Walk In Interview For Production, Quality Control And Quality Assurance Department At Ajanta Pharma - Job Engine

Latest Updates

Wednesday, 12 February 2025

Walk In Interview For Production, Quality Control And Quality Assurance Department At Ajanta Pharma

Walk In Interview Ahmedabad
Plant Location:-Dahej, Gujarat

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.

Dept. PRODUCTION Officer/Sr. Officer

Qualification/Experience
B. Pharm/M. Pharm 02 to 08 yrs,

Job Description
Exposure to OSD Manufacturing operations like Granulation, Compression, Pellet coating, Capsule filling, Primary Packing & Secondary Packing. Expertise in e-BPR and e-log will be added advantage.

Department 
PRODUCTION Associate/Operator

Qualification 
10th, 12th I.T.I, Diploma, D. Pharm 02 to 10 yrs.

Job Description 
Exposure to OSD Manufacturing operations like Granulation, Compression, Pellet coating, Capsule filling, Primary Packing & Secondary Packing. Expertise in e-BPR and e-log will be added advantage.

Department 
QUALITY CONTROL Officer/Sr. Officer

Qualification 
B. Pharm/B.Sc./M. Sc 02 to 08 yrs.

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.

Department 
QUALITY ASSURANCE Officer/Sr. Officer

Qualification 
B. Pharm/B.Sc./M. Sc 02 to 08 yrs.

Job Description 
Experience in DRA, IPQA, Validation & AQA Section. Currently working in USFDA approved facility.

Sunday- Feb 16, 2025

Between 09.00 a.m. to 04.00 p.m.

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: resume.dahej@ajantapharma.com

No comments:

Post a Comment