Job opening for Content writer in Gurugram  location

The ideal candidate possesses a passion for writing and an innovative ability
to create successful marketing campaigns and aid in creating company
growth.

Create high-quality content , aligning
with brand voice, objectives, and target audience.
Write daily blog posts with attention-grabbing titles to drive traffic and
engage our audience.
Conduct thorough research on relevant topics to ensure accuracy and
credibility.
Collaborate with our marketing team to develop content strategies and
achieve content goals.
Optimize content for search engines (SEO) to improve website visibility and
ranking.
Proven experience as a content writer, preferably in a product compliance
industry.
Excellent writing and editing skills with impeccable grammar and
punctuation.
Strong research skills and the ability to generate creative content ideas.
Familiarity with SEO best practices and the ability to optimize content for
search engines.
Ability to work independently and meet tight deadlines.
Bachelor’s degree in English, Journalism, Communications, or a related field
(preferred).

#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 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.