Pharmaceutical Guidance Complete Pharma Solution
Shilpa Medicare Limited – Urgent Requirement of Senior Positions in Regulatory Affairs / QA / Engineering & Projects – Apply Now
We are looking for Regulatory Affairs (ROW Market) professional having experience 4-12 years for Hyderabad based pharmaceutical corporate office
Interested candidates, please forward your resume to: smsaravanapharma@gmail.com
saravanakumar.m@shilpatherapeutics.com
Note: Telephonic interview will be conducted
Male candidate is preferred
We are looking for Regulatory Affairs (ROW Market- RUSSIA and LATAM) professional having experience 7-10 years for Hyderabad based pharmaceutical corporate office
Interested candidates, please forward your resume to: smsaravanapharma@gmail.com
saravanakumar.m@shilpatherapeutics.com
Note: Telephonic interview will be conducted
Male candidate is preferred
We are looking for Head QA having experience 20 plus years in Sterile and OSD formulation (Oncology experience is preferred) for USFDA approved pharmaceutical Company based at Hyderabad.
Interested candidates, please forward your resume to: smsaravanapharma@gmail.com
saravanakumar.m@shilpatherapeutics.com
Note: Expert in USFDA, UKMHRA, TGA, WHOGMP requirements etc. is preferred
We are looking for Head -Engineering and Projects having experience 20 plus years in pharmaceutical industry -engineering activities and projects for USFDA approved pharmaceutical company based at Hyderabad.
Interested candidates, please forward your resume to: smsaravanapharma@gmail.com
saravanakumar.m@shilpatherapeutics.com
Note: Expert in Engineering activities and projects as per recent regulatory requirements.
Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 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
