Job Summary
* Position: Junior Executive – Quality Assurance (QA)
* Company: Chemveda Life Sciences
* Employment Type: Full-Time
* Location: IDA Uppal, Hyderabad
* Interview Dates: May 5th to May 7th
* Interview Time: 10:00 AM – 12:00 PM
Company Overview
Chemveda Life Sciences is a rapidly growing, innovation-driven organization dedicated to providing high-quality research and development services to the global pharmaceutical and biotechnology industries. We pride ourselves on maintaining the highest standards of scientific integrity and operational excellence. As we continue to expand our research capabilities, we are looking for a dedicated and detail-oriented Quality Assurance professional to join our team as a Junior Executive.
Role Overview
The Junior Executive in Quality Assurance will play a critical role in maintaining the integrity of our laboratory and manufacturing processes. You will be responsible for ensuring that all analytical methods and quality management systems adhere to internal protocols and regulatory standards. The ideal candidate is someone who is meticulous, has a strong grasp of GLP (Good Laboratory Practice) guidelines, and possesses a keen interest in maintaining compliance across complex analytical environments.
Key Responsibilities
The successful candidate will be tasked with several core functions designed to uphold our quality standards:
Analytical Method Validation: You will be deeply involved in the review of Analytical Method Validations. This includes verifying data across various instrumental analysis techniques to ensure that our methodologies are precise, reliable, and compliant with established standards.
Quality Management Systems (QMS): You will gain hands-on experience in managing and maintaining QMS protocols specific to our QC and GLP laboratory environments. This involves documenting processes, handling deviations, and ensuring that all activities align with organizational quality policies.
Audit Trails and Calibration: A significant portion of your responsibilities will involve reviewing audit trails for laboratory instrumentation. You will ensure that all data is traceable and accurate. Furthermore, you will oversee the calibration processes for essential equipment, such as HPLC and GC systems, ensuring that all machinery is performing within validated parameters.
Process Knowledge: We require an individual who has a solid foundational understanding of the equipment and processes used in process R&D and manufacturing. Your ability to bridge the gap between laboratory quality and real-world manufacturing applications is essential for this role.
Regulatory Compliance: While the primary focus is on internal quality, you will gain exposure to customer audits and regulatory inspections. Candidates with previous experience in preparing for or participating in such audits will be highly regarded, as this is a key component of our commitment to transparency and quality excellence.
Professional Requirements
To be considered for this position, candidates should possess:
* A degree in Chemistry, Pharmacy, or a related scientific field.
* Proven knowledge of QC and GLP laboratory procedures.
* Technical proficiency in reviewing data from analytical instruments such as HPLC and GC.
* Strong attention to detail and a systematic approach to documentation and record-keeping.
* Excellent analytical and problem-solving skills.
* The ability to thrive in a collaborative team environment.
Application Process and Walk-In Interview Details
We are conducting a series of walk-in interviews to find the right talent for this position. If you meet the criteria outlined above, we invite you to attend our recruitment drive.
Interview Schedule:
* Dates: May 5th, May 6th, and May 7th
* Time: 10:00 AM to 12:00 PM
* Venue: Chemveda Life Sciences, Admin Building, 1st Floor, IDA Uppal.
Preparation:
Please bring an updated copy of your resume, copies of your educational certificates, and any relevant experience documentation.
For those unable to attend the walk-in or who wish to apply in advance, please submit your professional profile via email to [email protected]. Alternatively, you may send your CV via WhatsApp to 9100490347.
Why Join Chemveda Life Sciences?
At Chemveda, we believe that our employees are our greatest asset. We provide a professional, growth-oriented environment where innovation is encouraged and excellence is rewarded. Working as a Junior Executive in our Quality Assurance department offers an excellent opportunity to gain exposure to advanced analytical processes, sharpen your knowledge of global regulatory standards, and contribute to the development of life-saving pharmaceutical solutions.
We look forward to meeting with motivated professionals who are eager to advance their careers in quality assurance and make a meaningful impact within our organization. If you are passionate about quality, compliance, and scientific rigor, we encourage you to join us for an interview this week.