Biotech Healthcare Group is a global healthcare company founded back in 1999 in India. Today, after an exponential growth, Biotech Healthcare products are available in more than 106 countries. Sales and marketing headquarter is based in Luzern, Switzerland and two main research & development centers and state-of-the-art manufacturing facilities are in Roscommon, Ireland and Ahmedabad, India.
- Important Details :
- Location: Ahmedabad
- Post of date:10/09/2024
- Selection Process: The selection will be on the basis of Interview.
Job Description : Greeting from BIOTECH VISION CARE PVT. LTD.!!!!
Openings Details
- Post Name: QMS/Chemical/ Mechanical Engineer – Validation
- Experience: 2 to 4 years
Walk In Interview Details
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Date: 14-September-2024 – Saturday
Time: 10:00 AM to 4:00 PM
Venue: BIOTECH VISION CARE PVT. LTD Block 1, Abhishree Corporate Park, Opp. Swagat Bungalow, BRTS Stop, Bopal – Ambli Road, Ahmedabad Gujarat, India – 380 058.
Biotech Vision Walk In Interview For QMS Position
Senior Officer / Officer – QMS (For Medical Devices Indsutry)Â
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Required Experience: 2 to 4 years
•Maintain and improve the QMS to ensure compliance with regulatory requirements and company policies.
•Support the creation, review, and updating of company procedures and documentation in alignmentwith QMS guidelines.Â
•Execute and monitor QMS activities, including complaint handling, non-conformance management, CAPA, documentation control, and management reviews.
•Collaborate with process owners to develop and implement necessary procedures and protocols.
•Conduct internal audits and inspections to evaluate the effectiveness of the QMS and ensure continuous improvement.
Lead investigations of non-conformances and customer complaints, coordinating corrective and preventive actions to resolve issues.
•Conduct routine GMP audits, mock recalls, traceability exercises, and plant inspections.
•Provide ongoing quality assurance support to all departments and ensure supplier quality compliance.
•Develop and deliver training programs on quality-related topics to maintain awareness of QMS requirements.
•Assist in regulatory compliance activities in coordination with Regulatory Affairs.
•Ensure timely follow-up on quality issues and ensure all tasks are completed within established timelines.
•Perform additional tasks or projects as assigned by the Quality Manager.
Please Note: This Event is for Experienced Professionals Only. Candidates from Medical Devices or pharmaceutical companies operating within an SAP environment are strongly preferred.
Send Resume to prachi.shah@biotechhealthcare.com
Senior Officer / Officer – Validation (Chemical / Mechanial Engineers) (For Medical Devices Indsutry)Â
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Required Experience: 0 to 2 years
•Support senior validation staff in performing Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities.
•Assist in collecting data during validation activities and performing basic tests on equipment and processes under guidance.
•Execute validation protocols for equipment, processes, and systems to ensure they meet industry regulations.
Assist in preparing validation documents, such as protocols, test plans, and reports, ensuring proper filing and maintenance of documentation. Record test results, deviations, and corrective actions accurately and support the review of validation data.
•Ensure validation documentation complies with internal standards and regulatory requirements.
•Adhere to GMP, GDP, and internal quality management systems (QMS) while performing validation tasks.
•Assist in ensuring compliance with FDA, ISO 13485, and other relevant regulatory guidelines in validation activities.
•Support the preparation of documentation for internal audits and regulatory inspections. Participate in addressing audit findings or corrective actions related to validation processes.
•Collaborate with cross-functional teams, including manufacturing, engineering, and quality assurance, to assist in validation activities.
•Attend training and meetings to enhance knowledge of validation processes and regulatory requirements.
•Provide updates on assigned tasks and progress to senior validation staff.
Please Note: This Event is for Experienced Professionals Only. Candidates from Medical Devices or pharmaceutical companies operating within an SAP environment are strongly preferred.
