Drug Regulatory Affairs - Chandigarh

We're looking for a driven Regulatory Affairs leader to help shape and expand pharmaceutical products across India and global markets. · We are hiring a Regulatory Affairs Manager / Senior Regulatory Affairs Executive who will play a critical role in product development, registra ...

We're looking for a driven Regulatory Affairs leader to help shape and expand pharmaceutical products across India and global markets.As a key member of our regulatory team, you will play a critical role in product development, registration, and lifecycle management across multip ...

We are seeking a detail-oriented and experienced Drug Regulatory Affairs professional to manage and support regulatory submissions, approvals, and lifecycle maintenance for pharmaceutical products. · Prepare, review, and submit regulatory dossiers for pharmaceuticals,Mange regula ...

This role is for one of the Weekday's clients. We are seeking a detail-oriented and experienced Drug Regulatory Affairs professional to manage and support regulatory submissions, approvals, and lifecycle maintenance for pharmaceutical products. · ...

Regulatory affairs manager for pharmaceutical industry. Responsibilities: · Prepare regulatory dossiers for product registration and variations. · ...

Everva Lifecare is seeking a proactive Regulatory Affairs Executive to handle product registrations and regulatory compliance for pharmaceutical products across international markets. · ...

We are looking for a detail-oriented Regulatory Affairs Executive to ensure compliance with FSSAI and other regulations for our nutraceutical ingredients portfolio in India. · ...

This is a full-time on-site role for a Quality Head at Sysmed Medical Technologies headquartered at Chandigarh and having manufacturing plant at Nabha Punjab under make in India project. · ...

This is a full-time on-site role for a Quality Head at Sysmed Medical Technologies (sister concern of Sysmed Exim Private Limited) headquartered at Chandigarh and having manufacturing plant at Nabha Punjab under make in India project. · ...

The Regulatory Affairs Manager will prepare and submit dossiers for product registrations in various markets, coordinate with internal departments to compile technical documentation, liaise with regulatory authorities and consultants to facilitate approvals. · $ensure$compliance; ...

Evaluate the feasibility of new products and verify their Recommended Dietary Allowance (RDA) values in accordance with FSSAI standards. · ...

We are looking for a skilled and motivated Senior Executive Drug Regulatory Affairs to support the registration and maintenance of injectable pharmaceutical products across ROW markets. The ideal candidate will have experience in compiling and submitting dossiers in accordance wi ...

This is to inform you regarding the post of Drug Regulatory Affairs Specialist at our organization. The candidate should have minimum 7 years of experience in pharmaceutical industry. · The Responsibilities include Compile review and submit high-quality regulatory dossiers for ne ...

Manage regulatory affairs in Japan Korea China US. · ...

Lead UK and EU food supplement regulatory compliance including labelling claims dossiers and authority submissions ensure end to end approval readiness hands on experience with UK/EU frameworks mandatory India based role. · ...

We are Hiring Walk - in Interview Drive - Theon Pharmaceutical Ltd. · We are hiring drug regulatory affairs executive for our company. ...

B.Pharm job description varies by role but generally involves ensuring safe, effective and compliant medication use from dispensing in pharmacies/hospitals to developing new drugs overseeing production managing clinical trials and handling regulatory compliance in the pharmaceuti ...

We are seeking a highly skilled Regulatory Manager to join our team. The successful candidate will have a strong understanding of global regulatory requirements and experience in preparation and review of regulatory dossiers. · ...

Assist in managing the technology transfer process for new products and processes from R&D to commercial production. · ...

The Regulatory Manager will be responsible for preparing, reviewing and submitting regulatory dossiers to the Food and Drug Administration (FDA) and other global authorities. The role requires strong understanding of the Indian pharma market and licensing processes. · ...