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Belco Pharma

3 Job openings at Belco Pharma
Production Supervisor Bahadurgarh 0 - 5 years INR 1.5 - 3.0 Lacs P.A. Work from Office Full Time

Role & responsibilities The candidate will be required to learn and supervise the particular section they are assigned too. They will be involved in day to day production process along with man and material handling. The candidate will be required to learn the operation and maintenance of the machine/s in the assigned sections. Preferred candidate profile Experienced candidates in pharma production and machine operation will be preferred. They should be hard working and honest towards their work. English writing is required.

QC Chemist Bahadurgarh,Delhi / NCR 1 - 6 years INR 2.0 - 6.0 Lacs P.A. Work from Office Full Time

Role & responsibilities: The candidate would be required to take on the responsibility of testing of pharma formulations and ensure quality product and production efficiency. Some of the key responsibilities are: 1. Perform QC tests on raw materials, in process samples, and finished products. 2. Conduct analytical testing using instruments like HPLC ,UV , Ph meter, and titration. 3. Maintain proper documentation as per GMP/GLP guidelines. 4. Prepare and review SOPs, quality reports, and calibration records. 5. Ensure compliance with company standards and regulatory guidelines. 6. Report deviations or non-conformances to the QA team. Preferred candidate profile: The candidate should be hardworking and honest. Should be able to manage time, prioritize work accordingly and work well within a team. Proficiency in MS Word/excel and English is mandatory. Experience in testing is desirable but Freshers may apply

QA Chemist Bahadurgarh,Delhi / NCR 1 - 6 years INR 2.0 - 6.0 Lacs P.A. Work from Office Full Time

Role & responsibilities: The candidate would be required to take on the responsibility of ensuring quality product and production efficiency. Some of the key responsibilities that may be given are: 1. Review and maintain batch records, SOPs and quality documentation. 2. Conduct in-process checks and ensure GMP compliances. 3. Perform internal audits and assist in external audits (FDA, WHO, ISO, etc.) 4. Handle deviations, CAPA, change controls, and OOS investigations. 5. Ensure data integrity and documentation as per regulatory requirements. 6. Coordinate with QA, QC and Production teams to maintain quality standards. 7. Carry out validations and risk assessments Preferred candidate profile: The candidate should be hardworking and honest. Should be able to manage time, prioritize work accordingly and work well within a team. Proficiency in MS Word/excel and English is mandatory. Experience in testing is desirable but Freshers may apply