Oral Liquids Manufacturing Chemist – Walk-in Interview
A leading pharmaceutical manufacturing company is actively seeking skilled and dedicated Oral Liquids Manufacturing Chemists to join our production team. We are conducting a comprehensive series of walk-in interviews for professionals who possess strong expertise in the manufacturing of various oral liquid formulations and are committed to upholding the highest standards of quality and regulatory compliance. If you are passionate about pharmaceutical manufacturing and meet the specified criteria, we encourage you to attend.
Job Summary:
As an Oral Liquids Manufacturing Chemist, you will be a crucial part of our production unit, responsible for the efficient and compliant manufacturing of a range of oral liquid pharmaceutical products. This role demands a thorough understanding of manufacturing processes, equipment operation, and stringent adherence to quality and regulatory guidelines.
Key Responsibilities:
- Execute and oversee the end-to-end manufacturing processes for diverse oral liquid formulations, including Syrups, Suspensions, Oral solutions, Emulsions, and Oral drops.
- Operate, monitor, and troubleshoot various manufacturing process equipment, ensuring optimal performance and safety standards.
- Strictly implement and maintain Good Manufacturing Practices (GMP) throughout all stages of the production cycle.
- Prepare and maintain accurate and comprehensive documentation of all manufacturing activities, batch records, and process logs.
- Conduct In-Process Quality Assurance (IPQA) checks to ensure product quality and consistency at critical manufacturing stages.
- Actively participate in process problem-solving, optimization, and validation activities to enhance efficiency and product quality.
- Ensure all manufacturing operations comply with relevant national and international regulatory requirements.
Qualifications & Skills:
- Proven hands-on experience and in-depth knowledge of manufacturing processes for oral liquid dosage forms such as Syrups, Suspensions, Oral solutions, Emulsions, and Oral drops.
- Demonstrated proficiency in operating manufacturing process equipment specific to liquid oral production.
- A strong foundation and practical application of Good Manufacturing Practices (GMP).
- Exceptional documentation skills with attention to detail.
- Familiarity with In-Process Quality Assurance (IPQA) protocols and implementation.
- Experience in process validation and effective problem-solving within a pharmaceutical manufacturing environment.
- Up-to-date knowledge of regulatory guidelines pertinent to the pharmaceutical industry.
Walk-in Interview Details:
We invite all qualified and interested candidates to attend our walk-in interviews.
Dates: August 4th – September 30th
Time: 9:30 AM – 5:30 PM
Venue: Ace Sapphire, Unit 303, Above CENTRO, Vanasthalipuram
Contact Person for Queries: RAMYA (8247752316)
How to Prepare:
Please ensure you bring your most recent resume, copies of your educational qualifications, experience certificates, and a valid government-issued photo identification to the interview. We look forward to meeting you.
