Vimta Labs Ltd- Interviews for Scientist/ Sr.Scientist/ CRA/ SCRA on Sunday, 31-Mar-2024

Vimta Labs Ltd- Interviews for Scientist/ Sr.Scientist/ CRA/ SCRA on Sunday, 31-Mar-2024

Vimta Labs Ltd- Interviews

Vimta Labs Ltd. Walk-in Interviews for Research Scientist/ Sr.Scientist/ CRA/ SCRA – Clinical Research, Clinical Trial & Preclinical on Sunday, 31-Mar-2024

We welcome you to join and build a promising career and evolve as a scientific professional with India’s leading Contract Research and Testing Organization.

Department:

Clinical Research (CRBASC)

Clinical Trial (CTCRA)

Preclinical (PCDTX)

Preclinical (PCDDM)

Position: Research Scientist/ Sr.Scientist/ CRA/S CRA

Location: Hyderabad (Cherlapally)

QUALIFICATION: M.Sc./ B.Pharmacy/ M.Pharmacy

Experience: 3 to 8 years

SKILLS: Experience in Bioanalytical, Method Development and Validation using LCMS-MS Bioanalytical, Method Development, Validation, and study samples analysis

Experience in Clinical Trial Monitoring (Patient Monitoring) including site evaluation, EC dossier preparation and multiple vendor coordination.

Having the skillset in handling multiple therapeutic area and multi-site experience

Study Director/ Study Person for General and Reproductive Toxicology studies.

Study Director/ Study Person for ADME/Invitro DMPK studies Experience with cell culture, IVPT, IVRT, Flow Cytometry expertise

Date and Time: On Sunday, 31-Mar-2024 at 10 AM onwards

Venue:
Address: Hotel Gravity, 9th Phase KPHB Colony, Plot No 53, 54, & 55, Near to Forum Sujana Mall, Hyderabad, Telangana 500085

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

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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