20 Johnson Johnson jobs in Hyderabad

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
**The Position**
**Procurement Manager - Research & Development**
**Roche India - Roche Services & Solutions**
**Hyderabad**
A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love.
That's what makes us Roche.
Healthcare is evolving, and Global Procurement is responding by continuously striving for the highest possible performance, taking innovative and strategic approaches to business and supplier partnerships. Global Procurement proactively manages the entire supplier ecosystem, making a vital contribution to improving health outcomes, reducing costs for patients and global healthcare systems, and ensuring that Roche continues doing now what patients need next.
**Your Opportunity:**
This role sits within the Indirect Procurement Delivery group, which covers the core procurement activities from category management, strategic and operational sourcing, supplier management, contracting, content strategy definition, and execution. The Indirect Procurement Delivery group comprises many communities grouping categories of the same value chain or having commonality, including Research & Development, Commercial and Corporate Services, Digital & Technology, and Facilities. The communities are key enablers of strong category expertise while allowing flexibility in the procurement delivery response to the evolving needs of our customers.
As a Procurement Manager in Research Services, you will bring analytical thinking, planning, execution, and focus to the procurement sourcing and delivery capability area. Applying both general procurement and specialized knowledge or expertise in a specific commodity or spend area, you will ensure effective and efficient delivery of core procurement services and continuous improvement of automation and content availability.
You will collaborate closely with internal procurement (i.e. Chapters and capability areas such as customer relationship management, contracting, solutions, analytics, etc.) and business stakeholders to translate business needs into sourcing and spend management activities and content enhancement.
You will work closely with other team members to support customer demand, improve the customer buying experience, deliver on day-to day operational activities, and provide capacity and expertise to deliver productivity and other customer oriented projects/solutions.
As a Procurement Manager in Research & Development, you will play a variety of roles according to your experience, knowledge, and general business requirements, including but not limited to:
+ You are a Category and sourcing subject matter specialist in Research & Development conducting market and internal analysis to develop strategies and tactical plans for how Roche should source and negotiate for third party goods and services in order to satisfy stakeholder requirements.
+ You are a Procurement delivery practitioner delivering and executing sourcing strategies by leveraging spend, category know-how, robust sourcing, negotiation, contracting, supplier management methodologies and frameworks and project management skills.
+ You develop content and automation, translating sourcing outcomes and opportunities into content and automated buying channels that improve business adoption, satisfaction, and overall efficiency.
**Who you are:**
+ You hold a university degree, preferably in business or a scientific related discipline like Biological/Life Sciences, Chemistry, Biochemistry or related field.
+ You have 5+ year's procurement experience in strategic sourcing, category strategy building and strategic project execution with general contracting understanding and proficiency or relevant related commodity experience, preferably in the Pharmaceutical industry.
+ You have experience in procurement systems and processes, and implementation of procurement procedures and strategies across different EU sites
+ RFPs, RFIs, RFQs, market scan/benchmarking
+ Sourcing services for various research functions within Early Discovery across all Europe sites
+ You possess knowledge and experience in the Research Services commodity area (listed below) and awareness of adjacent commodities:
+ Chemistry Services - Medicinal Chemistry, Chemical synthesis, pCMC
+ Toxicology & Pharmacology Toxicology, Safety Pharmacology, Pharmacokinetics, ADME/DMPK
+ Early Drug Discovery Services - Research Biology (in vitro, in vivo), Protein Sciences, HTS, Lead Discovery, assay development
+ Live Animals, Transgenic & Breeding Services
+ You are proficient in collaborating with internal procurement teams and business stakeholders to translate needs into sourcing and spend management activities.
+ You have deep knowledge and experience in supplier management, contract negotiations, cost optimization, market research & analysis in R&D categories, and understand the related R&D regulations (e.g. GLP, animal welfare, SHE/K15).
+ You have experience negotiating Research Service Agreement Contracts (FTE agreements, Fee for Service agreements) with global suppliers (EU/US/UK/China/India), CROs, Universities, start-ups to industry leading providers to obtain savings and business partnering.
+ You have experience working closely with legal departments to implement and negotiate contracts, including knowledge around legal issues relating to IP, patents, data privacy, data ownership, confidentiality, insurance/liability, and Cell Line Permits/Licenses.
+ You have experience providing commercial/contracting support for business stakeholders throughout Europe sites and research functions, including supporting customer demand, improving buying experience, and facilitating day-to-day operational activities.
+ You demonstrate curiosity, active listening and a willingness to experiment and test new ideas when appropriate, with the focus very much on continuous learning and improvement.
+ You are open-minded and inclusive, generously sharing ideas and knowledge, while being receptive to ideas and feedback from others.
+ You have skills in project management.
+ You are fluent in English to a Business level.
+ Experience with the following suppliers is an asset: Aurigene Pharma Services, Bharat Biotech, Biological E, Chemo, Cohance, Ferring, Indian Immunologicals, Novartis, Sai Life Sciences, and Syngene
Join our team and enable the strong capability expertise needed to meet the evolving needs of our customers.
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
**The Position**
**Senior Procurement Manager - Research & Development**
**Roche India - Roche Services & solutions**
**Hyderabad**
A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love.
That's what makes us Roche.
Roche has defined an exciting 10-year ambition plan, requiring us to adapt and transform to our evolving ecosystem and challenges ahead of us. We have redesigned our Global Procurement (GP) organization to ensure we can succeed in this new environment and deliver on our mission for patients by building new capabilities and creating a more agile organization. Our goal is to improve our ability to deliver on our vision to "accelerate Roche's goal to bring innovative solutions to patients quickly and efficiently through business and supplier partnerships." If you are excited about driving this change and catalyzing the future in the R&D procurement capability, the Sr. Procurement Manager - R&D role is for you.
**What is the Delivery capability?**
The Delivery capability covers the core procurement activities from category management, strategic and operational sourcing, supplier management, content strategy definition, and execution. The Delivery capability comprises many communities grouping categories of the same value chain or having commonality. The communities are key enablers of strong category expertise while allowing flexibility in the procurement delivery response to the evolving needs of our customers.
This position is part of the Indirect Procurement Operations team reporting into the Procurement Delivery Operations Lead - Research & Development.
Are you wondering what is in it for you?
Are you interested in further developing and leveraging your market knowledge, business partnering, and influencing skills? Here is why we think the Sr. Procurement Manager - R&D role is a fantastic job to consider!
As a **Senior Procurement Manager - Research & Development** , you will work in a dynamic global environment where you bring analytical thinking, planning, execution, and focus to the procurement sourcing and delivery capability area. Thanks to your strong problem solving and core procurement skills, you will effectively collaborate with internal procurement (customer relationship management, contracting, solutions, etc.) and business stakeholders to translate business needs into sourcing, spend management activities, and content enhancement. Based on your R&D procurement and commodity expertise linked to clinical trials management and pre-clinical research, you ensure the effective and efficient delivery of core procurement services and continuous improvement of automation and content availability.
You will work closely with team members to support customer demand, improve the customer buying experience, deliver on day-to-day operational activities, and provide capacity and expertise to provide productivity and other customer-oriented projects/solutions.
Your key responsibilities include:
Your successful performance and contribution depend on the full embodiment and demonstration of core mindsets and behaviors, including an entrepreneurial spirit, enterprise thinking, inclusive collaboration, and desire for continuous learning that underpin our culture and ways of working.
As a **Senior Procurement Manager - Research & Development** , you will play a variety of roles according to your experience, knowledge, and the general business/team requirements, such as:
+ Sourcing and category subject matter specialist conducting internal analysis to develop and implement strategies and tactical plans for Roche to source and negotiate for third-party goods and services that satisfy stakeholder requirements.
+ Procurement practitioner delivering and executing sourcing strategies by leveraging spend, category know-how, robust sourcing, negotiation, contracting, supplier management, and project management skills to achieve objectives and key results.
+ Content and automation advocate translating sourcing outcomes and opportunities into content and automated buying channels that improve business adoption, satisfaction, and overall efficiency.
+ Manage day to day operations of the R&D team, organizing and overseeing workload, team statistics, information and trainings
+ Lead the local R&D team meetings, virtual and on-site
+ 1 on 1 check-ins with the local R&D team
+ Act as the local R&D team's main point of contact for sourcing and contracting queries, supporting the team's training and knowledge sharing (clarifying sourcing questions, ensuring quality of contracts and due diligence, organizing meetings with Category Managers when needed and organizing internal training for the team, supporting the team spirit and motivation
+ Collaborate cross functionally with other Procurement teams to share knowledge and improve Stakeholder support
+ Understand processes and support requests across multiple R&D categories (Clinical Trial management, Clinical Biomarkers, and Pre-clinical Research Services)
+ Follow global sourcing and contracting strategies to ensure alignment across regions
+ Manage team recruitments, onboarding and training of new starters.
+ Participate in monthly Regional R&D Meetings, supporting initiatives and proposing ideas to streamline work and processes
+ Ensure correct usage of myBuy Sourcing & Contracting platform by local R&D team, and myBuy Navigator by Stakeholders, providing support as needed
You will work within the broader team and GP networks and squads to determine the various roles needed to deliver project and foundational work.
You bring the following capabilities, mindset, and behaviors:
**Skills**
You hold a university degree, with a Life Science degree preferable. You also have demonstrable extensive experience in sourcing, simple contracting, people management, operational efficiency projects, or relevant commodity experience.
In addition, you have:
+ The ability to explain general capability area information to others or collect/translate moderate complexity stakeholder requirements in straightforward situations
+ Knowledgeable in procurement systems and operational processes, such as contracting, e-Sourcing, and spot buying is desired
+ Knowledge in the Clinical Development and/or Clinical Technologies area (e.g. Clinical Research Organisations, Imaging, eCOA, etc.)
+ Knowledge in the pre-clinical area (e.g. in vitro research, animal breeding, PK/PD)
+ Experience supporting Life Science research scientists (eg. biologist, biochemist)
+ Proven capability in negotiating project budgets and contracts
+ Demonstrated project management skills
+ Proven leadership skills with ability to motivate and influence
+ Business level fluency in English
**Mindset & Behaviors**
+ You strive to act as an enterprise thinker and leverage knowledge and expertise to create solutions for business customers by proactively fostering collaboration, including across the procurement network.
+ You are action-oriented and can make decisions and influence others to do the same; you repurpose work and ideas in favor of starting from scratch.
+ You demonstrate curiosity, active listening, and a willingness to experiment and test new ideas when appropriate, focusing on continuous learning and improvement.
+ You work with colleagues across procurement, business, and the broader Roche organization to broaden knowledge and expertise, better understand customer needs, and connect the dots.
+ You are open-minded and inclusive, generously sharing ideas and knowledge while being receptive to ideas and feedback from others.
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**

**Description**
At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.
USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds-regardless of background-to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.
**Brief Job Overview**
This is a non-supervisory position to support process development and scale-up of Active Pharmaceutical Ingredient (API) and related materials. The successful applicant in this role will work on projects including Analytical Method Development and evaluation for in-process samples for synthetic chemistry. The successful candidate will also perform a variety of non-routine and routine analytical tests, maintains safety & GLP environment in the lab including development/validation of methods, stability studies and research projects in analytical chemistry. The successful applicant will direct, troubleshoot, and share insights on complex projects while drawing independent conclusions about the results and determining how to proceed with the project. They closely collaborate with other scientists and/or other USP personnel.
**How will YOU create impact here at USP?**
As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.
Additionally, USP's People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.
The Scientist IV has the following responsibilities:
+ Support reaction monitoring, scale-up and final analysis of samples as per monograph /in-house procedures including method development/validation if required. Prepare development reports for Synthetic Support projects. Execute projects per the approved test protocols if assigned.
+ In collaboration with the synthetics team evaluate, implement and grow Process Analytical Technologies (PAT) capabilities and expertise. This includes evaluation of process monitoring, understanding, and control via in line, online and at line techniques. Serve as technical expert and champion for PAT and/or process model building.
+ Plan, execute, and complete the projects as per specifications, timelines, and budget.
+ Responsible for preparation and review of SOPs, protocols, reports, etc.
+ Ensure project requirements by coordinating with external vendors and all internal relevant departments.
+ Responsible for ensuring the required maintenance and calibrations of the equipment
+ Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments as assigned
+ Preparation and planning for ISO-9001 certification/recertification by participating actively, verification of protocols and related documents and take an active role in the internal as well as external QA audits and address the audit issues in a timely manner.
+ Maintain GLP & implement safety procedures while working in Lab.
+ Work on any other assigned tasks/ lab management activities.
+ Conversant with lab safety norms and strictly follow them.
+ Collaborate within the team and cross functional teams
+ Learn and practice Diversity, Equity, Inclusion & Belonging culture
**Who is USP Looking For?**
The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:
The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:
+ MSc. in Analytical Chemistry / Organic Chemistry/M. Pharm, having 8-10 years of experience in Analytical Research and Development or Ph.D. with 4-7 years of experience in Analytical Research and Development.
+ Must have hands on experience in working with chemical methods and handling instruments like HPLC, GC, LC-MS, GC-MS, FTIR, UV-Visible, wet chemistry, etc.
+ Understanding of process analytical technology, chemometrics, and knowledge of in-line, online, at line process analytical tools (e.g., IR, Raman, HPLC)
+ Experience in analytical testing and development with focus on process analytical chemistry and to understand, monitor and control chemical processes/reactions.
+ A comprehensive understanding of the science involved in the development of synthetic organic molecules and analytical chemistry.
+ Ability to perform analytical method developments and method validations as and when required.
+ Excellent technical writing and verbal communication skills
+ Good interpersonal skills and proven ability to function in a team-oriented environment are necessary.
We especially welcome applications from those who hold historically marginalized and/or underrepresented identities. This job description provides a portrait of an ideal candidate. Candidates who possess many, though perhaps not all, qualifications are encouraged to apply.
**Additional Desired Preferences**
+ Hands on experience with PAT instruments, techniques, and models such as in line, at line, or online IR, Raman, HPLC, NMR, etc.
+ Experience with a wide variety of software and laboratory information systems, including chemometric modeling software
+ Working knowledge of API manufacturing and product testing (e.g. ICH guidelines, USP general chapters and monographs)
+ Expertise with USP compendial methods and requirements (e.g. monographs and general chapter) and ICH quality guidelines
+ Pharmaceutical laboratory experience, method development and method implementation in manufacturing environments, and/or continuous manufacturing experience.
+ Strong project management skills with ability to be effective both independently and in collaborative teams
+ Skilled in evaluation and interpretation of data; Ability to multi-task.
+ Skilled in anticipating, troubleshooting, and solving technical problems.
+ Takes personal responsibility to ensure work is delivered on time and is of the highest quality.
**Supervisory Responsibilities**
NA
**Benefits**
USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.
**Job Category** Chemistry & Scientific Standards
**Job Type** Full-Time

**Description**
At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.
USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds-regardless of background-to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.
**Brief Job Overview**
This is a supervisory position in USP-India's NMR Laboratory. In this role, the Senior scientist-II works on projects including Characterization of molecules for synthetic chemistry, CDL and reference standard/ General Chapter development for Biologics and Verification Labs. The successful candidate will review/monitor a variety of non-routine and routine NMR tests, maintains safety & GLP environment in the lab including evaluation of reference standards, development/validation (as per requirement) of official methods, stability studies, and research projects in NMR department.
**How will YOU create impact here at USP?**
As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.
Additionally, USP's People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.
The Sr. Scientist II, TL has the following responsibilities:
+ (70%) Review NMR sample analysis reports as per monograph / in-house procedures including reaction monitoring. Prepare NMR reports, involve in project acceptance & approvals. Ensure the project's requirement by coordinating with the purchase department. Coordinate with lab scientists to complete projects within timelines. Prepare/review lab reports and documents.
+ (10%) Ensure that the calibrations of the equipment's are performed as per the schedule.
Prepare, Execute and complete IQ/OQ/PQ of new instruments. Indent the required glass ware and chemicals for the NMR projects. Maintain GLP & implement safety procedures
while working in Lab. Perform additional Projects/activities as per the requirement.
+ (10%) Assist in the development and implementation of safety projects impacting all USP Laboratory personnel. Participates in USP cross-functional teams as appropriate. Develop Standard Operating Procedures and policies in NMR Lab. Coordinate with Quality Assurance staff to ensure the implementation of corrective actions. Responsible for internal, method, ISO-9001 & ISO-17025 audits
+ (10%) Promote Diversity, Equity, Inclusion, and Belonging principles at USP India.
**Who is USP Looking For?**
The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:
+ MSc. in Analytical Chemistry / Organic Chemistry/ M. Pharm, having 13-15 years' experience in NMR or Ph.D. with 10-13 years of experience in NMR.
+ Must have hands on experience in handling NMR instruments.
+ Proficient in small molecule structure elucidation using NMR. Exposure to GMP/GLP environment and documentation procedures required.
+ Expertise with Bruker NMR software- automation software & hardware including cryo-probes.
+ Knowledge of solid state NMR and multinuclear NMR operations.
+ A comprehensive understanding of the science involved in the development of synthetic organic molecules and analytical chemistry.
+ Must be able to communicate effectively with both internal and external customers. Preferably familiar with electronic notebook documentation of experimental procedures.
+ Must possess a strong work ethic and a solid record of problem solving and technical results.
Excellent technical writing and verbal communication skills are required.
+ Good interpersonal skills and proven ability to function in a team-oriented environment are necessary. Proven self-effectiveness skills are a must. Understanding of GMP / ISO-IEC 17025 Guidelines is a requirement
+ Effective coach and mentor to staff. Ability to identify and develop talent.
+ Demonstrated stakeholder collaboration experience, with the ability to quickly develop and manage internal and external relationships and contacts.
**- Ability to lead in a fast paced environment with changing deadlines and priorities.**
**Additional Desired Preferences**
Desired preferences are to showcase any additional preferred levels of expertise to perform the role. Reminder: any items listed in this section are not requirements nor disqualifies for candidate consideration.
+ Experience on biological molecules such as peptides, proteins and vaccines would be an added advantage.
+ General chapter information, ELN, Empower and NuGenesis will be an added advantage.
+ Skilled in evaluation and interpretation of data; Ability to multi-task.
+ Skilled in anticipating, troubleshooting, and solving technical problems.
+ Takes personal responsibility to ensure work is delivered on time and is of the highest quality.
**Supervisory Responsibilities**
Six direct reports. TA, Scientist-I, Scientist-II, Scientist-III and two Scientist-IV
**Benefits**
USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.
**Job Category** Chemistry & Scientific Standards
**Job Type** Full-Time

About the Role
We are looking for a Medical Device Regulatory Lead with 4–6 years of proven hands-on experience in medical device regulatory submissions and compliance. The ideal candidate will have strong expertise in preparing and submitting applications to Health Authorities including US FDA (510k), Europe (CE Marking), MDSAP, CDSCO , and other global regulatory agencies. This role requires leadership, ownership, and the ability to guide cross-functional teams through complex regulatory pathways.

Key Responsibilities
Lead the preparation, submission, and management of medical device applications (US FDA 510k, CE Marking, MDSAP, CDSCO, and other markets).
Ensure compliance with regulatory standards including ISO 13485, 21 CFR 820 , and other applicable regulations.
Act as the primary contact for Health Authorities, managing queries and responses effectively.
Oversee regulatory strategy, project planning, and execution for medical device submissions.
Provide guidance on Quality Management Systems (QMS) and support audits/inspections.
Collaborate with cross-functional teams (R&D, Quality, Manufacturing, Clinical, Commercial) to align regulatory requirements with business objectives.
Take ownership of projects, demonstrating leadership and accountability in delivery.

Qualifications
4–6 years of experience in medical device regulatory affairs .
Proven track record with submissions to FDA (510k), CE Marking, CDSCO, and other agencies .
Strong knowledge of ISO 13485, 21 CFR 820, QMS practices, and international medical device regulations .
Experience in responding to Health Authority queries and managing regulatory communications.
Excellent project management, organizational, and leadership skills.
Ability to work independently, take ownership, and drive results.

Why Join Us
Opportunity to lead regulatory projects across global markets.
Work in a dynamic, entrepreneurial, and collaborative environment.
Be at the forefront of advancing compliance and patient safety in medical devices.
Apply now via LinkedIn or connect with us to explore this opportunity