Aurobindo Pharma Ltd. (APL), a leading multinational pharmaceutical manufacturing company, invites applications for immediate openings at its state-of-the-art facility in Naidupeta, Andhra Pradesh. With over US$2.8 billion in revenue (2018-19) and a global presence spanning 155 countries, APL is a rapidly expanding force in the pharmaceutical industry. Notably, APL ranks as the second largest generic company in the USA based on prescriptions dispensed and is among the top 10 generic players in key European markets including France, Germany, Portugal, the UK, Italy, Czech Republic, Netherlands, and Belgium. This is a fantastic opportunity to join a dynamic, growing organization making a significant impact on global healthcare.
Job Details: Quality Control/Assurance Executive/Senior Executive
Location: APL Health Care Limited., Unit IV, SEZ Menakur, Naidupeta, Tirupati District, Andhra Pradesh, 524421, India.
Department: Quality Control/Quality Assurance
Position: Executive/Senior Executive
Experience: 2 to 8 years (OSD Formulation Only)
Qualifications: M.Sc, B.Pharm, or M.Pharm
Key Responsibilities:
This position requires a highly motivated and experienced professional with a strong background in Oral Solid Dosage (OSD) formulation quality control and assurance. Responsibilities include, but are not limited to:
- Analytical Testing: Performing routine and non-routine analytical testing of raw materials, in-process materials, and finished products using various analytical techniques. This includes hands-on experience with HPLC, LCMS, GCMS, and GC.
- Data Analysis & Reporting: Accurate recording, analysis, and interpretation of test results; preparing comprehensive reports detailing findings and conclusions.
- Regulatory Compliance: Ensuring adherence to all relevant regulatory guidelines (e.g., GMP, GLP) and maintaining accurate documentation.
- Method Validation: Participation in method validation studies and troubleshooting analytical methodologies.
- Quality Management System (QMS): Contributing to the maintenance and improvement of the QMS and related documentation.
- Market Compliance: Understanding and adhering to market-specific compliance requirements.
Successful candidates will demonstrate a strong understanding of quality control principles in pharmaceutical manufacturing, specifically within OSD formulation. Experience in one or more of the following areas is preferred: Finished Product (FP), In-process (IP), Good Laboratory Practices (GLP), Raw Materials (RM), Validation, and Quality Management Systems (QMS).
Essential Skills and Experience:
- Proven experience (2-8 years) in a quality control/assurance role within OSD formulation in a pharmaceutical manufacturing environment.
- Hands-on expertise with advanced analytical instrumentation (HPLC, LCMS, GCMS, GC).
- Strong understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant regulatory requirements.
- Excellent data analysis, interpretation, and reporting skills.
- Proficiency in Microsoft Office Suite.
- Strong problem-solving and troubleshooting abilities.
- Ability to work independently and as part of a team.
- Excellent communication and interpersonal skills.
How to Apply:
We encourage immediate joiners to apply. Please submit your resume to the email address below:
Email: naidupetahr@aurobindo.com
Contact: Zuha HR, +91-9581444337
Note: Only candidates with relevant experience in OSD formulation will be considered. Please mention “Quality Control/Assurance Executive/Senior Executive Application” in the subject line of your email.
Aurobindo Pharma is an equal opportunity employer committed to diversity and inclusion. We encourage applications from all qualified individuals regardless of race, religion, gender, nationality, disability, or other protected characteristic. We offer a competitive salary and benefits package, along with opportunities for professional growth and development within a dynamic and globally recognized pharmaceutical organization. We look forward to hearing from you!
