Abryl Laboratories Pvt Ltd Jobs – FR&D, QC, IPQA, Production, Microbiology

The Quality Control (Documentation) department in a pharmaceutical company plays a critical role in ensuring that the drugs manufactured meet the required standards of quality, safety, and efficacy. The main role of this department is to ensure that the correct documentation is in place for all aspects of the drug manufacturing process and to ensure that the documentation accurately reflects the actual process. Some specific responsibilities of the Quality Control (Documentation) department include:

1. Reviewing and approving Standard Operating Procedures (SOPs) and Master Production Records (MPRs).
2. Monitoring the implementation of SOPs and MPRs in the production process.
3. Reviewing Batch Production Records (BPRs) to ensure that they accurately reflect the production process and that all required tests have been performed.
4. Verifying the accuracy and completeness of Quality Control (QC) Test Reports.
5. Reviewing Validation Reports to ensure that the production processes, equipment, and systems are capable of consistently producing products that meet the specified requirements.
6. Investigating and documenting deviations from established procedures and processes.
7. Maintaining an audit trail of all documentation, including SOPs, MPRs, BPRs, QC Test Reports, Validation Reports, and Deviation and Investigation Reports.

Overall, the role of the Quality Control (Documentation) department is to ensure that the drug manufacturing process is thoroughly documented and that the documentation accurately reflects the actual process, so that the manufactured drugs meet the required quality standards.

Designation:- Executive / Sr. Executive

Experience:– 4-8 years.

Formulation Research & Development; The Formulation Research & Development department in a pharmaceutical company is responsible for the development of new drug formulations and the improvement of existing ones. The main goal of this department is to develop effective and stable drug products that meet the needs of patients.

Designation:-  Sr. Executive / Assistant manager

Experience:– 5-10 years.

IPQA; IPQA stands for In-Process Quality Assurance in the pharmaceutical industry. The main role of IPQA is to monitor and control the quality of the drug manufacturing process in real-time, to ensure that the finished product meets the required standards of quality, safety, and efficacy.

Designation:- Executive

Experience:– 3-5 years.

Production (Vial/Ampule filling, Vial washing, compounding); Production (Vial/Ampule filling, Vial washing, compounding) refers to the process of manufacturing pharmaceutical products, specifically, filling vials or ampules with the liquid or semi-solid drug product, washing the containers, and compounding the ingredients to create the final product.

Designation:- Technician

Experience:– 2-6 years.

Micro (Environment monitoring); Microbiology (Environment Monitoring) in the pharmaceutical industry involves monitoring the environmental conditions in which drugs are manufactured to ensure that they are free from contaminants and that the final product meets the required standards of quality, safety, and efficacy.

Designation:- Jr Executive

Experience:– 2-4 years.

APPLICATION PROCESS; Interested candidates can share their cv’s on- hr.2@abryl.in