SMS Pharmaceuticals Ltd-Interview for Freshers and Experienced Candidates in Production / QC/QA/Maintenance -API Division on 13th & 14th April’ 2024 at Hyderabad.

SMS Pharmaceuticals Ltd-Interview for Freshers and Experienced Candidates in Production / QC/QA/Maintenance -API Division on 13th & 14th April’ 2024 @ Hyderabad.

SMS Pharmaceuticals Ltd-Interview

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.
SMS Pharmaceuticals Ltd is conducting Walk-In-Interview for Freshers and Experienced Candidates in Production / QC/QA/Maintenance -API Division on 13th & 14th April’ 2024 at Hyderabad.

Job Description:
·
Departments: Production / QC/QA/ Maintenance
Qualification: B.Sc, M.Sc, B.Pharm, M.Pharm, ITI, Diploma, B.Tech, Any Degree Experience: 00-09 yrs
Division: API
Location: Bachupally, Hyderabad
Please bring the following documents:
Latest Update copy of Resume
Latest three months Pay slips & Bank statement
Academic certificates
Walk-In Interview Details:
• Date: 13th & 14th April’ 2024
Time: 09:00 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: Preferable for Male candidates with Regulatory API plant exposure will be considered.
Registration Link: https://forms.office.com/r/km UuvbB4a1?
origin=QRCode&qrcodeorigin=presentation

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

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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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