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Urgent Vacancy for Senior Manager / Manager – Formulation QC (Guwahati) @ Natco Pharma Limited

Urgent Vacancy for Senior Manager / Manager – Formulation QC (Guwahati) @ Natco Pharma Limited

Post : Senior Manager / Manager – Formulation QC

Job Description
• Ensuring Laboratory compliance as per GMP and GLP on day to day activity.
• 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.
• Responsible for maintenance of Chemicals, Reagents, Solvents, Columns, Medias, Cultures Stock for smooth functioning of QC activities.
• Responsible for complying the customer and internal audit observations.
• Responsible for overall compliance of microbiological section as per GMP and GLP.
• Responsible for timely execution of method transfer/method verification activities for new products and drug substances in coordination with ARD and project management team.

Important Note:
• Please do not apply if you are from API experience and other than pharma background.
• You may also refer this mail / posting to your friends who are looking for an opportunity.
• Should have good leadership and communication skills

Additional Information:
Experience : 16-20 years
Qualification : M.Sc / M.Pharm / B.Pharm
Location : MIRZA, GUWAHATI
Industry Type :  Pharma / Biotech / Clinical Research
Functional Area : QC
Last date : 10th July, 2020

Interested candidates are requested to share the profiles to Mail id: gwhr@natcopharma.co.in  (or) usharani@natcopharma.co.in

Apply for this position

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About Pharmaceutical Guidanace

Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 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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