2.0 - 7.0 years

0 Lacs

vadodara, gujarat

On-site

Job Overview: As a Contracts Engineer, you will play a crucial role in overseeing the contractual aspects of EPC construction projects. Your primary responsibility will be to ensure that contracts are implemented in accordance with relevant legal frameworks, industry norms, and project specifications. Collaboration with project managers, legal teams, procurement, and other stakeholders will be essential to ensure the smooth execution of projects, while also minimizing risks and upholding contract terms. Key Responsibilities: - **Contractual Letter Drafting & Review:** Your duties will involve drafting, reviewing, and negotiating EPC contracts, subcontracts, and other relevant agreements. It will be your responsibility to ensure that the terms and conditions align with the company's objectives and meet legal standards. - **Risk Management:** You will be tasked with identifying and evaluating potential risks associated with contracts. Developing strategies to mitigate these risks and safeguard the company's interests will be a key aspect of your role. - **Dispute Resolution:** Addressing and resolving disputes or issues that may arise during the contract lifecycle will be part of your responsibilities. This may involve collaborating with legal teams or external lawyers as needed. - **Change Management:** Managing contract modifications and alterations in the scope of work will be crucial. You will need to ensure that proper documentation and approval procedures are followed for any changes. - **Compliance & Reporting:** Your role will also involve ensuring that all contracts and related documents comply with statutory regulations, industry norms, and company policies. Providing regular updates and reports to senior management regarding contract status, risks, and any emerging issues will be essential for effective communication and decision-making. Minimum Qualification: - **Graduate in Civil Engineering** Skills Required: - **Leadership Abilities** - **Analytical Skills** - **Estimations** - **Disciplinary & Grievance Procedures** If you have 2 to 7 years of experience in the field and possess the qualifications and skills mentioned above, this position as a Contracts Engineer could be an exciting opportunity for you.,

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Analyzer Technician KESHAV ENCON PRIVATE LIMITED

4.0 - 6.0 years

0 - 0 Lacs

mumbai city, mehsana

Remote

Dear All, Greetings from Keshav Encon! We are urgently hiring for the position of Analyzer Technician for our reputed client ABB , on third-party contract through Keshav Encon. Position: Analyzer Technician Location 1: Wanakbori Thermal Power Station Site, Kheda Location 2: Mumbai (Deepak Fertilizers Site) Client: ABB Experience: 4-6 Years Qualification: Diploma in Instrumentation / Electronics & Communication Role Type: TPC 1-Year Contract (Payroll of Keshav Encon Pvt. Ltd.) (Extendable based on performance) To Apply: Kindly share your updated CV at hrexec2@keshavencon.com For more details, WhatsApp: +91 9023185694 (Nirali Chauhan) We request you to circulate this requirement among your contacts and references who may be suitable for the above roles. Best Regards, Nirali Chauhan

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Junior Design Engineer Chetan Meditech Pvt Ltd

0.0 - 2.0 years

3 - 4 Lacs

Sanand

Work from Office

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.

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