Ajanta Pharma is a specialty pharmaceutical company engaged in development, manufacturing and marketing of quality finished-dosages. Committed to Serve Health Care Needs Worldwide, it produces comprehensive range of 1st to market products in specialty therapeutic segments, customized for each market it is present in, is looking for suitable candidates for its Formulation facility.
ajanta pharma limited
Walk In Interview @, Indore
Plant Location :- Dahej, Gujarat
1.Department: PRODUCTION Officer/ Sr. Officer
Experience: 02 to 08 yrs.
Qualification: B. Pharm / M. Pharm
Job description: Exposure to OSD Manufacturing operations like Granulation, Compression, Coating, Pellet coating, Capsule filling, Primary Packing & Secondary Packing.
Expertise in e-BPR and e-log will be added advantage.
2.Department: PRODUCTION (e-BMR/MES/PAS-X) Officer/ Sr.Officer
Experience: 02 to 08 yrs.
Qualification:B. Pharm/ M.Pharm
Job description: Experience of MBR designing, troubleshooting and simplification in MES (e-BMR).
Experience of PCS element & Alias preparation and configuration between equipment and MES.
Exposure to MM and PP Module of SAP and MES.
3.Department: PRODUCTION
Associate/Operator/ Technician
Experience: 02 to 10 yrs.
Qualification: 10th, 12th + I.T.I, Diploma, D. Pharm
Job description: Exposure to OSD Manufacturing operations like Gianulation, Compression, Coating, Pellet coating, Capsule filling, Primary Packing & Secondary Packing
4.Department: QUALITY CONTROL
Officer/ Sr. Officer
Experience: 02 to 08 yIs.
Qualification: B. Pharm/ B.Sc./M. Sc
Job description: Experience in analysis of HPLC, RM, XRD, ICPMS, LCMS, FP, IP, PV and stability samples and method validation and method transfer. Experience of handling of various instruments and expertise in Chromatography and Spectroscopy analysis.
Sunday- Oct 20, 2024
Between 09.00 a.m. to 05.00 p.m.
Venue: Papaya Tree Hotel Rau-Indore, Bypass Square, A.B. Road, Opp Dr.
Hardia Eye Hospital Rau-Indore.
453331,M.P. India.
1) For all the positions, candidates having exposure to regulatory requirements of documentation cGMP /GDP and worked in regulated plants shall be preferred.
2) Interested candidates who are working with USFDA/MHRA approved facilities only, may attend interview along with updated CV, current CTC structure, 3 recent salary slips, documents of educational qualification and previous employments.
3) Candidates already appeared for an interview in last 06 months will not be eligible for the interview.
If unable to attend the interview, please forward your updated CV at: [email protected]
