Open Jobs (Temp) | Max Corp Services

Open Jobs

Name of the Job	Last Submission Date	Number of Posts	Qualification/ Experience	Emolument & Age	Place of Posting	Nature of Duties	Application Link	General Instructions:
Pharmacovigilance Assistant	24/08/2026 (Walk-In)	12	Master’s degree in Pharmacology/ Clinical Pharmacology/ Pharmacy Practice/Clinical Research. OR Pharm.D/ MBBS/ BDS from a recognized University/Institute. Desirable: 1 year experience in drug safety/ Pharmacovigilance	32000.00 Not exceeding 28 years	National Coordination Center – Pharmacovigilance Programme of India (NCC-PvPI), Indian Pharmacopoeia Commission, Ghaziabad OR any AMC under PvPI	1. Processing of Individual Case Safety Reports (ICSRs) and managing them in VigiFlow. 2. Quality review, Clinical Review & Statistical review of ICSRs in Safety database. 3. Any other work assigned by Competent Authority from time to time.		1. Candidates appearing for the walk-in interview are required to bring two sets of their updated CV/resume, along with four recent passport-size photographs, copies of their educational qualification certificates, experience certificates, Aadhaar Card, PAN Card, UAN details, and bank account details. 2. Candidates must bring all original documents required for verification at the time of the interview. Failure to produce the original documents may result in disqualification from the selection process. 3. No TA/DA shall be admissible for attending the walk-in interview. 4. Mere fulfilment of the prescribed essential qualifications and experience does not confer any right to selection or appointment. 5. The educational qualifications and experience must be relevant to the respective post/discipline and should have been obtained from a recognized institution or organization of repute. Unless otherwise specified, experience shall be counted only after acquiring the prescribed minimum educational qualification. 6. Furnishing false, incorrect, misleading, or suppressed information at any stage of the recruitment process shall result in disqualification of the candidature. In such cases, the candidature may be cancelled at any stage, including after selection or engagement. 7. All positions are purely contractual and outsourced in nature. Engagement against any of the advertised positions shall not confer upon the selected candidates any right, claim, or entitlement, either directly or indirectly, to seek or claim regular, permanent, or contractual employment with MAX CORPORATE SERVICES, HITES and Posted Centre. The selected candidates shall not be deemed to be employees of MAX CORPORATE SERVICES, HITES and posted centre and shall have no right to claim absorption, regularization, or appointment against any post of MAX CORPORATE SERVICES, HITES or Posted centre at any time in the future. 8. The engagement will be subject to the terms and conditions prescribed by the competent authority and the service provider. 9. Candidates are advised to carefully read the detailed eligibility criteria and instructions before appearing for the walk-in interview. Note: Candidates are requested to report to the venue Indian Pharmacopoeia Commission, Sector-23, Raj Nagar, Ghaziabad between 9.00 to 10.00 AM. Latecomers will not be entertained.
Pharmacopoeial Associate Grade-1	20/08/2026	02	Essential Qualification Master's Degree in Pharmaceutical Sciences/Pharmaceutical Chemistry/Medicinal Chemistry/Pharmaceutica l Analysis/Pharmaceutical Biotechnology or equivalent from a recognized University/Institute M.Sc. in Radiochemistry/ Chemistry/Nuclear Chemistry/Medical Physics. Essential Experiences 1 year of experience in the field of radiopharmaceuticals/drugs in a recognized institution, nuclear medicine department/ cyclotron facility/ radio-pharmacy laboratory/ research organization, or pharmaceutical industry/ laboratory. Desirable Experience Experience in the preparation, quality control, validation, and regulatory aspects of diagnostic and/or therapeutic radiopharmaceuticals/ drugs. Working knowledge of analytical techniques such as HPLC, GC, gamma spectrometry, radionuclidic and Radiochemical purity testing. Knowledge of GMP, Pharmacopoeial requirements, and national and international regulatory frameworks including CDSCO, ICH, WHO, US FDA, EMA, USP, EP, and other relevant pharmacopoeias. Publications in peer-reviewed journals related to radiopharmaceuticals, nuclear medicine, radiochemistry, or pharmaceutical quality assurance. Preferred Competencies Scientific writing and technical documentation. Data analysis and interpretation. Proficiency in MS Office and scientific software. Good communication and coordination skills.	Rs. 35,000/-(PM)	Indian Pharmacopoeia Commission	Development, revision, and Upgradation of radiopharmaceutical monographs and general chapters for inclusion in the Indian Pharmacopoeia. Review of national and international guidelines, pharmacopoeial texts,and regulatory requirements. Preparation of technical reports, draft monographs, and supporting documents. Review of Scientific literature and preparation of manuscript related to radiopharmaceutical preparations. Coordination with Expert Working Groups and stakeholders. Any other work assigned related to Pharmacopoeial standard setting and radiopharmaceutical quality assurance.	https://docs.google.com/forms/d/e/1FAIpQLSeTGvTAMiVE8dobe3teGtSuEJrvMqoW7Igg6jsDNmMzLrWzIw/viewform?usp=preview
Scientific Consultant	20/08/2026	01	Essential Qualification Master's Degree in Biotechnology, Molecular Biology, Cell Biology, Genetic Engineering, Pharmaceutical Biotechnology, Life Sciences, Genomics, Pharmacy (M. Pharm), Regulatory Sciences, or equivalent from a recognized University/Institute. Essential Experience Minimum 5 years of post-qualification experience in Cell and Gene Therapy Products (CGT), Advanced Therapy Medicinal Products (ATMPs), biological products,regenerative medicine, stem cell-based products, gene therapy medicinal products, tissue-engineered products, or related areas Desirable Experience Demonstrated expertise in development/ quality assessment/ manufacturing, characterization, regulatory evaluation, or standardization of CGT/ATMP products. Experience with regulatory submissions, quality standards, and product evaluation. Thorough knowledge of international regulatory and pharmacopoeial requirements including CDSCO, WHO, US FDA, EMA, ICH, USP, European Pharmacopoeia and British Pharmacopoeia Experience in drafting pharmacopoeial monographs, general chapters, guidance documents, or regulatory standards. Publications in peer-reviewed journals related to CGT/ATMPs. Experience in leading scientific committees, expert groups, or multidisciplinary projects.	Rs. 75,000/- (PM)	Indian Pharmacopoeia Commission, Sector-23, Raj Nagar, Ghaziabad	Development of quality standards, monographs, and general chapters for Cell and Gene Therapy Products in Indian Pharmacopoeia. Provide scientific and regulatory guidance to IPC on CGT/ATMP- related activities. Review and harmonize standards with international pharmacopoeias and regulatory agencies. Coordinate with national and international experts, regulatory agencies, academia, and industry stakeholders. Facilitate training programs, workshops, and expert consultations on CGT products. Identify emerging technologies and recommend future pharmacopoeial initiatives in advanced therapies	https://docs.google.com/forms/d/14ShS9CQen9YIUxS4pufdVhfAy2GNa_ZPmDeNmg4BfSg/preview
Pharmacopoeial Associate Grade-1	20/08/2026	01	Essential Qualification Master's Degree in Biotechnology, Molecular Biology, Cell Biology, Genetic Engineering, Pharmaceutical Biotechnology, Life Sciences, Genomics, Pharmacy (M.Pharm), Regulatory Sciences, or equivalent from a recognized University/Institute. Essential Experience Minimum 1 years of experience in Cell and Gene Therapy (CGT), Advanced Therapy Medicinal Products (ATMPs), regenerative medicine, tissue engineered products, stem cell products, viral vector-based products, gene-editing technologies, or related biological products. Experience in preparation, review, or implementation of quality standards, specifications, analytical methods, regulatory dossiers, pharmacopoeial monographs, or guidelines related to CGT products. Working knowledge of national and international regulatory frameworks including CDSCO, ICH, WHO, US FDA, EMA, USP, EP, and other relevant pharmacopoeias. Experience in analytical characterization and quality evaluation of CGT products. Desirable Experience Experience in drafting pharmacopoeial monographs, general chapters, guidance documents, or regulatory standards. Experience in viral vector characterization, cell-based assays, molecular biology techniques, next-generation sequencing (NGS), flow cytometry, qPCR/ddPCR, potency assays, and sterility/mycoplasma testing. Publications, patents, or research work related to CGT products.	Rs. 35.000/- (PM)	Indian Pharmacopoe ia Commission, Sector-23, Raj Nagar, Ghaziabad	Development and revision of Indian Pharmacopoeia standards such as general requirements, monographs and general chapters related to Cell and Gene Therapy Products. Review of national and international guidelines, pharmacopoeial texts, and regulatory requirements. Coordination with Expert Working Groups and stakeholders. Scientific literature review and analysis for emerging CGT technologies. Support analytical method development, verification, and standard-setting activities.	https://docs.google.com/forms/d/1hT0gloGjFU4m0NkLlSFN1YWJyabsvEq0K3flkR1CMFo/preview