Maiva Pharma Private Limited (FDA Approved Sterile Injectables)
Website:
maivapharma.com
Job details:
Company Description
Maiva Pharma Private Limited, formerly known as Global Pharmatech, is a leading manufacturer of high-quality sterile injectables, specializing in liquid sterile formulations in glass vials and ampoules. Established in 1996, Maiva is renowned in the pharmaceutical industry for its strong commitment to quality and regulatory compliance. The company's state-of-the-art manufacturing facility, located in Hosur, Tamil Nadu, is equipped to produce both aseptically filled and terminally sterilized products. With accreditations such as USFDA, EU-GMP, Health Canada, and PIC/S, Maiva delivers end-to-end pharmaceutical solutions, including formulation development, stability studies, cGMP manufacturing, and global supply of commercial injectables. By leveraging advanced technology, skilled scientific talent, and cost efficiencies, Maiva has become a prominent name in sterile injectables.
Role Description
This is a full-time, on-site role for a Shift Incharge based at Maiva Pharma's manufacturing facility in Hosur, Tamil Nadu. The Shift Incharge will oversee daily manufacturing operations, ensuring compliance with cGMP requirements and regulatory standards. Responsibilities include managing production schedules, supervising staff, monitoring equipment functionality, ensuring product quality, and preparing detailed production reports. The candidate will also play a key role in resolving operational issues, driving efficiency, and ensuring safety protocols are adhered to during their shift.
Qualifications
- Strong understanding of cGMP, regulatory standards, and sterile manufacturing processes
- Experience in creating production schedules, managing staff, and overseeing day-to-day manufacturing operations
- Knowledge of quality control processes and the ability to ensure the production of high-quality sterile injectables
- Technical knowledge in operating and maintaining sterile manufacturing equipment
- Excellent leadership, problem-solving, and decision-making skills
- Strong communication skills to effectively interact with team members and other departments
- A Bachelor's degree in Pharmacy, Microbiology, or a relevant discipline
- Prior experience in a similar role within a sterile injectables or pharmaceutical facility is preferred
- Familiarity with regulatory audit processes and documentation is a plus.
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