Cronus Pharma Hiring for QA Executive/Sr. Executive – Validation (Injectable/OSD Formulation)
Job Overview
| Job Title | QA Executive/Sr. Executive – Validation (Injectable/OSD Formulation) |
|---|---|
| Company | Cronus Pharma |
| Location | Telangana (Hotel Millennium Grand, Miyapur) |
| Eligibility | 3 to 7 years experience in QA Validation (Injectable/OSD) |
| Interview Date | October 6, 2024 |
| Interview Time | 10 AM – 4 PM |
| Skills Required | Validation management, QMS, SOP preparation, equipment qualification |
| Contact | hra@cronuspharma.com, planthr@cronuspharma.com, 7337445157 / 7337445197 |
Elevate Your Career with Cronus Pharma – QA Validation (Injectable/OSD Formulation)
Are you a skilled QA Validation professional with experience in Injectable or OSD (Oral Solid Dosage) formulations? Cronus Pharma is offering an exciting opportunity for professionals with 3 to 7 years of experience in the field. Join us for an in-person interview on October 6, 2024, and take the next step in your career at one of the leading pharmaceutical companies in Telangana.
Why Choose Cronus Pharma?
Cronus Pharma is a trusted name in the pharmaceutical industry, known for its cutting-edge solutions in the Injectable and Oral Solid Dosage segments. The company is dedicated to ensuring the highest quality standards in drug development and manufacturing, making it an ideal place for quality professionals to thrive. With a commitment to continuous improvement and regulatory compliance, Cronus offers an environment where you can apply your expertise in validation processes while growing alongside industry leaders.
What Does the Role Involve?
As a QA Executive or Senior Executive specializing in validation for Injectable and OSD formulations, you will be responsible for ensuring that production processes and equipment meet rigorous quality standards. Here’s a breakdown of your key responsibilities:
- Validation Management: Oversee the validation of OSD and Injectable lines, ensuring that all processes adhere to regulatory and company standards.
- Process and Cleaning Validation: Manage the complete validation process for both production lines, including cleaning validation and the associated documentation.
- Equipment Qualification: Perform qualification for production equipment and utilities, ensuring that all systems function correctly and meet Good Manufacturing Practice (GMP) standards.
- Documentation and SOPs: Prepare and review Standard Operating Procedures (SOPs), validation protocols, and reports to ensure compliance and accuracy.
- Cephalosporin Block Validation: Handle validation tasks specific to Cephalosporin Block, ensuring that all related equipment and processes are properly validated.
- QMS and CAPA Management: Collaborate with the Quality Management System (QMS) team to manage non-conformances, implement Corrective and Preventive Actions (CAPA), and ensure timely resolution of any issues.
- Collaboration: Work closely with external agencies to coordinate requalification activities and ensure all regulatory requirements are met.
- Training: Provide training to staff on validation processes and qualification planning.
This position is not just about technical proficiency; it requires excellent time management, problem-solving skills, and the ability to work collaboratively with both internal teams and external partners.
Event Details – Walk-In Interview
The interview will take place at Hotel Millennium Grand, Miyapur, Telangana. Be sure to bring your updated resume, and prepare to discuss your experience in validation and equipment qualification. The event will be a great opportunity to meet with key decision-makers and potentially secure a position in Cronus Pharma’s thriving QA Validation team.
- Date: October 6, 2024 (Sunday)
- Time: 10 AM – 4 PM
- Location: Hotel Millennium Grand, Miyapur, Telangana
How to Apply:
Even if you cannot attend the walk-in interview, you can still apply by sending your CV to:
- 📧 hra@cronuspharma.com
- 📧 planthr@cronuspharma.com
For more information, feel free to contact the HR department at:
- 📞 7337445157 / 7337445197
What You Need to Succeed
To qualify for this role, you’ll need 3 to 7 years of hands-on experience in QA validation for Injectable or OSD formulations. Specific qualifications include:
- Proven experience in validation protocols, equipment qualification, and process validation.
- Familiarity with the QMS and CAPA processes.
- Ability to prepare and review critical SOPs and other documentation.
- Experience in coordinating with external agencies for requalification and equipment validation.
A Career in QA Validation with Cronus Pharma
Joining Cronus Pharma means working for a company that prioritizes quality, innovation, and excellence. With a focus on Injectable and OSD formulation validation, you’ll have the chance to work in a challenging and rewarding environment where your skills and expertise will make a direct impact on the success of the company. This role is ideal for those who thrive in a fast-paced environment, enjoy problem-solving, and are committed to upholding high-quality standards.
If you’re ready to take the next step in your career, don’t miss this chance to join Cronus Pharma’s exceptional team!