Job Title: Executive - Quality Assurance Company: SAVA Healthcare is amongst the fastest emerging pharmaceutical company in India with global reach to customers in Canada, Ukraine and the CIS, Asia, Latin America, Africa & FWA. With manufacturing units in Surendranagar, Malur and in near future in Indore holds various accreditations and produces wide variety of dosage forms across therapeutic categories. Our GMP compliant, State of Art manufacturing facility for Tablet, Oral Dry Powder, Capsule, Nasal sprays, DPIs, Cream, Gel and Ointment formulations with dedicated manufacturing sections supported by In-House R&D Center, focuses on Formulation and Analytical Development with an annual turnover of more than 200 crores and manpower of 500+ employees engaged across locations. Job Location: Surendranagar Plant Job Summary We are seeking a dedicated and detail-oriented Quality Assurance (QA) Personnel to join our Pharma Manufacturing Plant. The ideal candidate will be responsible for ensuring that our manufacturing processes comply with regulatory standards and internal quality protocols. This role is critical in maintaining product quality, safety, and efficacy, and ensuring our products meet all required specifications before reaching the market. Key Responsibilities Quality Management System (QMS): Maintain and enhance the Quality Management System (QMS) to ensure compliance with GMP (Good Manufacturing Practices) and other regulatory requirements. Develop, review, and update quality assurance policies, procedures, and SOPs. Documentation And Records Ensure all quality-related documentation is accurate, complete, and maintained according to regulatory standards. Review and approve batch records, quality control reports, and other manufacturing documentation. Compliance And Audits Conduct internal audits and support external audits to ensure compliance with regulatory requirements and company standards. Prepare audit reports, identify non-conformances, and implement corrective and preventive actions (CAPAs). Product Quality Assurance Monitor and verify the quality of raw materials, in-process materials, and finished products through regular inspections and testing. Investigate and resolve quality issues, deviations, and complaints related to manufacturing processes and products. Process Validation And Improvement Participate in process validation activities to ensure manufacturing processes are robust and reproducible. Identify areas for process improvement and implement quality enhancement initiatives. Training And Development Provide training and guidance to manufacturing staff on quality assurance practices, GMP, and regulatory requirements. Stay updated on the latest industry trends, regulations, and best practices in quality assurance. Risk Management Conduct risk assessments to identify potential quality issues and implement strategies to mitigate risks. Monitor and analyze quality metrics to identify trends and areas for improvement. Qualifications Education: Bachelor’s degree in Pharmacy, Chemistry, Microbiology, or a related field. Advanced degree or professional certification (e.g., Certified Quality Auditor) is a plus. Experience Minimum of 3-5 years of experience in quality assurance within the pharmaceutical manufacturing industry. Strong understanding of GMP, regulatory requirements (e.g., FDA, EMA), and quality management systems. Skills Excellent analytical, problem-solving, and decision-making skills. Strong attention to detail and organizational skills. Effective communication and interpersonal skills. Proficiency in using quality management software and MS Office Suite (Word, Excel, PowerPoint). Personal Attributes High level of integrity and commitment to maintaining quality standards. Ability to work independently and collaboratively in a team-oriented environment. Proactive and results-oriented with a focus on continuous improvement. Show more Show less

Job Description: Operator - Nasal Spray Manufacturing, Filling & Packaging Job Title: Operator – Nasal Manufacturing, Filling & Packaging Location: Indore – Regulated Pharma Manufacturing Plant Department: Production – Respiratory (Nasal Spray) Reporting To: Executive / Officer – Production Job Type: Full-Time | Operator Level Job Purpose To execute routine operations related to nasal spray filling and packaging , ensuring adherence to cGMP, safety standards, and regulatory norms in a sterile/cleanroom environment. Key Responsibilities 🔹 1. Nasal Filling Operations Operate And Assist In Activities Involving Sterile filtration setup Filling machine setup (semi-automatic / automatic nasal filling) Bottle positioning and nozzle placement Crimping and sealing of nasal containers Perform in-process checks for fill volume, crimp integrity, and visual inspection. Maintain cleanroom discipline and aseptic techniques during operations. 🔹 2. Nasal Packaging Operations Operate Machines For Primary and secondary packaging of nasal sprays (cartoning, labeling, overwrapping) Online batch coding and serialization (if applicable) Assist in leaflet insertion, outer box packing, and visual verification of final packs. 🔹 3. Cleaning & Line Clearance Clean machines and areas before and after production as per SOPs . Support line clearance and reconciliation activities with production/QA. 🔹 4. Documentation & Reporting Record entries in logbooks, equipment usage logs, and process registers accurately. Report any equipment malfunctions, abnormalities, or product quality issues to supervisor. 🔹 5. Compliance & Safety Follow cGMP, GDP, and safety practices as per regulatory guidelines. Wear appropriate PPE and follow gowning procedures for cleanroom entry. Maintain hygiene and housekeeping in the designated manufacturing/packaging areas. Skills & Competencies Basic machine operation skills (filling, crimping, packaging). Understanding of cleanroom behavior , aseptic area discipline, and basic quality checks. Ability to read and follow SOPs (in English/Hindi). Teamwork and alertness during operations. Educational Qualifications ITI / 12th Pass / Diploma (Engineering or Pharma) Experience 1–4 years of experience in sterile/Nasal spray filling and packaging in a regulated pharmaceutical environment (USFDA / MHRA / WHO-GMP preferred). Show more Show less

Job Title: General Manager – Quality Assurance Department: Quality Assurance Location: Indore Plant Reports To: Vice President – Technical Industry: Pharmaceuticals – Regulated Market Manufacturing Employment Type: Full Time Position Overview The General Manager – Quality Assurance (QA) will be responsible for leading and overseeing all QA functions at the pharmaceutical manufacturing site to ensure compliance with cGMP, regulatory guidelines (USFDA, EU, MHRA, TGA, etc.), and company quality standards. The role is pivotal in establishing a robust Quality Management System (QMS), driving a culture of compliance, and ensuring the release of safe and effective pharmaceutical products. Key Responsibilities Strategic Leadership & Quality Oversight: Lead the QA department to ensure strict adherence to current Good Manufacturing Practices (cGMP). Define and implement site-wide QA strategies in line with global quality policies. Establish robust systems for product quality assurance, documentation, and compliance. Compliance & Regulatory Ensure the site remains audit-ready at all times and leads all external inspections (USFDA, MHRA, EU, WHO, etc.). Manage responses and CAPA implementation for regulatory inspections and customer audits. Stay updated with changes in global regulatory requirements and align site practices accordingly. Quality Management System (QMS) Oversee implementation and continuous improvement of QMS elements including: Deviation, Change Control, CAPA, and OOS management Quality Risk Management Document and Record Control Annual Product Review (APR/PQR) Vendor Qualification and Audits Batch Release & Documentation Review and approve batch manufacturing and packing records. Authorize batch release as per regulatory and internal requirements. Oversee document control systems ensuring timely and accurate documentation. Cross-functional Collaboration Work closely with Production, QC, Engineering, Regulatory Affairs, and R&D teams. Support in technology transfers, process validations, and new product introductions from QA perspective. People Management Lead, mentor, and develop a team of QA professionals. Promote a quality-driven culture across the site. Conduct training and competency programs on cGMP and quality systems. Education Desired Candidate Profile: M. Pharm / B. Pharm / M.Sc. in Chemistry, Microbiology, or related life sciences field. Experience Minimum 18–22 years of experience in the pharmaceutical industry with at least 5 years in a senior QA leadership role in a regulated environment. Hands-on experience in facing global regulatory inspections (e.g., USFDA, MHRA, ANVISA, TGA). Sound knowledge of GMP, ICH, WHO, and other international quality guidelines. Skills & Attributes Strong leadership and decision-making ability. Excellent communication, interpersonal, and presentation skills. High attention to detail and ability to handle complex quality issues. Analytical mindset with risk-based thinking. Show more Show less

Job Description: Executive - Production (Respiratory – Nasal Spray) Job Title: Executive – Production (Respiratory – Nasal Spray) Location: Indore – Regulated Pharma Manufacturing Plant Department: Production – Respiratory (Nasal Spray) Reporting To: Manager / Sr. Manager – Production Job Type: Full-Time | Executive Level Job Purpose To execute day-to-day manufacturing activities related to Nasal Spray formulations , ensuring compliance with cGMP, safety, and regulatory standards while supporting batch execution, documentation, and process control. Key Responsibilities 🔹 1. Batch Execution Execute Manufacturing Operations For Nasal Sprays Including Dispensing of raw materials Solution preparation Sterile filtration and filling Crimping, sealing, and leak testing Ensure adherence to Batch Manufacturing Records (BMR) and Standard Operating Procedures (SOPs) . 🔹 2. Equipment Operation Operate And Monitor Equipment Such As Filling machines (manual/semi-auto/auto) Crimping and sealing machines Visual inspection stations Coordinate with engineering for equipment readiness and maintenance. 🔹 3. Documentation & Compliance Complete and review BMRs, logbooks, checklists, and other documents as per Good Documentation Practices (GDP) . Report any deviations, breakdowns, or abnormalities to the supervisor. Support change control, deviation investigations, and CAPA implementation. 🔹 4. Regulatory & GMP Compliance Ensure compliance with cGMP, data integrity , and site-specific regulatory standards (USFDA, MHRA, WHO-GMP). Participate in self-inspections , internal audits , and assist in audit readiness. 🔹 5. Safety & Hygiene Follow safety protocols and wear appropriate PPE while working in classified areas. Maintain cleanroom behavior , hygiene, and area sanitation as per SOPs. Skills & Competencies Hands-on experience in sterile/Nasal Spray manufacturing operations. Good understanding of cGMP, GDP, and regulatory expectations . Ability to handle critical documentation and execute tasks with attention to detail. Familiarity with equipment cleaning, area cleaning, and aseptic practices. Qualifications B.Pharm / M.Pharm / B.Sc. in Chemistry, Microbiology, or equivalent discipline. Experience 2–5 years of experience in regulated pharmaceutical manufacturing , preferably in nasal spray/respiratory or sterile dosage forms . Show more Show less

Job Description – Executive - Tablet Packaging Job Title: Executive – Tablet Packaging Location: Indore – Regulated Pharma Manufacturing Plant Department: Production – Packaging (OSD) Reporting To: Manager / Sr. Manager – Packaging Job Type: Full-Time | Executive Level Job Purpose To execute primary and secondary packaging of tablets in compliance with packaging plans, cGMP, and regulatory requirements while maintaining quality and efficiency. Key Responsibilities Execute blister / alu-alu / strip / bottle packaging as per approved Batch Packaging Records (BPR). Operate packaging line equipment like blister pack machines, cartonators, inkjet/online printers, deblistering machines . Carry out line clearance in coordination with QA. Perform in-process checks: batch coding, leaflet insertion, sealing, pack integrity, and labeling . Maintain cleanliness and hygiene of the packaging area and equipment. Ensure proper usage and accountability of packaging material (PM). Record entries in logbooks, BPRs, and online systems (LIMS/SAP). Adhere to data integrity, safety norms , and regulatory compliance requirements. Skills & Competencies Knowledge of primary and secondary packaging processes and equipment. Understanding of SOPs, GMP , and packaging documentation requirements. Good coordination and observation skills. Experience in facing regulatory audits is a plus. Qualifications B.Pharm / M.Pharm / B.Sc. (Science) 2–5 years of experience in regulated pharmaceutical packaging environments. Show more Show less

Job Title: Executive / Senior Executive - Production Company: SAVA Healthcare is amongst the fastest emerging pharmaceutical company in India with global reach to customers in Canada, Ukraine and the CIS, Asia, Latin America, Africa & FWA. With manufacturing units in Surendranagar, Malur and in near future in Indore holds various accreditations and produces wide variety of dosage forms across therapeutic categories. Our GMP compliant, State of Art manufacturing facility for Tablet, Oral Dry Powder, Capsule, Nasal sprays, DPIs, Cream, Gel and Ointment formulations with dedicated manufacturing sections supported by In-House R&D Center, focuses on Formulation and Analytical Development with an annual turnover of more than 200 crores and manpower of 500+ employees engaged across locations. Job Location: Surendranagar Plant Job Summary Production Management: Supervise and coordinate the activities of the production team to meet production schedules and targets. Ensure efficient use of resources and equipment to maximize productivity. Monitor production processes and adjust schedules as needed to meet changing demands. Quality Assurance: Ensure all production activities comply with GMP (Good Manufacturing Practices) and FDA regulations. Conduct regular inspections and audits to ensure adherence to quality standards. Address and resolve any quality issues that arise during production. Process Optimization: Identify areas for improvement in production processes and implement changes to enhance efficiency and reduce waste. Utilize lean manufacturing principles and other continuous improvement methodologies. Collaborate with the engineering and quality assurance teams to optimize equipment performance and product quality. Team Leadership: Lead, train, and mentor production staff to ensure they have the skills and knowledge required to perform their duties effectively. Conduct performance evaluations and provide feedback to team members. Foster a positive and collaborative work environment. Documentation and Reporting: Maintain accurate and up-to-date records of production activities, including batch records, logbooks, and production reports. Prepare and submit regular reports on production performance, including output, efficiency, and quality metrics. Ensure all documentation is compliant with regulatory requirements. Compliance and Safety: Ensure all production activities are carried out in compliance with safety regulations and company policies. Conduct regular safety training and drills for production staff. Investigate and report any accidents or incidents in the production area. Inventory Management: Monitor inventory levels of raw materials, packaging materials, and finished products. Coordinate with the procurement department to ensure timely availability of materials required for production. Implement inventory control measures to minimize stockouts and excess inventory. Qualifications Bachelor’s degree in Pharmacy, Chemistry, Engineering, or a related field. A minimum of 3-8 years of experience in pharmaceutical manufacturing or a similar production environment. Strong knowledge of GMP, FDA regulations, and pharmaceutical manufacturing processes. Proven experience in managing production teams and processes. Excellent problem-solving skills and the ability to make quick decisions. Strong organizational and time management skills. Proficiency in using production management software and tools. Effective communication and leadership skills. Working Conditions This position requires working in a pharmaceutical manufacturing plant environment, which may involve exposure to chemicals, noise, and varying temperatures. Must be able to work shifts, including weekends and holidays, as required by the production schedule. Occasional travel may be required for training, meetings, or conferences. Show more Show less

Job Description: Operator - Tablet Manufacturing / Packaging Job Title: Operator – Tablet Manufacturing / Packaging Location: Indore – Regulated Pharma Manufacturing Plant Department: Production – Oral Solid Dosage (OSD) Reporting To: Executive / Officer – Production Job Type: Full-Time | Operator Level Job Purpose To operate, clean, and maintain machines and perform assigned tasks in tablet manufacturing or packaging areas , ensuring compliance with cGMP, safety standards, and production targets. Key Responsibilities 🔹 For Tablet Manufacturing: Operate machines used in granulation, compression, and coating (e.g., RMG, FBD, compression machines, auto coaters). Clean and assemble equipment as per SOPs and maintain cleaning records. Assist in batch changeovers and perform machine setup under supervision. Follow BMR instructions and carry out in-process checks (weight, hardness, thickness, etc.). Ensure cleanliness and housekeeping in the manufacturing area. 🔹 For Tablet Packaging Operate machines for blister packing, alu-alu packing, strip packing, bottle filling, cartonators , etc. Load and unload packaging materials (foils, cartons, labels, leaflets) properly. Support in line clearance and material reconciliation activities. Maintain equipment and work area cleanliness. Ensure proper labelling, batch coding, and visual inspection of finished packs. 🔹 Common Responsibilities Strictly follow cGMP, safety, hygiene, and data integrity guidelines. Report any equipment breakdowns, deviations, or abnormalities to the supervisor. Record activities in logbooks/registers accurately and timely. Participate in on-the-job training and continuous improvement activities. Wear appropriate PPE (Personal Protective Equipment) at all times. Skills & Competencies Basic machine handling skills. Understanding of SOPs, hygiene, and safety standards . Ability to read and follow instructions (Hindi/English). Good observation and attention to detail. Qualifications ITI / 12th Pass / Diploma in Engineering or Pharmacy Experience 1–5 years of hands-on experience in OSD tablet manufacturing or packaging in a regulated pharma plant (USFDA / WHO / MHRA preferred). Show more Show less

Location: Indore, Madhya Pradesh Department: EHS (Environment, Health & Safety) About SAVA Healthcare Limited SAVA Healthcare is committed to delivering high-quality pharmaceutical, herbal, and veterinary products across global markets. With our mission to "Make Life Feel Good," we uphold excellence, compliance, and safety in every aspect of our operations. Join us in building a safer workplace as we expand our manufacturing capabilities at Indore. Role & Responsibilities Develop and implement workplace health and safety plans in alignment with local and national regulations. Prepare, update, and enforce health and safety policies to establish a culture of safety. Evaluate existing procedures and facilities to identify risks and ensure legal compliance. Conduct training programs, workshops, and presentations on accident prevention and safety practices. Monitor adherence to health and safety protocols through regular inspections and audits. Inspect equipment and machinery to detect and address potential hazards. Investigate accidents/incidents to determine root causes and manage workers' compensation claims. Recommend corrective actions, preventive measures, and process improvements to enhance workplace safety. Maintain and present reports on health and safety performance, incidents, and compliance statistics. Preferred Candidate Profile Proven experience as a Health & Safety Manager or similar role in a manufacturing setup. Strong understanding of occupational health and safety laws and regulatory compliance. Experience in creating reports, policies, and conducting risk assessments. Proficient in data analysis and safety metrics. Exceptional attention to detail with strong observation and documentation skills. Excellent communication, training, and interpersonal skills. Strong organizational and leadership capabilities. Qualifications Graduate / B.E. / B.Tech in a relevant field. ADIS / PDIS certification (Advanced/Post Diploma in Industrial Safety) is mandatory. Certification in Occupational Health & Safety is highly desirable. Show more Show less

Job Title: QC Executive – (RM / FG / Stability / AMV & PV / Microbiology) Location: Indore – Regulated Pharma Manufacturing Plant Department: Quality Control Reporting To: QC Manager / Head – Quality Control Job Type: Full-Time | Executive Level Job Purpose To perform quality control testing and analysis of raw materials, finished products, stability samples, and microbiological parameters as per current Good Manufacturing Practices (cGMP), standard operating procedures (SOPs), pharmacopeial standards, and regulatory requirements to ensure product quality and compliance. Key Responsibilities Testing and Analysis Perform chemical and instrumental testing of Raw Materials (RM) and Finished Goods (FG) as per pharmacopeial and in-house specifications. Conduct Stability Studies in line with ICH guidelines and maintain records of stability trends. Execute Analytical Method Validations (AMV) and support Process Validation (PV) testing. Carry out Microbiological analysis of samples, including environmental monitoring, water testing, and microbial limit tests. Documentation and Compliance Maintain accurate, complete, and timely documentation (analytical reports, logbooks, LIMS/ERP entries). Ensure compliance with cGMP, GLP, and regulatory standards (USFDA, EU-GMP, WHO, etc.) . Participate in internal audits, external regulatory inspections , and implement CAPAs. Prepare and review standard operating procedures (SOPs), specifications, and testing protocols. Equipment Operation & Calibration Operate and calibrate instruments like HPLC, GC, UV, IR, Dissolution Apparatus, FTIR, etc. Ensure timely preventive maintenance and validation of QC instruments. Cross-functional Coordination Coordinate with Production, QA, Regulatory Affairs, and other relevant departments to resolve testing issues and support product release timelines. Participate in investigations of OOS/OOT results, deviations, and change controls. Key Skills & Competencies Sound knowledge of cGMP/GLP and ICH guidelines. Hands-on experience with analytical instruments and microbiology techniques. Strong documentation and data integrity practices. Good communication and team collaboration skills. Eye for detail and high level of integrity. Educational Qualifications B.Pharm / M.Pharm / M.Sc. (Chemistry / Microbiology / Pharmaceutical Sciences) Experience 2–5 years of relevant experience in a regulated pharmaceutical manufacturing environment. Preferred Certifications Training in Data Integrity, cGMP, QMS, or Instrument Handling is an advantage. Show more Show less

Job Title: Manager – Section Head (Validation / Qualification / CSV) Location: Indore Plant Department: Quality Assurance (QA) Reports to: Head – Quality Assurance / Site Quality Head Role Summary We are seeking a highly experienced and self-driven professional to lead the Validation & Qualification section within the QA department. The incumbent will be responsible for overseeing end-to-end activities related to Process Validation, Cleaning Validation, Equipment & Facility Qualification , and Computer System Validation (CSV) . This is a managerial role requiring strong cross-functional collaboration, team leadership, and audit readiness for domestic and international regulatory inspections. Key Responsibilities Strategic Planning & Oversight: Lead the development and implementation of the site Validation Master Plan (VMP). Oversee all validation and qualification activities (Process, Cleaning, Equipment, Facility, CSV) to ensure compliance with cGMP and regulatory expectations. Allocate resources and manage workload for validation team to ensure timely execution. Process & Cleaning Validation Review and approve process validation protocols and reports in line with lifecycle approach. Ensure cleaning validation activities meet regulatory expectations and site-specific risk assessments. Support risk-based re-validation and continued process verification programs. Equipment / Facility / Utility Qualification Oversee IQ, OQ, PQ of new and existing equipment, HVAC systems, and utilities. Ensure periodic requalification and deviation handling. Review and approve all qualification documents and summary reports. Computer System Validation (CSV) Ensure GxP software and computer systems are validated as per GAMP 5 and 21 CFR Part 11 requirements. Collaborate with IT, Engineering, and external vendors for new system qualification, periodic reviews, and change management. Review and approve CSV documentation (URS, RA, IQ/OQ/PQ). Compliance & Audit Readiness Ensure all validation activities are audit-ready and compliant with USFDA, MHRA, EU-GMP, WHO, and other regulatory guidelines. Lead responses to regulatory queries and participate in audits and inspections. Maintain robust document control and support data integrity compliance across systems. Team Leadership & Development Lead a team of executives and senior executives in the validation function. Provide technical guidance, training, and performance feedback. Foster a culture of continuous improvement and compliance. Candidate Profile Qualification: B.Pharm / M.Pharm / M.Sc. (Life Sciences, Chemistry, Microbiology) Experience: 10–15 years in Pharmaceutical Quality Assurance, with minimum 5 years in handling validation/qualification/CSV independently Sound knowledge of GMP guidelines, ICH Q8–Q10, GAMP 5, and regulatory requirements Prior experience in handling regulatory audits (USFDA / MHRA / EU-GMP / WHO / ANVISA, etc.) Desired Skills Strong leadership and decision-making capabilities Excellent documentation, communication, and cross-functional coordination skills Proficiency in QMS systems, validation documentation tools, and MS Office Problem-solving mindset with a focus on risk-based, data-driven validation Employment Type: Full-Time Position Level: Manager – Section Head CTC: As per industry standards and candidate profile Show more Show less

Job Title: Executive / Senior Executive – QA (Validation & Qualification) Location: Indore Plant Department: Quality Assurance (QA) Reports to: QA Manager – Validation / Head QA Role Summary We are looking for dedicated and experienced professionals to join our Quality Assurance (QA) Department as Executive / Senior Executive . The role involves supporting Validation & Qualification activities in any of the following areas: Process Validation Cleaning Validation Facility & Equipment Qualification Computer System Validation (CSV) Candidates with hands-on experience in one or more of these areas are encouraged to apply. Process Validation Key Responsibilities (based on area of expertise): Prepare and review Process Validation Protocols and Reports (PV). Coordinate validation batches with cross-functional teams. Monitor critical process parameters and ensure adherence to approved specifications. Perform risk assessments and gap analysis as required. Cleaning Validation Develop and execute cleaning validation protocols and sampling plans. Perform visual inspection and swab/rinse sampling for various equipment. Review analytical data and calculate MACO/Residue Limits. Maintain cleaning validation matrix and revalidation schedules. Facility & Equipment Qualification Support IQ, OQ, PQ of equipment, systems, and utilities as per validation master plan. Participate in installation, commissioning, and qualification activities. Ensure periodic qualification and requalification as per schedule. Maintain GMP-compliant records and reports for audits and inspections. Computer System Validation (CSV) Prepare and review URS, RA, IQ/OQ/PQ protocols for GxP systems. Ensure compliance with 21 CFR Part 11, GAMP 5, and data integrity principles. Coordinate with IT, QA, and software vendors during validation life cycle. Maintain validation documentation and change control records. Candidate Profile Qualification: B.Pharm / M.Pharm / M.Sc. (Life Sciences / Chemistry / Microbiology) Experience: 2–6 years in regulated pharmaceutical / API / sterile manufacturing environments Exposure to GMP, ICH, WHO, USFDA, and other regulatory guidelines is essential Experience in one or more of the following: Process Validation, Cleaning Validation, Equipment Qualification, or CSV Desired Skills Strong understanding of validation life cycle and risk-based approach Good documentation and data review skills Ability to coordinate with cross-functional teams (Production, QA, QC, Engineering, IT) Audit readiness and familiarity with regulatory expectations Proficiency in MS Office and documentation systems Employment Type: Full-Time CTC: As per industry norms and candidate’s experience Show more Show less

Job Title: Assistant Manager – Engineering Department Location: Indore Plant Department: Engineering Reports to: Manager / Head – Engineering Role Summary We are seeking experienced and result-oriented professionals for the role of Assistant Manager – Engineering . This role is open to candidates with expertise in one or more of the following areas: Electrical / Instrumentation / Control Systems (CS) Mechanical Process Maintenance HVAC / AHU / Utilities Process Engineering The incumbent will play a key role in ensuring engineering excellence, regulatory compliance, system uptime, and continuous improvement in a pharmaceutical manufacturing setup. Key Responsibilities (based On Area Of Expertise) Electrical / Instrumentation / Control Systems (CS): Oversee installation, maintenance, and troubleshooting of electrical panels, drives, and automation systems (PLC/SCADA). Lead calibration programs for critical instruments as per GMP. Ensure statutory compliance related to electrical safety, energy audits, and load management. Develop preventive maintenance schedules and drive cost-effective energy usage. Mechanical Process Maintenance Lead preventive, predictive, and breakdown maintenance of production and packaging machinery. Coordinate with production, quality, and validation teams to minimize downtime. Support CAPEX projects, vendor management, and equipment procurement. Conduct root cause analysis (RCA) and implement CAPAs. AHU / Utilities (HVAC, Boilers, Compressors, WTP, Etc.) Manage the operation and performance of HVAC and utility systems ensuring compliance with GMP & environmental standards. Ensure temperature, humidity, and differential pressure compliance in classified areas. Coordinate HVAC validation, requalification, and maintenance activities. Monitor utility consumption and drive efficiency improvement projects. Process Engineering Support process design improvements for enhanced efficiency and compliance. Participate in equipment and process validation, scale-up, and technology transfer. Collaborate on continuous improvement projects (Lean, Kaizen, TPM, etc.). Support qualification of new processes, change control management, and documentation. Candidate Profile Qualification: B.E. / B.Tech in Electrical, Mechanical, Instrumentation, or related Engineering field Experience: 6–10 years in pharmaceutical / API / chemical / FMCG manufacturing industry Sound knowledge of GMP, regulatory audits (MHRA/USFDA), safety practices, and documentation Hands-on experience in one or more of the mentioned areas is mandatory Experience in handling a small team will be an added advantage Desired Skills Strong leadership and team coordination skills Proactive approach in troubleshooting and decision-making Excellent communication and documentation capabilities Familiarity with SAP / ERP systems, MS Office Ability to work under pressure and manage multiple priorities Employment Type: Full-Time Shift: General / Rotational (based on business needs) CTC: As per company norms and experience level Show more Show less

Location: Indore, Madhya Pradesh Department: EHS (Environment, Health & Safety) About SAVA Healthcare Limited SAVA Healthcare is committed to delivering high-quality pharmaceutical, herbal, and veterinary products across global markets. With our mission to "Make Life Feel Good," we uphold excellence, compliance, and safety in every aspect of our operations. Join us in building a safer workplace as we expand our manufacturing capabilities at Indore. Role & Responsibilities Develop and implement workplace health and safety plans in alignment with local and national regulations. Prepare, update, and enforce health and safety policies to establish a culture of safety. Evaluate existing procedures and facilities to identify risks and ensure legal compliance. Conduct training programs, workshops, and presentations on accident prevention and safety practices. Monitor adherence to health and safety protocols through regular inspections and audits. Inspect equipment and machinery to detect and address potential hazards. Investigate accidents/incidents to determine root causes and manage workers' compensation claims. Recommend corrective actions, preventive measures, and process improvements to enhance workplace safety. Maintain and present reports on health and safety performance, incidents, and compliance statistics. Preferred Candidate Profile Proven experience as a Health & Safety Manager or similar role in a manufacturing setup. Strong understanding of occupational health and safety laws and regulatory compliance. Experience in creating reports, policies, and conducting risk assessments. Proficient in data analysis and safety metrics. Exceptional attention to detail with strong observation and documentation skills. Excellent communication, training, and interpersonal skills. Strong organizational and leadership capabilities. Qualifications Graduate / B.E. / B.Tech in a relevant field. ADIS / PDIS certification (Advanced/Post Diploma in Industrial Safety) is mandatory. Certification in Occupational Health & Safety is highly desirable. Show more Show less

Job Description: Technician - Tablet Manufacturing / Packaging Job Title: Technician – Tablet Manufacturing / Packaging Location: Indore – Regulated Pharma Manufacturing Plant Department: Production – Oral Solid Dosage (OSD) Reporting To: Executive / Officer – Production Job Type: Full-Time | Operator Level Job Purpose To operate, clean, and maintain machines and perform assigned tasks in tablet manufacturing or packaging areas , ensuring compliance with cGMP, safety standards, and production targets. Key Responsibilities 🔹 For Tablet Manufacturing: Operate machines used in granulation, compression, and coating (e.g., RMG, FBD, compression machines, auto coaters). Clean and assemble equipment as per SOPs and maintain cleaning records. Assist in batch changeovers and perform machine setup under supervision. Follow BMR instructions and carry out in-process checks (weight, hardness, thickness, etc.). Ensure cleanliness and housekeeping in the manufacturing area. 🔹 For Tablet Packaging Operate machines for blister packing, alu-alu packing, strip packing, bottle filling, cartonators , etc. Load and unload packaging materials (foils, cartons, labels, leaflets) properly. Support in line clearance and material reconciliation activities. Maintain equipment and work area cleanliness. Ensure proper labelling, batch coding, and visual inspection of finished packs. 🔹 Common Responsibilities Strictly follow cGMP, safety, hygiene, and data integrity guidelines. Report any equipment breakdowns, deviations, or abnormalities to the supervisor. Record activities in logbooks/registers accurately and timely. Participate in on-the-job training and continuous improvement activities. Wear appropriate PPE (Personal Protective Equipment) at all times. Skills & Competencies Basic machine handling skills. Understanding of SOPs, hygiene, and safety standards . Ability to read and follow instructions (Hindi/English). Good observation and attention to detail. Qualifications ITI / 12th Pass / Diploma in Engineering or Pharmacy Experience 1–5 years of hands-on experience in OSD tablet manufacturing or packaging in a regulated pharma plant (USFDA / WHO / MHRA preferred). Show more Show less

About Us SAVA Healthcare is amongst the fastest emerging pharmaceutical company in India with global reach to customers in Canada, Ukraine and the CIS, Asia, Latin America, Africa & FWA. With manufacturing units in Surendranagar, Malur and in near future in Indore holds various accreditations and produces wide variety of dosage forms across therapeutic categories. Our GMP compliant, State of Art manufacturing facility for Tablet, Oral Dry Powder, Capsule, Nasal sprays, DPIs, Cream, Gel and Ointment formulations with dedicated manufacturing sections supported by In-House R&D Center, focuses on Formulation and Analytical Development with an annual turnover of more than 250 crores and manpower of 500+ employees engaged across locations. As we continue to grow and evolve, we are seeking for talented and experienced in pharma company candidates to join our R&D Center located at Pimpri-Chinchwad, Pune. Job Title: Area Sales Manager (ASM) Location: Ahmedabad, Ghaziabad, Hubli, Hyderabad, Indore, Jaipur, Karnal, Ludhiana, Nagpur, Namakkal, Patna, Pune, Varanasi, Vijayawada. CTC to be offered: 6 LPA to 6.5 LPA Job Overview Area Sales Manager (ASM) is responsible for achievement of sales targets of territories in his or her region by building and retaining a strong sales team, ensuring flawless execution of marketing strategies, building strong rapport amongst key opinion leaders, and monitoring adherence to business unit norms. Key Responsibility Sales Management: Ensure achievement of Area and Regional Sales Targets; Drive team to achieve collection and POB targets. Foster a growth-oriented mindset within the sales team. Direct selling activities and prioritize tasks effectively. Perform Sales Tracking and provide Monthly Sales Forecasting. Maintain accurate and up-to-date sales data for the territory. Ensure adequate coverage of channel partners to maintain inventory availability. Ensure 100% compliance with ethical practices set forth by the organization. Key Opinion Leader Engagement: Build and develop personal rapport with core KOLs in the area/region. Engage customers through scientific platforms, camps/campaigns, etc., adhering to organizational practices. People Management: Communicate job expectations to the sales team; plan, monitor, appraise, and review job contributions. Orient, Train, Assign, Schedule, Coach, Counsel, and Discipline employees in assigned areas/regions. Demonstrate and detail products to all stakeholders for sales objective achievement. Train Territory Sales Officer to sell brand value to target customer groups. Evaluate performance of VSOs at pre-set intervals. Aim to retain a high-performing sales team. Market Development: Ensure 100% coverage of all stakeholders in the area/region including Veterinarians, Livestock specialists, Veterinary/Animal Husbandry institutions, and Channel partners. Record and communicate market trends and competitor information; identify trends impacting business. Recommend launch of new products by identifying unmet clinical needs and therapy gaps. Major Challenges: Proactively plan for market and customer-related uncertainties. Coach, train, and nurture the sales team to address attrition. Key Decisions: Plan allocation of time and resources among different parts of the area/region. Qualifications Graduate in Science are preferred. Non-science graduate with previous experience in farm animal business can also apply. 5 years of experience in frontline or 2 years of managerial experience in livestock business. Ability to handle scientific communication with customers. Eagerness to build relationships, nurture, and manage people. Strong sales planning and negotiating skills. Additional Information This position offers competitive compensation including base salary, commission, Insurance and benefits package. Travel within the assigned territory is required. Application Process Interested candidates are encouraged to submit their resume and a cover letter detailing their relevant experience, qualifications and prefer location to careers@savaglobal.com. Show more Show less

Job Title: Area Sales Manager - Companion Animal Healthcare Business Company: SAVA Healthcare is amongst the fastest emerging pharmaceutical company in India with global reach to customers in Canada, Ukraine and the CIS, Asia, Latin America, Africa & FWA. With manufacturing units in Surendranagar, Malur and in near future in Indore holds various accreditations and produces wide variety of dosage forms across therapeutic categories. Our GMP compliant, State of Art manufacturing facility for Tablet, Oral Dry Powder, Capsule, Nasal sprays, DPIs, Cream, Gel and Ointment formulations with dedicated manufacturing sections supported by In-House R&D Center, focuses on Formulation and Analytical Development with an annual turnover of more than 200 crores and manpower of 500+ employees engaged across locations. Job Location: Pune Overview The Area Sales Manager will be responsible for driving sales and managing the business operations for veterinary medicines in the assigned territory. This role involves building and maintaining strong customer relationships, leading a sales team, and achieving sales targets. The ideal candidate will have a deep understanding of the veterinary pharmaceutical market, strong sales acumen, and excellent leadership skills. Key Responsibilities Sales Strategy and Planning: Develop and implement sales strategies to achieve sales targets for veterinary medicines in the assigned area. Monitor market trends, competitor activities, and customer needs to identify business opportunities. Prepare and execute sales plans and budgets for the territory. Team Leadership Recruit, train, and manage a team of sales representatives. Set performance targets and provide coaching to the sales team to ensure their success. Conduct regular performance reviews and provide feedback to team members. Customer Relationship Management Build and maintain strong relationships with veterinary doctors, clinics, distributors, and key stakeholders in the territory. Address customer inquiries and resolve issues promptly to ensure customer satisfaction. Organize and participate in veterinary conferences, seminars, and workshops to promote products. Business Development Identify and pursue new business opportunities to expand the customer base and increase market share. Develop and execute promotional activities and campaigns to drive sales growth. Collaborate with marketing and product development teams to align sales efforts with overall company objectives. Reporting And Analysis Monitor sales performance and prepare regular reports on sales activities, customer feedback, and market trends. Analyze sales data to identify areas for improvement and implement corrective actions. Provide insights and recommendations to the Regional Sales Manager on sales strategies and market opportunities. Compliance Ensure compliance with all company policies, industry regulations, and ethical standards in sales activities. Stay updated on relevant veterinary pharmaceutical regulations and ensure the team’s adherence. Qualifications Education: Bachelor's degree in Veterinary Science, Animal Husbandry, Pharmacy, or a related field. MBA or equivalent in Sales/Marketing is a plus. Experience: Minimum of 5-7 years of sales experience in the veterinary pharmaceutical industry, with at least 2 years in a managerial role. Skills: Strong leadership and team management skills. Excellent communication, negotiation, and interpersonal skills. In-depth knowledge of the veterinary pharmaceutical market and products. Ability to analyze market data and trends. Proficiency in MS Office and CRM software. Key Competencies Customer-focused approach with strong problem-solving abilities. Ability to work under pressure and meet deadlines. Strategic thinking and planning skills. High ethical standards and integrity. Work Environment Field-based role with regular travel within the assigned territory. Interaction with veterinary professionals, distributors, and internal teams. Compensation Competitive salary with performance-based incentives. Other benefits as per company policy. Show more Show less

Job Title: Stores Executive / Sr. Executive Location: Surendranagar Department: Stores / Warehouse Reports To: Head Stores Job Purpose The Stores Executive will be responsible for the overall management of the store's dispensing activities, including receipt, stock handling, verification, and control of Raw Materials (RM), Packaging Materials (PM), and other materials. The candidate will ensure compliance with regulatory standards and contribute to efficient inventory management. Key Responsibilities Responsible for the receipt, proper storage, and dispensing of Raw Materials (RM), Packaging Materials (PM), and other materials. Ensure accurate material issuance to production and other departments as per requirements. Maintain up-to-date records of all material movements (receipt, issuance, returns, etc.). Perform regular stock verification and physical inventory checks as per schedule. Monitor stock levels and initiate timely requisitions to avoid shortages or overstocking. Ensure compliance with Good Storage Practices (GSP) and applicable regulatory requirements. Coordinate with Quality Assurance (QA) and other relevant departments for material clearance and other related activities. Assist in documentation related to regulatory inspections and audits. Maintain hygiene, safety, and security standards in the storage area. Identify and report any discrepancies or non-conformities related to materials. Support continuous improvement initiatives related to inventory control and store management. Candidate Profile Education: Graduate in Science / Commerce / Pharmacy or equivalent qualification. Experience 2–5 years of relevant experience in pharmaceutical/regulated industries. Experience in RM/PM material handling, stock management, and compliance activities. Preferred Background Candidates with prior exposure to regulatory audits (USFDA, EU, WHO, etc.) will be preferred. Knowledge of ERP systems for inventory management is an added advantage. Skills Required Good organizational and record-keeping skills. Attention to detail and accuracy. Understanding of regulatory and quality standards. Show more Show less

Job Description – Executive: Tablet Manufacturing Job Title: Executive – Tablet Manufacturing Location: Indore – Regulated Pharma Manufacturing Plant Department: Production – Oral Solid Dosage (OSD) Reporting To: Manager / Sr. Manager – Manufacturing Job Type: Full-Time | Executive Level Job Purpose To execute and monitor day-to-day operations in tablet manufacturing (Granulation, Compression, Coating) ensuring compliance with production plans, cGMP, and regulatory standards. Key Responsibilities Execute operations related to granulation, compression, and coating as per Batch Manufacturing Records (BMR) and SOPs. Operate, clean, and maintain equipment such as RMG, FBD, tablet press (compression machines), auto coaters, etc. Perform line clearance in coordination with QA. Ensure in-process checks like weight variation, hardness, thickness, disintegration, friability, etc. Maintain all documentation in compliance with GDP (Good Documentation Practices) and Data Integrity . Report deviations, breakdowns, and process abnormalities to supervisors. Monitor adherence to safety protocols , hygiene, and housekeeping in the manufacturing area. Participate in validation and qualification activities (equipment/process). Skills & Competencies Good understanding of cGMP , SOPs , and manufacturing operations. Hands-on experience in operating tablet manufacturing equipment. Ability to work in shifts and under regulatory-compliant environments. Documentation and observation skills. Qualifications B.Pharm / M.Pharm / B.Sc. (Science) 2–5 years of relevant experience in regulated pharmaceutical manufacturing (USFDA / MHRA / WHO-GMP). Show more Show less

Job Title: Territory Sales Executive - Companion Animal Healthcare Business Company: SAVA Healthcare is amongst the fastest emerging pharmaceutical company in India with global reach to customers in Canada, Ukraine and the CIS, Asia, Latin America, Africa & FWA. With manufacturing units in Surendranagar, Malur and in near future in Indore holds various accreditations and produces wide variety of dosage forms across therapeutic categories. Our GMP compliant, State of Art manufacturing facility for Tablet, Oral Dry Powder, Capsule, Nasal sprays, DPIs, Cream, Gel and Ointment formulations with dedicated manufacturing sections supported by In-House R&D Center, focuses on Formulation and Analytical Development with an annual turnover of more than 200 crores and manpower of 500+ employees engaged across locations. Job Location: Pan India Locations (Pune, Goa, Mumbai, Nagpur, Kolhapur, Sambhajinagar, Lucknow, Delhi, Ghaziabad, Muzaffarpur, Bhagalpur, Patna, Rourkela, Bhubaneswar, Guwahati) CTC to be offered: 3 LPA to 4 LPA Overview We are looking for a Territory Sales Executive to join our Companion Animal Healthcare Business team. The ideal candidate will be responsible for driving sales and achieving targets within their designated territory. They will play a crucial role in promoting our products, building relationships with key stakeholders, and providing excellent customer service to veterinary clinics, pet stores, and other relevant outlets. Key Responsibilities Sales and Business Development: Develop and execute strategic sales plans to achieve sales targets and expand market share within the assigned territory. Identify new business opportunities and establish strong relationships with veterinary clinics, pet stores, and other potential customers. Conduct product presentations, demonstrations, and training sessions for veterinarians and other professionals. Customer Relationship Management: Build and maintain strong relationships with existing customers, understanding their needs and providing solutions. Address customer inquiries, concerns, and complaints promptly and professionally. Collaborate with internal teams to ensure timely delivery of products and resolution of customer issues. Market Analysis and Reporting: Monitor market trends, competitor activities, and customer feedback to identify opportunities and challenges. Prepare regular reports on sales performance, market trends, and competitor activities, providing insights and recommendations for improvement. Product Promotion and Marketing: Implement marketing strategies and promotional campaigns to increase awareness and demand for our products. Organize and participate in trade shows, conferences, and other events to showcase our products and network with industry professionals. Qualification B.Sc B.Pharma Additional Information This position offers competitive compensation including base salary, incentive, Insurance and benefits package. Travel within the assigned territory is required. Driving License is Mandatory. Show more Show less

Job Title: Assistant Manager - Engineering Company: SAVA Healthcare is amongst the fastest emerging pharmaceutical company in India with global reach to customers in Canada, Ukraine and the CIS, Asia, Latin America, Africa & FWA. With manufacturing units in Surendranagar, Malur and in near future in Indore holds various accreditations and produces wide variety of dosage forms across therapeutic categories. Our GMP compliant, State of Art manufacturing facility for Tablet, Oral Dry Powder, Capsule, Nasal sprays, DPIs, Cream, Gel and Ointment formulations with dedicated manufacturing sections supported by In-House R&D Center, focuses on Formulation and Analytical Development with an annual turnover of more than 200 crores and manpower of 500+ employees engaged across locations. Job Location: Surendranagar Plant Job Summary The Assistant Manager of Engineering will support the Engineering Head in ensuring the smooth operation and maintenance of all engineering aspects within the pharmaceutical manufacturing plant. This role involves overseeing equipment maintenance, ensuring compliance with industry standards, managing engineering projects, and leading a team of technicians and engineers. The Assistant Manager will play a critical role in optimizing production efficiency, maintaining safety standards, and implementing continuous improvement initiatives. Key Responsibilities Maintenance Management: Oversee routine and preventive maintenance of manufacturing equipment and utilities. Ensure timely response to equipment breakdowns to minimize downtime. Coordinate with vendors and contractors for specialized maintenance and repair work. Compliance and Quality Assurance: Ensure all engineering activities comply with GMP (Good Manufacturing Practices), FDA regulations, and other relevant industry standards. Conduct regular audits and inspections to maintain compliance with safety and quality standards. Collaborate with the Quality Assurance team to address engineering-related quality issues. Project Management: Assist in planning and executing engineering projects, including equipment upgrades, facility expansions, and process improvements. Prepare project proposals, budgets, and timelines. Monitor project progress and ensure projects are completed on time and within budget. Team Leadership: Supervise and mentor a team of engineers and technicians. Conduct performance reviews and provide ongoing training and development. Foster a culture of safety, teamwork, and continuous improvement. Process Optimization: Identify and implement opportunities for improving manufacturing processes and equipment efficiency. Utilize data and metrics to drive decision-making and process enhancements. Lead root cause analysis and problem-solving initiatives for recurring issues. Documentation and Reporting: Maintain accurate records of maintenance activities, equipment performance, and project status. Prepare regular reports for senior management on engineering performance and project updates. Ensure all engineering documentation is up-to-date and compliant with regulatory requirements. Budget Management: Assist in the preparation and management of the engineering department’s budget. Monitor expenses and identify cost-saving opportunities without compromising on quality and safety. Qualifications Bachelor’s degree in Mechanical Engineering, Electrical Engineering, or a related field. A minimum of 5 years of experience in engineering roles within the pharmaceutical or related manufacturing industry. Proven experience in maintenance management, project management, and team leadership. Strong knowledge of GMP, FDA regulations, and industry standards. Excellent problem-solving skills and the ability to work under pressure. Proficiency in using engineering software and tools. Strong communication and interpersonal skills. Working Conditions This position requires working in a manufacturing plant environment, which may involve exposure to hazardous materials, noise, and varying temperatures. Occasional travel may be required for vendor meetings, training, and conferences. Show more Show less