Regulatory Affairs Specialist

3 days ago


Pune India Atlas Copco Group Full time

Job Description Our solutions are a key part of most industries - electronics, medical research, renewable energy, food production, infrastructure and many more. Working with us means working with the latest technologies and groundbreaking, sustainable innovations. Join us on our journey for a better tomorrow. Your Role- Purpose - Gecia is supporting Atlas Copco entities in different activities like Trade Compliance (Customs Classifications, Conflict Minerals reporting, Dangerous Goods, SCRM, etc.), aftermarket, sourcing, vendor management etc. The above activities have become quite vast & need a well-coordinated, focussed & integrated approach to deal with these. Also, to improve efficiency there is need to explore & implement digitalisations & automations in these activities to reduce the monotonic elements & improve accuracy. Do you like chemical compliance Atlas Copco Group is a global leader in innovative solutions, providing sustainable productivity through innovative compressors, vacuum solutions, generators, pumps, power tools, and assembly systems. All these machines require a whole range of chemical products to properly function. Also, during the manufacturing process various chemicals are used. Job Description We are seeking a passionate and detail-oriented Regulatory Affairs Specialist to join our dynamic team. In this role, you will provide entities around the world the necessary support to ensure compliance with all relevant chemical regulations and the availability of accurate and up-to-date safety data sheets (SDS) and labels. You are responsible for creating manuals and providing comprehensive trainings to staff. This role is crucial for supporting our commitment to safety and regulatory adherence. Roles And Responsibilities - Regulatory Compliance: Monitor and interpret chemical regulations and standards (e.g., CLP, REACH, GHS) to ensure company compliance. - Documentation Management: Support the availability of up-to-date safety data sheets (SDS), product labels, and technical manuals in accordance with regulatory requirements. - Training and Support: Develop and deliver training programs for employees on chemical safety, handling procedures, and regulatory compliance. - Audit and Inspection: Conduct internal audits to ensure compliance with chemical safety regulations and prepare for external audits. - Risk Assessment: Perform risk assessments related to chemical products and processes and recommend corrective actions as needed. - Cross-Functional Collaboration: Work closely with Engineering, Sourcing, SHEQ and other departments to support product development and ensure compliance throughout the product lifecycle. - Problem-Solving: Address and resolve any issues related to chemical management and provide expert guidance to internal stakeholders. Educational Requirements - Education: Bachelor's degree in Applied Sciences (biology, chemistry, medical, environmental or engineering) or a related field. A master's degree is a plus. - Experience: Minimum of 3-8 years of experience in compliance, or a similar role within a global organization. - Skills: - Strong understanding of global regulatory environments. - Excellent project management and organizational skills. - Ability to work independently and as part of a team. - Strong communication and interpersonal skills. - Analytical and problem-solving abilities. Personality Requirements - Optimistic & Never give up attitude; - Driven, motivated and take initiative; - Curious, interested in new systems and processes; - Accurate, independent, disciplined; - Creative, innovative attitude; - Good communicative skills; - Team player - Flexible What You Can Except From Us - An excellent culture - Ample opportunities for professional development - New challenges and opportunities to learn every day - A culture known for respectful interaction, ethical behaviour,and integrity - Drive your Career, Explore Opportunities, Realize your Passion - Have multiple interactions with different stakeholders internally and externally - Potential to see your ideas realized and to make an impact on interesting projects - Plenty of opportunities to grow and develop - A Pivotal Role with large group of people management Diverse by nature and inclusive by choice Bright ideas come from all of us. The more unique perspectives we embrace, the more innovative we are. Together we build a culture where difference is valued, and we share a deep sense of purpose and belonging. Location: Pune Last Date To Apply 11-Dec-24 Diverse by nature and inclusive by choice Bright ideas come from all of us. The more unique perspectives we embrace, the more innovative we are. Together we build a culture where difference is valued and we share a deep sense of purpose and belonging.


  • Regulatory Affairs

    2 days ago


    Pune, India Statistical Pharma Full time

    The **Regulatory Affairs Specialist** stays with the same company for an average of 10 to 15 years; the rate of turnaround is therefore low. Networking is very much encouraged, through joining various associations to participate in conferences and exhibitions, and also to access current literature. Presently, there is a strong demand for Regulatory Affairs...


  • India Concept Medical Full time

    About Us: Concept Medical is at the forefront of developing and manufacturing innovative medical devices for interventional cardiology and radiology. Our commitment to excellence in healthcare and patient outcomes drives us to provide the best-in-class stents and balloon catheters. With a growing presence in the global market, we are expanding our team in...


  • India, Cochin / Kochi / Ernakulam Bayfield Food Ingredients Full time

    Job Description About Bayfield Food Ingredients Bayfield Food Ingredients is a pioneering provider of innovative, high-quality food ingredients, specializing in natural flavors, extracts, and sustainable solutions. Our mission is to empower healthier food choices for consumers while prioritizing ethical sourcing and environmental responsibility. At Bayfield,...


  • Noida, India Gentell Full time

    Job Description Gentell is one of the largest vertically integrated wound care companies in the world. Based in Yardley, PA and with offices, distribution centers and manufacturing plants around the world, our purpose is to make a positive difference in the quality of life for the injured, the chronically ill and those near the end of life. Our success is a...


  • Gurugram, India Respironics Inc Full time

    Job 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...


  • Pune, India Atlas Copco Full time

    Job Description Our solutions are a key part of most industries - electronics, medical research, renewable energy, food production, infrastructure and many more. Working with us means working with the latest technologies and groundbreaking, sustainable innovations. Join us on our journey for a better tomorrow. Your Role- Purpose - Gecia is supporting Atlas...


  • India G&L Scientific Full time

    We are seeking three Global Regulatory Affairs Specialists to provide critical subject matter expertise and backfill internal SMEs during a major regulatory transformation initiative. These roles will ensure continuity of day-to-day regulatory operations - particularly across CMC, labelling, and lifecycle management activities. This opportunity can be...


  • Pune, India Whatjobs IN C2 Full time

    Dear Candidate, We are hiring for the Regulatory Affairs role-handling the below job responsibilities, Job Title: Regulatory Affairs Manager Company: Brinton Pharmaceuticals Ltd. Location: Kharadi, Pune Salary: Best in Industry Joining: Immediately Job Description: Regulatory Affairs Manager Position Overview: We are seeking an experienced and resourceful...

  • Senior Compliance

    2 weeks ago


    Mumbai, India Hemant Surgical Industries Limited Full time

    Job Description Job Title: Senior Compliance & Regulatory Affairs Specialist (Medical Devices) Location: Mumbai Department: Regulatory Affairs / Quality Assurance Experience Required: 712+ years Industry: Medical Devices / Healthcare / Pharma ______________ Job Summary: The Senior Compliance & Regulatory Affairs Specialist will lead and manage all activities...


  • Pune, India Atlas Copco Full time

    .fit_to_content{width:%;height:auto}Our solutions are a key part of most industries - electronics, medical research, renewable energy, food production, infrastructure and many more. Working with us means working with the latest technologies and groundbreaking, sustainable innovations. Join us on our journey for a better tomorrow. Your Role-  Purpose  -...