Regulatory Affairs Coordinator Otsuka Pharmaceutical India

3.0 - 5.0 years

3 - 5 Lacs

ahmedabad

Work from Office

Job Responsibilities: Dossier preparation/review as per country specific guideline/CTD guideline Timely query response submission to Distributor/ MOH Review of documents for its correctness and compliance with respective regulatory guidelines (as per country requirement) Preparation, review & release of artworks & sales order as per country approval Variation documents preparation and filing as per country requirements Timely dispatch of tender documents to country/parties as per deadline Candidate profile Should be able to review & interpret the requirement as per country specific/ tender guideline/Query received from MOH Should be able to review various plant documents for dossier preparat...

Posted 3 weeks ago

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2D Spine Animator Gamix Labs

0.0 - 3.0 years

0 Lacs

noida, uttar pradesh

On-site

As a 2D Spine Animator at Gamix Labs, you will have the exciting opportunity to work on creating rich graphics games by utilizing your expertise in 2D spine animation. You will collaborate with the Art Director and 2D Artists to bring various characters, effects, and UI elements to life using tools such as Spine and After Effects. Your role will involve applying advanced animation principles like timing, staging, anticipation, squash, and stretch to produce high-quality animations. In this position, you will be responsible for providing artwork at different stages of the project for review and incorporating feedback in a timely manner. Additionally, you will work closely with the Software te...

Posted 1 month ago

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CQA Executive Meyer Organics

2.0 - 5.0 years

3 - 6 Lacs

Thane

Work from Office

ERP Management: Create and update Bill of Process (BOP) entries for in-house and loan license (LL) manufacturing sites. Generate and revise Item Master Codes for packaging materials and finished goods. Maintain ERP item master update records as per Format No. QAD-FR-89. Raw Material Specification (RMS): Prepare and revise RMS documents in line with regulatory and internal requirements. Draft RMS for product registration, including compliance with UK market norms. Finalize and issue authorized RMS for submission to regulatory bodies. Sample Coordination & Analysis: Coordinate dispatch of AVD raw material and NPD samples for lab testing. Maintain records of sent samples in Format No. QAD/FR-42...

Posted 3 months ago

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