Anthea Pharma Pvt Ltd, a prominent player in the pharmaceutical industry with a USFDA-approved facility, is actively seeking qualified and passionate professionals to join our dedicated team. We are offering a remarkable opportunity within our sterile injectable division located in the vibrant city of Hyderabad. If you are eager to advance your career in a dynamic environment, we would love to hear from you!
Position Available: Executive to Senior Executive
Department: Quality Control Validation
Experience Required: 2 to 8 years
Qualification: B Pharm / M Pharm / M.Sc
About Us:
Anthea Pharma Pvt Ltd prides itself on adhering to the highest standards of manufacturing and quality assurance in the pharmaceutical sector. Our commitment to delivering safe and effective sterile injectable products underscores our dedication to patient care and compliance with global regulations.
Key Responsibilities:
As a successful candidate, you will play a crucial role in our Quality Control Validation department. Your responsibilities will include, but are not limited to, the following:
- Analytical Method Validation:
- Conduct comprehensive validation of analytical methods, ensuring robustness and reliability.
- Method Verification and Transfer:
- Execute method verification processes and facilitate seamless method transfers between departments to uphold quality standards.
- Hands-On Instrumentation Expertise:
- Utilize state-of-the-art laboratory instrumentation such as:
- High-Performance Liquid Chromatography (HPLC)
- Gas Chromatography (GC)
- Ion Chromatography (IC)
- Dissolution Testing (USP Type IV)
- Osmometer
- Leak Test Apparatus
- Karl Fischer Autotitrator
- UV-Visible Spectrophotometer
- Dealing with Laboratory Incidents:
- Actively participate in laboratory incident investigations and deviation management to ensure compliance with established protocols.
- Regulatory Compliance:
- Maintain a thorough understanding of regulatory requirements related to documentation, including Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
Qualifications and Skills:
To thrive in this role, candidates should possess the following qualifications and skills:
- A degree in Pharmacy (B Pharm / M Pharm) or a Master’s degree in Science (M.Sc) from a recognized institution.
- A minimum of 2 years to a maximum of 8 years of experience in quality control and validation within the pharmaceutical industry.
- Strong analytical skills, attention to detail, and proficiency in using laboratory instrumentation.
- Familiarity with regulatory guidelines and a commitment to maintaining high-quality standards.
- Excellent communication and teamwork abilities to foster a collaborative work environment.
Why Join Anthea Pharma Pvt Ltd?
- Innovative Work Environment: Be part of a forward-thinking organization that values innovation and quality.
- Career Advancement: Opportunities for professional development and growth within a well-established company.
- Competitive Compensation: Receive a competitive salary and benefits package commensurate with your skills and experience.
How to Apply:
If you are excited about the opportunity to contribute to a leading pharmaceutical company and meet the qualifications outlined above, we encourage you to apply. Please send your updated resume to recruitment@antheapharma.com. We look forward to welcoming talented individuals who share our mission of enhancing patient health and well-being.
Conclusion:
At Anthea Pharma Pvt Ltd, we understand that our greatest asset is our people. Join us in our pursuit of excellence, and help us shape the future of healthcare. If you are ready to take the next step in your career, don’t hesitate to reach out!
This job opening represents an excellent career opportunity in the pharmaceutical sector, specifically in Quality Control Validation. By ensuring that this role is filled with qualified professionals, we continue our commitment to quality and compliance in the pharmaceutical industry.
