Ajanta Pharma Ltd Released Job Openings On 22/06/2022.Ajanta Pharma is a specialty pharmaceutical company engaged in development, manufacturing and marketing of quality finished dosages. Committed to ‘Serve Health Care Needs Worldwide’, we produce a comprehensive range of specialty products targeting different therapeutic segments for treatment of patients, customised to each market we are present in.
Vacancy Details:
Ajanta Pharma Ltd Recruiting B.Pharm,M.Pharm,M.Sc Candidates with 02+ Years of Experience for QC,QA,Production,Manufacturing,Packing Position.
Important Details :
- Location: Goa
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application: 22/06/2022
- Mode of application : Walk In
- Time And Venue:  26th June 2022,10:00 AM to 05:00 PM,The Fern Kesarval Hotel & Spa Verna Plateau, Kesarval Cortalim Goa – 403710
- Contact : If unable to attend interview then forward updated CV at manish.datta@ajantapharma.com / rahul.bhat@ajantapharma.com
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Job Description/Skills Required
Department: Quality Control
- Officer / Asst. Officer (QC):Â B.Pharm / M.Pharm / M.Sc. Experience range: 02 to 05 years
- Over all experience in analysis of FP, IP, PV and Stablity samples. Handling of various instruments like IR, UV and HPLC. Expertise in Chromatography and Spectroscopy analysis.
Department: Production ( Manufacturing OSD )
- Sr. Officer / Officer (Production):Â B.Pharm / M.Pharm with 03 to 06 years of experience. Candidates should have experience of granulation, compression, coating & capsules areas.
- Sr. Executive (Production):Â B.Pharm / M.Pharm with 12 to 13 years of experience. Should have worked in capacity of Shift in-charge. Experience with E-BMR systems is preferred.
Department: Quality Assurance
- Officer: B.Pharm / M.Pharm / M.Sc. with 02 to 03 years of experience. The candidate should have exposure in preparation of BMR / BPR. Experience with E – BMR systems is preferred.
- Officer (Lab QA):Â B.Pharm / M.Pharm / M.Sc with 03 to 04 years experience. The candidate should have exposure of review of analytical reports ( QC ), instrument log books, compliance of procedure in lab, co ordination with DRA, ensure integrity of data.
Note:
- For all positions, candidates having exposure to regulatory requirements of documentation CGMP / GDP and worked in regulated plants shall be preferred.
- Wearing of mask is compulsory at the venue. Maintain social distancing.
- 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.



