Meiji Group’s Medreich Limited is conducting a walk-in interview for experienced Quality Control specialists. This is an excellent opportunity for skilled professionals with a background in Chemistry and Pharmacy to join a leading pharmaceutical company. If you’re seeking a challenging and rewarding career in the pharmaceutical industry, we encourage you to attend this walk-in interview.
Date and Time: Saturday, April 19th, 2025, 10:00 AM to 2:30 PM
Location:
Medreich Limited
Unit III, Survey No. 4/3, Avalahalli,
Anjanapura Post, Off. Kanakapura Road,
Bengaluru – 560 062, India
About Medreich Limited:
Medreich Limited, a part of the prestigious Meiji Group, is a renowned pharmaceutical company dedicated to developing and manufacturing high-quality pharmaceutical products. We are committed to innovation, patient safety, and employing skilled professionals who share our passion for excellence. Our state-of-the-art facilities in Bengaluru offer a dynamic and stimulating work environment. Joining Medreich means becoming part of a global organization with a strong commitment to ethical practices and continuous improvement. We foster a culture of collaboration, learning, and professional growth, providing ample opportunities for career advancement.
Job Description: Quality Control Specialist (6 Openings)
We are seeking highly motivated and experienced Quality Control Specialists to join our team in Bengaluru. The successful candidates will play a vital role in ensuring the quality and compliance of our pharmaceutical products. Key responsibilities include, but are not limited to:
Key Responsibilities:
- Analytical Testing: Conducting a comprehensive range of analytical tests, including physical and wet chemical analysis, to ensure product quality and consistency.
- Instrumental Analysis: Demonstrating expertise in operating and maintaining sophisticated laboratory instruments such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet-Visible Spectroscopy (UV), and Infrared Spectroscopy (IR). Proficiency in troubleshooting and instrument calibration is essential.
- Regulatory Compliance: Maintaining meticulous records and ensuring strict adherence to Current Good Laboratory Practices (cGLP) and data integrity guidelines. A deep understanding of regulatory requirements within the pharmaceutical industry is crucial.
- Out-of-Specification (OOS) and Out-of-Trend (OOT) Investigations: Conducting thorough investigations of OOS and OOT results, identifying root causes, and implementing corrective and preventive actions (CAPA). This includes expertise in drug product analysis.
- Reagent Preparation and Standardization: Preparing and standardizing various reagents and volumetric solutions according to established procedures. Accuracy and precision are paramount in this role.
- Method Validation and Development (if applicable based on experience): Participation in method validation and development projects may be required depending on experience level.
Qualifications and Experience:
- Education: Master of Science (M.Sc.) in Chemistry or Bachelor of Pharmacy (B.Pharm) is required.
- Experience: A minimum of 2 to 6 years of relevant experience in a pharmaceutical quality control laboratory is mandatory.
- Skills: Excellent analytical and problem-solving skills are essential. Strong attention to detail and meticulous record-keeping are critical for success in this position. Proficiency in Microsoft Office Suite is necessary.
Preferred Candidate Profile:
Candidates with immediate availability are highly preferred. The ability and willingness to work in a shift-based environment is a must.
How to Apply:
Interested and qualified candidates are encouraged to attend the walk-in interview on the date and time specified above. Please bring your updated resume and relevant certificates.
Contact Information:
For any inquiries, please contact:
- Mr. Naveena: naveena.at@medreich.com
- Ms. Hemavathi: hemavathi.r@medreich.com
This revised article incorporates SEO best practices, including relevant keywords, clear headings, a structured format, and a comprehensive description of the job and company. Remember to also consider submitting this job posting to relevant job boards and online platforms to maximize its reach.
