Quality Control (OSD)

Job Description

Sri Krishna Pharmaceuticals Limited are searching for a  diligent and technically proficient professional for the role of Quality Control (OSD) to join their growing team at the Nacharam facility. This role is vital because the professional will be   maintaining the safety, efficacy, and regulatory compliance of Oral Solid Dosage (OSD) forms such as tablets and capsules. As a QC professional the job is very crucial as you will be responsible for the rigorous testing and validation of raw materials which are used for the oral solid dosage, in-process samples which are used for testing, and finished pharmaceutical products which are about to be sold  to ensure  that they meet stringent pharmacopeial specifications according to the industry standards. As a quality control professional it is   very  much necessary to be due diligent and must  be willing  to work within a data-driven laboratory environment, As a quality control professional is a mandatory to strictly follow the (GMP) and  (GLP)  as these  Oral Solid Dosages are  used for medical purposes and so to safeguard  them for  patient’s health is necessary.  

Key Responsibilities

• Analytical Testing:  The raw materials used for the Oral Solid Dosage is very much necessary and so the  potency of the raw material is really important and so performing routine analysis of raw materials, active pharmaceutical ingredients (APIs), packaging materials, and finished OSD products and that’s why the analytical testing is a major requirement.

• Instrumental Analysis: The process of creating OSD is very crucial and so operating and handling advanced analytical instruments including HPLC, GC, and KF Titration equipment becomes a must.

• Wet Analysis: In the OSD manufacturing the potency and purity is important and so conducting essential wet chemistry tests and assays to confirm the purity and potency of active ingredients is a huge responsibility for QC.

• In-Process Monitoring: The OSD is specifically designed for specific illness and so the OSD needs to be perfect for the use of the patient’s because of which testing parameters such as weight variation, disintegration time, and dissolution to ensure consistency throughout the manufacturing process and all this monitoring is done by a QC.

• Data Documentation:  While manufacturing the OSD everything done in the laboratory is crucial and so maintaining accurate, real-time analytical data and records in laboratory notebooks and electronic systems, ensuring strict data integrity now this data integrity is maintained by the quality control professional.

• Equipment Calibration: While manufacturing the OSD  the laboratory instruments need regular maintenance to prevent malfunction and ensure precise results  and so the regular calibration and maintenance of the  laboratory instruments is done by the quality control professional.

• Regulatory Compliance: The Quality Control professional makes sure that all the activities comply with ICH, USP, BP, or IP guidelines and so the quality control professional needs to participate in method validation, stability studies

Skills Required

• Analytical Proficiency:  As the manufacturing of the OSD is so crucial the professional needs to be a master of Wet Analysis, HPLC, GC, and KF Titration techniques.

• OSD Industry Expertise: To maintain the potency and purity of the OSD the professional needs to have a deep understanding of quality control processes specifically for oral solid dosage manufacturing.

• Attention to Detail: The manufacturing of the OSD is a intense chemical process which asks for attention to detail and needs to be precise and a keen eye for identifying subtle deviations in quality or out-of-specification (OOS) results is a vital skill.

• Technical Accuracy: The whole process of manufacturing is dependent on how precisely the quantities are used to create the respective OSD and so the ability to follow Standard Operating Procedures (SOPs) with precision and interpret complex technical data makes it a very needed skill to have for the professional.

• Communication:  The manufacturing involves various steps and so effective verbal and written communication skills for clear documentation and cross-departmental coordination.

Qualification Required

• Education: B.Pharm or M.Pharm degree from a recognised institution.

• Industry Experience: The manufacturing is a vital process for the pharmaceutical industry and so the candidates must be from the OSD industry; and should have a prior experience in QC roles within pharmaceutical manufacturing .

• Technical Knowledge: Keeping the gravity of the process in mind solid grounding in analytical chemistry and a thorough understanding of GMP/GLP guidelines.

Benefits 

• Professional Advancement: The role is positioned in such a way which will give you an opportunity to "Build your career with Natus Hospital,

• Skill Development: The one who applies for the job will work in an environment dedicated to "Quality, Innovation, and Healthcare,"  which will provide exposure to cutting-edge laboratory techniques and global standards.

• Statutory Benefits: An additional benefit is that  there  are standard provisions of  Provident Fund (PF) and Gratuity are typically provided to permanent employees.

• Cultural Values: Joining a "Growing Team"  which are centered on the pillars of "Grow, Innovate, and Excel" this will  ensure a collaborative and high-performance workplace.

• Technical Excellence: State-of-the-art analytical units (like Unit-IV)  will allow you to get  hands-on mastery of  the complex instrumentation