Are you passionate about regulatory compliance and quality assurance in the pharmaceutical industry? Fortrea, a leading global Contract Research Organization (CRO), is hiring a QA Controlled Docs Coordinator in Bangalore and Mumbai. This entry-level role is perfect for recent graduates or professionals with less than one year of experience looking to kickstart their career in pharmaceutical document management. Join a dynamic team dedicated to maintaining high standards in controlled document administration, ensuring compliance and quality in every task.
Job Responsibilities
As a QA Controlled Docs Coordinator at Fortrea, you will play a critical role in managing controlled documents to ensure regulatory compliance and operational efficiency. Your key responsibilities include:
- Following Standard Operating Procedures (SOPs): Adhere to departmental SOPs and Work Instructions to maintain consistency and compliance.
- Completing Required Trainings: Finish all mandatory training programs within specified timelines to stay updated on protocols.
- Managing Day-to-Day Tasks: Handle daily tasks with a focus on quality and productivity to support operational goals.
- Administering Controlled Documents: Ensure controlled documents are accessible and properly maintained for end users.
- Maintaining Document Inventory: Keep an accurate and organized inventory of all controlled documents.
- Performing Quality Checks: Conduct thorough checks to ensure the accuracy and quality of completed work.
- Escalating Issues Promptly: Identify and escalate issues impacting document release and manage resolutions effectively.
- Ensuring Regulatory Compliance: Follow RC and QA guidelines as outlined in controlled documents.
- Additional Duties: Take on other tasks as assigned to support team objectives.
Qualifications and Experience
To excel in this role, candidates should meet the following requirements:
- Education: Minimum Bachelor’s degree. Fortrea may consider equivalent experience in lieu of educational requirements.
- Experience: Less than 1 year of professional experience, making this an ideal role for fresh graduates or early-career professionals.
- Skills:
- Strong organizational and communication skills to manage documents and collaborate with teams.
- High attention to detail to ensure accuracy in document management and quality checks.
- Ability to work well with others in a fast-paced environment.
- Proficiency in using computers and departmental tools to manage tasks efficiently.
- Consistent delivery of high-quality work under tight deadlines.
Benefits of Joining Fortrea
Working at Fortrea offers an excellent opportunity to grow in the pharmaceutical industry. Benefits include:
- Career Growth: Gain hands-on experience in regulatory compliance and quality assurance, paving the way for future roles in the CRO industry.
- Supportive Environment: Collaborate with a team of professionals dedicated to excellence in pharmaceutical research.
- Training Opportunities: Access comprehensive training programs to enhance your skills and knowledge.
- Work-Life Balance: Engage in tasks that involve prolonged computer work but offer a structured and supportive work environment.
How to Apply
