The HPLC Operator is responsible for Operating Maintaining , And troubleshooting High Performance Liquid Chromatography ( HPLC) Syastem to perform qualitative and quantitave anaysis of Pharmaceutical Product ensuring compliance with regulatory and company quality standard KEY RESPONSIBILITY Perform HPLC analysis of raw material, in process samples, finished product, and stability samples prepare samples and standards following SOP and test protocols. calibrate and maintain HPLC Instrument Troubleshoot HPLC System - Identify and resolve system errors, baseline issue, leaks, pressure problem. Document result maintain accurate and complete record of chromatograms and obervation Ensure compliance with GMP and regulatory Requirement Participate in method validation verification activities Experience 2-4 Year ( Expert HPLC Operator) Preferred Experience : Hand on Experience With HPLC Software (eg. Emplower Chemstation, Labsolutions.) Knowledge method Development and Validation Familitarity With other analytical Techniques ( GC, UV-VIs, Dissolution) Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Health insurance Paid sick time Provident Fund Schedule: Day shift Rotational shift Supplemental Pay: Yearly bonus Ability to commute/relocate: Makarpura, Vadodara, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Work Location: In person
Job Responsibility : Analysis of Finished Pwroduct / raw material/ in process & stability To issue release note, testing protocol time to time to QA department calibration of instrument as per defined procedure and sechdule preparation of certificate of analysis preparation of protocol to prepared and maintain working standard as per SOP. Instrument Handling : HPLC operator UV spectore GC and Other Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹48,579.45 per month Benefits: Health insurance Paid sick time Provident Fund Schedule: Rotational shift Work Location: In person
Job Responsibility : Analysis of Finished Pwroduct / raw material/ in process & stability To issue release note, testing protocol time to time to QA department calibration of instrument as per defined procedure and sechdule preparation of certificate of analysis preparation of protocol to prepared and maintain working standard as per SOP. Instrument Handling : HPLC operator UV spectore GC and Other Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹48,579.45 per month Benefits: Health insurance Paid sick time Provident Fund Schedule: Rotational shift Work Location: In person
Job Title: Granulation Operator Department: Manufacturing / Production Location: [Insert Location] Reports To: Production Supervisor / Manufacturing Manager Employment Type: Full-time Job Summary: The Granulation Operator is responsible for performing granulation activities as per the batch manufacturing records (BMR) and standard operating procedures (SOPs) in a cGMP-compliant pharmaceutical manufacturing facility. The role ensures the accurate processing of raw materials into granules used for tablet and capsule production. Key Responsibilities: Operate granulation equipment such as high shear mixer, fluid bed dryer (FBD), multi-mill, oscillating granulator, sifter, and blenders. Review and follow batch manufacturing records (BMR), SOPs, and GMP guidelines. Perform equipment set-up, cleaning, and changeover as per defined procedures. Monitor granulation parameters such as mixing time, binder addition, drying time, and temperature. Accurately record data in logbooks and BMRs. Coordinate with QA/QC for in-process sampling and approvals. Ensure proper usage and handling of raw materials and granulated intermediates. Maintain cleanliness and hygiene in the granulation area at all times. Troubleshoot minor equipment issues and report maintenance needs promptly. Participate in deviation reporting, investigations, and CAPA implementation. Adhere to EHS (Environment, Health & Safety) regulations. Required Qualifications: Education: ITI / Diploma in Pharmacy / B.Sc / M.Pharm or equivalent Experience: 1–3 years of experience in granulation operations within a pharmaceutical (formulations) environment Knowledge: Understanding of granulation processes (dry and wet) Working knowledge of cGMP, GDP, and EHS guidelines Familiar with regulatory requirements (USFDA, EU, WHO) Skills & Competencies: Ability to read and interpret SOPs and BMRs Basic mechanical aptitude for equipment operation Attention to detail and accuracy in documentation Good communication and teamwork skills Time management and ability to work in shifts Working Conditions: Shift-based work (Day/Night) Exposure to noise, powders, and temperature-controlled environments Requires wearing PPE (Personal Protective Equipment) Let me know if you'd like this as a Word or PDF file, or if you want a version tailored to a specific dosage form (e.g., tablets, capsules, etc.). Ask ChatGPT Job Types: Full-time, Permanent Schedule: Rotational shift Work Location: In person
Key Responsibilities: Operate capsule-filling machines such as Bosch, ACG-PAM, Sejong, or other automatic capsule fillers . Perform machine setup, calibration, and cleaning as per SOPs and batch manufacturing records (BMRs). Load capsules and powder/granules into hoppers as required. Monitor the capsule filling process to ensure proper weight, lock integrity, and production efficiency. Troubleshoot and resolve machine issues or minor breakdowns during production. Perform in-process checks (IPC) for capsule weight, defects, and locking as per quality standards. Record production and machine parameters accurately in logbooks and BMRs. Follow standard operating procedures (SOPs), Good Manufacturing Practices (GMP), and safety protocols at all times. Coordinate with Quality Assurance (QA) and Maintenance teams for any deviations or repairs. Maintain cleanliness and hygiene in the machine area, including proper gowning and PPE usage. Assist during validations, audits, and inventory of tooling and machine parts. Required Qualifications: Education: ITI / Diploma in Pharmacy / B.Sc / D.Pharm or equivalent Experience: 1–3 years in capsule-filling machine operations in a pharmaceutical formulation unit Knowledge: Familiar with automatic capsule-filling machines Knowledge of GMP, GDP, and EHS compliance Understanding of production documentation and in-process control procedures Skills & Competencies: Mechanical aptitude and troubleshooting ability Basic understanding of capsule formulations (powder, pellets, etc.) Attention to detail and accuracy in recording data Good communication and teamwork skills Ability to work under shift schedules and production deadlines Working Conditions: Shift-based role (including night shifts if required) Standing for extended periods and handling fine powder Working in controlled and cleanroom environments Required to wear PPE (gloves, mask, gown, etc Job Types: Full-time, Permanent Pay: ₹9,781.41 - ₹28,386.25 per month Benefits: Health insurance Paid sick time Provident Fund Schedule: Rotational shift Supplemental Pay: Quarterly bonus Work Location: In person
Job Title: IPQA Officer / Executive Department: Quality Assurance Location: MAKARPURA GIDC (Formulation Company) Reporting To: IPQA Manager / QA Head Job Purpose: To ensure in-process quality checks and compliance during manufacturing and packaging operations in accordance with cGMP, regulatory guidelines, and company SOPs. IPQA ensures that quality is built into the product during manufacturing and packaging processes. Key Responsibilities:1. In-Process Checks: Perform in-process checks during manufacturing and packaging (e.g., weight variation, hardness, friability, disintegration, etc. for tablets). Monitor critical process parameters (CPP) and ensure adherence to batch manufacturing records (BMR) and batch packaging records (BPR). Line clearance at every stage (dispensing, granulation, compression, coating, primary and secondary packaging). Check cleanliness and status labeling of equipment and manufacturing areas. 2. Documentation and Compliance: Review and ensure correctness of in-process documents like BMRs and BPRs. Real-time documentation of deviations, incidents, and change controls. Ensure compliance with GMP, GDP, and company policies. 3. Sampling and Testing: Perform sampling of in-process materials, intermediates, and finished products as per SOP. Collect environmental and line clearance samples, if applicable. 4. Deviation and Incident Handling: Identify and report process deviations, incidents, or non-conformities. Support investigation and implementation of CAPA (Corrective and Preventive Actions). 5. Training and Audit Support: Provide on-the-job GMP training to operators and production personnel. Support internal/external audits (regulatory and customer). Ensure readiness of manufacturing area for audit and inspections. Key Skills and Competencies: Knowledge of GMP, GDP, and regulatory compliance. Good documentation practices. Attention to detail and problem-solving attitude. Basic knowledge of instruments like pH meter, balance, hardness tester, etc. Communication and coordination skills. Qualifications and Experience: Education: B.Pharm / M.Pharm / B.Sc / M.Sc in relevant field. Experience: 1–5 years of experience in IPQA in a pharmaceutical formulation/API manufacturing unit. Job Type: Full-time Pay: ₹9,605.87 - ₹25,000.00 per month Benefits: Paid sick time Provident Fund Schedule: Day shift Morning shift Night shift Rotational shift Weekend availability Supplemental Pay: Overtime pay Yearly bonus Work Location: In person
Job Title: IPQA Officer / Executive Department: Quality Assurance Location: MAKARPURA GIDC (Formulation Company) Reporting To: IPQA Manager / QA Head Job Purpose: To ensure in-process quality checks and compliance during manufacturing and packaging operations in accordance with cGMP, regulatory guidelines, and company SOPs. IPQA ensures that quality is built into the product during manufacturing and packaging processes. Key Responsibilities:1. In-Process Checks: Perform in-process checks during manufacturing and packaging (e.g., weight variation, hardness, friability, disintegration, etc. for tablets). Monitor critical process parameters (CPP) and ensure adherence to batch manufacturing records (BMR) and batch packaging records (BPR). Line clearance at every stage (dispensing, granulation, compression, coating, primary and secondary packaging). Check cleanliness and status labeling of equipment and manufacturing areas. 2. Documentation and Compliance: Review and ensure correctness of in-process documents like BMRs and BPRs. Real-time documentation of deviations, incidents, and change controls. Ensure compliance with GMP, GDP, and company policies. 3. Sampling and Testing: Perform sampling of in-process materials, intermediates, and finished products as per SOP. Collect environmental and line clearance samples, if applicable. 4. Deviation and Incident Handling: Identify and report process deviations, incidents, or non-conformities. Support investigation and implementation of CAPA (Corrective and Preventive Actions). 5. Training and Audit Support: Provide on-the-job GMP training to operators and production personnel. Support internal/external audits (regulatory and customer). Ensure readiness of manufacturing area for audit and inspections. Key Skills and Competencies: Knowledge of GMP, GDP, and regulatory compliance. Good documentation practices. Attention to detail and problem-solving attitude. Basic knowledge of instruments like pH meter, balance, hardness tester, etc. Communication and coordination skills. Qualifications and Experience: Education: B.Pharm / M.Pharm / B.Sc / M.Sc in relevant field. Experience: 1–5 years of experience in IPQA in a pharmaceutical formulation/API manufacturing unit. Job Type: Full-time Pay: ₹9,605.87 - ₹25,000.00 per month Benefits: Paid sick time Provident Fund Schedule: Day shift Morning shift Night shift Rotational shift Weekend availability Supplemental Pay: Overtime pay Yearly bonus Work Location: In person
Key Responsibilities Prospecting & Lead Generation: Identify, research, and target potential clients through networking, cold calling, social media, and industry events. Client Relationship Management: Build and maintain strong relationships with new and existing clients to ensure customer satisfaction and long-term partnerships. Sales Strategy Execution: Work closely with the sales and marketing teams to implement business growth strategies. Market Research: Analyze market trends, competitor activities, and customer needs to identify opportunities. Proposal Development: Prepare and deliver compelling business proposals and presentations tailored to client requirements. Negotiation & Closing: Negotiate terms and close deals to meet or exceed sales targets. Reporting: Maintain accurate records of sales activities and prepare regular progress reports for management. Collaboration: Coordinate with internal departments (marketing, operations, finance) to ensure smooth project execution . Qualifications & Skills Bachelor’s degree in Business Administration, Marketing, or a related field (MBA is a plus). Proven experience (1–3 years) in business development, or a related role. Strong communication, presentation, and interpersonal skills. Ability to build rapport and maintain long-term client relationships. Negotiation and persuasion skills. Self-motivated, target-driven, and able to work independently. Knowledge of CRM tools and MS Office Suite. Willingness to travel when required. Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Experience: Business development executive: 1 year (Preferred) Language: Hindi (Preferred) English (Preferred) Work Location: In person
ACCOUNT , PURCHASE AND OTHER ADMINISTRATION WORK QUALIFICATION : COMMRACE GRADUCATE MINIMUM : 1 YEAR EXEPERIANCE IN ACCOUNT Job Type: Full-time Pay: ₹20,000.00 - ₹22,000.00 per month Benefits: Paid sick time Provident Fund Work Location: In person
ACCOUNT , PURCHASE AND OTHER ADMINISTRATION WORK QUALIFICATION : COMMRACE GRADUCATE MINIMUM : 1 YEAR EXEPERIANCE IN ACCOUNT Job Type: Full-time Pay: ₹20,000.00 - ₹22,000.00 per month Benefits: Paid sick time Provident Fund Work Location: In person