Regulatory Affairs Professional

3 weeks ago


Hyderabad, India Eastman Full time

**Responsibilities**:
Job Responsibilities:
Assists in the planning, development, maintenance, and implementation of the **SDS authoring process.**
Partners across all areas of expertise within the **PSRA** organization to monitor, promote, and deliver high quality, and fully compliant SDSs.
Identifies key measures to assist in driving continuous improvements and adherence to applicable regulatory requirements.
Actively fosters an organizational culture that is based on collaboration, partnership, innovation, customer service, driving change, and teamwork.
SDS and label data maintenance for new and existing products, intermediates and experimental products. Position works under direct supervision as needed.
Maintain regulatory and compositional information from raw materials suppliers and our businesses.
Manage our translation process with a 3rd party vendor.
Enter and maintain hazard assessment and regulatory data into product compliance support and MSDS authoring systems.
Provide internal and external customer support related to hazard communication including SDS distribution.
Actively participate in projects to continue to maintain compliance with global hazard communication regulations and related regulatory requirements.
Use product compliance tools to retrieve/query production models, specifications, recipes, labeling information, global database searches.
Support Eastman’s Product Stewardship and Regulatory Affairs activities.
Assist in special assignments and accepting new responsibilities as needed.

**Functional Skills and capabilities**:
Associate’s degree in Chemistry, Biological Sciences, Toxicology or HSE related field, computer technologies or equivalent experience in these fields.
One to three years’ experience, desired.
Ability to multi-task and adapt to changing work priorities in a dynamic environment
Strong interpersonal skills required to facilitate team building and partnering with colleagues and peers
Demonstrated ability to focus on details, work autonomously and lead projects
SAP EHS module experience a plus.
Results driven with excellent communication skills
Ability to handle multiple tasks/priorities and deal with ambiguity to meet specified deadlines.
Good analytical, problem solving and organizational skills.
Self-motivated, detail-oriented and comfortable working in a team environment.
Experience with innovative methodology for capturing and identifying metrics of key performance indicators.

Eastman is committed to creating a powerfully diverse workforce and a broadly inclusive workplace, where everyone can contribute to their fullest potential each day



  • Hyderabad, India Cellix Bio Full time

    Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. You will help make an impact on people’s lives and change futures every day. We are equally committed to bringing out your best and fostering a collaborative workplace built on trust and respect. We empower our people to take charge of their potential. We offer...


  • Hyderabad, India Eastman Full time

    Founded in 1920, Eastman is a global specialty materials company that produces a broad range of products found in items people use every day. With the purpose of enhancing the quality of life in a material way, Eastman works with customers to deliver innovative products and solutions while maintaining a commitment to safety and sustainability. The...


  • hyderabad, India Medtronic Full time

    Careers that Change Lives Collaborate and partner with Design QA, R&D, Sustaining Engineering, Clinical Affairs, Marketing and Operations.Supports the Global Operating Unit Regulatory Affairs function as the local representative for ensuring requirements are met.Responsible for supporting the needs of the MEIC with regulatory support for research and...


  • Hyderabad, India Medtronic Full time

    Careers that Change Lives Collaborate and partner with Design QA, R&D, Sustaining Engineering, Clinical Affairs, Marketing and Operations.Supports the Global Operating Unit Regulatory Affairs function as the local representative for ensuring requirements are met.Responsible for supporting the needs of the MEIC with regulatory support for research and...


  • Hyderabad, Telangana, India Parexel Full time

    Regulatory Affairs LabelingBachelor's Degree plus at least 5 to 8 years of experience in drug development especially in labeling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs, or quality.Good working knowledge of key labeling regulations/guidance and past experience in label development (CCDS, USPI, packaging)The...


  • Hyderabad, Telangana, India Parexel Full time

    Regulatory Affairs Consultant.8+ years' experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresLead and / or contribute...


  • Hyderabad, India Parexel Full time

    When our values align, there's no limit to what we can achieve.   Regulatory Affairs Consultant. 8+ years’ experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market. Good understanding of regulatory framework, including regional...


  • Hyderabad, India Parexel Full time

    Regulatory Affairs AssociateAround 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of  drug products (small molecules as well as biologics) in various markets.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresContribute to preparation...


  • Hyderabad, Telangana, India Parexel Full time

    Regulatory Affairs Associate Around 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologics) in various markets. Good understanding of regulatory framework, including regional trends, for various types of applications and procedures Contribute to preparation...


  • hyderabad, India IQ-EQ Full time

    Job DescriptionResponsibilities The Senior Associate: Enterprise Risk and Regulatory Affairs will provide support: to the attainment of the overall objectives of the Enterprise Risk and Regulatory Affairs Department. in the planning, design and implementation of the enterprise-wide risk governance framework. to formulate regulatory and personal compliance...


  • hyderabad, India Parexel Full time

    When our values align, there's no limit to what we can achieve.   Regulatory Affairs Associate Around 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologics) in various markets. Good understanding of regulatory framework, including regional trends,...


  • Hyderabad, India Parexel Full time

    When our values align, there's no limit to what we can achieve.   Regulatory Affairs Associate Around 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologics) in various markets. Good understanding of regulatory framework, including regional trends, for...


  • Hyderabad, India Eastman Full time

    **Role Description**: To support business growth within the Southeast Asia (SEA) and India, Eastman is looking for a highly motivated individual to join our Product Steward & Regulatory Affairs (PSRA) team. The **_PSRA _**Representative is a key member of the company that links Eastman’s Business Units (BUs, excluding Coating & Inks, Animal Nutrition and...


  • Hyderabad, India AMN LIFE SCIENCE PVT LTD Full time

    1. Preparation of technical documents like, Specs, COA, Method of analysis of raw materials and finished products and stability summary sheet etc. 2. Co-ordinate with different departments in plant to arrange the data for documents preparation. 3. Provide the required technical documents of the products to the regulatory team in corporate office. 4. Takes...


  • Hyderabad, India HETERO LABS LIMITED - India Full time

    · Should have experience in Regulatory Affairs pre & post approvals (Life cycle management).·  9-12 yrs of experience in Pharmaceutical industry.


  • Hyderabad, India HETERO LABS LIMITED - India Full time

    · Should have experience in Regulatory Affairs pre & post approvals (Life cycle management).·  9-12 yrs of experience in Pharmaceutical industry.


  • hyderabad, India HETERO LABS LIMITED - India Full time

    · Should have experience in Regulatory Affairs pre & post approvals (Life cycle management). ·  9-12 yrs of experience in Pharmaceutical industry.


  • hyderabad, India Seven Consultancy Full time

    JOB DETAILS 1.Review all data and documents related to product registrations for various health authoritiesCompilation of Drug Master Files2.Registration Dossiers & Technical Data Packages/OpenParts 3.In-House developed APIs manufactured at In-House API manufacturing sites and ensuring their updation.4.Prepare responses to deficiency letters...


  • Hyderabad, India Parexel Full time

    When our values align, there's no limit to what we can achieve.   Senior Regulatory Affairs Associate Around 4-8 y ears of relevant experience in handling of pre and post approval life cycle management of drug products (Biologics) in various markets. Good understanding of regulatory framework, including regional trends, for various types of...


  • Hyderabad, India Parexel Full time

    When our values align, there's no limit to what we can achieve.   8+ years’ experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market. Good understanding of regulatory framework, including regional trends, for various types of...