123 Capsules 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.

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

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/

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

Job Description Department: Production Designation: Jr. Officer - Production (E0) Working Section: Granulation / Compression / Coating Comply with all cGMP, GxP and any other applicable regulatory requirement, including EH&S requirements. Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task. Conduct all tasks/activities as per the applicable SOPs. Report any difficulty or deviation in following the procedure/instruction to immediate supervisor/managers. Report any quality concern or suggestion for improvement to supervisors/ managers. Manufacturing / processing of batches of assigned products under supervision as per instructions given in the BMR. Handling and movement of raw material, bulk, semi-finished and finished goods. Operation, washing and cleaning of equipment’s and accessories used in related production activities as per respective SOP. Up-keeping area and machines as per GMP requirements. To Support Quality Management Systems and to report any discrepancy, abnormity, non-conformance or any incidence observed to the Department Head and QA Head. Receipt of RM and PM from Warehouse and ensuring overall cleanliness of areas. Doing operations as per the SOPs and BMR with online recording in respective documents as applicable. To ensure self-hygiene before entering in the production area and follow all the other rules & regulation set by HR department. Performing in-process checks as per respective BMR and recording of results of in respective documents as applicable. To fulfil the training need as per current needs with respect to cGMP, Job, safety, health & Hygiene by attending the training programmes. Cost effectiveness in production operation by controlling overtime, revenue expenses and achieving standard yield. Critically monitoring of the environmental conditions with a view to meet the standards mentioned in BMR and SOP. Ensure calibration and preventive maintenance of manufacturing equipment and instruments as per approved schedule and the results of same meeting the standards. To perform line clearance activity during batch to batch and product to product change over and ensure the compliance as per SOP. Issuance, retrieval and destruction of dies and punches, product dedicated bags and sieves, silicon sleeves, pipes, hose pipes and screens. To ensure the audit compliance. Trouble-shooting: To attend the problems of machine and process as and when necessary. Any other assignment allocated by production Head. To attend required cGMP/ On Job /Functional training activities as per planner. Work Experience Minimum 3 years, maximum 5 years Education Diploma Vocational Competencies Customer Centricity Developing Talent Collaboration Strategic Agility Process Excellence Stakeholder Management Innovation & Creativity Result Orientation

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

Walk In Drive For Production OSD In Formulation Division @ Kothur Department:- Production OSD Qualification :-ITI | Diploma | BSC | B Pharmacy | M Sc | M Pharmacy Experience :- 2 To 8 Years Skills :- Packing Operators :- Primary Packing:- Cam MNX | ACG|B Max|BQS|IMAPG||EL Mach|Pharma Pack|CVC Secondary Packing:- HI-Cart|IC-150|CAMHV1|CVC| IMA A 300 Cartonator & Pharma Pack| Labelling Packing Supervisors| Inchargers|Bottle Line Supervisors QMS Supervisors : Handling deviation|Change Controls|Market Complaint&Investigations|Audit Complaince&Intiations of Quality Intiatives Manufacturing:- Compression | Coating | Granulation | Capsule Filling| Executives | Operators| Supervisors Division :- Formulation Interview Date:- 06-10-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- MSNF-II , Kothur Venue Location:- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those who have experience in Coating , Granulation , Compression, Capsule Filling , Blister Packing , Cam Cartontor, Hi Cartonator, Primary Packing , Secondary Packing, Documentation. About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Walk In Drive for Production OSD Department In Formulation Division @ Mekaguda Qualification :- Diploma | BSC Experience:- Fresher Interview Date:- 06-09-2025 (Saturday) Interview Time:- 9.00AM TO 2.0PM Work Location :- MSNF- IV, Mekaguda Venue Location :- MSN Laboratories Pvt Ltd,. Formulation Unit-04-Mekaguda 37XJ+W82, Mekaguda, Telangana 509228 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Walk In Drive for Production OSD Department In Formulation Division @ Mekaguda Qualification :- Diploma | B Tech | B Sc | B Pharmacy | M Sc | M Pharmacy Experience:- 2 to 8 Years Interview Date:- 06-09-2025 (Saturday) Interview Time:- 9.00AM TO 2.0PM Work Location :- MSNF- IV, Mekaguda Venue Location :- MSN Laboratories Pvt Ltd,. Formulation Unit-04-Mekaguda 37XJ+W82, Mekaguda, Telangana 509228 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidates those who have experience in Packing Operators :- Blister Primary & Secondary | Capsule Filling | Oral Liquid | Cartornator | CVC | Production Documentation | Granulation Executive | Executive Manufacturing | Executive Packing Operators :- Coating Operator | Granulation Operator | B Max Operator About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top management level professionals according to clients specific needs. We are BEST-FIT Recruitment Riders do exactly what our name tells. To know more about us please visit our website: www.bestfitrecruitment.co.in We would like to inform you that presently we have professional career opportunity matching to your profile with one of our esteemed client. Please see the following position summary: Client Name: USA based Pharma Company Position: Executive - Regulatory Affairs (Formulations for USA market) Department: Regulatory Affairs Location: Ahmedabad, Gujarat Special Note: Immediate Joiner Required Job Profile: Responsible for supporting the Regulatory Affairs department in its efforts to remain in compliance with the regulations of all intended market territories (USA Market). Regulatory support for assigned projects through product development and lifecycle management of products for US market. Review and approve labels in line with US regulatory requirements for assigned products. Prepare, develop, and maintain internal Regulatory informational trackers. Prepare technical documents required for submission of dossier as per country specific requirements. Respond to consumer inquiries based on approved labels and product information. Coordinate the receipt of raw material regulatory documents from vendors. Preparation of module 1 sections including labelling sections. Perform drug listing of assigned products for US market. Support publishing of ANDA submissions Support manufacturing site for commercialization and life cycle management of the approved products. Other projects and duties as assigned by Senior Management. Desired Profile: B.Sc / B.Pharm / M.Sc / M.Pharm with 2 to 5 years experience in US regulatory affairs Labelling department with growing & well established pharmaceuticals. Immediate Joiner Required OTC products Experience is a Plus. Must have good exposure in supporting role of ANDA filling for USA market. Exposure in Solid Oral (Tablets & Capsules) for regulated markets (USA) would be preferred. Exposure to working in US Markets is Mandatory. Ability to compile, manage and interpret data. Ability to work both independently and within a team environment. Ability to manage several tasks simultaneously. Ability to co-ordinate & manage the project with external stake holder. Effective communicator with excellent relationship building & interpersonal skills. Proficiency in Microsoft Office and Adobe Acrobat. Strong communication skills, both verbal and written. Strong organizational skills. Recruiter's Contact Details: BEST-FIT Recruitment Riders G-7, Amrit Complex, R.V. Desai Road, Near Goyagate Circle, Vadodara-390001, Gujarat Mobile: 09722042906 E-Mail: post@bfrr.in Website: www.bestfitrecruitment.co.in

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.

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.,

* Oversee nutraceutical product development from concept to launch. * Collaborate with R&D team on new formulations and recipes. knows how to handle , manage and operate machinary and process of tablets, capsules , powders etc

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.,

For Operator /Technician Role - OSD Manufacturing Qualification Diploma Eng/ITI Category – Operator Role - Officer / Staff / Supervisor Qualification – B. Pharm/M. Pharm Category – Staff

Interview for SVP / Injectable & OSD Pharma Formulation Plant in Bharuch on Company / Permanent Payroll Exp: 0 to 13 Yrs CTC: As per Interview Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch & Call 9727755486 Free Job Required Candidate profile Qualification: BE / Diploma Mech / Elec / Inst Vacancies Instrument: 3 Mechanical: 3 Electrical: 3 Experience in SVP & OSD Plant in Must Share with Your Colleagues & Seniors Free Job Placement

Interview for SVP / Injectable & OSD Pharma Formulation Plant in Bharuch on Company / Permanent Payroll Exp: 0 to 13 Yrs CTC: As per Interview Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch & Call 9727755486 Free Job Required Candidate profile Qualification: BE / Diploma Mech / Elec / Inst Vacancies Instrument: 3 Mechanical: 3 Electrical: 3 Experience in SVP & OSD Plant in Must Share with Your Colleagues & Seniors Free Job Placement

As a Production Area Handling Specialist, you will be responsible for overseeing the manufacturing processes of tablets and capsules. This includes ensuring smooth operations, monitoring equipment performance, and maintaining quality standards. Your duties will also involve the preparation and filing of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) in compliance with regulatory guidelines. Attention to detail and accuracy are crucial in this aspect of the role. In addition, you will be tasked with managing the manpower within the production area, ensuring optimal utilization of resources and manpower efficiency. Effective communication and leadership skills will be essential in coordinating the workforce. Collaboration with the In-Process Quality Assurance (IPQA) team and Quality Control (QC) department will be a key part of your role to maintain product quality and compliance. Your experience of 2 to 4 years in a similar role will enable you to contribute effectively to these functions. If you are ready to take on this challenging role, please send your application to hrd@stravahealthcare.com.,