Regulatory Affairs Executive

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...

Dear Candidates Greetings from Randstad India ! We have an openingfor the role of Executive Regulatory Affairs with a leading pharmacompany in India. Interested candidates can drop your resume to the mailid The details arebelow: Qualification: B.Pharm / M. PharmExperience: 48 years Market:Canada Location: Pune Review of compilation...

Job Req ID: 39631- Location: Pune, IN- Function: Other- About: - Vodafone Idea Limited is an Aditya Birla Group and Vodafone Group partnership. It is India’s leading telecom service provider. The Company provides pan India Voice and Data services across 2G, 3G and 4G platform. With the large spectrum portfolio to support the growing demand for data and...

Designation : Regulatory SpecialistExperience : 7+Location : PuneQualificationsBachelor of Science in science and/or engineering field8 - 12years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered)Thorough working knowledge of applicable FDA, ISO, EU and/or other region-specific medical device...

Designation : Regulatory Specialist Experience : 7+ Location : Pune Qualifications Bachelor of Science in science and/or engineering field 8 - 12years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered) Thorough working knowledge of applicable FDA, ISO, EU and/or other region-specific medical...

Designation : Regulatory SpecialistExperience : 7+Location : PuneQualificationsBachelor of Science in science and/or engineering field8 - 12years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered)Thorough working knowledge of applicable FDA, ISO, EU and/or other region-specific medical device...

Designation : Regulatory SpecialistExperience : 7+Location : PuneQualificationsBachelor of Science in science and/or engineering field8 - 12years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered)Thorough working knowledge of applicable FDA, ISO, EU and/or other region-specific medical device...

**Eligibility**: - Masters in Chemistry or Bachelors in Food Tech. - A minimum of 3 -4 years of experience in Food Ingredients, Food or Analytical Laboratory company - Your past profile could be of Quality Assurance (QA), Product / Regulatory Documentation or Quality Management (QM). - SAP experience is must - Good communication skills in English are...

Designation : Regulatory SpecialistExperience : 7+Location : PuneQualifications- Bachelor of Science in science and/or engineering field- 8 - 12years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered)- Thorough working knowledge of applicable FDA, ISO, EU and/or other region-specific medical...

About First Energy Private LimitedThermax expands its business in the renewable spaceThe fight against the biggest existential threat that is ‘climate change’ can be addressed if industries adopt clean energy and transition to more sustainable manufacturing practices.Fostering our presence in the renewable energy segment, Thermax’s group company, First...

About First Energy Private Limited Thermax expands its business in the renewable space The fight against the biggest existential threat that is ‘climate change’ can be addressed if industries adopt clean energy and transition to more sustainable manufacturing practices. Fostering our presence in the renewable energy segment, Thermax’s group...

**Job Types**: Full-time, Regular / Permanent, Fresher **Salary**: ₹15,000.00 - ₹25,000.00 per month **Benefits**: - Cell phone reimbursement - Health insurance - Paid sick time Schedule: - Day shift Supplemental pay types: - Performance bonus - Yearly bonus **Education**: - Bachelor's (preferred) **Language**: - English,Hindi (preferred)

**Roles and Responsibilities for Lorenz Docubridge Technical Resource**: - Well versed with Drug Regulatory Affairs domain and Operations - Experience in Lorenz Docubridge and ISI Tool Box - Experience in sequence building and document level publishing - Good knowledge on the CTD,eCTD and NeSS - Hands on implementation and upgrade of Lorenz Suite of...

Key Responsibilities: - Statutory Compliance Ensure all compliance with the Companies Act, and other applicable laws and regulations. Due diligence, committee formation, and overlooking other routine compliances - Board and Committee Meetings: Assist in the organization and coordination of board and committee meetings. Prepare and circulate meeting...

Job Summary: Key Responsibilities: Statutory Compliance: Ensure all the compliance with the Companies Act other applicable laws and regulations. Due diligence, committees formation and overlook Other routine compliances Board and Committee Meetings: Assist in the organization and coordination of board and committee meetings. Prepare and circulate...

Overview Regulatory Analysis and Reporting - S2Under moderate supervision, helps compile, synthesize and report on BNY Mellon or market data sources. Assists with access, maintenance and security activities. May manage databases, feeds and other data sources of low-to-moderate complexity. May assist with more complex data sources. Conducts preliminary, basic...

Regulatory Analysis and Reporting - S2Under moderate supervision, helps compile, synthesize and report on BNY Mellon or market data sources. Assists with access, maintenance and security activities. May manage databases, feeds and other data sources of low-to-moderate complexity. May assist with more complex data sources. Conducts preliminary, basic...

**Job Type - Fresher or Internship level** Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe. **Responsibilities**: **1. Assist in Protocol Development**: -...

About the internship:Selected intern's day-to-day responsibilities include: 1. Taking care of the regulatory affairs of the company and Working on statutory compliances2. Drafting legal contracts and agreements with company's associates and clients.3. Identifying Collaborators and establishing collaboration or joint ventures to carry out company's...

**Job Title: - **Safety and compliance - HR **Experience: - ** 4-5 Years **Job Location: - ** Pune **Department: - ** HR **Job Type: - ** Full Time **Qualification: - ** MBA in HR **Company Description**: HYT engineering company Pvt. Ltd formerly known as HYT Engineering Corporation started its operation in 1977 with manufacturing drilling...