Piramal Pharma- Walk-in drive for Multiple Positions on 20th August 2023 

Piramal Pharma- Walk-in Drive for Multiple Positions on 20th August 2023 

Piramal Pharma- Walk-in Drive

Piramal Pharma Solutions
QUALIFICATION AND EXPERIENCE
1. Research Associate – Analytical R&D (API)
M.Sc. (Analytical Chem) with 02-06 years’ in Analytical R&D. Experience in handling Method development by HPLC. Timely analysis & release of In-process, RM, Intermediates and finished products as per procedure to support for R&D.
3. Research Associate – Process/Synthesis R&D (API)
MSc, M.Pharm with 2-6 years of experience in Pharma R&D (API), Experienced on IUT, VQ, LFR/PDR reports documentation, vendor qualification, investigation, and root cause analysis.
Executive – Quality Control (API)
M.Sc./B Pharm/B.Sc. with 04-08 years in QC. Knowledge on handling HPLC. Preferred candidates from API Industry and Regulatory Approved Sites. Knowledge on Empower 3 software.
4. Executive – Production (API)
M.Sc./B.Sc. with 1-5 years’ in Production, execution of BMR, BPR. Knowledge on CGMP and safety practices.
5. Executive-TSD (API)
B.Tech/M.Tech (Chemical) with 4-6 yrs. of exp in Trail & Validations, PFD’s PID’s & process mapping & HAZOP studies
Walk In Drive On 20th Auguest’23 (Sunday) at Hyderabad.
Venue: Piramal Pharma Limited,

Timings: 9:30am – 4 pm
Ground Floor, D3T Tech Hub, 1-98/8/6&7, Image Garden Road, VIP Hills, Silicon Valley, Madhapur, Hyderabad -81, Telangana
and Mark: Metro Pillar no-1765 Muthoot Finance D3T Tech Hub
For queries/Applicants can send in their CVs to:
hr.general@piramal.com

Job Category: pharma
Job Type: Full Time
Job Location: Hyderabad

Apply for this position

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About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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