B.Pharmacy JobsB.Sc JobsExperienced JobsM.Pharmacy JobsM.Sc jobsPharma JobsProduction JobsQuality Assurance JobsQuality Control JobsRaghava Life Sciences

Raghava Life Sciences – Walk-in for Production/ QA/ QC on 24th June 2022

Raghava Life Science is end-to-end contract research, development, and manufacturing organization (CRO-CDMO) offering products and services across the drug development spectrum to enable our partners to turn their concepts into commercials. We work with global pharma companies to accelerate the discovery, development, and manufacture of complex small molecules, consistently delivering values based on quality, responsiveness, and transparency. Raghava Life Science is a young and fast-growing company. Founded in 2018, it is headquartered in one of the fastest-growing ISO-certified metropolitan cities, Hyderabad, India

Walk-In Interviews for QA / QC / PROD Departments on 24th June 2022 at Corporate Office: Raghava Pride,
#6-2-603/1/27, Krishnapuram Street, Road No 10, Banjara hills, Hyderabad, Telangana
Email: [email protected]

Department: Quality Assurance
Posts: Executives / Sr. Executives – 30 Nos.
Experience: 0-5 years.
Qualification: B.Sc/M.Sc/B.Pharm/M.Pharm
Job Description:

  • IPQA– Daily plant online monitoring, In-process samples monitoring, Line Clearance, raising of any deviations, Incidents during the online monitoring, Monitoring of IM, API, RM Sampling and packing
  • Doc. Control team – Issuance and Retrieval, Doc. Distribution, Obsolete doc., Archival maintenance and Labelling, General Stationary indent and maintenance, Batch Release /QA release for dispatched products, Customer samples, Responsible for Production Department, Executed BPRs, ECRs Review, Master BPRs, ECRs Review, Responsible for PD department, PD change controls
  • Validations & Qualifications – Process Validations, Cleaning Validations, DEHT Validations, CEHT Validations, Water system validations, Utensils cleaning validation, Equipment Qualifications, Facility Qualifications, Preventive Maintenance, Calibrations, Schedules, Utility qualifications, Responsible for ENG department, Responsible for ENG, HR, SE, ENG, HR &SE change controls
  • Vendor Qualifications – Vendor Qualification all materials, WH SOPs review, Vendor Evaluation, RM trending, Approved Vendor list, RM data filing, WH department related documents monitoring, Responsible for WH monitoring, WH change controls QMS – Deviations, Incidents, Internal Audits, MRM, VMP, Trainings, APQRs, CAPA, Complaints, Return Goods, Recalls, OOS/OOT, Errata, Responsible for QA, QA change controls
  • AQA – Analytical Data Review, SOPs review, INP data, Intermediate data, FP data, Cleaning Samples, DM water, Lab incidents, Lab deviations, OOS/OOT, working stand qualifications, QC schedules, Stability chambers monitoring, holding data, Stability data, Calibrations, Method validations, Method transfers, Method verifications, Software validations, Computer system Validations, Responsible for QC and change controls
  • Audit Compliance team and RA, License – Audits preparation and report preparation compilation, Customer VQ, DMF/RA support, Customer /RA Queries, Mails Response, License documents, WHO GMP/ EU written confirmations, ISO certifications and any regulatory….

Department: Quality Control
Post: Analyst/Executives / Senior Executives – 30 Nos
Qualification: B.Sc/M.Sc/B.Pharm/M.Pharm
Experience: From 1 to 6 year(s) of experience
Job Description: Experience in handling of instruments like HPLC, GC, KF apparatus etc.& software like Empower 3, Lab Solutions. Knowledge in investigations i.e., Incidents(Laboratory), OOS, OOT, Complaints, Audit trail review, QMS review.

Department: Production
Post: Chemists / Sr. Chemists – 70 Nos

  • Qualification: B.Sc. /M.Sc. In Chemistry, B.Pharm/ M.Pharm,
  • Experience: From 2 to 8 year(s) of experience

Post: Block In-charge / Shift In-charge – 20 nos

  • Qualification: B.Sc. /M.Sc. In Chemistry, B.Pharm/ M.Pharm,
  • Experience: From 10 to 12 year(s) of experience

Job Description: Must have API Manufacturing Experience., Execute production batches as per plan, following relevant SOPs, Verification of cleaning area / equipment and completion of Logs, To comply with cGMP standard during the entire manufacturing activity, Concurrent completion of batch process records. To maintain the manufacturing facility as per the regulatory norms, To comply with EHS standards, Purely knowledge on shop floor, Clean rooms, Pilot Plant, Intermediate areas.

Interested candidates who cannot attend walk in can send their resumes to [email protected] along with CTC, Expected CTC, and Notice Period info.

Date of interview: 24th June 2022
Venue: Corporate Office: Raghava Pride, #6-2-603/1/27, Krishnapuram Street, Road No 10, Banjara hills, Hyderabad, Telangana.

Back to top button