inventia -INTERVIEW For Quality Control& Production on 5th APRIL 2024

inventia -Interview For Quality Control& Production on 5th APRIL 2024

inventia -Interview
inventia WALK-IN INTERVIEW
Quality Control I Production

Important Note:
• Current pharma (formulation) background is must.

• Aware of all required regulatory norms, good in read, write & understanding of English language.
• Only relevant experienced candidates as per criteria mentioned are invited.
• Experienced applications will be entertained only as per specific interview schedule.
QUALITY CONTROL (IPFP/Stability/RM/PV)
Education & Experience: B Sc/MSc with 1 to 5 years of relevant Oral Solid Dosage formulation plant experience only. (No API Plant). Instrument Expertise: HPLC, Dissolution, GC, UV.
Other Qualities: Aware of all required Regulatory
norms like GLP, GDP, GMP, LIMS.
PRODUCTION (Tablet/Pellets/Packing)
Education & Experience: ITI/D Pharm with 2 to 5 years of relevant experience only. Instrument Expertise: Compression (Bi-Layer), Coating pan, Encapsulation, Cartonator, Blister packing.
Other Qualities: Aware of all required Regulatory norms like GLP, GDP, GMP, LIMS.
Interview | Hotel Nakshatra, Lot No. K-1, Additional MIDC, Near Anand Nagar,

5th APRIL 2024
Time:9 am to 1 pm 

Venue Ambernath (E), Thane Dist., MH – 421506
Note: Candidate should bring Resume, Aadhar Copy, Education Certificates, Current CTC
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Job Category: pharma
Job Type: Full Time
Job Location: Ambernath (E)

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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