Apotex is a Canadian-based, globally recognized pharmaceutical company with a strong presence in the industry for over 50 years. Known for its dedication to providing affordable healthcare solutions, Apotex prides itself on offering high-quality, effective medicines that cater to a diverse range of therapeutic needs. As a top employer, Apotex has been certified as a “Great Place to Work,” demonstrating its commitment to fostering a positive and dynamic work environment. The company continues to expand, creating new opportunities for talented professionals who want to make a meaningful impact in the world of healthcare.
Responsibilities in the Job: Quality Control – Stability Analysis Team
Apotex is currently hiring for the position of Quality Control – Stability Analysis Team. This role is crucial for maintaining the high standards of quality and compliance that the company is known for. The key responsibilities include:
- Timely Completion of Analysis and Data: Ensure that all analyses and associated data are completed on time for laboratory samples and stability tests.
- Quality Control Laboratory Activities: Oversee all activities within the Quality Control Laboratory, ensuring compliance with current Good Laboratory Practices (CGLP), documentation, and quality systems.
- In-Process and Finished Product Testing: Conduct testing of in-process and finished products, stability samples, and cleaning validation.
- Stability Trend Reports: Prepare comprehensive stability trend reports for laboratory samples to track product performance.
- Sample Collection and Maintenance: Collect, maintain, and manage various laboratory samples in an organized and compliant manner.
- Regulatory Compliance: Ensure all work adheres to regulatory, compliance, and safety standards to maintain Apotex’s reputation for high-quality production.
Qualifications and Experience Required
Apotex seeks professionals with the following qualifications and experience:
- Educational Qualification: A Master’s in Science (M.Sc.), Bachelor of Pharmacy (BPharm), or any relevant degree.
- Experience: Candidates should have 2 to 6 years of experience working in the GMP-regulated pharmaceutical industry, particularly within quality control or stability analysis.
- Industry Knowledge: Familiarity with industry standards and regulatory practices such as GMP (Good Manufacturing Practices) is essential.
- Technical Expertise: Ability to perform and report analysis on in-process samples, finished products, stability samples, and cleaning validation procedures.
Key Skills for Success in the Role
To excel in this role, the following skills are essential:
- Analytical Skills: Strong analytical abilities to interpret laboratory results, ensuring accurate and reliable data.
- Attention to Detail: High attention to detail to comply with regulatory guidelines and ensure the quality of pharmaceutical products.
- Problem-Solving: Ability to address any issues that arise in the testing process, ensuring smooth operations.
- Time Management: Excellent organizational skills to manage multiple tasks and deadlines effectively.
- Teamwork: Strong collaboration skills to work effectively within a team while maintaining a focus on quality and compliance.
How to Apply: Join Our Team at Apotex
Apotex is excited to meet potential candidates for the Quality Control – Stability Analysis position. Here’s how you can apply:
- Walk-In Interview:
- Date: 16th February 2025
- Timing: 9 AM to 2 PM
- Location: Lemon Tree Premier HITEC City, Madhapur, Hyderabad, 500081, Telangana State, India.
- Work Location: The role will be based in Bengaluru.
To reduce wait time during the walk-in interview, scan the QR code provided in the job advertisement or call 080-63611681 for more details.
