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.
DATE AND TIME:
- Date: Sunday- 29th Dec, 2024
- Time: 09.00 a.m. to 05.00 p.m.
- Venue: Hotel Silver Leaf, Plot No-CM-14 & 15, Raghuvir Complex, Opp. Vapi Industries Association Ground, GIDC, Vapi – 396195
If unable to attend the interview, please forward your updated CV at: resume.dahej@ajantapharma.com
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
- Designation: 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 Granulation, Compression, Coating, Pellet coating, Capsule filling, Primary Packing & Secondary Packing.
- Expertise in e-BPR and e-log will be added advantage
3. Department: QUALITY CONTROL
- Designation: Officer/ Sr. Officer
- Experience: 02 to 08 yrs.
- Qualification: B.Pharm/ B.Sc. /M.Sc
- Job description: Experience in analysis of Solid Oral – FP, In-process or Stability samples. Experience of HPLC, UV spectrophotometer and Dissolution Tester operation. Experience of Analytical Method Validation/Transfer (Solid Oral). Experience of GC, ICPMS and/or LCMS operation.
4. Department: QUALITY ASSURANCE
- Designation: Officer / Sr. Officer
- Experience: 02 to 08 yrs.
- Qualification: B.Pharm/ M.Pharm / M.Sc
- Job description: Experience in DRA, IPQA, Validation & AQA Section. Currently working in USFDA approved facility.
Note:
- For all the positions, candidates having exposure to regulatory requirements of documentation cGMP /GDP and worked in regulated plants shall be preferred.
- 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.
- Candidates already appeared for an interview in last 06 months will not be eligible for the interview.
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