Open Positions
For any Questions, please send an Email at: hr1@mediwinpharma.com or call us at: +91-8238810025 (Mon-Sat from 10:00 AM-6:30 PM)
Note: Mediwin Pharmaceuticals conducts all hiring processes through direct recruitment and has not engaged any third-party recruitment agencies. As such, we do not charge any fees from candidates at any stage of the recruitment process. Please be cautious of potential scams or fraudulent activities conducted by individuals or agencies falsely claiming association with our company.
Job Posting Details
Job title: Export Executive
Required Qualifications:
- Bachelors or Master’s Degree / BBA / BMS with experience in pharma export operations
- Diploma or Certification in Export–Import Management, International Trade, or Logistics (an added advantage).
- At least 2 to 3 year experience in Back office/Export.
Job Profile:
An Export Executive with 2 to 3 years of experience in a pharmaceutical company is primarily responsible for managing end-to-end export logistics and documentation, ensuring strict compliance with international trade laws and pharmaceutical regulations.
Roles & Responsibilities:
- Oversee end-to-end export documentation ensuring accuracy, compliance, and timely submission.
- Manage air and sea shipments and courier export/import operations, coordinating with airlines, freight forwarders, and logistics partners.
- Coordinate with the logistics team to arrange transportation and track shipments to ensure on-time delivery and resolve any issues or delays.
- Coordinate with CHA and Clearing & Forwarding agents for smooth customs clearance and shipment processing.
- Prepare and submit license applications, technical assistance agreements and other request for license and approval to the State Department and Commerce Department.
- Track all outbound and inbound shipments, maintaining complete and up-to-date documentation to support export incentives and statutory requirements.
- Prepare and present periodic MIS reports to the Head of Export, highlighting shipment status, documentation performance, and process improvements.
- Perform other duties as assigned
Candidate Profile / Skill required:
- Strong knowledge of pharma export regulations, including WHO, EU and country-specific requirements for formulations.
- Good understanding of shipping regulations, international trade policies, and documentation standards for pharmaceutical products.
- Hands-on experience with customs regulations, customs clearance procedures, and coordination with CHA/C&F agents (Preferred).
- 2–3 years of proven experience in pharma import–export operations, logistics coordination, air freight handling, and courier shipments (Required).
- Ability to prepare and review pharma-specific documents such as COA, MSDS, COO, AWB, packing lists, batch documents, and compliance certificates.
- Strong command of English with excellent verbal and written communication skills for interaction with customers, agents, and regulatory teams.
- Proficiency in MS Word, Excel, and email communication platforms; familiarity with ERP systems (Pharma cloud) is an advantage.
- Excellent organizational, time-management, and multitasking skills, with the ability to handle high-volume shipments and tight timelines.
- Strong attention to detail and accuracy in documentation to ensure compliance with pharma regulatory and export standards.
Job Posting Details
Job title: Quality Control Executive
Required Qualifications:
- Masters of Science “M.Sc” (Chemistry) or B.Pharm degree.
- A minimum of 4-5 years related experience in QC pharmaceutical manufacturing company.
Job Profile:
A Quality Control Officer is a professional who is Responsible for the Raw materials. in process and finished product and also stabling samples analysis and had knowledge of handling instruments like HPLC , UV-visible spectrophotometer , Dissolution Apparatus, pH meter , viscometer , KF, Polarimeter , Refractometer, Friabilator, D.T. Apparatus etc.
Roles & Responsibilities:
Responsible for in-process and finished product analysis and also analysis of stability samples. Handling instrument like HPLC, UV-visible spectrophotometer, Dissolution Apparatus, pH meter, viscometer, KF, Polarimeter, Refractometer, Friabilator, D.T. Apparatus etc.
- Analysis of finished product, stability product and raw material.
- Preparation of SOP for related to instrument and system.
- Preparation of protocol, worksheet for raw material and finish product.
- Documentation like ATP, Development report, Validation protocol, Validation report, STP preparation.
- Performing sample based check, monitor transactions & provide feedback on quality.
- Sampling of Raw material, entry, packaging and labeling.
- Supporting completion of audit checklist in advance for all internal/ external audits.
- Assisting company’s external auditors for preparation of documentation for control weakness/ error remediation.
- Standardisation and Calibration of Instruments.
- Water analysis.
- Perform other duties as assigned.
Candidate Profile / Skill required:
- Knowledge of cGMP & GLP guidelines, ICH/ USFDA guidelines.
- Working knowledge of Analytical Method development and validation.
- Working knowledge of process, Reflux process, Carbon treatment, Purification process, Addition process and Separation process.
- Handling of instruments like HPLC/Spectrophotometer etc.
- In-depth understanding of company standards
- Up-to-date knowledge of federal and industry standards and best practices
- Basic computer and math skills to calibrate and measure specifications
- A keen eye for detail
- Good verbal and written Communication skills
- Proficiency in Microsoft Office
- Knowledge of pharmasuite software