Job Title: Drug Regulatory Affairs Specialist Location: Parwanoo, Himachal Pradesh (Bus Service Available from Panchkula, Pinjore, Kalka in HARYANA) Experience: 2-3 Years in Pharmaceutical Industry Job Description: We are seeking a highly motivated Drug Regulatory Affairs Specialist to join our team. The ideal candidate will have 2-3 years of experience in the pharmaceutical industry with a strong understanding of regulatory requirements and dossier compilation. The role requires close collaboration with internal teams and external clients to ensure timely submission of regulatory documents. Key Responsibilities: Compile, review, and submit high-quality regulatory dossiers (e.g., CTD, ACTD) for new product registrations, renewals, and variations. Communicate effectively with international clients to deliver necessary documents and information for dossier preparation and submission. Coordinate with internal departments (e.g., R&D, QA/QC, Production) to gather technical documents required for regulatory submissions. Maintain and update regulatory databases, records, and documentation for ongoing projects. Monitor changes in regulatory guidelines and ensure adherence to current regulations. Support product registrations, renewals, and variations across different markets. Liaise with regulatory agencies and respond to their queries in a timely manner. Qualifications and Skills: Bachelor's degree in Pharmacy, Life Sciences, or a related field. A Master's degree is a plus. 2-3 years of experience in a Drug Regulatory Affairs role within the pharmaceutical industry. Expertise in dossier compilation (CTD, ACTD format). Strong knowledge of global regulatory requirements (FDA, WHO, etc.). Excellent communication skills to interact with clients and internal teams. Attention to detail and the ability to handle multiple projects simultaneously. Proficiency in Microsoft Office and regulatory submission software. Please submit your application here or email your resume to hr.unit2@hanuchemlabs.com with the subject line "Regulatory." Show more Show less

Job Title: Drug Regulatory Affairs Specialist Location: Ghaziabad, Delhi NCR Experience: 3-5 Years in Pharmaceutical Industry Job Description: We are seeking a highly motivated Drug Regulatory Affairs Specialist to join our team. The ideal candidate will have 3-5 years of experience in the pharmaceutical industry with a strong understanding of regulatory requirements and dossier compilation. The role requires close collaboration with internal teams and external clients to ensure timely submission of regulatory documents. Key Responsibilities: Compile, review, and submit high-quality regulatory dossiers (e.g., CTD, ACTD) for new product registrations, renewals, and variations. Communicate effectively with international clients to deliver necessary documents and information for dossier preparation and submission. Coordinate with internal departments (e.g., R&D, QA/QC, Production) to gather technical documents required for regulatory submissions. Maintain and update regulatory databases, records, and documentation for ongoing projects. Monitor changes in regulatory guidelines and ensure adherence to current regulations. Support product registrations, renewals, and variations across different markets. Liaise with regulatory agencies and respond to their queries in a timely manner. Qualifications and Skills: Bachelor's degree in Pharmacy, Life Sciences, or a related field. A Master's degree is a plus. 3-5 years of experience in a Drug Regulatory Affairs role within the pharmaceutical industry. Expertise in dossier compilation (CTD, ACTD format). Strong knowledge of global regulatory requirements (FDA, WHO, etc.). Excellent communication skills to interact with clients and internal teams. Attention to detail and the ability to handle multiple projects simultaneously. Proficiency in Microsoft Office and regulatory submission software. Please submit your application here or email your resume to hr.unit2@hanuchemlabs.com with the subject line "Regulatory." Show more Show less

Job Title: Accounting Executive Location: Baddi, Himachal Pradesh (Bus Service Available) Experience: 2-3 Years in Pharmaceutical Industry Job Summary: We are looking for a versatile professional to manage accounts, store inventory, and HR tasks. Key Responsibilities: Maintain daily accounts (vouchers, ledgers, bank reconciliation). Manage store GRNs, material receipts/issues, and stock records. Handle HR tasks: attendance, leaves, onboarding, and basic payroll. Qualifications: Graduate (B.Com/BBA) with 2–4 years of experience. Proficiency in Marg/Tally/Excel and basic HR practices. Strong organizational and communication skills. Please submit your application here or email your resume to hr.unit2@hanuchemlabs.com with the subject line "Baddi Accounts" Show more Show less

Job Title: Production Officer Location: Parwanoo, Himachal Pradesh (Bus Service Available from Panchkula, Pinjore, Kalka in HARYANA) Experience: 2-3 Years in Pharmaceutical Industry Job Summary: We are seeking a Production Officer with 2–5 years of experience in sterile manufacturing (eye drops/sterile liquids) to oversee day-to-day production activities, ensure documentation, and maintain cGMP compliance. Key Responsibilities: Supervise and manage eye drop production processes, including filling operations. Ensure proper filling documentation (batch records, in-process checks, line clearance records, yield calculations). Adhere to cleanroom and cGMP standards during manufacturing. Troubleshoot production issues and coordinate with QA/QC teams. Train staff on procedures and ensure safety and compliance in the manufacturing area. Qualifications: B.Pharm / M.Pharm / B.Sc in Chemistry or related field. Experience in ophthalmic dosage form manufacturing is preferable Strong understanding of aseptic techniques, documentation practices, and cGMP. Good documentation and communication skills. Please submit your application here or email your resume to hr.unit2@hanuchemlabs.com with the subject line "Production" Show more Show less