "WOW" experiences for millions of device users across the country.,

As a recruiter, your primary responsibility will be to find qualified candidates for our company's open positions. This involves designing and updating job descriptions, sourcing potential candidates from various online channels such as social media and professional platforms, and crafting recruiting emails to attract passive candidates. You will also be involved in agreements, hiring operators, helpers, full-time employees, and apprentices while closely working with contractors. It will be your responsibility to define the hiring policy, manage the onboarding process of new employees, and oversee the joining process. Additionally, you will be in charge of handling grievances and providing necessary support to the employees. To be successful in this role, you must have at least 5 to 8 years of experience in the field of recruitment. Candidates with experience in the Pharma Finished products sector, particularly in tablets and capsules units, will be preferred. If you meet the qualifications and are interested in this position, please send your CV to hrd@stravahealthcare.com.,