8 Manufacturing Feasibility Jobs

As a Food Technologist at Apple Edibles and Logistics Pvt Ltd., you will be responsible for innovating new products for tiffin snacks and meals catering to children aged 3 - 12 years old. Your passion for developing food products for kids and commitment to delivering fun experiences for them will be key in this role. You will work at our in-house kitchen and lead R&D events alongside food technicians and process technologists to design new dishes and food products aligning with consumer trends and market demands. Key Responsibilities: - Product Creation: Develop new snack recipes and products like snack bars, chips, and crackers that cater to consumer preferences for healthier and more convenient options. - Manufacturing Feasibility: Ensure efficient production of developed recipes from the kitchen to the shelf while maintaining cost-effectiveness and product quality. - Regulatory Compliance: Ensure all new products comply with local and international food safety regulations. - Market Awareness: Stay updated on consumer trends to inform product development decisions. - Collaboration: Work closely with food technologists to ensure recipes align with factory processes and meet quality standards. - Sensory and Taste Panels: Refine product recipes based on feedback from sensory and taste panels to meet consumer preferences. - Innovation: Integrate innovative ingredients and packaging solutions to enhance product appeal and sustainability. - Quality Assurances: Ensure compliance with food safety regulations and industry standards throughout the factory development process. Skills and Qualifications: - Experience in food sciences with practical experience in food development. - Education: PHD or degree in food technology, culinary arts, or related field. - Skills: Creative and innovative thinking, understanding of ingredients and nutrition, knowledge of FSSAI and food safety regulations, and computer literacy. Location: Mumbai The compensation for this role is as per industry standards and negotiable.,

Job Description: 1. Understanding the brand&aposs design-aesthetic - help build differentiate product Designs (segment and price-specific range, collections, etc.,) 2. Create detailed hand-drawn designs for jewellery pieces. 3. Prepare sketches and illustrations for approval. 4. Developing a comprehensive understanding of product trends 5. Create bespoke designs specific to their needs 6. Proposing design stories and ideas 7. Research work and Design trend forecasts 8. Proficiency in Sketch Making Skills and Requirements: Proven experience in designing high-end fine jewellery, with a strong understanding of luxury aesthetics, craftsmanship, and precious materials. Proficiency in hand sketching and translating creative ideas into detailed design concepts. Working knowledge of Rhino and AutoCAD is an added advantage. Familiarity with digital sketching tools such as Procreate is preferable. Strong understanding of gemstones, settings, and manufacturing feasibility is a plus. Ability to interpret client briefs and create bespoke, one-of-a-kind designs. Show more Show less

You will be responsible for reviewing drawings to ensure manufacturing feasibility in sheet metal fabrication and product assembly processes. This includes initiating the necessary facilities for new or modified processes, conducting trials with the Cross-Functional Team (CFT), and ensuring the timely implementation of engineering changes. Your role will also involve identifying and implementing process improvements to enhance efficiency and quality.,

Position Title: Manager Formulation & Development – Tech Transfer Department: Formulation & Development Location: Vadodara Reports To: Job Overview: The Manager – Formulation & Development will oversee the successful transition of products from development (R&D or other manufacturing sites) to commercial manufacturing. This role requires in-depth expertise in technology transfer, quality control, scale-up processes, and regulatory compliance, ensuring seamless manufacturing operations and product quality. Key Responsibilities: Review of Technology Transfer Dossier (TTD): Conduct detailed reviews of TTDs to ensure accuracy, completeness, and alignment with manufacturing capabilities. Assess process flow, raw material specifications, equipment needs, and facility requirements. Evaluate scalability and identify bottlenecks or challenges in transitioning from lab scale to full-scale production. Assessment of Manufacturing Feasibility: Analyse the feasibility of transferring technologies to manufacturing, including processes, equipment, and facilities. Mitigate potential issues related to scale-up and manufacturing variability. Ensure reproducibility of the process in a commercial manufacturing environment while maintaining product quality. Collaboration with Cross-functional Teams: Partner with R&D, Regulatory Affairs, Quality Assurance, and Production teams to streamline the technology transfer process. Act as a bridge between development and manufacturing teams, addressing concerns and optimizing processes. Participate in and facilitate meetings to review progress and provide actionable feedback. Evaluation of Process Validation Plans: Review process validation strategies, protocols, and acceptance criteria. Ensure validations align with manufacturing capacity and regulatory requirements. Assess results of process qualification and validation batches to guarantee robustness. Risk Assessment and Mitigation: Conduct risk assessments to identify critical control points, potential failure modes, and quality risks. Develop and implement quality control measures in collaboration with the quality team. Propose process, equipment, or material modifications to enhance manufacturability and reduce costs or risks. Compliance and Documentation: Ensure adherence to local and international regulatory requirements (e.g., FDA, EMA, ICH). Review TTD documentation for regulatory alignment and maintain accurate records for inspections. Troubleshooting and Problem Solving: Provide technical support during initial manufacturing runs and address product or process issues. Identify gaps or inconsistencies in the process and implement corrective actions. Continuous Improvement: Recommend improvements based on TTD reviews and manufacturing performance. Identify opportunities to enhance efficiency, cost-effectiveness, and product quality. Key Skills: Technical Skills: Expertise in manufacturing processes, equipment, and scale-up principles. Knowledge of analytical techniques and quality control measures. Ability to interpret complex technical documents and implement actionable manufacturing strategies. Soft Skills: Strong communication and interpersonal skills for effective cross-functional collaboration. Problem-solving skills to address complex manufacturing challenges. Analytical thinking and attention to detail. Qualifications & Experience: Education: Master's degree in Pharmaceuticals (M. Pharm) or equivalent. Experience: 10-15 years of experience in manufacturing, product development, and technology transfer. Proven ability to lead and manage a team of approximately 10 members. Skills: Deep knowledge of GMP, process validation, and regulatory standards. Strong leadership abilities and a proactive approach to process optimization.

You are invited to join OSC Atelier, a renowned High Jewellery Atelier in Mumbai, as a Senior CAD Jewellery Designer. With a focus on exceptional craftsmanship and couture design, we are seeking an individual with at least 10 years of experience in CAD jewellery designing. Your expertise should include fine and high jewellery CAD modeling with precision, proportion, and technical accuracy. A strong understanding of manufacturing feasibility and gemstone setting styles is essential for this role. At OSC Atelier, you will have the opportunity to work on exclusive high jewellery creations tailored for global luxury clients. We value design innovation, luxury aesthetics, and craftsmanship. This position offers the chance to explore creative and technical boundaries while contributing to a dedicated atelier that upholds trust, artistry, and design excellence. If you possess the required experience, creativity, and dedication to shape the future of high jewellery, we encourage you to apply now or reach out to us directly to explore this exciting opportunity further.,

???? Were Hiring: Senior CAD Jewellery Designer ???? Location: Mumbai | Work Mode: On-Site Only OSC Atelier a High Jewellery Atelier known for exceptional craftsmanship and couture design is seeking an experienced Senior CAD Jewellery Designer to join our creative team. Requirements: 10+ years of proven experience in CAD jewellery designing Expertise in fine and high jewellery CAD modeling (precision, proportion, technical accuracy) Strong understanding of manufacturing feasibility and gemstone setting styles Passion for design innovation, luxury aesthetics, and craftsmanship Why OSC Atelier At OSC, youll work onexclusive high jewellery creations crafted for global luxury clients. This role offers the chance to push creative and technical boundaries while being part of a dedicated atelier that values trust, artistry, and design excellence . ???? If you have the experience, creativity, and dedication to shape the future of high jewellery with us, apply now or DM us to connect. Show more Show less

As a Sourcing & Development Engineer at TVS Motor Company, your primary responsibility will be to ensure the development of parts and purchasing activities to meet the QCDD targets and achieve business goals. You will work within the CP department, specifically in the Super Premium & Co-Operation projects section located at the Hosur Plant in Tamil Nadu. Your role involves understanding, aligning, and finalizing requirements for parts between TVS and suppliers, including SRS, design validation, part level validation, and testing after SOP according to AOI/AOT standards. You will also need to comprehend EV related standards such as functional safety per ISO 26262, EMI/EMC, software development procedures like ASPICE, and country-specific homologation, and translate them into part level specifications. Additionally, you will be responsible for preparing manufacturing feasibility and APQP with suppliers, estimating costs for tooling development efforts and part levels, negotiating with suppliers, and overseeing the development of parts from Alpha to SOP for BO parts as per agreed build-wise product maturity requirements. You will also be involved in initiating and completing PO/SA release for CBU/CKD/Imports/Spares, mapping and implementing traceability requirements, and conducting packing sign off activities with suppliers, especially for EV products like ESD packing. Your role will also require you to prepare analysis, identify root causes, develop solutions, and implement them from Stage 30 to 90 using the PQM Methodology. You will need to obtain PPAP, SPTR audit, sign off PSW, and effect file transfer for all BO parts, as well as prepare process, timeline, and cost analysis for Gams/CR with R&D QAD/Supplier and implement them based on agreed timelines. Furthermore, you will be responsible for monitoring the validity of regulatory requirements such as IMDS, country-specific homologation requirements, QMS, EHS, OHSAS, and PCB for suppliers. It will also be part of your duties to monitor tool life through supply quantity and additional indicators like appearance issues, porosity rejections, and supplier rejection levels, and initiate tool replacement activities as necessary. Your role as a Sourcing & Development Engineer at TVS Motor Company will play a crucial part in ensuring the quality, efficiency, and success of the company's sourcing and development activities within the CP department at the Hosur Plant in Tamil Nadu.,

Job Title: Senior Design Engineer Reports to: D&D Head Job Summary: The Senior Design Engineer will lead the design and development of innovative medical devices, ensuring compliance with regulatory and industry standards. This role involves mentoring junior team members, managing complex design projects, coordinating with cross-functional departments, and preparing comprehensive design documentation for regulatory submissions. The candidate must have a strong understanding of manufacturing processes, regulatory expectations, and design control principles. Key Responsibilities: 1. Design & Product Development Lead the design and development of new products and improvements to existing devices using SolidWorks and AutoCAD. Translate clinical and market requirements into functional designs while ensuring manufacturability and cost-effectiveness. Validate engineering calculations, tolerance stack-ups, and material selection for implantable devices and surgical instruments. 2. Project Leadership Plan and execute design activities in alignment with project timelines. Coordinate design reviews, risk analysis, and design verification/validation. Collaborate with the D&D Head to define design strategy and resource allocation. 3. Mentorship & Team Development Guide and mentor Junior Design Engineers in modeling, drafting, design analysis, and documentation. Review work submitted by junior staff and provide constructive feedback. 4. Manufacturing Integration Ensure designs are optimized for manufacturing processes such as CNC machining, laser marking, anodizing, and PEEK/titanium-specific considerations. Work closely with production, quality, and supply chain teams to ensure smooth handover from design to production. 5. Regulatory & Documentation Prepare and review Design History Files (DHF), Technical Files, Risk Management Reports, and Engineering Change Requests (ECRs). Ensure all designs and documentation meet CE MDR, US FDA, and CDSCO regulatory requirements. Support audits and regulatory submissions with accurate and complete documentation. 6. Design Evaluation & Predicate Comparison Conduct design benchmarking and engineering justification reports. Compare new designs against predicate or competitive devices for clinical and functional performance. 7. Innovation & Continuous Improvement Research new design trends, technologies, and surgical techniques in arthroscopy and orthopedics. Contribute to IP development, design patents, and publications where applicable. Qualifications: Education: Bachelors or Master’s degree in Mechanical, Biomedical, or Product Design Engineering. Experience: 3–6 years of experience in medical device design, preferably with exposure to orthopedic/arthroscopic implants and instruments. Skills: Advanced proficiency in SolidWorks and AutoCAD. Strong knowledge of GD&T, DFMA, FMEA, and design verification protocols. Familiarity with regulatory frameworks (CE MDR, US FDA 21 CFR 820, ISO 13485). Hands-on experience with prototype evaluation, testing fixtures, and validation tools. Good communication, leadership, and documentation skills.