168 Jobs in Gajraula

Urgent Vacancies for Teaching Faculties in Dept. of Radiology in Medical College and Hospitals in Pan India. Locations: Jodhpur, Bhopal, Gajraula, Durgapur, Delhi NCR, Bihar, Kanpur, Mathura, MP, Shahjahapur.

Delivering direct Patient care under supervision of the doctor Administrating medications Monitoring patients health Performing basic nursing health Collaborating with doctors and seniors Doccumenting care Develope the skills to improve quality during work Should be BSc Nursing/GNM should have minimum of 2 years and above can join soon. Send your CV to amr1.vims@svu.edu.in

Greetings from Venkateshwara Institute of Medical Sciences & Hospital, Gajraula, UP We are inviting applications from GNM/B.Sc. Nursing for the post of Staff nurse in the nursing department Qualification - GNM/B.Sc. Nursing Experience- Minimum 2 Years of experience Department- nursing Salary best as industry Candidate should have excellent communication skills and should have good knowledge in her department. If Interested kindly call or what's app at 9971796967 or email your resume at amr.vims@svu.edu.in Thanks & Regards Yashwant Singh HR VIMS

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description 🚀 We’re looking for a dynamic Manager – MS&T (Manufacturing Science & Technology) with deep expertise in Chemical Engineering and CDMO operations . If you thrive in high-impact, cross-functional environments and can lead Process Engineering calculations, Technology Transfer, project delivery, and regulatory compliance with precision, this opportunity in Gajraula, UP is for you. 📋 Key Responsibilities Performs technical evaluations of incoming RFPs and existing program extensions across capabilities including proposed scope of work, costing, timelines, and budgets with limited guidance from more senior level technical Evaluations Specialists and Management. Ensure project delivery as per plan and QA norms Provide technical guidance and lead project reviews. Ensure and regularly review compliance with all statutory, legal, environmental, licensing, regulatory, and safety norms and fulfill commitments to regulatory agencies, customers, and quality management Complete technical evaluation into appropriate cost model and proposal templates for proposal generation. The successful candidate will have a background in Chemical Engineering with experience in a relevant pharmaceutical or CDMO industry Assesses with Operations and Management and recommends capabilities to meet Client requirements as part of technical evaluations. Represents technical operations in front of Client in support of project acquisition with Sales & Business Development, Project Management, and/or Partnership Management. Attends Client site visits, presentations for new, and extension of existing opportunities. Ensuring that equipment works to its specification and to appropriate capacities of products Contribute novel ideas by way of participation during technical discussion with superiors/ Colleagues Preparation of Capex Proposals (Concept notes, Savings/Payback calculations) for purchase of new Process Intensification technologies, co-ordination with cross functional teams for purchase, installation and commissioning related activities Knowledge to use process modelling tools like Dyno Chem ,VISMIX for reaction, crystallization, filtration, solubility and mixing studies Study the process and recycling of solvents, performing experiments in PD Lab, generating data, proposing changes/modifications in recovery processes and establishing recovery process for new solvent streams for target improvement in the solvent recovery. Person will have demonstrated expertise in the scale-up and process understanding of chemical process unit operations in the manufacture of APIs, intermediates and raw materials. Experience in Quality by Design, process safety, technology transfer and commercial production would be advantageous. In-depth, hands-on expertise and up-to-date knowledge of a wide range of chemistry unit operations such as reactions, distillation, separation, filtration and drying. Strong scientific record of accomplishment, ability to handle several projects in different stages of development at the same time. Person will be responsible to Investigate and troubleshoot in case of issues in scale up/validation and support troubleshooting activities in case of issues in scale up/validation batches Key Attributes Excellent communication skills to interact internally with project teams and externally with customers Good understanding on CDMO business, RFP preparations in stretched timelines Good project management and supervisory skills. Collaboration and influencing skills to build partnerships with the other disciplines, similar groups, Conscientious with a can-do attitude and thorough attention to detail. Experience in working to GMP & FDA adherence Qualifications The ideal candidate will have: Qualification: B. Tech/ M. Tech Chemical Experience: 12 to 15 Years Key Skills: Good understanding of CDMO Business, Equipment mapping, RFP preparation, CFT alignment & Collaboration, Process Engineering calculations, Technology Transfer, knowledge of FDA regulations/ ICH guideline, OH cost calculations. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description 🚀 We’re seeking a seasoned Senior Manager – Mechanical Maintenance / Engineering with proven expertise in utility systems, preventive maintenance, and engineering operations. If you excel in managing plant-wide mechanical infrastructure, driving GMP compliance, leading Capex evaluations, and optimizing maintenance costs while ensuring safety and regulatory adherence, this leadership opportunity in Gajraula, UP is for you. 📋 Key Responsibilities To ensure plaining and scheduling for annual preventive maintenance of all mechanical and utility installations in the plant. To attend and timely response for all emergency breakdowns of mechanical and utility installations in the plant. To ensure and implement GMP requirements in function. Aligning SOP corporate SOP and guideline. To ensure spare part inventory of the mechanical and utility equipment items in Engineering Stores. To evaluate new equipment/facility proposals for Capex & modification and its procurement with timely execution. Support site project team for evaluation and timely completion of project. To ensure renewal of registrations and licenses related to Utility & Mechanical equipment for concerned Government Department as per standards. To ensure the safety of persons, plant & Equipment while carrying out the maintenance job. Work procedure update and training. To critically analyze the expenditure on procurement of items and overall equipment and utility maintenance expenditure periodically and find out ways and means to control the same at optimum level. To review the planning and implementation of energy conversion schemes and maintenance excellence schemes. To ensure timely closely of permanent change Control, temporary change control, deviation, CAPA and service calls. Is accountable for the performance and results of a team with own disciplined & Function. Defines Team operating standard and ensures essential procedure are followed based on knowledge of own disciplined, to ensure completion of assigned the training of self & Team members. Excretive limited management authority, sets employee performance objectives, conducts performance reviews and recommends pay actions. To ensure all the activities perform in own discipline for self and team should follow the compliance requirements. Qualifications The ideal candidate will have: Qualification: B.E. / B. Tech. in Mechanical Engineering Experience: Minimum 18 Years Key Skills: Good understanding of Mechanical and Utilities Operation, Understanding of GMP and EHS procedures. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Location Name: Gajraula Job Purpose “This position is open with Bajaj Finance ltd.”Culture Anchor:Work Hard - Consistently puts in effort. plans and tracks daily progress to achieve targetsExecute with Rigor - Takes responsibility for meeting targets with focus and effortOwn It - Maintains honesty and fairness in all interactions in line with organization’s policiesAct with Integrity Duties And Responsibilities ХTo achieve collection targets of the Respective Branch assigned, ensuring meeting PI Targets.ХMeeting the Target on Cost of Collections. Ensuring meeting PI Targets within cost limit specified on monthly basis.ХEnsuring legal guidelines are complied for entire collection structure in letter and sprits.ХEnsure that the collection agencies and executives adhere to the legal guidelines provided by the law in force.ХEnsure adherence to the Code of Conduct.ХContinuously monitoring collection agencies and collection executives to identify fraudulent practices and ensure that no loss is incurred due to such activities. Required Qualifications And Experience ХPeople Management skills.ХDemonstrated success & achievement orientation. ХExcellent communication skills.ХNegotiation SkillsХStrong bias for action & driving results in a high performance environment. ХDemonstrated ability to lead from the front. ХExcellent relationship skills. ХAffirmative in nature, Strong Leadership Skills, Clarity of thought and perseverance..ХExceptionally high motivational levels and needs to be a self starter.ХWorking knowledge of computers.

Now Hiring: Medical Educator in the Department of Obstetrics & Gynecology Institution :Venkateshwara Institute of Medical Sciences Location: Gajraula, Uttar Pradesh Institution Type: Reputable UG & PG Medical College About the Role We are currently seeking a dedicated and passionate Medical Educator to join our Department of Obstetrics & Gynecology at a leading UG/PG medical college VIMS Gajraula UP. This is an exciting opportunity for an experienced academician or clinician who is committed to excellence in teaching, research, and clinical education. Qualifications & Requirements MD/MS/DNB in Obstetrics & Gynecology from an NMC-recognized institution. Academic and/or clinical teaching experience as per NMC norms. Excellent communication, leadership, and organizational skills. A strong commitment to medical education, clinical excellence, and continuous learning. What We Offer Competitive salary and benefits package based on experience and designation. Opportunities for professional development, research, and academic leadership. Access to modern teaching tools and well-equipped clinical facilities. Supportive, inclusive, and collaborative academic environment. How to Apply To apply, please submit the updated CV/Resume to: dmr.vims@svu.edu.in +91-9837201984 (Whatsapp) Make a meaningful impact in the field of Womens Health and Medical Education. Join a legacy of excellence in teaching, innovation, and patient care.

Job Opportunity: Physiotherapist (Preferably Male) Venkateshwara Institute of Medical Sciences. Location: Gajraula, Uttar Pradesh About the Role: A well-established Medical College/Hospital VIMS is seeking a qualified and compassionate Physiotherapist (Preferably Male) to join its clinical team. The role involves delivering personalized physiotherapy treatments, assisting in patient rehabilitation, and contributing to a multidisciplinary care environment. Required Qualifications & Skills: Bachelor's in Physiotherapy (BPT) from a recognized institution Registration with the relevant Physiotherapy Council 2-5 years of clinical experience preferred. Excellent interpersonal and communication skills Patient-focused, empathetic, and professional in approach What We Offer: Attractive and competitive salary A collaborative and growth-oriented work environment Opportunity to work in a modern, well-equipped physiotherapy unit Learning and professional development opportunities How to Apply: Send your resume to dmr.vims@svu.edu.in with the subject line: "Application for Physiotherapist" For further information, contact: +91-9837201984 Make a meaningful impact on patients lives through skilled, hands-on rehabilitation. Join our healthcare team today!

Job Opening: Office Coordinator Venkateshwara Institute of Medical Sciences Location: Gajraula, Uttar Pradesh. We are seeking a dynamic, well-organized, and proactive Office Coordinator to join our administrative team at a reputed UG (MBBS)/PG (MS/MD) Medical College VIMS Gajraula. The ideal candidate will be responsible for ensuring smooth office operations while acting as a communication bridge across departments. Key Responsibilities: Coordinate daily administrative activities and support academic departments. Serve as the point of contact for internal and external communications. Manage scheduling, meetings, documentation, and inter-departmental coordination. Assist with correspondence, report preparation, and official communication in both Hindi and English . Ensure efficient office functioning and support the leadership team in administrative tasks. Required Qualifications & Skills: MBA in HR, Administration, or related field (mandatory) Minimum 1–5 years of relevant experience in office coordination or administration Excellent communication skills in both Hindi & English (spoken and written) Proficient in MS Office Suite (Word, Excel, PowerPoint, Outlook) Strong organizational, interpersonal, and multitasking abilities Professional attitude and ability to work in a fast-paced academic environment What We Offer: Competitive salary based on qualifications and experience A supportive and professional work culture Opportunity to work with experienced academicians and administrators Career growth opportunities within the institution How to Apply: Send your resume and cover letter to dmr.vims@svu.edu.in with the subject line: "Application for Office Coordinator" For queries, contact: +91-9837201984 Take the next step in your career with us and be the backbone of our academic administration!

Job Opportunity: Computer Operator at Venkateshwara Institute of Medical Sciences. Are you a tech-savvy professional with a passion for accuracy and efficiency? Join our esteemed Medical College as a Computer Operator and be part of a dynamic and mission-driven academic environment. Position: Computer Operator Location: Gajraula, UP Key Responsibilities: Manage and maintain data entry operations with high accuracy. Handle daily administrative computer tasks including documentation, record keeping, and report generation. Support faculty and administrative staff. Ensure proper functioning of computer systems and software used across departments. Coordinate with IT support team for troubleshooting and maintenance. Requirements: Graduate in any discipline. Minimum 2-5 years of relevant experience Proficiency in MS Office (Word, Excel, PowerPoint) and basic database handling. Fast and accurate typing skills. Ability to multitask and manage time efficiently. Strong communication and interpersonal skills. We Offer: Competitive salary based on qualifications and experience Supportive and professional work environment Opportunities for skill development and career advancement Exposure to the academic and healthcare sector How to Apply: Send your updated resume with a cover letter to dmr.vims@svu.edu.in mentioning "Application for Computer Operator" in the subject line. For more details, contact us at +91-9837201984 . Join us and contribute to the backbone of medical education through your technical expertise.

Job Opening: Senior Resident Department of Radiology Institution: Venkateshwara Institute of Medical Sciences Location: Gajraula, Distt Amroha , Uttar Pradesh Industry: Education / Medical / Healthcare/Hospital Functional Area: Healthcare Role Category: Medical P Experience: 02 years (Freshers with required qualifications are welcome) About the Institution Venkateshwara Institute of Medical Sciences Gajraula UP is a leading UG/PG Medical College and hospital dedicated to academic excellence, clinical innovation, and community-centered care. Our Radiology Department is equipped with the latest imaging technology and run by a team of expert faculty committed to high-impact diagnostics and training. We are looking for a dynamic and committed Senior Resident Radiology to join our department and be an integral part of our teaching hospitals growth and patient care excellence. Eligibility Criteria Educational Qualification: MD/DNB in Radiology from an institution recognized by the National Medical Commission (NMC). Experience: 0–2 years post-PG Why Join Us? Apply Now! If you're ready to elevate your radiology career in a collaborative, high-tech, and academic environment — we invite you to apply for the role of Senior Resident – Radiology at VIMS. Contact for Application & Queries HR Department Email: dmr.vims@svu.edu.in Phone: +91-9837201984

Job Opening: Assistant Professor Department of ENT Institution: Venkateshwara Institute of Medical Sciences Location: Gajraula, District Amroha, Uttar Pradesh Industry: Medical College /Hospital Functional Area: Teaching / Education/Clinical Experience: Minimum 1-3 Years About Us Venkateshwara Institute of Medical Sciences (VIMS) is a leading medical college and healthcare institution committed to academic excellence, groundbreaking research, and holistic medical education. Our Department of ENT (Otorhinolaryngology) is known for its advanced clinical infrastructure, dynamic faculty, and a strong focus on interdisciplinary learning. We are currently seeking an enthusiastic and qualified Assistant Professor ENT to join our team and contribute to nurturing the next generation of healthcare professionals. Key Responsibilities Deliver high-quality lectures, clinical teaching, and practical training to undergraduate and postgraduate medical students. Supervise student projects, theses, and clinical postings. Contribute to departmental academic activities, workshops, and seminars. Engage in research activities and publish in reputed journals. Collaborate with senior faculty in curriculum development and department growth. Desired Candidate Profile Educational Qualification: MS/DNB (ENT) from a recognized institution (as per NMC norms). Experience: 13 years of teaching or clinical experience preferred. Skills: Excellent communication and presentation skills Passion for teaching and mentoring Strong clinical acumen and academic integrity Ability to work collaboratively in a team environment What We Offer Competitive salary package aligned with experience and qualifications Opportunities for academic growth and research funding Access to state-of-the-art medical infrastructure and labs Supportive, collegial, and inclusive work environment Continuing professional development and career advancement pathways Join Us! If you’re passionate about shaping the future of medical education and want to be a part of a forward-thinking, academically driven institution, we invite you to apply. Apply Now – and take the next step in your academic journey with VIMS Gajraula UP Contact Information HR Department Email: dmr.vims@svu.edu.in Phone: +91-9837201984

Role & responsibilities Manage day-to-day HR operations Handle employee files, joining formalities, induction, credential verification and HR record-keeping for audits. Oversee the attendance, payroll processing, Performance appraisals & exit processes Assist in disciplinary actions, grievance handling, and maintaining workplace ethics and compliance. Ensure accurate and timely salary disbursements, reimbursements, and statutory deductions (PF, ESI, TDS, PT, etc.). Monitor manpower planning, deployment to meet service requirements effectively. Coordination for training and development programs Maintain and update HR policies, SOPs, and documentation in line with accreditation requirement Ensure all the documentation process as per the guidelines of UGC / NAAC for strict compliance Maintain Staff credentials, training records and other data for HR audit Liaise with statutory bodies for compliance-related documentation and inspections. Support internal and external audits to ensure prompt resolution of HR-related audit findings. Prior work experience in any reputed University/Medical college/ Hospital is preferred Preferred candidate profile Strong HR operational knowledge Good understanding of UGC/NAAC standards and documentation Excellent command on MS Excel and HRMS / Payroll software's Good communication, high level of integrity, confidentiality, and accuracy Ability to work in a high-pressure, compliance-driven environment. Strong organizational, people management and problem-solving abilities How to Apply? Interested candidates can forward their resume to recruitment@svu.edu.in and may call on 9368731732 / Neeraja

Role & responsibilities Oversee and manage monthly payroll processing for University, Hospital, and Medical College staff. Ensure accurate and timely salary disbursements, reimbursements, and statutory deductions (PF, ESI, TDS, PT, etc.). Maintain employee data across payroll systems, ensuring integrity and confidentiality. Manage leave encashment, bonus, gratuity, and final settlements. Generate payroll reports, audit trails, and MIS for internal and external stakeholders. Work closely with finance and audit departments to support payroll-related queries and reconciliations. Ensure compliance with all applicable labor laws, tax regulations, and statutory guidelines. Regularly update and maintain payroll software (SARAL / COSEC / ESSL) and handle troubleshooting or escalations. Coordinate with HR and IT departments for system upgrades, employee onboarding, and data flow integration. Support audits and ensure payroll documentation is maintained as per regulatory standards. Prior work experience in any reputed University/Medical college/ Hospital is preferred Preferred candidate profile : Minimum 10+ years of experience in managing payroll operations in a multi-unit organization. Proficient in payroll software SARAL, COSEC, ESSL (any one or more). Strong knowledge of statutory compliance, payroll taxation, and labor laws. Excellent Excel skills and familiarity with HRMS/payroll systems. High level of integrity, confidentiality, and accuracy. Good communication skills and ability to work collaboratively across departments. How to Apply? Interested candidates can forward their resume to recruitment@svu.edu.in then may call on 9368731732 / Neeraja

Role & responsibilities The candidate will play a key role in managing communication, coordination and day-to-day operational support to the senior management. Ensures the smooth execution of the assigned tasks. Key Responsibilities: Handle phone calls, emails, and visitors in a professional and courteous manner. Manage and organise the daily schedule, meetings, appointments, and travel plans. Coordinate with internal departments and external vendors for related activities. Prepare and manage correspondence, reports, presentations, and documentation. Follow up on tasks and deadlines on behalf of the seniors and ensuring timely completion. Attend meetings (when required), take minutes, and follow up on action items. Maintain confidentiality in handling sensitive business and operational information. Coordinate withe internal & external partners. Support the seniors in administrative and operational matters as needed. Prior work experience in any reputed University/Medical college/Hospital is preferred. Preferred candidate profile . Minimum 5 years experience in a similar PA/EA/Coordinator/Office Management role, Strong written and verbal communication skills. Proficient in MS Office (Word, Excel, PowerPoint, Outlook). Excellent organizational, coordination, and multitasking abilities. High degree of professionalism, discretion, and reliability. Ability to work independently and handle pressure in a fast-paced environment. How To Apply? Please confirm your Interest by sending your updated resume to recruitment@svu.edu .in then you may call on 9368731732 / Neeraja

Job Title: HR Executive / Senior HR Executive Department: Human Resources Institution: Venkateshwara Institute of Medical Sciences (VIMS) Location: Gajraula, Uttar Pradesh, India Employment Type: Full-Time About Us: Venkateshwara Institute of Medical Sciences (VIMS), is a premier institution committed to excellence in medical education, patient care, and research. Located in Gajraula, Uttar Pradesh, VIMS is dedicated to building a strong and ethical healthcare system through professional development and institutional growth. Position Summary: We are seeking dynamic and dedicated professionals to join our Human Resources department as HR Executive and Senior HR Executive . The selected candidates will be responsible for supporting and executing a wide range of HR functions, including employee relations, end to end Recruitment, employee grievances, etc. Key Responsibilities: Assist in end-to-end recruitment processes including sourcing, screening, interviewing, and onboarding of staff and faculty. Maintain and update employee records in accordance with legal requirements and institutional policies. Ensure compliance with statutory requirements and institutional policies. Handle employee grievances and assist in disciplinary procedures when necessary. Support the performance management cycle and annual appraisal process. Collaborate with departmental heads to support manpower planning and resource deployment. Knowledge of NMC (National Medical Commission): Working knowledge of NMC guidelines and regulatory requirements relevant to HR in a medical college/hospital setting. Understanding of NMC norms related to faculty recruitment, qualifications, documentation, and staffing ratios . Experience with HR documentation and institutional preparedness for NMC inspections and audits . Qualifications & Experience: For HR Executive: Bachelors degree in Human Resources, Business Administration, or a related field. MBA/PGDM in HR preferred. 1 to 3 years of relevant HR experience, in a medical education institution. For Senior HR Executive: Masters degree in Human Resources Management or a related field. 2 to 5 years of progressive HR experience, with exposure to core HR functions in a medical or academic institution. Demonstrated experience working within regulatory frameworks and HR compliance. Skills & Competencies: Proficiency in MS Office Suite and HR software tools. Strong interpersonal, communication, and organizational skills. High level of integrity, discretion, and professionalism. Ability to multitask and perform under pressure in a deadline-driven environment. Remuneration: Compensation will be competitive and commensurate with qualifications and experience, as per institutional norms. Application Process: Interested candidates are invited to submit their updated resume/CV , along with a cover letter specifying the position applied for ( HR Executive or Senior HR Executive ), to the following email address: Email: dmr.vims@svu.edu.in Join Venkateshwara Institute of Medical Sciences and contribute to shaping the future of healthcare through excellence in human resources and regulatory compliance. Contact HR Department VIMS Gajraula UP +91-9837201984 Email : dmr.vims@svu.edu.in

Greetings from Venkateshwara Institute of Medical Sciences, Gajraula, UP. We are inviting application from the General Medicine/Internal Medicine department. Job Location - Gajraula, Amroha, UP Position - Senior Resident/Assistant Professor Experience- Fresher also can apply. Salary best as the industry. If interested Kindly call or what's app @ 997171796967 or email your CV at amr.vims@svu.edu.in About Institution- College Name: Venkateshwara Institute of Medical Sciences (VIMS) Established: 2016 Academic Programs: Undergraduate (MBBS): Initial intake: 150 students (2016) Increased intake: 250 students (2023) Postgraduate (MD/MS): Started in 2021 with Dermatology and Anesthesia Expanded in 2023 to include: Pathology General Surgery Medicine Dermatology Anesthesia Radiology ENT Orthopedics Ophthalmology Obstetrics & Gynecology (OBG) Pediatrics Total PG Intake: 60 students per year Location Details: Situated on Delhi-Nainital Highway Approximately 110 km from Delhi Near Moradabad Thanks & Regards HR VIMS

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description We’re seeking a detail-oriented and technically skilled professional to take on the role of QC Technician - ATS at our cutting-edge manufacturing facility. This role is critical to ensuring the integrity, compliance, and reliability of our stability testing and analytical operations. 📌 Key Responsibilities Perform analysis of stability samples and working standard qualification as per defined procedures and pharmacopeial monographs. Operate and maintain analytical instruments, ensuring smooth function and troubleshooting following GLP standards. Maintain accurate documentation of methods, specifications, logbooks, certificates, and stability reports, including archiving data. Monitor stability studies in accordance with ICH Q1 guidelines. Conduct analytical method validation activities as per ICH Q2 standards. Initiate LIR/OOS investigations for any deviations or gaps related to SOPs or monographs during routine operations. Ensure qualifications and calibrations of all analytical instruments within the stability section. Comply strictly with laboratory safety procedures during daily activities. 🛠 Minimum Required Skills Solid understanding of Quality Control procedures. Strong knowledge of GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices). Hands-on expertise with HPLC, GC, KF, Auto titrator, and Vacuum oven operations. Ability to handle instrument troubleshooting and follow documentation protocols. Qualifications The ideal candidate must have: Experience Level: 4+ Years Industry Experience: API Experience is required Qualification: B.Sc. / M.Sc. in Chemistry or B. Pharmacy Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description 🚀 We’re looking for a proactive engineering lead with a passion for capital project execution and GMP excellence—if you thrive in high-impact environments, this opportunity is for you. 📋 Key Responsibilities 🧩 Project Leadership & Execution Lead delivery of electrical and instrumentation capital projects, ensuring timeline, budget, and customer expectations are met Plan, develop, and track annual capital spending plans Drive cost optimization and project execution efficiency through best practices Ensure adherence to Global Engineering policies, standards, and procedures Consult on engineering designs for new processes, equipment, and facilities for FDA/GMP compliance Contribute to long-range infrastructure and product/process planning 👥 Team Development & Collaboration Identify skill gaps within the project team and implement development or hiring strategies Collaborate with procurement for equipment selection and techno-commercial evaluations Finalize Capital Expenditure Requests (CERs) and secure global approvals Provide monthly reporting on Capex spends and forecasts Prepare and analyze Annual Operating Plan (AOP) and Long Range Plan (LRP) for Capex projects Establish Capex governance and tracking mechanisms ⚠️ Safety, Compliance & EHS Oversight Ensure full implementation of safety guidelines for the department and contractor teams, including HR compliance Achieve local and global EHS KPIs without delays Conduct regular Safety GEMBA walks and participate in risk assessments Ensure every shift has trained Emergency Response Team (ERT) and first aid members Perform any additional tasks as assigned by the Department Head Qualifications We’re looking for candidates with a strong engineering site project management background. The ideal candidate will have: Education: B.E. / B.Tech. in Electrical/EEE Engineering. Experience: Minimum 10 years of experience in Engineering Site Project management. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description We’re seeking a detail-driven and strategic leader to take on the role of the Quality Senior Specialist at our state-of-the-art manufacturing facility. This role is critical to ensuring compliance, safeguarding product integrity, and driving continuous improvement across all quality systems. Key Responsibilities: Review of all documentation (i.e. batch records, test results, deviation, LIR, OOS, CAPA, validation, COA, Change Controls, etc.) prior to disposition (release or rejection) of batch. Review of executed document like batch record, analytical data etc. and also to ensure on time compliance of errors/deviations identified (if any). Review of step-by-step performance and compliance to batch manufacturing and packaging record requirements and resolution of any errors/deviations identified. Monitoring and follow-up of corrective and preventive actions (review, approval, and on time closure of the CAPA) in order to resolve an event. Review Process/documentation (i.e. Protocol/report) of reviewing effectiveness to determine the effectiveness of a corrective or preventive action. Involving in investigation and ensuring on time closure of the investigation and event with resolution including corrective and preventive actions along with effectiveness determination. Initiating NTM to Senior Quality Unit Management, Operations, and other applicable functions for the purpose of expedited communication of critical quality/compliance related issues. Ensuring Quality interface with internal and external customers when dealing with activities such as issue resolution, product information, or for movement of materials, products, or process from site to site. Developing Process for observing, reviewing, and auditing operations activities in order to facilitate batch review and to assure compliance. Also, ensure self availability on shop floor as per requirement i.e. support to investigation etc. Responsible for assuring / coordinating for timely shipment, delivery, and/or receipt to assure compliance with regulatory requirements. In addition, responsible to assure appropriate shipping instructions, coordinate/approve route validation and investigation of temperature excursions as required for materials, components, drug substance, and drug product. Responsible for oversight and review of R&D product development & product tech transfer at the site and batch manufacture in GMP areas including resolution of deviations. Provide and ensuring support to Regulatory Affairs for Market Authorization (MA) application and maintenance. Responsible for Collection, compilation, analysis, and review of all data (i.e. manufacturing, packaging, testing, sourcing, deviations, stability, and changes etc.) and information supporting to validation status of a product’s. Responsible for Review of all documentation associated with the validation of the procedure(s) used to clean the equipment train for a product’s manufacturing and packaging process and cleaning verifications. This includes cleaning to remove active ingredients and cleaning agents. Responsible for Review of all documentation including protocols and reports associated with the validation of a product’s manufacturing (and packaging process, if required) and continuous process verification (CPV). Assessment of stability requirements based on the type of validation. Responsible for Performing, reporting of observations and verification of compliance reports of internal audit. Qualifications The ideal candidate will have: Education: M.Sc. in Chemistry or B.Tech/BE (Chemical Engineering) Experience: Minimum 4 to 6 years of industrial experience. Preferred Industries: API / Pharma. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description We’re seeking a meticulous and strategic professional to take on a pivotal role in our Quality Assurance team. This position demands a sharp eye for detail, a deep understanding of GMP compliance, and a proactive approach to quality oversight across the product lifecycle. Key Responsibilities Review of all documentation (i.e. batch records, test results, deviation, LIR, OOS, CAPA, validation, COA, Change Controls, etc. except analytical data related to batch release) prior to disposition (release or rejection) of batch. Review of executed document like batch record etc. and also to ensure on time compliance of errors/deviations identified (if any). Review of step-by-step performance and compliance to batch manufacturing and packaging record requirements and resolution of any errors/deviations identified. Monitoring and follow-up of corrective and preventive actions (review, approval, and on time closure of the CAPA) in order to resolve an event. Review Process/documentation (i.e. Protocol/report) of reviewing effectiveness to determine the effectiveness of a corrective or preventive action. Involving in investigation and ensuring on time closure of the investigation and event with resolution including corrective and preventive actions along with effectiveness determination. Initiating NTM to Senior Quality Unit Management, Operations, and other applicable functions for the purpose of expedited communication of critical quality/compliance related issues. Ensuring Quality interface with internal and external customers when dealing with activities such as issue resolution, product information, or for movement of materials, products, or process from site to site. Developing Process for observing, reviewing, and auditing operations activities in order to facilitate batch review and to assure compliance. Also, ensure self availability on shop floor as per requirement i.e. support to investigation etc. Responsible for assuring / coordinating for timely shipment, delivery, and/or receipt to assure compliance with regulatory requirements. In addition, responsible to assure appropriate shipping instructions, coordinate/approve route validation and investigation of temperature excursions as required for materials, components, drug substance, and drug product. Responsible for oversight and review of R&D product development & product tech transfer at the site and batch manufacture in GMP areas including resolution of deviations. Provide and ensuring support to Regulatory Affairs for Market Authorization (MA) application and maintenance. Responsible for Collection, compilation, analysis, and review of all data (i.e. manufacturing, packaging, testing, sourcing, deviations, stability, and changes etc.) and information supporting to validation status of a product’s. Responsible for Review of all documentation associated with the validation of the procedure(s) used to clean the equipment train for a product’s manufacturing and packaging process and cleaning verifications. This includes cleaning to remove active ingredients and cleaning agents. Responsible for Review of all documentation including protocols and reports associated with the validation of a product’s manufacturing (and packaging process, if required) and continuous process verification (CPV). Assessment of stability requirements based on the type of validation. Responsible for Performing, reporting of observations and verification of compliance reports of internal audit. Qualifications The ideal candidate will have: Education: B.Sc. / M.Sc. in Chemistry or B.Tech/BE (Chemical Engineering) Experience: Minimum 7 to 10 years of industrial experience. Preferred Industries: API / Pharma. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description We’re seeking a detail-driven and strategic leader to take on the role of the Quality Senior Specialist at our state-of-the-art manufacturing facility. This role is critical to ensuring compliance, safeguarding product integrity, and driving continuous improvement across all quality systems. Key Responsibilities Review of all documentation (i.e. batch records, test results, deviation, LIR, OOS, CAPA, validation, COA, Change Controls, etc.) prior to disposition (release or rejection) of batch. Review of executed document like batch record, analytical data etc. and also to ensure on time compliance of errors/deviations identified (if any). Review of step-by-step performance and compliance to batch manufacturing and packaging record requirements and resolution of any errors/deviations identified. Monitoring and follow-up of corrective and preventive actions (review, approval, and on time closure of the CAPA) in order to resolve an event. Review Process/documentation (i.e. Protocol/report) of reviewing effectiveness to determine the effectiveness of a corrective or preventive action. Involving in investigation and ensuring on time closure of the investigation and event with resolution including corrective and preventive actions along with effectiveness determination. Initiating NTM to Senior Quality Unit Management, Operations, and other applicable functions for the purpose of expedited communication of critical quality/compliance related issues. Ensuring Quality interface with internal and external customers when dealing with activities such as issue resolution, product information, or for movement of materials, products, or process from site to site. Developing Process for observing, reviewing, and auditing operations activities in order to facilitate batch review and to assure compliance. Also, ensure self availability on shop floor as per requirement i.e. support to investigation etc. Responsible for assuring / coordinating for timely shipment, delivery, and/or receipt to assure compliance with regulatory requirements. In addition, responsible to assure appropriate shipping instructions, coordinate/approve route validation and investigation of temperature excursions as required for materials, components, drug substance, and drug product. Responsible for oversight and review of R&D product development & product tech transfer at the site and batch manufacture in GMP areas including resolution of deviations. Provide and ensuring support to Regulatory Affairs for Market Authorization (MA) application and maintenance. Responsible for Collection, compilation, analysis, and review of all data (i.e. manufacturing, packaging, testing, sourcing, deviations, stability, and changes etc.) and information supporting to validation status of a product’s. Responsible for Review of all documentation associated with the validation of the procedure(s) used to clean the equipment train for a product’s manufacturing and packaging process and cleaning verifications. This includes cleaning to remove active ingredients and cleaning agents. Responsible for Review of all documentation including protocols and reports associated with the validation of a product’s manufacturing (and packaging process, if required) and continuous process verification (CPV). Assessment of stability requirements based on the type of validation. Responsible for Performing, reporting of observations and verification of compliance reports of internal audit. Qualifications The ideal candidate will have: Education: M.Sc. in Chemistry or B.Tech/BE (Chemical Engineering) Experience: Minimum 4 to 6 years of industrial experience. Preferred Industries: API / Pharma. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description 🚀 We’re seeking a hands-on production expert with deep GMP knowledge, ERP proficiency, and operational expertise in documentation, safety. Key Responsibilities Carrying out dispensing activities as per applicable procedure. Carrying out process and sampling activities during the production of Intermediate /API’s according to approved batch cards. Responsible for recording the observations of reaction parameters on the batch card as per approved procedure. Filling of all the batch cards (production cleaning) as per approved instructions. Ensure verification of pH meters and weigh balances as per applicable procedures. Maintain work procedure, safety precaution and cGMP. Ensure housekeeping of plant and cleanliness of the equipments, update the equipment Report accidents and irregularities at the work station to the Shift Officer. Knowledge to perform trouble shooting and root cause analysis. Develops solutions to complex problems requiring resourcefulness and creativity/innovation and ensures solutions are consistent with organization’s objectives. Work is performed without appreciable direction while exercising considerable latitude in determining objectives and approaches to assignment Good organizational skills, basic first-line management skills for daily operation, situational Leadership and decision-making skills Coordination of production tasks to meet assigned schedule Knowledge about the Spray drying & Liquide column chromatography Skills & Competencies Good understanding of Production procedures. Good Understating of GMP & Safety Good communication and teamwork skills. ✅ Preferred Experience Prior experience in regulated environments (USFDA, WHO-GMP, etc.) Exposure to API manufacturing in pharma. Qualifications The ideal candidate will have: Minimum 3 years of experience with M.Sc./ Diploma (Chemistry) or 1 to 3 years of experience with B.E. / B.Tech. in Chemical Engineering. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description 🚀 We’re seeking a hands-on production expert with deep GMP knowledge, ERP proficiency, and operational expertise in documentation, safety. 🔧 Key Responsibilities Carrying out dispensing activities as per applicable procedure. Carrying out process and sampling activities during the production of Intermediate /API’s according to approved batch cards. Responsible for recording the observations of reaction parameters on the batch card as per approved procedure. Filling of all the batch cards (production cleaning) as per approved instructions. Ensure verification of pH meters and weigh balances as per applicable procedures. Maintain work procedure, safety precaution and cGMP. Ensure housekeeping of plant and cleanliness of the equipment, update the equipment Report accidents and irregularities at the work station to the Shift Officer. Knowledge to perform trouble shooting and root cause analysis. Develops solutions to complex problems requiring resourcefulness and creativity/innovation and ensures solutions are consistent with organization’s objectives. Work is performed without appreciable direction while exercising considerable latitude in determining objectives and approaches to assignment. Good organizational skills, basic first-line management skills for daily operation, situational Leadership and decision-making skills. Coordination of production tasks to meet assigned schedule. Knowledge of Liquide chromatography Operations. 🧪 Skills & Competencies Good understanding of Production procedures. Good Understating of GMP & Safety Good communication and teamwork skills. ✅ Preferred Experience Prior experience in regulated environments (USFDA, WHO-GMP, etc.) Exposure to API manufacturing in pharma. 💼 What We Offer Competitive salary. Opportunity to work in a world-class API facility Training and career development programs Safe and inclusive work environment Qualifications The ideal candidate will have: Education: M.Sc./ Diploma (Chemistry) or B.E. / B.Tech. in Chemical Engineering. Experience: Minimum 4 years of experience. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description We’re looking for a dynamic Manager – MS&T (Manufacturing Science & Technology) with deep expertise in Chemical Engineering and CDMO operations . If you thrive in high-impact, cross-functional environments and can lead Process Engineering calculations, Technology Transfer, project delivery, and regulatory compliance with precision, this opportunity in Gajraula, UP is for you. Key Responsibilities: Performs technical evaluations of incoming RFPs and existing program extensions across capabilities including proposed scope of work, costing, timelines, and budgets with limited guidance from more senior level technical Evaluations Specialists and Management. Ensure project delivery as per plan and QA norms Provide technical guidance and lead project reviews. Ensure and regularly review compliance with all statutory, legal, environmental, licensing, regulatory, and safety norms and fulfill commitments to regulatory agencies, customers, and quality management Complete technical evaluation into appropriate cost model and proposal templates for proposal generation. The successful candidate will have a background in Chemical Engineering with experience in a relevant pharmaceutical or CDMO industry Assesses with Operations and Management and recommends capabilities to meet Client requirements as part of technical evaluations. Represents technical operations in front of Client in support of project acquisition with Sales & Business Development, Project Management, and/or Partnership Management. Attends Client site visits, presentations for new, and extension of existing opportunities. Ensuring that equipment works to its specification and to appropriate capacities of products Contribute novel ideas by way of participation during technical discussion with superiors/ Colleagues Preparation of Capex Proposals (Concept notes, Savings/Payback calculations) for purchase of new Process Intensification technologies, co-ordination with cross functional teams for purchase, installation and commissioning related activities Knowledge to use process modelling tools like Dyno Chem ,VISMIX for reaction, crystallization, filtration, solubility and mixing studies Study the process and recycling of solvents, performing experiments in PD Lab, generating data, proposing changes/modifications in recovery processes and establishing recovery process for new solvent streams for target improvement in the solvent recovery. Person will have demonstrated expertise in the scale-up and process understanding of chemical process unit operations in the manufacture of APIs, intermediates and raw materials. Experience in Quality by Design, process safety, technology transfer and commercial production would be advantageous. In-depth, hands-on expertise and up-to-date knowledge of a wide range of chemistry unit operations such as reactions, distillation, separation, filtration and drying. Strong scientific record of accomplishment, ability to handle several projects in different stages of development at the same time. Person will be responsible to Investigate and troubleshoot in case of issues in scale up/validation and support troubleshooting activities in case of issues in scale up/validation batches Key Attributes: Excellent communication skills to interact internally with project teams and externally with customers Good understanding on CDMO business, RFP preparations in stretched timelines Good project management and supervisory skills. Collaboration and influencing skills to build partnerships with the other disciplines, similar groups, Conscientious with a can-do attitude and thorough attention to detail. Experience in working to GMP & FDA adherence Qualifications The ideal candidate will have: Qualification: B. Tech/ M. Tech Chemical Experience: 12 to 15 Years Key Skills: Good understanding of CDMO Business, Equipment mapping, RFP preparation, CFT alignment & Collaboration, Process Engineering calculations, Technology Transfer, knowledge of FDA regulations/ ICH guideline, OH cost calculations. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!