Urgent hiring for EA for Chandigarh location.

Job Responsibilities:

1. Provide comprehensive administrative support to the Managing Director, including managing schedules, appointments, and meetings.
2. Handle correspondence, emails, and phone calls on behalf of the MD, ensuring effective communication and follow-up.
3. Prepare reports, presentations, and documents as required, using MS Office tools such as Word, Excel, and PowerPoint.
4. Maintain a high level of confidentiality and discretion in all tasks.
5. Coordinate and organize meetings, conferences, and travel arrangements for the MD.
6. Monitor and follow up on assigned tasks to ensure timely completion.

Required Skills:

• Excellent Follow-Up: Ability to track tasks and ensure completion without reminders.
• Proficiency in MS Office: Strong skills in MS Excel, Word, and PowerPoint.
• Good Communication Skills: Strong command of English, both written and verbal.
• Organizational Skills: Ability to prioritize tasks and manage time effectively.

Qualifications:

• Minimum 3 years of experience as an Executive Assistant or Secretary to the Managing Director or top management of a company.
• Bachelor’s degree in any field preferred.

Other Requirements:

• Ability to work long hours and adapt to a dynamic work environment.
• A proactive and professional approach to managing responsibilities.

Urgent hiring for Quality Assurance Executive for Sonipat location.

Key skills:
Thorough Knowledge of Medical Device Directive (MDD) 93/42/EEC, ISO 13485:2016, ISO 14971:2012 & Medical device Rules 2017

Desired Candidate Profile
• Implementation and improvement in Quality Management System as per ISO 13485:2016.
• Implementation & Formation of Standard Operating Procedure (SOP) & Protocols as per GMP.
• Maintain complete documents of various departments like Site Master File, Device Master File with easy archival/retrieval.
• Involve onsite into the calibration & Validation activities. Preparation of Calibration calendar and preventive maintenance.
• Assist in preparation of Batch Manufacturing Record as per manufacturing and their review before release of the batch.
• Giving line clearance before starting the New Batch.
• Review and analysis of Environmental Monitoring plan to monitor environmental condition and hygiene of Personnel working in manufacturing areas and other controlled areas.
• Experience of CE, ISO 13485:2016 and GMP Inspections.
• Experience of Risk Management as per ISO 14971
• Experience of Design & development file as per ISO 13485:2016
• Knowledge of Post Market Surveillance and Post Market Clinical Follow Up, Product recall-

Handling and handling market complaints as per SOP and maintaining its records.

Education- UG: B Tech in Mechanical, BE – Bio Medical, B. Pharma, B. Tech Medical Science

#JobOpening #Hiring #JobSearch #NowHiring #CareerOpportunity #Employment #JobOpportunity #JobListing #JobPosting #JobAlert #recruitment  If interested can forward your updated resumes on hr5@tasolutions.in and can directly contact us on 8427933492 also can provide our reference to your friends and colleagues.

Urgent hiring for Regulatory Affairs Executive for Sonipat location.

Job Description

Preparation of documentation for submission to FDA for medical device approval and/or response to FDA inquiries
Responsible for Compliance of Medical Device Directive (MDD) 93/42/EEC, ISO 13485:2016, ISO 14971:2012 & Medical device Rules 2017.
Key skills:
Thorough Knowledge of Medical Device Directive (MDD) 93/42/EEC, ISO 13485:2016, ISO 14971:2012 & Medical device Rules 2017

Desired Candidate Profile
Minimum B. Tech in Mechanical, Bio Medical, B. Pharma, B. Tech Bio Medical Science or a science discipline
· 2+ years of experience implementing test strategies, test plans and test cases for validation and verification in FDA-compliant medical device industry
· Demonstrated success in a start-up, entrepreneurial work environment
· Thorough knowledge of FDA Quality System requirements, ISO 13485:2012 (Quality System) requirements, ISO 14971 (Risk Management) requirements, Medical Device Directives (MDD) requirements, Knowledge of Good Manufacturing Practices (GMP) and applicable Quality System Standards
· 2+ years of experience in verification/validation of products incorporating scalable data acquisition, processing, management, and reporting functionalities.
· 2 or more years of experience with QMS implementation that complies with, MDD /93/42/EEC, ISO 13485 and ISO 14971 standards.
· Lead role (administrative or technical) in one or more FDA submissions for approval of a medical device
· Project management skills and proficiency and analysing and interpreting test data

Education-
UG: B Tech in Mechanical, Bio Medical, B. Pharma, B. Tech Medical Science or a Science

#JobOpening #Hiring #JobSearch #NowHiring #CareerOpportunity #Employment #JobOpportunity #JobListing #JobPosting #JobAlert #recruitment  If interested can forward your updated resumes on hr5@tasolutions.in and can directly contact us on 8427933492 also can provide our reference to your friends and colleagues.