Vital Therapeutics & Formulations- Walk In For Manager Quality Control Department on 1st July 2023

Vital Therapeutics & Formulations- Walk In For Manager Quality Control Department on 1st July 2023

RESOURCES-THE QUALITY SYSTEMS MODEL

1. Dept: Manager – Head QC Department

Qualification: M. Pharmacy & MSc (Organic & Analytical)

Exp: 12-16years

Job Responsible: –

Responsibility: Handle the entire QC department.

a) Ensuring Laboratory compliance as per GMP and GLP on day to day activity

b) Exposure of the especially formulation oral liquid & oral solid Dosage.

c) Responsible for the approval of the all Standard Operating Procedures, Standard Testing Procedures, General Testing Procedures, Validation protocols, Specifications, Record of Results related to Quality Control Dept.

d) Responsible for maintenance of Chemicals, Reagents, Solvents, Columns, Medias, Cultures Stock for smooth functioning of QC activities.

e) Responsible for complying the customer and internal audit observations.

f) Responsible for overall compliance of microbiological section as per GMP and GLP.

g) Should have good leadership and communication skills.

h) Please do not apply if you are from API experience and other than Formulation Exposure.

Date: 1st July’2023 

Time:-10:00 am to 12:30 pm

Venue: Vital Therapeutics & Formulations Pvt. Ltd., D.No:6.2-119/1, Near Bhoiguda Bharath Petrol Bunk, Pillar No: 1010B Opposite. New Bhoiguda, Secunderabad.

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

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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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