Quality assurance and regulatory affairs
4 weeks ago
Job Description Hello Connections, We have immediate openings for the following positions. Open Positions in theQARA-DQARole Greetings from Tekaccel Job Title:QARA-DQA Experience: 5+ years Location:Gurgaon Work mode: WFO NP: 0-30 Days Hire type: Full-time Key Responsibilities: Be a part of the sustaining project team and work in the design quality engineering across the entire product cycle. Ensure appropriate project/sustaining quality deliverables are created and properly executed (e.g., project design & development plan, risk management plan, hazard analysis, use and design FMEA, field assessment plan, and software validation plan if applicable). Working on product DHF, design input, design output, product risk management, usability, verification, and validation efforts (if required) for commercial products. Ensure adherence to the quality systems and design assurance SOPs and the customer's PLCP. Provide quality and regulatory compliance guidance as needed to product development or design change project teams to assure country-specific compliance with the laws and regulations of the targeted market for distribution. Lead in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements. In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all other documented quality processes and procedures. For those individuals who supervise others, the following statements are applicable: Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the Customer's Quality Policy. Job Scope and Leveling Guidelines. Functional Knowledge. Requires expanded conceptual, technical, and/or functional knowledge in the medical device design quality domain. Plans and organizes non-routine tasks with approval. Initiates or maintains work schedule and priorities. Plans and organizes project assignments and maintains project schedules. Uses and exercises judgment to solve problems in straightforward situations and determine appropriate action/solutions. Works under general direction from more senior-level roles/managers. Candidate should have 5+ years of experience. Please share your resume with [HIDDEN TEXT] and call/WhatsApp me at 7997763537 Tekaccel Software Services India
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Gurugram, India Medtronic (Medtronic)(279) Full timeAt Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. Youll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the Life.Role Summary. The QARA Director for India will be responsible for leading a team supporting Quality...
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Quality Assurance
1 week ago
Gurugram, Haryana, India Ethics Group Of Companies Full timeQuality Systems Management: Develop, implement, and maintain quality systems and processes to ensure compliance with regulatory requirements, including Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and Good Documentation Practices (GDP). - Document Control: Manage document control processes, including document creation, review,...
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Associate - Regulatory Affairs
2 weeks ago
Gurugram, Haryana, India DDReg Pharma Full time-Full Time Gurgaon Posted 5 days ago Job title Associate - Regulatory Affairs - Reports to Senior Associate/Astt Manager/Manager - Regulatory Affairs - **Job purpose**: To carry out Regulatory Review and Compilation of Technical documentation & dossiers for - Various Markets in compliance to applicable regulations and guidelines. - **Duties and...
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▷ [Urgent] Regulatory Affairs Specialist
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Gurugram, India Respironics Inc Full timeJob Description Job Title Regulatory Affairs Specialist Job Description Job title: Regulatory Affairs Specialist Your role: Regulatory Affairs Specialist - ISC will have an exciting opportunity to work with the ISC Commercial Regulatory Affairs Team and help business with product registration in the India Sub Continent, actively providing value-added...
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Assistant Manager- Regulatory affairs
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Gurugram, India myGwork - LGBTQ+ Business Community Full timeJob Description This job is with Johnson & Johnson, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are...
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Regulatory Affairs
2 weeks ago
Gurugram, Haryana, India Ethics Group Of Companies Full time**Responsibilities**: - **Regulatory Compliance**: - Stay abreast of current and evolving regulations related to Drug License and FSSAI requirements. - Ensure the organization's adherence to all applicable government regulations and standards. - **Drug License Application**: - Coordinate with regulatory authorities for timely approvals and compliance...
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Gurugram, Gurugram, India Fresenius Medical Care Full timeJob Description - Responsible for Medical Device and Drug registration in CDSCO, State FDA office and other government office. Lead negotiations with key health authority agencies during development, registration, and product lifecycle activities to resolve regulatory issues and/or negotiate approvals; establish and maintain proactive and professional...
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▷ Apply Now! Commercial
2 weeks ago
Gurugram, Gurugram, India Opten Power Full timeJob Description About Opten Power Opten Power is pioneering India's digital marketplace for clean energy commerce, connecting power producers, buyers and advisors on a unified platform. We're transforming renewable energy procurement through technology-driven solutions that streamline transactions, enhance transparency, and accelerate India's clean energy...
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Regulatory Affairs Executive
6 hours ago
Gurugram, Haryana, India A2Z Jobs Consultancy Full time**_Job Descriptions: _** - Â- Prepare and review technical documents, and dossiers in the format of CTD/ACTD. _ - Â- Check the compliance status of the Quality Systems. _ - Â- Evaluate and comment on requirements of Clinical studies. _ - Â- Prepare artwork of packaging materials as per current rules and regulations. _ - Â- Must have worked on ASEAN,...
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Gurugram, India Chakr Innovation Private Limited Full timeAbout the Role:- We are seeking an accomplished Quality Assurance Manager with a strong management background to lead our organization's quality function. This role requires a professional who can design and execute quality strategies, manage cross-functional collaboration, and ensure that all quality operations align with business objectives. The QA...