SMS Pharmaceuticals Ltd-Walk-In-Interview for Production / QA / Store / Maintenance -API on1st & 2nd Dec’ 2023

SMS Pharmaceuticals Ltd-Walk-In-Interview for Production / QA / Store / Maintenance -API on1st & 2nd Dec’ 2023

 

SMS Pharmaceuticals Ltd is one of the leading pharmaceutical manufacturing companies in India with world-class facilities, with a wide range of process equipment fully compliant with the cGMP and WHO Standards. SMS Pharmaceuticals Ltd. is a global player in API manufacturing having a strong research and manufacturing team supported by state of the art facilities. What started off as a single facility – single product manufacturing company in 1990 grew to be a multi-location group having product list spreading across an array of therapeutic segments.

SMS Pharmaceuticals Ltd is conducting Walk-In-Interview for Freshers and
Experienced Candidates in Production / QA / Store / Maintenance -API Division on 1st & 2nd Dec’ 2023 at Hyderabad.

• Departments: Production / QA/ Store / Maintenance
. Qualification: B.Sc, M.Sc, B.Com, M.Com, B.Tech, Any Degree
• Experience: 0-09 yrs
. Division: API
Location: Bachupally, Hyderabad

Walk-In-Interview
. Date: 1st & 2nd Dec’ 2023 .Time: 09:30 AM to 12:30 PM
. Venue:

SMS Pharmaceuticals Ltd, Unit-II, Plot No.: 24 & 24B, 36 & 37, S.V. Co- Operative Industrial Estate, Bachupally, Miyapur, Hyderabad
. Note: Carry out all relevant documents and Preferable for Male Candidates & Immediate Joining.

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

Apply for this position

Allowed Type(s): .rtf

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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