We are seeking highly motivated MEP Design Engineers (Mechanical/Electrical) to join our pharmaceutical project team. The ideal candidate will be responsible for designing layouts and drawings using AUTOCAD and REVIT software in compliance with WHO-GMP , EU-GMP , and USFDA guidelines. This role also involves coordinating with various stakeholders and executing turnkey pharmaceutical projects, both locally and internationally. Key Responsibilities: Assist in the conceptual design and execution of pharmaceutical projects as per WHO/cGMP norms . Prepare layouts and drawings in AUTOCAD/REVIT software under senior supervision. Participate in site visits (local & overseas) to assess site conditions and support design verification. Coordinate with internal teams, vendors, and clients for design data and approvals. Prepare equipment lists and bill of quantities (BOQ) as per project requirements. Support documentation work like URS, FAT, checklists, SOPs under guidance. Develop 3D layouts in REVIT software for client presentations. Learn and assist in preparing validation documents like DQ, IQ, OQ, PQ . Qualifications & Skills: Bachelor’s / Diploma in Mechanical or Electrical Engineering . Basic to advanced proficiency in AUTOCAD and REVIT . Good communication and interpersonal skills. Ability to work independently or as part of a team. Willingness to travel locally and internationally for project assignments. Proactive, self-motivated, with effective time management skills. Send your updated CV to: hrm@sushenmed.com/hrm2@sushenmed.com Subject Line: Application for MEP Design Engineer – [Fresher/Experienced] Show more Show less
About the Role: We are seeking a dedicated Production Officer/Executive with experience in pharmaceutical manufacturing to join our team. The ideal candidate will ensure smooth production operations, compliance with cGMP standards, and timely delivery of quality products. Key Responsibilities: Production Planning and Scheduling Assist in creating and managing daily and weekly production schedules for OSD manufacturing to ensure timely execution of batch orders. Monitor production progress and adjust timelines as required based on operational priorities or customer requirements. Resource Management and Stock Control Ensure availability of required raw materials, packaging materials, and equipment for planned production. Quality Standards and Compliance Ensure adherence to cGMP, GDP, and internal SOPs during all stages of production. Support in maintaining product quality standards as per specifications and regulatory requirements. Assist in implementing in-process checks and quality monitoring during manufacturing. Production Process Monitoring Supervise and monitor OSD manufacturing processes such as granulation, compression, coating, and packing. Identify bottlenecks and take corrective actions to ensure smooth workflow and improved efficiency. Cross-Functional Coordination Collaborate with QA, QC, Maintenance, and Supply Chain teams to ensure uninterrupted operations. Support in resolving issues impacting production timelines or quality. Health and Safety Compliance Ensure compliance with health, safety, and environmental guidelines in the production area. Promote safe work practices and report unsafe conditions promptly. Customer Order Fulfillment Ensure production is aligned with customer delivery schedules and quality expectations. Coordinate with logistics to support timely dispatch of finished products. QMS Activities Participate in Quality Management System (QMS) activities, including documentation, deviation handling, and CAPA implementation. Support in preparation for internal and external audits and regulatory inspections. Requirements: B.Pharm / M.Pharm / B.Sc / M.Sc. 1–5 years’ experience in pharmaceutical production. Knowledge of cGMP, documentation, and regulatory requirements. Strong problem-solving, communication, and teamwork skills.
📝 Job Summary We are seeking a detail-oriented and skilled Machine Operator to join our pharmaceutical manufacturing team. The ideal candidate will be responsible for operating, monitoring, and maintaining production machinery to ensure the efficient and compliant manufacturing of pharmaceutical products. This role requires adherence to GMP standards and Standard Operating Procedures (SOPs) to maintain product quality and safety. 🔧 Key Responsibilities Machine Operation : Set up, operate, and monitor pharmaceutical manufacturing equipment, such as tablet presses, capsule fillers, and packaging machines, ensuring optimal performance and minimal downtime. Process Monitoring : Continuously observe production processes, making necessary adjustments to maintain product quality and consistency. Maintenance : Perform routine maintenance and cleaning of equipment, promptly reporting any malfunctions or irregularities to the maintenance team. Quality Assurance : Conduct in-process quality checks and inspections to ensure products meet specified standards, documenting results accurately. Compliance : Strictly adhere to GMP, SOPs, and safety protocols to ensure compliance with regulatory requirements. Documentation : Maintain accurate and detailed records of production activities, including batch records, equipment logs, and maintenance reports. Collaboration : Work closely with cross-functional teams, including Quality Control and Maintenance, to resolve issues and improve processes. 🎓 Qualifications Education : ITI Diploma or related field. Experience : Minimum of 1-2 years of experience operating machinery in a pharmaceutical or regulated manufacturing environment. Technical Skills : Proficiency in operating and troubleshooting manufacturing equipment; familiarity with GMP and SOPs. 🧰 Preferred Skills Experience with specific pharmaceutical equipment such as granulators, blenders, or coating machines. Knowledge of cleanroom procedures and contamination control. Ability to interpret technical documents. 📩 Application Process Interested candidates should send their resume : careers@sushenmed.com
Objective: To enhance brand visibility, strengthen outreach, and support ongoing marketing and business development initiatives across Sushen Medicamentos and its New Ventures . Role Overview: A dedicated Marketing / Business Development professional responsible for managing digital visibility, creating marketing assets, and driving outreach and growth initiatives across all verticals. Key Responsibilities: Marketing Assets Development: Create brochures, product flyers, and comprehensive product booklets with key information for customer engagement. Develop marketing content for internal and external use. Outreach & Events: Execute targeted cold-email campaigns in key markets to generate leads and partnerships. Support participation in industry events and organize promotional activities for marketing, early adopters, and beta testing. Market Research: Conduct in-depth market research and prepare reports on new markets, competitors, and product opportunities. Pitch Deck Optimization: Refine and update investor and customer presentations to ensure consistency, clarity, and impact. New Venture Support: Assist in scaling new initiatives, partnerships, and go-to-market efforts under Healta and QuadAssure . Content & Visibility: Manage social media and digital campaigns, publish marketing content, and run newsletters aimed at improving brand visibility and SEO. Note: This is a dynamic, startup-style role—flexibility and initiative beyond defined responsibilities are expected to drive company growth. Desired Profile: Creative, entrepreneurial, and driven individual with a passion for healthcare innovation, digital engagement, and business growth. Candidate Type & Compensation: Recent Graduates / Open to interns (final-year students or recent graduates). Only requirement is to have the passion to bring change. flexible for the right candidate.