Position: Production Head Experience: 10 To 20 Yrs Location: Bangalore Department: Manufacturing Industry: Medical Devices / Healthcare Technology Role Summary We are looking for an experienced and strategic Production Head to lead our manufacturing operations in the medical device domain. The ideal candidate will have deep knowledge of regulated production environments, strong people management skills, and a passion for driving quality, safety, and efficiency. This role is critical to ensuring that our products meet global standards and are delivered on time and within budget. Key Responsibilities Lead and oversee all daily manufacturing activities, ensuring production targets, timelines, and quality standards are met. Develop and implement effective production strategies aligned with company goals. Ensure full compliance with regulatory and quality standards, including ISO 13485, FDA21 CFR Part 820, and EU MDR. Manage cleanroom operations and ensure adherence to safety and hygiene protocols. Plan and optimize resource allocation including manpower, materials, and machines. Implement and promote Lean Manufacturing, 5S, Six Sigma, and other process improvement techniques. Coordinate with cross-functional teams such as Quality, R&D, Regulatory Affairs, SCM, and Maintenance. Oversee preventive and corrective maintenance of production equipment and ensure minimal downtime. Ensure documentation practices meet Good Manufacturing Practices (GMP), including DMR, DHR, CAPA, NCR, etc. Train, mentor, and lead the production team to drive productivity and accountability. Participate in internal, external, and regulatory audits. Qualifications Bachelors/Masters degree in Mechanical / Industrial / Biomedical Engineering or related field. Certifications in Lean, Six Sigma (Green/Black Belt), or ISO 13485 are an advantage. Experience 12-20 years of experience in manufacturing, with at least 5 years in the medical device or pharma industry. Prior leadership role in managing large-scale, regulated production lines. Key Competencies In-depth knowledge of regulatory standards (ISO 13485, GMP, FDA, EU MDR). Excellent team leadership, communication, and conflict-resolution skills. Proven track record in implementing continuous improvement and cost-saving initiatives. Hands-on experience with ERP/MES systems. Strong analytical and decision-making abilities. Why Join Us? Opportunity to lead in a fast-growing, innovation-driven organization Work on cutting-edge medical technologies that impact lives A culture that values quality, teamwork, and continuous learning
Job Title: Finance Manager / Financial Controller (Chartered Accountant) Location: Bangalore, India Company: Happy Reliable Surgeries Pvt. Ltd. Industry: Healthcare / Medical Technology Experience Required: 57 Years Qualification: CA (Preferred), or MBA in Finance About Us Happy Reliable Surgeries Pvt. Ltd. (HRS Navigation) is a leading provider of advanced healthcare solutions. We're passionate about transforming patient care through cutting-edge technology and innovation. As part of our strategic growth, we are looking for a dynamic finance professional to lead our financial operations with precision and strategic foresight. Key Responsibilities Lead and oversee financial planning, budgeting, and forecasting processes. Manage end-to-end financial reporting , MIS reporting , and monthly/quarterly/annual closings. Ensure compliance with direct and indirect taxation laws (GST, TDS, Income Tax). Handle internal and statutory audits and maintain robust audit readiness. Oversee regulatory compliance , company secretarial matters, and timely filing of returns. Implement and maintain risk and control frameworks , internal controls, and governance. Provide actionable insights through financial planning & analysis (FP&A) to support strategic decisions. Administer ERP systems and ensure optimal use of tools like SAP, Oracle Financials, Tally ERP, or Zoho Books . Liaise with auditors, banks, and external stakeholders to manage relationships and reporting. Monitor and optimize working capital , cash flow , and cost efficiency initiatives. Candidate Profile Chartered Accountant (CA) or MBA Finance from a reputed institution. 57 years of relevant experience in financial services , healthcare, or similar industries. Sound knowledge of IFRS / Indian GAAP , taxation laws, and financial compliance. Strong command of Advanced Excel and financial modeling. Familiarity with finance modules of tools such as SAP , Oracle , Tally ERP , or Zoho Books . Proven leadership, team management, and stakeholder engagement skills. Why Join Us? Thrive in a fast-paced, high-impact healthcare environment. Opportunity to influence key business decisions through financial insights. Cross-functional exposure with technology, operations, and leadership teams. Competitive compensation and a collaborative work culture that values excellence and innovation.
Job brief We are looking for an experienced Product Manager who is passionate about building products that customers love. You will join a dynamic and fast-paced environment and work with cross-functional teams to design, build and roll-out products that deliver the company's vision and strategy. Role: Product Manager Location: Bangalore Experience: 5 to 7 Responsibilities Gain a deep understanding of customer experience, identify and fill product gaps and generate new ideas that grow market share, improve customer experience and drive growth Create buy-in for the product vision both internally and with key external partners Develop product pricing and positioning strategies Translate product strategy into detailed requirements and prototypes Scope and prioritize activities based on business and customer impact Work closely with engineering teams to deliver with quick time-to-market and optimal resources Drive product launches including working with public relations team, executives, and other product management team members Evaluate promotional plans to ensure that they are consistent with product line strategy and that the message is effectively conveyed Act as a product evangelist to build awareness and understanding Represent the company by visiting customers to solicit feedback on company products and services Requirements Proven work experience in product management or as an associate product manager Proven track record of managing all aspects of a successful product throughout its lifecycle Proven ability to develop product and marketing strategies and effectively communicate recommendations to executive management Solid technical background with understanding and/or hands-on experience in software development and web technologies Strong problem solving skills and willingness to roll up ones sleeves to get the job Skilled at working effectively with cross functional teams in a matrix organization Excellent written and verbal communication skills MS/BS degree in Computer Science, Engineering or equivalent preferred
Bachelors degree in Life Sciences, Engineering, or a related field. 3-5 years of experience in QA roles with strong focus ondocumentation and compliance in the medical device industry. In-depth knowledge of ISO 13485, FDA QSR, EU MDR, and risk management (ISO 14971). Proven experience with QMS documentation management and inspection/audit readiness. Familiarity with risk management tools (e.g., FMEA, Hazard Analysis). Strong attention to detail and high standards for documentation accuracy. Experience in a startup or fast-paced, resource constrained environment preferred. Excellent written and verbal communication skills. Preferred Qualifications: Certified Quality Auditor (CQA), Six Sigma, or similar certifications. Experience with software as a medical device (SaMD) is a plus. Familiarity with electronic QMS systems (e.g., MasterControl, Greenlight Guru, Qualio, SimplerQMS, ETQ, and Qualityze EQMS). Skill Required: Contribute to building and maintaining our QMS in line with ISO 13485, FDA 21 CFR Part 820, EU MDR and so on. Own and manage CAPAs, non-conformances, and change controls. Support risk management activities (ISO 14971) and product lifecycle management. Work cross-functionally with engineering, regulatory, and manufacturing teams to support design controls and risk management. Support and prepare for audits and inspections (internal and external). Assist in regulatory inspection readiness and participate as SME where needed. Develop, revise, and maintain quality documentation (SOPs, work instructions, protocols). Support the development and maintenance of Design History File (DHF) and Device Master Record (DMR). Help implement electronic QMS tools suitable for a growing organization. Monitor and analyze quality metrics and trends to identify improvement opportunities. Participate in supplier evaluations, audits and ensure ongoing quality compliance. Review and approve quality documents including SOPs, work instructions, protocols, and reports. Maintain document control and training systems per QMS requirements. Ensure quality-related training programs are current, effective, and fully documented. Support complaint handling and post-market surveillance activities (as applicable).
Lead and oversee all daily manufacturing activities, ensuring production targets, t imelines, and quality standards are met. Develop and implement effective production strategies aligned with company goals. Ensure full compliance with regulatory and quality standards, including ISO 13485, FDA 21 CFR Part 820, and EU MDR. Manage cleanroom operations and ensure adherence to safety and hygiene protocols. Plan and optimize resource allocation including manpower, materials, and machines. Implement and promote Lean Manufacturing, 5S, Six Sigma, and other process improvement techniques. Coordinate with cross-functional teams such as Quality, R&D, Regulatory Affairs, SCM, and Maintenance. Oversee preventive and corrective maintenance of production equipment and ensure minimal downtime. Ensure documentation practices meet Good Manufacturing Practices (GMP), including DMR, DHR, CAPA, NCR, etc. Train, mentor, and lead the production team to drive productivity and accountability. Participate in internal, external, and regulatory audits. Qualifications: Bachelor s/Master s degree in Mechanical / Industrial / Biomedical Engineering or related field. Certifications in Lean, Six Sigma (Green/Black Belt), or ISO 13485 are an advantage.