About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. We are seeking a dynamic and motivated Candidate to join our team. Key Responsibilities: Perform accurate and timely data entry into software systems. Prepare and maintain reports, records, and documentation. Handle email communications and manage digital files. Operate office equipment such as printers, scanners, and photocopiers. Support administrative tasks as required. Ensure data security and confidentiality. Requirements: Diploma in Computer Applications or Graduate. Proven experience as a computer operator or data entry operator preferred Proficiency in MS Office (Word, Excel, Outlook) Strong organizational and communication skills Freshers can also apply. How to Apply: Send your resume to hrd@fidopharma.com . Job Type: Full-time Benefits: Health insurance Provident Fund Ability to commute/relocate: Panchkula, Haryana: Reliably commute or planning to relocate before starting work (Required) Experience: Computer operation: 1 year (Required) Language: English (Preferred) Work Location: In person
About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. We are seeking a dynamic and motivated R&D Scientis t to join our pharmaceutical team. Key Responsibilities: Lead and execute R&D projects related to formulation and process development of APIs and/or finished dosage forms. Conduct method development, validation, and optimization for analytical procedures. Design and perform experiments for the synthesis and characterization of new chemical entities (NCEs) or generics. Interpret analytical data and prepare comprehensive technical reports. Collaborate with cross-functional teams including QA, QC, production, and regulatory affairs. Ensure compliance with cGMP, GLP, and regulatory guidelines. Stay updated on current trends, techniques, and advancements in pharmaceutical R&D. Requirements: M.Sc. in Chemistry (preferably Organic, Analytical, or Pharmaceutical Chemistry). Minimum 5 years of hands-on R&D experience in a pharmaceutical company. Proficient in analytical instruments (e.g., HPLC, GC, FTIR, UV, NMR). Strong understanding of ICH guidelines and regulatory frameworks. Excellent documentation, problem-solving, and communication skills. Preferred Qualities: Experience in formulation development or API process optimization. Exposure to regulatory filing (ANDA, DMF, etc.). Self-motivated, detail-oriented, and results-driven. What We Offer: Competitive salary and benefits A collaborative and innovative work environment Opportunities for professional growth and development How to Apply: Send your resume to hrd@fidopharma.com Job Type: Full-time Benefits: Cell phone reimbursement Life insurance Provident Fund Ability to commute/relocate: Panchkula, Haryana: Reliably commute or planning to relocate before starting work (Required) Experience: APIs: 5 years (Required) Work Location: In person
About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. We are seeking a dynamic and motivated R&D Scientis t to join our pharmaceutical team. Key Responsibilities: Lead and execute R&D projects related to formulation and process development of APIs and/or finished dosage forms. Conduct method development, validation, and optimization for analytical procedures. Design and perform experiments for the synthesis and characterization of new chemical entities (NCEs) or generics. Interpret analytical data and prepare comprehensive technical reports. Collaborate with cross-functional teams including QA, QC, production, and regulatory affairs. Ensure compliance with cGMP, GLP, and regulatory guidelines. Stay updated on current trends, techniques, and advancements in pharmaceutical R&D. Requirements: M.Sc. in Chemistry (preferably Organic, Analytical, or Pharmaceutical Chemistry). Minimum 5 years of hands-on R&D experience in a pharmaceutical company. Proficient in analytical instruments (e.g., HPLC, GC, FTIR, UV, NMR). Strong understanding of ICH guidelines and regulatory frameworks. Excellent documentation, problem-solving, and communication skills. Preferred Qualities: Experience in formulation development or API process optimization. Exposure to regulatory filing (ANDA, DMF, etc.). Self-motivated, detail-oriented, and results-driven. What We Offer: Competitive salary and benefits A collaborative and innovative work environment Opportunities for professional growth and development How to Apply: Send your resume to hrd@fidopharma.com Job Type: Full-time Benefits: Cell phone reimbursement Life insurance Provident Fund Ability to commute/relocate: Panchkula, Haryana: Reliably commute or planning to relocate before starting work (Required) Experience: APIs: 5 years (Required) Work Location: In person
About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. We are currently seeking a highly organized and detail-oriented Quality Assurance Documentation Specialist to join our Quality team. Job Summary The QA Documentation Specialist is responsible for managing, reviewing, and maintaining controlled documents to ensure compliance with GMP (Good Manufacturing Practices), company policies, and applicable regulatory requirements. This role plays a critical part in ensuring that our products meet the highest quality standards through proper documentation practices. Key Responsibilities Maintain and control Quality Assurance documentation including SOPs, protocols, batch records, specifications, reports, and training records. Assist in the preparation, revision, issuance, and archiving of controlled documents. Ensure documents are accurate, up-to-date, properly formatted, and comply with internal and regulatory standards. Support document change control processes and maintain document lifecycle tracking. Coordinate with cross-functional departments to ensure timely review and approval of documents. Assist in internal and external audits by preparing documentation and supporting audit readiness. Maintain electronic document management systems (EDMS), if applicable. Ensure proper filing and secure storage of all QA records and documents. Qualifications Bachelor’s degree in Life Sciences, Pharmacy, Chemistry, or a related field. 2-5 years of experience in a QA documentation or regulatory documentation role within the pharmaceutical, biotech, or medical device industry. Knowledge of GMP, GDP, and relevant regulatory guidelines (e.g., FDA, EMA, ICH). Proficiency in MS Office (Word, Excel, Outlook); experience with EDMS or QMS software is a plus. Excellent written and verbal communication skills. Strong attention to detail and organizational skills. Ability to manage multiple tasks and deadlines effectively. Why Join Us? Competitive salary and benefits package Opportunity to work in a growth-driven, innovative environment Supportive team and leadership Ongoing training and professional development opportunities How to Apply: Send your resume to hrd@fidopharma.com Job Type: Full-time Benefits: Cell phone reimbursement Health insurance Provident Fund Ability to commute/relocate: Panchkula, Haryana: Reliably commute or planning to relocate before starting work (Required) Experience: Document management: 2 years (Required) Work Location: In person
About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. We are currently seeking a highly organized and detail-oriented Quality Assurance Documentation Specialist to join our Quality team. Job Summary The QA Documentation Specialist is responsible for managing, reviewing, and maintaining controlled documents to ensure compliance with GMP (Good Manufacturing Practices), company policies, and applicable regulatory requirements. This role plays a critical part in ensuring that our products meet the highest quality standards through proper documentation practices. Key Responsibilities Maintain and control Quality Assurance documentation including SOPs, protocols, batch records, specifications, reports, and training records. Assist in the preparation, revision, issuance, and archiving of controlled documents. Ensure documents are accurate, up-to-date, properly formatted, and comply with internal and regulatory standards. Support document change control processes and maintain document lifecycle tracking. Coordinate with cross-functional departments to ensure timely review and approval of documents. Assist in internal and external audits by preparing documentation and supporting audit readiness. Maintain electronic document management systems (EDMS), if applicable. Ensure proper filing and secure storage of all QA records and documents. Qualifications Bachelor’s degree in Life Sciences, Pharmacy, Chemistry, or a related field. 2-5 years of experience in a QA documentation or regulatory documentation role within the pharmaceutical, biotech, or medical device industry. Knowledge of GMP, GDP, and relevant regulatory guidelines (e.g., FDA, EMA, ICH). Proficiency in MS Office (Word, Excel, Outlook); experience with EDMS or QMS software is a plus. Excellent written and verbal communication skills. Strong attention to detail and organizational skills. Ability to manage multiple tasks and deadlines effectively. Why Join Us? Competitive salary and benefits package Opportunity to work in a growth-driven, innovative environment Supportive team and leadership Ongoing training and professional development opportunities How to Apply: Send your resume to hrd@fidopharma.com Job Type: Full-time Benefits: Cell phone reimbursement Health insurance Provident Fund Ability to commute/relocate: Panchkula, Haryana: Reliably commute or planning to relocate before starting work (Required) Experience: Document management: 2 years (Required) Work Location: In person
About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. With state-of-the-art facilities and a commitment to compliance and innovation, we are expanding our team and seeking a qualified Senior Chemist to join our solid dosage manufacturing division. Job Description: We are looking for an experienced Senior Chemist to oversee and support the manufacturing processes of tablets and capsules . The ideal candidate will have hands-on experience in formulation, troubleshooting, and optimization of solid oral dosage forms in a cGMP-compliant environment. Key Responsibilities: Supervise and support the manufacturing processes of tablets and capsules from raw material dispensing to finished product. Develop and optimize formulations and processes for scale-up and commercial manufacturing. Conduct troubleshooting during manufacturing and recommend improvements to enhance yield, quality, and efficiency. Collaborate with cross-functional teams including Quality Assurance, R&D, and Engineering. Ensure compliance with cGMP, SOPs, and regulatory requirements. Maintain detailed documentation of processes, investigations, and technical reports. Train and mentor junior chemists and production staff. Requirements: Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, or a related field. 2*- 5 years* of experience in pharmaceutical manufacturing, specifically in tablet and capsule production . Strong understanding of cGMP regulations and quality systems. Familiarity with granulation, blending, compression, coating, and encapsulation equipment. Excellent problem-solving, communication, and organizational skills. Benefits: Competitive salary and performance-based bonuses Health insurance and other statutory benefits Professional development opportunities Supportive and collaborative work environment How to Apply: Send your resume to hrd@fidopharma.com Job Type: Full-time Pay: ₹14,517.36 - ₹35,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Ability to commute/relocate: Panchkula, Haryana: Reliably commute or planning to relocate before starting work (Required) Experience: Manufacturing tablet: 2 years (Required) Work Location: In person
About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. With state-of-the-art facilities and a commitment to compliance and innovation, we are expanding our team and seeking a qualified Senior Chemist to join our solid dosage manufacturing division. Job Description: We are looking for an experienced Senior Chemist to oversee and support the manufacturing processes of tablets and capsules . The ideal candidate will have hands-on experience in formulation, troubleshooting, and optimization of solid oral dosage forms in a cGMP-compliant environment. Key Responsibilities: Supervise and support the manufacturing processes of tablets and capsules from raw material dispensing to finished product. Develop and optimize formulations and processes for scale-up and commercial manufacturing. Conduct troubleshooting during manufacturing and recommend improvements to enhance yield, quality, and efficiency. Collaborate with cross-functional teams including Quality Assurance, R&D, and Engineering. Ensure compliance with cGMP, SOPs, and regulatory requirements. Maintain detailed documentation of processes, investigations, and technical reports. Train and mentor junior chemists and production staff. Requirements: Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, or a related field. 2*- 5 years* of experience in pharmaceutical manufacturing, specifically in tablet and capsule production . Strong understanding of cGMP regulations and quality systems. Familiarity with granulation, blending, compression, coating, and encapsulation equipment. Excellent problem-solving, communication, and organizational skills. Benefits: Competitive salary and performance-based bonuses Health insurance and other statutory benefits Professional development opportunities Supportive and collaborative work environment How to Apply: Send your resume to hrd@fidopharma.com Job Type: Full-time Pay: ₹14,517.36 - ₹35,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Ability to commute/relocate: Panchkula, Haryana: Reliably commute or planning to relocate before starting work (Required) Experience: Manufacturing tablet: 2 years (Required) Work Location: In person
About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. We are seeking a dynamic and motivated Manufacturing Chemist / Operator – Tablet Manufacturing to join our pharmaceutical team. What You’ll * Operate and monitor tablet manufacturing equipment as per SOPs. Set up, clean, and maintain machines used in granulation, blending, compression, and coating processes. Ensure all production activities comply with GMP , safety, and quality standards. Accurately document batch manufacturing records and equipment logs. Troubleshoot machine issues and escalate problems to the maintenance team when necessary. What We’re Looking For: Diploma / B.Pharm / B.Sc or equivalent in Chemistry or Pharmaceutical Sciences or a related field 2-3 years of relevant experience in tablet manufacturing in a pharmaceutical environment. Sound knowledge of GMP, safety protocols, and documentation practices. Proficient in operating and maintaining pharmaceutical production machinery. Ability to work both independently and in a team environment Preferred Skills: Experience with compression machines like Fette, Cadmach, or Korsch is a plus. Basic understanding of process validation and calibration activities. Good communication and team coordination skills. Apply Now: Send your CV to [email protected] Job Type: Full-time Pay: ₹18,000.00 - ₹35,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. We are seeking a dynamic and motivated Manufacturing Chemist / Operator – Tablet Manufacturing to join our pharmaceutical team. What You’ll * Operate and monitor tablet manufacturing equipment as per SOPs. Set up, clean, and maintain machines used in granulation, blending, compression, and coating processes. Ensure all production activities comply with GMP , safety, and quality standards. Accurately document batch manufacturing records and equipment logs. Troubleshoot machine issues and escalate problems to the maintenance team when necessary. What We’re Looking For: Diploma / B.Pharm / B.Sc or equivalent in Chemistry or Pharmaceutical Sciences or a related field 2-3 years of relevant experience in tablet manufacturing in a pharmaceutical environment. Sound knowledge of GMP, safety protocols, and documentation practices. Proficient in operating and maintaining pharmaceutical production machinery. Ability to work both independently and in a team environment Preferred Skills: Experience with compression machines like Fette, Cadmach, or Korsch is a plus. Basic understanding of process validation and calibration activities. Good communication and team coordination skills. Apply Now: Send your CV to hrd@fidopharma.com Job Type: Full-time Pay: ₹18,000.00 - ₹35,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. We are seeking a dynamic and motivated R&D Executive – API Development to join our pharmaceutical team. Key Responsibilities: Develop and optimize synthetic routes for APIs in accordance with regulatory and quality standards. Perform lab-scale synthesis, process optimization, and scale-up activities. Support technology transfer to pilot plant and production facilities. Ensure compliance with cGMP, safety, and regulatory guidelines during R&D operations. Conduct literature reviews and patent analysis for new product development. Maintain proper documentation of experiments, observations, and results as per GLP practices. Collaborate with cross-functional teams including Analytical R&D, QA/QC, Regulatory Affairs, and Production. Required Qualifications: M.Sc. (Organic Chemistry) / M.Pharm /B.Pharm or in a relevant field. 3 - 4 years of hands-on experience in API R&D in a reputed pharmaceutical company. Strong understanding of process chemistry, reaction mechanisms, and impurity profiling. Familiarity with analytical tools like HPLC, GC, NMR, and LC-MS (in coordination with AR&D). Good documentation skills and understanding of regulatory expectations (ICH, FDA, etc.). Ability to manage multiple projects with strong problem-solving skills. What We Offer: Competitive compensation and benefits Opportunities for professional growth and learning Collaborative and innovation-driven work culture How to Apply: Send your resume to hrd@fidopharma.com Job Types: Full-time, Permanent Pay: ₹28,000.00 - ₹45,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
About Us: FIDO is a leading organization committed to excellence, innovation, and sustainability. We pride ourselves on delivering top-tier products and services while maintaining the highest standards of quality and compliance. As we continue to grow, we are looking for a dynamic and experienced Head of Quality to lead our Quality Assurance and Quality Control initiatives across the organization. Key Responsibilities: Lead and manage all quality assurance and control activities. Develop, implement, and monitor QMS and SOPs. Ensure compliance with national and international quality standards (e.g., ISO, GMP, HACCP, etc. as applicable). Oversee internal audits, external audits, and third-party certifications. Collaborate with cross-functional teams to drive quality improvements. Analyze data and generate reports on product quality, non-conformities, and root cause analysis. Drive supplier quality management and vendor audits. Mentor and develop the quality team to build organizational capability. Qualifications: Bachelor’s/Master’s degree in Engineering, Science, or a related field. 8–15 years of relevant experience in quality management (preferably in [your industry]). Strong knowledge of quality standards, tools, and methodologies. Proven leadership and team management skills. Excellent analytical, communication, and interpersonal skills. Preferred Candidate Profile: We value diversity and inclusion in our leadership roles. Female candidates with a passion for quality and leadership are encouraged to apply . Experience in managing diverse teams and driving culture change will be an added advantage. What We Offer: A leadership role with high visibility and impact. A supportive and inclusive work environment. Opportunities for professional growth and development. Competitive compensation and benefits. How To Apply: Please send your resume to hrd@fidopharma.com Job Types: Full-time, Permanent Benefits: Health insurance Provident Fund Work Location: In person
About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. We are seeking a dynamic and motivated API Warehouse Executive ( Active Pharmaceutical Ingredients (APIs) to join our pharmaceutical team. Key Responsibilities: Receive, inspect, and verify incoming API materials as per SOPs. Ensure proper storage conditions (temperature, humidity, segregation) for APIs. Maintain accurate records of stock, issue slips, and inventory reports. Coordinate with the Quality Control (QC) and Quality Assurance (QA) departments for sampling and release. Handle material dispatches and returns as per company procedures. Operate ERP/WMS systems for inventory management. Ensure compliance with all safety and regulatory guidelines. Participate in internal and external audits and assist in documentation. Requirements: Minimum 2 years of experience in an API warehouse or related role. Strong understanding of GMP, GDP , and warehouse protocols. Experience with ERP systems (SAP, Oracle, etc.) preferred. Good communication and documentation skills. Diploma/Bachelor’s degree in Pharmacy, Chemistry, or a related field. Preferred Qualifications: Experience in a regulated pharmaceutical manufacturing environment . How to Apply: Send your resume to [email protected] Job Type: Full-time Pay: ₹12,134.73 - ₹29,132.38 per month Work Location: In person
About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. We are looking for a skilled and responsible API Maintenance Executive to oversee and maintain equipment and utilities used in Active Pharmaceutical Ingredient (API) manufacturing. Key Responsibilities: Carry out preventive and corrective maintenance of all API plant equipment, utilities, and machinery. Troubleshoot mechanical, electrical, and utility-related issues to minimize downtime. Ensure compliance with GMP, safety, and environmental standards during maintenance activities. Maintain proper documentation of maintenance activities, logs, and calibration records. Coordinate with production, QA, and other departments for timely equipment readiness. Support in equipment installation, validation, and qualification activities. Monitor performance and condition of critical equipment (reactors, centrifuges, dryers, pumps, etc.). Participate in internal and external audits as required. Requirements: Minimum 2 years of hands-on experience in maintenance within an API manufacturing facility . Diploma / ITI / B.Tech in Mechanical / Electrical / Instrumentation Engineering. Sound knowledge of GMP practices, utility systems (chillers, boilers, compressors), and instrumentation . Ability to read and interpret technical drawings, manuals, and SOPs. Strong troubleshooting and analytical skills. How to Apply: Send your resume to [email protected] Job Type: Full-time Pay: ₹10,065.61 - ₹25,000.00 per month Work Location: In person
About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. We are seeking a dedicated and detail-oriented API Plant QMS Executive to support and maintain the Quality Management System within our API manufacturing facility. The ideal candidate will ensure compliance with regulatory standards and internal SOPs, driving continuous improvement and maintaining documentation integrity. Key Responsibilities: Implement, monitor, and maintain the Quality Management System (QMS) in the API plant. Ensure all activities comply with cGMP guidelines , regulatory requirements, and internal policies. Manage documentation related to QMS including SOPs, CAPAs, deviation reports, change controls, and audit records. Coordinate and support internal and external audits, inspections, and regulatory visits. Facilitate training programs related to QMS and GMP compliance for plant personnel. Track, investigate, and report on quality incidents, deviations, and non-conformances. Support continuous improvement initiatives to enhance quality standards and operational efficiency. Liaise with cross-functional teams including Production, QA, QC, and Engineering to ensure QMS adherence. Requirements: Minimum 2 years of experience working in Quality Management or Quality Assurance within an API manufacturing environment . Bachelor’s degree in Pharmacy, Chemistry, Microbiology, or a related discipline. Strong knowledge of cGMP, ISO standards, and regulatory compliance . Experience in documentation control, audit management, and CAPA processes. Excellent communication, organizational, and analytical skills. Proficiency with QMS software/tools and MS Office applications. Preferred Qualifications: Experience with regulatory audits (FDA, EU GMP, MHRA, etc.) is a plus. Knowledge of risk management and root cause analysis methodologies. How to Apply: Send your resume to [email protected] Job Type: Full-time Pay: ₹15,000.00 - ₹35,000.00 per month Work Location: In person
About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. We are seeking a dynamic and motivated API Warehouse Executive ( Active Pharmaceutical Ingredients (APIs) to join our pharmaceutical team. Key Responsibilities: Receive, inspect, and verify incoming API materials as per SOPs. Ensure proper storage conditions (temperature, humidity, segregation) for APIs. Maintain accurate records of stock, issue slips, and inventory reports. Coordinate with the Quality Control (QC) and Quality Assurance (QA) departments for sampling and release. Handle material dispatches and returns as per company procedures. Operate ERP/WMS systems for inventory management. Ensure compliance with all safety and regulatory guidelines. Participate in internal and external audits and assist in documentation. Requirements: Minimum 2 years of experience in an API warehouse or related role. Strong understanding of GMP, GDP , and warehouse protocols. Experience with ERP systems (SAP, Oracle, etc.) preferred. Good communication and documentation skills. Diploma/Bachelor’s degree in Pharmacy, Chemistry, or a related field. Preferred Qualifications: Experience in a regulated pharmaceutical manufacturing environment . How to Apply: Send your resume to hrd@fidopharma.com Job Type: Full-time Pay: ₹12,134.73 - ₹29,132.38 per month Work Location: In person
About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. We are seeking a dedicated and detail-oriented API Plant QMS Executive to support and maintain the Quality Management System within our API manufacturing facility. The ideal candidate will ensure compliance with regulatory standards and internal SOPs, driving continuous improvement and maintaining documentation integrity. Key Responsibilities: Implement, monitor, and maintain the Quality Management System (QMS) in the API plant. Ensure all activities comply with cGMP guidelines , regulatory requirements, and internal policies. Manage documentation related to QMS including SOPs, CAPAs, deviation reports, change controls, and audit records. Coordinate and support internal and external audits, inspections, and regulatory visits. Facilitate training programs related to QMS and GMP compliance for plant personnel. Track, investigate, and report on quality incidents, deviations, and non-conformances. Support continuous improvement initiatives to enhance quality standards and operational efficiency. Liaise with cross-functional teams including Production, QA, QC, and Engineering to ensure QMS adherence. Requirements: Minimum 2 years of experience working in Quality Management or Quality Assurance within an API manufacturing environment . Bachelor’s degree in Pharmacy, Chemistry, Microbiology, or a related discipline. Strong knowledge of cGMP, ISO standards, and regulatory compliance . Experience in documentation control, audit management, and CAPA processes. Excellent communication, organizational, and analytical skills. Proficiency with QMS software/tools and MS Office applications. Preferred Qualifications: Experience with regulatory audits (FDA, EU GMP, MHRA, etc.) is a plus. Knowledge of risk management and root cause analysis methodologies. How to Apply: Send your resume to hrd@fidopharma.com Job Type: Full-time Pay: ₹15,000.00 - ₹35,000.00 per month Work Location: In person
About Us: Fido Pharma is a leading pharmaceutical manufacturer committed to ensuring the highest standards of product quality, safety, and compliance. We are looking for a skilled and responsible API Maintenance Executive to oversee and maintain equipment and utilities used in Active Pharmaceutical Ingredient (API) manufacturing. Key Responsibilities: Carry out preventive and corrective maintenance of all API plant equipment, utilities, and machinery. Troubleshoot mechanical, electrical, and utility-related issues to minimize downtime. Ensure compliance with GMP, safety, and environmental standards during maintenance activities. Maintain proper documentation of maintenance activities, logs, and calibration records. Coordinate with production, QA, and other departments for timely equipment readiness. Support in equipment installation, validation, and qualification activities. Monitor performance and condition of critical equipment (reactors, centrifuges, dryers, pumps, etc.). Participate in internal and external audits as required. Requirements: Minimum 2 years of hands-on experience in maintenance within an API manufacturing facility . Diploma / ITI / B.Tech in Mechanical / Electrical / Instrumentation Engineering. Sound knowledge of GMP practices, utility systems (chillers, boilers, compressors), and instrumentation . Ability to read and interpret technical drawings, manuals, and SOPs. Strong troubleshooting and analytical skills. How to Apply: Send your resume to hrd@fidopharma.com Job Type: Full-time Pay: ₹10,065.61 - ₹25,000.00 per month Work Location: In person