Vadodara
INR 0.35 - 0.7 Lacs P.A.
On-site
Full Time
Business Development Manager (Pharmaceutical Export) Company We are a leading pharmaceutical company committed to improving healthcare through the development and distribution of high-quality products. Our global presence spans across multiple regions, and we are expanding our footprint in emerging markets. We are looking for a dynamic and experienced Business Development Manager to join our team in Vadodara and help drive our growth in both regulatory and non-regulatory markets. Place of Posting Vadodara- Gujarat Application to be submitted to hrmanager613@gmail.com Qualifications (Essential) (Any one of the following qualification) Bachelor’s degree in Pharmacy, Life Sciences, Business Administration, or a related field. MBA is a plus. Preference/ Experience At least 5 years of experience in business development within the pharmaceutical industry, with a strong understanding of both regulatory and non-regulatory requirements. Proven experience working in African and South Asian markets, with knowledge of local healthcare systems, regulations, and business environments. Skills Strong negotiation, communication (written and verbal) , and relationship-building skills. In-depth knowledge of pharmaceutical industry trends and regulations. Fluency in English; proficiency in additional languages spoken in target regions is a plus. Personal Attributes: Strategic thinker with a strong business acumen. Proactive, results-oriented, and adaptable to changing market conditions. Willingness to travel internationally as needed. Job Description Key Responsibilities: Market Research and Strategy Development: Conduct in-depth market research in the pharmaceutical industry, focusing on emerging trends in African and South Asian countries. Develop and implement business strategies to expand the company’s presence in both regulatory and non-regulatory markets. Identify new business opportunities, including partnerships, licensing, and distribution agreements in target regions. Regulatory and Non-Regulatory Expertise: Lead efforts in obtaining regulatory approvals for new products and navigating local regulations in key African and South Asian markets. Stay updated on changes in pharmaceutical regulations and ensure the company complies with all regulatory requirements. Oversee non-regulatory aspects of business development, including product marketing, branding, and market positioning. Relationship Building and Client Management: Develop and maintain strong relationships with key stakeholders, including regulatory authorities, distributors, healthcare professionals, and other partners across Africa and South Asia. Coordinate with internal teams to manage key client accounts and resolve issues related to product distribution, quality, and pricing. Negotiation and Deal Closure: Lead negotiations for contracts, strategic alliances, and joint ventures in the pharmaceutical sector. Work closely with the legal and compliance teams to ensure all agreements comply with local regulations and company policies. Cross-Functional Collaboration: Collaborate with the marketing, regulatory affairs, and sales teams to ensure successful execution of business development initiatives. Monitor and report on business performance, competitor activity, and market dynamics. Travel and Market Engagement: Travel extensively across African and South Asian countries to engage with key clients, regulators, and stakeholders, ensuring the company’s growth in the region. Represent the company at industry conferences, trade shows, and other professional events. Benefits: Competitive salary and performance-based incentives. Health and wellness benefits. Opportunities for professional growth and career advancement. A dynamic and inclusive work environment. Job Types: Full-time, Permanent Pay: ₹35,000.00 - ₹75,000.00 per month Benefits: Cell phone reimbursement Paid sick time Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Experience: in same field: 8 years (Preferred) Work Location: In person Job Type: Full-time Pay: ₹35,000.00 - ₹70,000.00 per month Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person Job Types: Full-time, Permanent Pay: ₹35,000.00 - ₹70,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Work Location: In person
Vadodara, Gujarat
INR 0.15 - 0.18 Lacs P.A.
On-site
Full Time
Company We are a leading pharmaceutical company committed to improving healthcare through the development and distribution of high-quality products. Our global presence spans across multiple regions, and we are expanding our footprint in emerging markets. We are looking for a dynamic and experienced maintenance engineer to join our team in Rani Plant, Savli, Vadodara. Place of Posting Rania, Savli, Vadodara- Gujarat Application to be submitted to [email protected] Qualifications (Essential) (Any one of the following qualification) · Bachelor's degree in Mechanical Engineering, Electrical Engineering, or a related field. Preference/ Experience · Experience in industrial maintenance, preferably within the pharmaceutical industry. · Knowledge of GMP regulations and quality standards · Strong mechanical and electrical troubleshooting skills · Proficiency in using computerized maintenance management systems (CMMS) Skills · Ability to work independently and as part of a team. Personal Attributes: A maintenance engineer in a pharmaceutical company is responsible for the upkeep and repair of all manufacturing equipment and plant utilities, ensuring their optimal functionality while adhering to strict Good Manufacturing Practices (GMP) and safety regulations, by performing routine maintenance, troubleshooting breakdowns, implementing preventive maintenance plans, and coordinating with production teams to minimize downtime and maintain product quality. Job Description · Preventive Maintenance: o Develop and execute scheduled maintenance plans for all production equipment, including reactors, centrifuges, dryers, and filling machines. o Inspect equipment for wear and tear, identify potential issues, and perform necessary preventative actions. o Maintain accurate documentation of maintenance activities and spare parts inventory. Breakdown Maintenance: Respond promptly to equipment failures, diagnose the root cause of malfunctions, and perform repairs efficiently. Coordinate with vendors for necessary parts and repairs when required. Compliance and Quality Assurance: Ensure all maintenance activities comply with GMP regulations, including documentation, validation, and cleaning procedures. Monitor and maintain critical parameters like temperature, pressure, and humidity within designated ranges. Plant Utilities Maintenance: Oversee the upkeep of essential plant utilities such as HVAC systems, water purification systems, compressed air lines, and electrical power generation. Project Management: Participate in equipment upgrades, modifications, and new installations, including commissioning and validation processes. Data Analysis and Improvement: Analyze maintenance data to identify trends and implement corrective actions to improve equipment reliability and reduce downtime. Propose and implement continuous improvement initiatives to optimize maintenance operations. Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person Job Type: Full-time Pay: ₹15,000.00 - ₹18,000.00 per month Work Location: In person
Makarpura, Vadodara, Gujarat
INR 0.3 - 0.5 Lacs P.A.
On-site
Full Time
EXPRIENCE : 3 - 5 years of experience as COMPANY SECRETARY in a limited company preferably in Pharmaceutical and Bulk drugs. Qualification: CS Completion Preference: 1. She/he should be good in Drafting, Statutory compliance, and all legal matters. 2. She/he should maintain Confidentiality of all information of organization and client information. 3. She/he should quick learner and adaptive to any process change in a minimal time. Rolls: Legal compliance: Ensuring the company complies with relevant laws, such as the Companies Act and SEBI regulations Corporate governance:Managing the company's corporate governance framework, including listing requirements and public disclosures. Communication: Acting as a point of communication between the board of directors. government agencies, and stakeholders Record keeping: Maintainirrg statutory books, including registerc gf mernbe,rs,directors, and secretaries o Poligy implementaf ion:Ensuring policies, regulatory,or statutory changes are up to date and approved by the committee Meetings: Facilitating the corivening of . meetings' and attending Board, cornmittee, and general meetings Legql documents: Ensuring the,security of the company's legal documents Board guidance: Providingstrategic guidance on corporate affairs matters relattrd to companies act and securities law Stakeholder relationships:Builcling relationships with stakeholders System improvements:undertaking and driving process and system improvements Job Type: Full-time Pay: ₹30,000.00 - ₹50,000.00 per month Application Question(s): Are you qualified Company Secretary Course form the Institute of Company Secretaries of India (ICSI)? Experience: total work: 3 years (Preferred) Work Location: In person
Vadodara
INR 0.4 - 1.0 Lacs P.A.
On-site
Full Time
EXPERIENCE: 10 YEAR (GELATIN CAPSULE MACHINE) QUALIFICATION:DIPLOMA IN ELECTRICAL/MECHANICAL ENGINEERING /TECHNICAL BOARD JOB ROLE: Production planning Production scheduling Resource utilization People management Meet Business Objectives Quality Assurance Cost Control Team Building Process Streamlining Process Improvement Documentation Training Customer Care Key skills: Strategic planning & leadership lean manufacturing processes Production planning & control Rejection Analysis & Control Good analytical skill Project Management Mechanical Maintenance Quality Assurance Generate MIS Good Knowledge of computers At least 10 Years' of working experience preferably in EHGC( Empty Hard Gelatin Capsule Production) as a Production Manager. Job Type: Full-time Work Location: In person Job Type: Full-time Pay: ₹40,000.00 - ₹100,000.00 per month Work Location: In person
India
INR 0.3 - 0.5 Lacs P.A.
On-site
Full Time
EXPRIENCE : 3 - 5 years of experience as COMPANY SECRETARY in a limited company preferably in Pharmaceutical and Bulk drugs. Qualification: CS Completion Preference: 1. She/he should be good in Drafting, Statutory compliance, and all legal matters. 2. She/he should maintain Confidentiality of all information of organization and client information. 3. She/he should quick learner and adaptive to any process change in a minimal time. Rolls: Legal compliance: Ensuring the company complies with relevant laws, such as the Companies Act and SEBI regulations Corporate governance:Managing the company's corporate governance framework, including listing requirements and public disclosures. Communication: Acting as a point of communication between the board of directors. government agencies, and stakeholders Record keeping: Maintainirrg statutory books, including registerc gf mernbe,rs,directors, and secretaries o Poligy implementaf ion:Ensuring policies, regulatory,or statutory changes are up to date and approved by the committee Meetings: Facilitating the corivening of . meetings' and attending Board, cornmittee, and general meetings Legql documents: Ensuring the,security of the company's legal documents Board guidance: Providingstrategic guidance on corporate affairs matters relattrd to companies act and securities law Stakeholder relationships:Builcling relationships with stakeholders System improvements:undertaking and driving process and system improvements Job Type: Full-time Pay: ₹30,000.00 - ₹50,000.00 per month Application Question(s): Are you qualified Company Secretary Course form the Institute of Company Secretaries of India (ICSI)? Experience: total work: 3 years (Preferred) Work Location: In person
Vadodara
INR 0.15 - 0.18 Lacs P.A.
On-site
Full Time
Company We are a leading pharmaceutical company committed to improving healthcare through the development and distribution of high-quality products. Our global presence spans across multiple regions, and we are expanding our footprint in emerging markets. We are looking for a dynamic and experienced maintenance engineer to join our team in Rani Plant, Savli, Vadodara. Place of Posting Rania, Savli, Vadodara- Gujarat Application to be submitted to hrmanager613@gmail.com Qualifications (Essential) (Any one of the following qualification) · Bachelor's degree in Mechanical Engineering, Electrical Engineering, or a related field. Preference/ Experience · Experience in industrial maintenance, preferably within the pharmaceutical industry. · Knowledge of GMP regulations and quality standards · Strong mechanical and electrical troubleshooting skills · Proficiency in using computerized maintenance management systems (CMMS) Skills · Ability to work independently and as part of a team. Personal Attributes: A maintenance engineer in a pharmaceutical company is responsible for the upkeep and repair of all manufacturing equipment and plant utilities, ensuring their optimal functionality while adhering to strict Good Manufacturing Practices (GMP) and safety regulations, by performing routine maintenance, troubleshooting breakdowns, implementing preventive maintenance plans, and coordinating with production teams to minimize downtime and maintain product quality. Job Description · Preventive Maintenance: o Develop and execute scheduled maintenance plans for all production equipment, including reactors, centrifuges, dryers, and filling machines. o Inspect equipment for wear and tear, identify potential issues, and perform necessary preventative actions. o Maintain accurate documentation of maintenance activities and spare parts inventory. Breakdown Maintenance: Respond promptly to equipment failures, diagnose the root cause of malfunctions, and perform repairs efficiently. Coordinate with vendors for necessary parts and repairs when required. Compliance and Quality Assurance: Ensure all maintenance activities comply with GMP regulations, including documentation, validation, and cleaning procedures. Monitor and maintain critical parameters like temperature, pressure, and humidity within designated ranges. Plant Utilities Maintenance: Oversee the upkeep of essential plant utilities such as HVAC systems, water purification systems, compressed air lines, and electrical power generation. Project Management: Participate in equipment upgrades, modifications, and new installations, including commissioning and validation processes. Data Analysis and Improvement: Analyze maintenance data to identify trends and implement corrective actions to improve equipment reliability and reduce downtime. Propose and implement continuous improvement initiatives to optimize maintenance operations. Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person Job Type: Full-time Pay: ₹15,000.00 - ₹18,000.00 per month Work Location: In person
Vadodara, Gujarat
INR Not disclosed
On-site
Full Time
Company We are a leading pharmaceutical company committed to improving healthcare through the development and distribution of high-quality products. Our global presence spans across multiple regions, and we are expanding our footprint in emerging markets. We are looking for a dynamic and experienced maintenance engineer to join our team in Rani Plant, Savli, Vadodara. Place of Posting Rania, Savli, Vadodara- Gujarat Application to be submitted to hrmanager613@gmail.com Qualifications (Essential) (Any one of the following qualification) · Bachelor's degree in Mechanical Engineering, Electrical Engineering, or a related field. Preference/ Experience · Experience in industrial maintenance, preferably within the pharmaceutical industry. · Knowledge of GMP regulations and quality standards · Strong mechanical and electrical troubleshooting skills · Proficiency in using computerized maintenance management systems (CMMS) Skills · Ability to work independently and as part of a team. Personal Attributes: A maintenance engineer in a pharmaceutical company is responsible for the upkeep and repair of all manufacturing equipment and plant utilities, ensuring their optimal functionality while adhering to strict Good Manufacturing Practices (GMP) and safety regulations, by performing routine maintenance, troubleshooting breakdowns, implementing preventive maintenance plans, and coordinating with production teams to minimize downtime and maintain product quality. Job Description · Preventive Maintenance: o Develop and execute scheduled maintenance plans for all production equipment, including reactors, centrifuges, dryers, and filling machines. o Inspect equipment for wear and tear, identify potential issues, and perform necessary preventative actions. o Maintain accurate documentation of maintenance activities and spare parts inventory. Breakdown Maintenance: Respond promptly to equipment failures, diagnose the root cause of malfunctions, and perform repairs efficiently. Coordinate with vendors for necessary parts and repairs when required. Compliance and Quality Assurance: Ensure all maintenance activities comply with GMP regulations, including documentation, validation, and cleaning procedures. Monitor and maintain critical parameters like temperature, pressure, and humidity within designated ranges. Plant Utilities Maintenance: Oversee the upkeep of essential plant utilities such as HVAC systems, water purification systems, compressed air lines, and electrical power generation. Project Management: Participate in equipment upgrades, modifications, and new installations, including commissioning and validation processes. Data Analysis and Improvement: Analyze maintenance data to identify trends and implement corrective actions to improve equipment reliability and reduce downtime. Propose and implement continuous improvement initiatives to optimize maintenance operations. Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person Job Type: Full-time Pay: ₹15,000.00 - ₹18,000.00 per month Work Location: In person
Vadodara, Gujarat
INR Not disclosed
On-site
Full Time
EXPERIENCE: 5+ YEAR IN REGULATORY AFFAIRS IN A PHARMACEUTICAL INDUSTRY QUALIFICATIONS : B.PHARM/M.PHARM JOB DESCRIPTION: Compiling & documentation of wide range of data and information of Regulatory Affairs. Knowledge of regulatory guidelines of various countries. Information of regulatory compliances, knowledge of various ICH guidelines and cGMP guidelines. Ensuring preparation of documentation according to the requirements of MOH of the concerned country for various dosage form. Monitoring and checking of registration and re-registration dossiers of formulations & EHGC. Sorting out technical queries received from agents and health authorities of respective countries for registration of products. Co-ordination with Quality Assurance, Quality Control, R&D, packing, Production for technical data from different manufacture. Checking for artwork development of packing material for product. Maintain the registration certificate and maintain the records of registered products for renewal of registration. Upgrading knowledge in line with ever changing regulatory requirements. Compilation of documents for company registration and inspection by overseas regulatory authorities. Furnishing the scientific responses to deficiency queries received from various regulatory bodies. Application of Manufacturing Licenses for new products and COPP Review of BMR, PDR, Process Validation Data, Validation of Analytical Procedure, stability data, dissolution data, specifications etc. Checking of Artwork as per the guidelines Have acquaintance with CTD filling to various regulatory bodies. Co-ordinate with various departments lime QA, QC, Production, F&D, Artwork development department for collecting and processing various technical documents required for dossier compilation. Coordinate with Third parties for procuring the documents required for registration as per the requirement. Compilation of dossier for Formulations Responsible for notarization and legalization of administrative documents , from Embassy as per country requirement. Document preparation for FDCA application like Product Permission, Free Sale Certificate, Certificate Of Pharmaceutical Products with or without WHO inclusion, Loan License Manufacturing application, GMP Certificate application, WHO GMP Certificate application, Product inclusion in WHOGMP list, Supervisory Chemist for LLM, Test License application, Product Permission with NOC, Non Standard Quality Certificate application, Query certificate for relevant country guideline as well as customer requirement. Control of online doc mentation according to FDCA reguirement and Freezing process. Good knowledge of Drugs and Cosmetics Acts. Job Type: Full-time Pay: ₹30,000.00 - ₹40,000.00 per month Work Location: In person Benefits: Provident Fund Schedule: Day shift Experience: total work: 1 year (Preferred) Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹40,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person Job Types: Full-time, Permanent Pay: ₹35,000.00 - ₹48,679.31 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Work Location: In person
Vadodara
INR 0.35 - 0.48679 Lacs P.A.
On-site
Full Time
EXPERIENCE: 5+ YEAR IN REGULATORY AFFAIRS IN A PHARMACEUTICAL INDUSTRY QUALIFICATIONS : B.PHARM/M.PHARM JOB DESCRIPTION: Compiling & documentation of wide range of data and information of Regulatory Affairs. Knowledge of regulatory guidelines of various countries. Information of regulatory compliances, knowledge of various ICH guidelines and cGMP guidelines. Ensuring preparation of documentation according to the requirements of MOH of the concerned country for various dosage form. Monitoring and checking of registration and re-registration dossiers of formulations & EHGC. Sorting out technical queries received from agents and health authorities of respective countries for registration of products. Co-ordination with Quality Assurance, Quality Control, R&D, packing, Production for technical data from different manufacture. Checking for artwork development of packing material for product. Maintain the registration certificate and maintain the records of registered products for renewal of registration. Upgrading knowledge in line with ever changing regulatory requirements. Compilation of documents for company registration and inspection by overseas regulatory authorities. Furnishing the scientific responses to deficiency queries received from various regulatory bodies. Application of Manufacturing Licenses for new products and COPP Review of BMR, PDR, Process Validation Data, Validation of Analytical Procedure, stability data, dissolution data, specifications etc. Checking of Artwork as per the guidelines Have acquaintance with CTD filling to various regulatory bodies. Co-ordinate with various departments lime QA, QC, Production, F&D, Artwork development department for collecting and processing various technical documents required for dossier compilation. Coordinate with Third parties for procuring the documents required for registration as per the requirement. Compilation of dossier for Formulations Responsible for notarization and legalization of administrative documents , from Embassy as per country requirement. Document preparation for FDCA application like Product Permission, Free Sale Certificate, Certificate Of Pharmaceutical Products with or without WHO inclusion, Loan License Manufacturing application, GMP Certificate application, WHO GMP Certificate application, Product inclusion in WHOGMP list, Supervisory Chemist for LLM, Test License application, Product Permission with NOC, Non Standard Quality Certificate application, Query certificate for relevant country guideline as well as customer requirement. Control of online doc mentation according to FDCA reguirement and Freezing process. Good knowledge of Drugs and Cosmetics Acts. Job Type: Full-time Pay: ₹30,000.00 - ₹40,000.00 per month Work Location: In person Benefits: Provident Fund Schedule: Day shift Experience: total work: 1 year (Preferred) Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹40,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person Job Types: Full-time, Permanent Pay: ₹35,000.00 - ₹48,679.31 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Work Location: In person
Vadodara, Gujarat
INR Not disclosed
On-site
Full Time
Business Development Manager (Pharmaceutical Export) Company We are a leading pharmaceutical company committed to improving healthcare through the development and distribution of high-quality products. Our global presence spans across multiple regions, and we are expanding our footprint in emerging markets. We are looking for a dynamic and experienced Business Development Manager to join our team in Vadodara and help drive our growth in both regulatory and non-regulatory markets. Place of Posting Vadodara- Gujarat Application to be submitted to hrmanager613@gmail.com Qualifications (Essential) (Any one of the following qualification) Bachelor’s degree in Pharmacy, Life Sciences, Business Administration, or a related field. MBA is a plus. Preference/ Experience At least 5 years of experience in business development within the pharmaceutical industry, with a strong understanding of both regulatory and non-regulatory requirements. Proven experience working in African and South Asian markets, with knowledge of local healthcare systems, regulations, and business environments. Skills Strong negotiation, communication (written and verbal) , and relationship-building skills. In-depth knowledge of pharmaceutical industry trends and regulations. Fluency in English; proficiency in additional languages spoken in target regions is a plus. Personal Attributes: Strategic thinker with a strong business acumen. Proactive, results-oriented, and adaptable to changing market conditions. Willingness to travel internationally as needed. Job Description Key Responsibilities: Market Research and Strategy Development: Conduct in-depth market research in the pharmaceutical industry, focusing on emerging trends in African and South Asian countries. Develop and implement business strategies to expand the company’s presence in both regulatory and non-regulatory markets. Identify new business opportunities, including partnerships, licensing, and distribution agreements in target regions. Regulatory and Non-Regulatory Expertise: Lead efforts in obtaining regulatory approvals for new products and navigating local regulations in key African and South Asian markets. Stay updated on changes in pharmaceutical regulations and ensure the company complies with all regulatory requirements. Oversee non-regulatory aspects of business development, including product marketing, branding, and market positioning. Relationship Building and Client Management: Develop and maintain strong relationships with key stakeholders, including regulatory authorities, distributors, healthcare professionals, and other partners across Africa and South Asia. Coordinate with internal teams to manage key client accounts and resolve issues related to product distribution, quality, and pricing. Negotiation and Deal Closure: Lead negotiations for contracts, strategic alliances, and joint ventures in the pharmaceutical sector. Work closely with the legal and compliance teams to ensure all agreements comply with local regulations and company policies. Cross-Functional Collaboration: Collaborate with the marketing, regulatory affairs, and sales teams to ensure successful execution of business development initiatives. Monitor and report on business performance, competitor activity, and market dynamics. Travel and Market Engagement: Travel extensively across African and South Asian countries to engage with key clients, regulators, and stakeholders, ensuring the company’s growth in the region. Represent the company at industry conferences, trade shows, and other professional events. Benefits: Competitive salary and performance-based incentives. Health and wellness benefits. Opportunities for professional growth and career advancement. A dynamic and inclusive work environment. Job Types: Full-time, Permanent Pay: ₹35,000.00 - ₹75,000.00 per month Benefits: Cell phone reimbursement Paid sick time Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Experience: in same field: 8 years (Preferred) Work Location: In person Job Type: Full-time Pay: ₹35,000.00 - ₹70,000.00 per month Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person Job Types: Full-time, Permanent Pay: ₹35,000.00 - ₹70,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Work Location: In person
Vadodara
INR 1.8 - 2.4 Lacs P.A.
On-site
Full Time
QUALIFICATION: B.PHARMA/M.PHARMA EXPERIENCE : 1.5 to 2 YEARS JOB DESCRIPTION: 1. Environmental monitoring of manufacturing clean room area. 2. Non-viable particle monitoring of manufacturing clean room area. 3. Compressed air /nitrogen gas monitor and Personnel monitoring. 4. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g. plates, swabs, etc. 5. To perform line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling and packing. 6. To perform Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP. 7. Perform Root Cause Analysis using tools such as Fishbone, KT, 5Whys, etc. 8. Develops applicable Standard Operating Procedures (SOPs) governing Quality Management Systems. 9. Supports regulatory inspections and audits. 10. Communicate results from Daily Compliance walkthroughs 11. As appropriate, use knowledge and experience to solve straightforward problems. 12. Ensures Operations are compliant with SOPs. 13. Use independent judgment, as necessary, in developing systems/processes for use within Quality. 14. Aid in the identification of Process Improvements on a continuous basis. 15. Aid in the monitoring of Key Performance Indicating (KPIs) for functional area and ensure systems are operating within target. Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per mon Experience: total work: 1 year (Required) Work Location: In person Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Work Location: In person Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Work Location: In person
Vadodara
INR 1.8 - 2.16 Lacs P.A.
On-site
Full Time
CANDIDATE MUST BE FDA APPROVED. Develop new pharmaceutical products, vaccines, medicines and compounds such as antiseptics Collecting samples from a variety of locations Provide laboratory services for health departments, for community environmental health programs and for physicians needing information for diagnosis and treatment Record, analyze and interpret data Write research papers, reports, and reviews Ensure data is recorded accurately in accordance with guidelines Remain up to date with scientific and research developments Validate microbiological methods to meet client requirements, as appropriate Qualifications for Microbiologist 2 years of pharma experience Able to knowledgeably and safely handle hazardous chemicals Enthusiastically serve customers and represent our laboratory professionally Deep knowledge in managing a laboratory project and collaborate with a wide variety of technical colleagues Proficiency in numeracy and IT skills Strong oral and written communication skills Superb problem-solving skills Able to work well in a team and to manage your own workload Job Type: Full-time Experience: total work: 2 years (Preferred) Ability to Commute: Vadodara, Gujarat (Required) Ability to Relocate: Vadodara, Gujarat: Relocate before starting work (Required) Work Location: In person Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Work Location: In person
Vadodara
INR 1.92 - 2.28 Lacs P.A.
On-site
Full Time
Experience: 3 years in pharmaceuticals Company. skills: The QC Chemist is responsible for conducting chemical and physical testing on raw materials, intermediate products, and finished goods to ensure they meet quality and safety standards. This role involves analyzing data, maintaining documentation,and contributing to quality control processes. Job Type: Full-time Pay: ₹16,000 - ₹19,000.00 per month Schedule: Rotational shift Work Location: In person Benefits: Provident Fund Schedule: Day shift Work Location: In person Job Type: Full-time Pay: ₹16,000.00 - ₹19,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Work Location: In person
Vadodara, Gujarat
INR 0.15 - 0.18 Lacs P.A.
On-site
Full Time
CANDIDATE MUST BE FDA APPROVED. Develop new pharmaceutical products, vaccines, medicines and compounds such as antiseptics Collecting samples from a variety of locations Provide laboratory services for health departments, for community environmental health programs and for physicians needing information for diagnosis and treatment Record, analyze and interpret data Write research papers, reports, and reviews Ensure data is recorded accurately in accordance with guidelines Remain up to date with scientific and research developments Validate microbiological methods to meet client requirements, as appropriate Qualifications for Microbiologist 2 years of pharma experience Able to knowledgeably and safely handle hazardous chemicals Enthusiastically serve customers and represent our laboratory professionally Deep knowledge in managing a laboratory project and collaborate with a wide variety of technical colleagues Proficiency in numeracy and IT skills Strong oral and written communication skills Superb problem-solving skills Able to work well in a team and to manage your own workload Job Type: Full-time Experience: total work: 2 years (Preferred) Ability to Commute: Vadodara, Gujarat (Required) Ability to Relocate: Vadodara, Gujarat: Relocate before starting work (Required) Work Location: In person Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Work Location: In person
Vadodara, Gujarat
INR 2.4 - 6.0 Lacs P.A.
On-site
Full Time
M.Pharm/B.Pharm having 4 to 5 years of experience in Regulatory affairs & Documentation in Pharma formulation. Job Type: Full-time Pay: ₹20,000.00 - ₹50,000.00 per month Benefits: Provident Fund Schedule: Day shift Experience: total work in Regulatory Affairs: 4 years (Required) Work Location: In person
Vadodara
INR 2.4 - 6.0 Lacs P.A.
On-site
Full Time
M.Pharm/B.Pharm having 4 to 5 years of experience in Regulatory affairs & Documentation in Pharma formulation. Job Type: Full-time Pay: ₹20,000.00 - ₹50,000.00 per month Benefits: Provident Fund Schedule: Day shift Experience: total work in Regulatory Affairs: 4 years (Required) Work Location: In person
Rania, Vadodara, Gujarat
INR 1.8 - 2.04 Lacs P.A.
On-site
Full Time
Education: B.Pharm/ M.Pharm Licence: Possession of certificate approved by FDA for Tablets/Capsules. Experience: 2-3 Years in Pharma Industry Roles & Responsibilities: Providing production schedules and necessary guidelines to production operators. Reviewing documentation and ensuring all in-process checks are carried out as per the standard operating process. Maintaining good manufacturing practices & conditions as per GMP & WHO. Communicating any equipment breakdown to the maintenance team. Following SOP to improve efficiency. Facilitating audits as a production team member. Coordinating with the shift supervisor, cross functional teams and within team. Knowledge of the ideal conditions for working of equipment, their calibrations, inspections and maintenance schedule. GMP training. Knowledge of documentation as per GMP & QMS guidelines. Knowledge of audits, importance of documentation and basics of production data analysis. Knowledge of process safety analysis and handling hazards. Basic knowledge of production planning, supervising and delegating. Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹17,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Work Location: In person
India
INR 1.8 - 2.04 Lacs P.A.
On-site
Full Time
Education: B.Pharm/ M.Pharm Licence: Possession of certificate approved by FDA for Tablets/Capsules. Experience: 2-3 Years in Pharma Industry Roles & Responsibilities: Providing production schedules and necessary guidelines to production operators. Reviewing documentation and ensuring all in-process checks are carried out as per the standard operating process. Maintaining good manufacturing practices & conditions as per GMP & WHO. Communicating any equipment breakdown to the maintenance team. Following SOP to improve efficiency. Facilitating audits as a production team member. Coordinating with the shift supervisor, cross functional teams and within team. Knowledge of the ideal conditions for working of equipment, their calibrations, inspections and maintenance schedule. GMP training. Knowledge of documentation as per GMP & QMS guidelines. Knowledge of audits, importance of documentation and basics of production data analysis. Knowledge of process safety analysis and handling hazards. Basic knowledge of production planning, supervising and delegating. Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹17,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Work Location: In person
Vadodara, Gujarat
INR 2.4 - 6.0 Lacs P.A.
On-site
Full Time
M.Pharm/B.Pharm having 4 to 5 years of experience in Regulatory affairs & Documentation in Pharma formulation. Job Type: Full-time Pay: ₹20,000.00 - ₹50,000.00 per month Benefits: Provident Fund Schedule: Day shift Experience: total work in Regulatory Affairs: 4 years (Required) Work Location: In person Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹50,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Work Location: In person
Vadodara, Gujarat
INR 1.8 - 2.16 Lacs P.A.
On-site
Full Time
Company We are a leading pharmaceutical company committed to improving healthcare through the development and distribution of high-quality products. Our global presence spans across multiple regions, and we are expanding our footprint in emerging markets. We are looking for a dynamic and experienced maintenance engineer to join our team in Rani Plant, Savli, Vadodara. Place of Posting Rania, Savli, Vadodara- Gujarat Application to be submitted to [email protected] Qualifications (Essential) (Any one of the following qualification) · Bachelor's degree in Mechanical Engineering, Electrical Engineering, or a related field. Preference/ Experience · Experience in industrial maintenance, preferably within the pharmaceutical industry. · Knowledge of GMP regulations and quality standards · Strong mechanical and electrical troubleshooting skills · Proficiency in using computerized maintenance management systems (CMMS) Skills · Ability to work independently and as part of a team. Personal Attributes: A maintenance engineer in a pharmaceutical company is responsible for the upkeep and repair of all manufacturing equipment and plant utilities, ensuring their optimal functionality while adhering to strict Good Manufacturing Practices (GMP) and safety regulations, by performing routine maintenance, troubleshooting breakdowns, implementing preventive maintenance plans, and coordinating with production teams to minimize downtime and maintain product quality. Job Description · Preventive Maintenance: o Develop and execute scheduled maintenance plans for all production equipment, including reactors, centrifuges, dryers, and filling machines. o Inspect equipment for wear and tear, identify potential issues, and perform necessary preventative actions. o Maintain accurate documentation of maintenance activities and spare parts inventory. Breakdown Maintenance: Respond promptly to equipment failures, diagnose the root cause of malfunctions, and perform repairs efficiently. Coordinate with vendors for necessary parts and repairs when required. Compliance and Quality Assurance: Ensure all maintenance activities comply with GMP regulations, including documentation, validation, and cleaning procedures. Monitor and maintain critical parameters like temperature, pressure, and humidity within designated ranges. Plant Utilities Maintenance: Oversee the upkeep of essential plant utilities such as HVAC systems, water purification systems, compressed air lines, and electrical power generation. Project Management: Participate in equipment upgrades, modifications, and new installations, including commissioning and validation processes. Data Analysis and Improvement: Analyze maintenance data to identify trends and implement corrective actions to improve equipment reliability and reduce downtime. Propose and implement continuous improvement initiatives to optimize maintenance operations. Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Work Location: In person
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