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Nivagen Pharma (india)

7 Job openings at Nivagen Pharma (india)
Trainee - Supply Chain Management Ahmedabad 0 - 1 years INR 0.5 - 3.0 Lacs P.A. Work from Office Full Time

We are looking for a dedicated team player to support our Supply Chain. It is a fast-paced work environment with many opportunities for career growth. Job Title : Trainee Supply Chain Management Job Location : Satellite, Ahmedabad Reporting: Manager, Supply chain Job Responsibilities. - Closely work with Logistics team to ensure smooth process. - Work on Inventory data for optimized planning - Co-ordinating with Sales and Marketing team for forecast - Co-ordinating with CMO and suppliers for Product Planning and dispatch planning - Use of Ms office as well as SAP to track planning and ensure data management. - Track manufacturing status of given planning - Track Purchase orders to make sure timely delivery of the products. - Identify, manage, and minimise the risks (for example operational or reputational) that could affect or interrupt the supply chain - Planning and implementing strategies and initiatives to ensure continuous improvement in both service and transit time performance - Liaise and coordinate with internal and external parties to ensure smooth and timely execution of shipments. Liaising with suppliers. - Ensure Complete track of Product planning. Requirements: - Masters degree (Preferred MBA) from an accredited university in Supply chain/Finance/Pharma. - Fresher Preferred Female candidate - Strong communication skills; ability to appropriately involve others in consultations and decisions. - Strong relationship building, networking, interpersonal and communication skills. - High degree of initiative, credibility, independence, integrity, confidentiality, and trust. Fluent in English (Speaking, writing & reading) is must

Apprentice Trainee Ahmedabad 1 - 2 years INR 1.75 - 2.0 Lacs P.A. Work from Office Full Time

Urgent Requirement Apprentice Trainee (Project Base Work) Designation apprentice Department - Finance Company - Pharmacist Company Location - Satellite, Ahmedabad KEY ACCOUNTABILITIES Accountabilities Key Performance Indicators Knowledge of Day to day Accounting, Cash & Bank entry, Sales Entry Knowledge of Book Keeping Knowledge of Debit Memo/ Credit memo. Invoice Processing Knowledge of Passing Entries in Software SKILLS AND KNOWLEDGE Bachelor's degree in any subject (Preference in Commerce) Additional Finance certification will be an advantage 1-2 years work experience in Accounts & Commercial (Finance) TECHNICAL SKILLS Knowledge and experience of SAP ERP system & MS Office Knowledge Understanding of accounting systems and processes Understanding of the AR collection (cash application) process Personal skills and attributes INTEGRITY AND TRUST Effective communication with ability to build successful teams Good written/oral communication skills. Ready to Work any time

Accounts Officer Ahmedabad 2 - 5 years INR 2.5 - 3.5 Lacs P.A. Work from Office Full Time

Accounts Officer- Experience 2-5 years in Accounts & Finance Processing Sales Order Processing Invoices Passing Remittance entries Remittance Knock off Preparing Sales Report Weekly Monthly Yearly Follow up with Customers for Collection Customer Ledger Reconciliation Pharma Industry knowledge is advantage SAP B1 , MS Excel Knowledge is must

Accounts Sr. Officer Ahmedabad 5 - 7 years INR 3.0 - 4.5 Lacs P.A. Work from Office Full Time

Accounts Sr. Officer: Experience 5-7 years in Finance Order & Invoice Processing Credit Memo& Debit memo Knowledge Aware of Sales Return Customer Ledger Reconciliation Knowledge of Profit sharing with Customer Pharma Industry knowledge is advantage for this candidate SAP B1 , MS Excel Knowledge is must

It Manager Ahmedabad 10 - 15 years INR 6.0 - 10.0 Lacs P.A. Remote Full Time

IT Manager General Summary: The Cloud & Security Engineer will work remotely from India, supporting our infrastructure, cloud environment, and cybersecurity posture. This senior-level role will collaborate directly with the Systems Administrator II, contributing to network and system security, Azure administration, automation, and compliance initiatives. This position requires working standard U.S. Pacific Time (PST) hours. Key Responsibilities: Administer and secure Microsoft Azure infrastructure and related services Manage firewalls, servers, and network configuration Support identity and access management using Azure AD and Entra ID Ensure systems are compliant with applicable frameworks (e.g., NIST, HIPAA, 21 CFR Part 11, etc) Develop and maintain IT documentation and SOPs for cloud and security operations Monitor logs, alerts, and events for signs of potential threats Respond to incidents and perform root cause analysis Automate operational tasks with PowerShell or other scripting tools Collaborate on IT strategy and infrastructure improvements Qualifications: 10+ years of experience in IT infrastructure, cloud, and cybersecurity roles Must be fluent in English, written and verbal Strong hands-on experience with Microsoft Azure and security tools Understanding of compliance frameworks and risk management Proficiency in scripting and automation Excellent written and verbal communication skills Must be available to work during U.S. Pacific Time (PST) hours Ideal Certs Azure Administrator Associate Azure Security Engineer Associate CCNA

Executive / Officer ahmedabad 1 - 5 years INR 5.0 - 10.0 Lacs P.A. Work from Office Full Time

Job description for Executive / Officer - Regulatory Affairs Department (USA market) Location: Nivagen Pharma (INDIA) Pvt. Ltd., Satellite, Ahmedabad, INDIA Report to : Manager, Regulatory Affairs, Nivagen Pharmaceuticals Job Description: 1. Compilation of various applications like CC / CGT / iPSP / PIND packages. 2. The planning, writing and review of all regulatory submissions to support PIND/IND/NDA/505(b)2/ANDA/PAS submissions including FDA meeting requests and technical DS, DP and Clinical packages. 3. Compilation and review of Labeling and SPLs for NDA/ANDA/PAS applications. 4. Review and compilation of DMF sections for NDA/ANDA/PAS filing. 5. Ensures that project timelines are developed and communicated; evaluates changes to maintain submission goals and timelines; communicates any delays along with the rationale. 6. Updates of status and trackers of Regulatory submission. Candidate Profile: 1. Minimum of M.Pharm./M.Sc./Ph.D. with 1 to 5 years experience in the pharmaceutical industry, with at least USFDA working experience. 2. Strong analytical skills; Operational activities and product launches in generics. 3. Cross-functional collaboration skills with the ability to network with different functional areas and integrate cross-functional deliverables. 4. Sterile injectable and Solid Oral Dosage form registration experience candidates are required. 5. Proficiency in eCTD software, SPL, MS Office & MS Project. 6. Strong oral interpersonal and written communications skills.

Assistant Manager / Sr. Executive ahmedabad 5 - 10 years INR 15.0 - 30.0 Lacs P.A. Work from Office Full Time

Job description for Asst. Manager/Sr. Executive - Regulatory Affairs Department (USA market) Location: Nivagen Pharma (INDIA) Pvt. Ltd., Satellite, Ahmedabad, INDIA Report to : Manager, Regulatory Affairs, Nivagen Pharmaceuticals Job Description: 1. Develops and implements submission strategies for PIND, 505(b)(2); NDAs; ANDA. 2. Leads and ensures implementation of the planning, writing and review of all regulatory submissions to support PIND/IND/NDA/505(b)2; ANDA submissions including FDA meeting requests and packages. 3. Critically reviews and approves documentation from clinical development, non-clinical development, iPSP, Research and Development (R&D), Quality, Technical Operations, Labeling and other appropriate departments, internal and stakeholders, vendors and consultants. 4. Ensures that project timelines are developed and communicated; evaluates changes to maintain submission goals and timelines; communicates any delays along with the rationale. 5. Interprets regulations and guidance documents and provides strong regulatory leadership to project teams to ensure regulatory success. Candidate Profile: 1. Minimum of M.Pharm./M.Sc./Ph.D. with 5 to 10 years experience in the pharmaceutical industry, with at least USFDA working experience. 2. Strong analytical skills and business acumen specific to operational activities and product launches in generics. 3. Cross-functional collaboration skills with the ability to network with different functional areas and integrate cross-functional deliverables. 4. Sterile injectable and Solid Oral Dosage form registration experience candidates are required. 5. Proficiency in eCTD software, SPL, MS Office, MS Project. 6. Strong oral interpersonal and written communications skills.