Walk-in | Production Documentation Chemist

Covalent Laboratories; Sangareddy; Presencial; INR 167 000 - 279 000; Tempo integral

Resumo da oferta

Covalent Laboratories Private Limited is a USFDA, EU-GMP & ISO 14001(2004) certified and reputed pharmaceutical company, leading in Cephalosporin products since 2003 in global and domestic markets.

Trainee or Jr Executive For Formulation FRD is invited to contribute to batch process knowledge, equipment handling, and document verification to ensure compliance and quality in production.

Qualificações

• UG: Any Graduate.
• Experience with GMP/SOPs is a plus.
• Familiarity with BMR/BPR requirements and data integrity.

Responsabilidades

• Responsible for preparing, reviewing, maintaining, and controlling production-related documents per GMP, SOPs, BMR/BPR and regulatory guidelines.

Conhecimentos

Documentation

GMP compliance

SOPs adherence

Regulatory guidelines

Data integrity

Document review

Formação académica

Any Graduate

Descrição da oferta de emprego

12th October- 13th October, 9.30 AM - 5.30 PM

Contact - Mahesh Reddy(9100132004)

Responsible for preparing, reviewing, maintaining, and controlling production-related documents in compliance with GMP, SOPs, BMR/BPR requirements, data integrity, and regulatory guidelines

Role Category: Production & Manufacturing - Other

Education

UG: Any Graduate

Key Skills

Skills highlighted with ‘‘ are preferred keyskills

Covalent Laboratories Private Limited is an USFDA,EU-GMP & ISO 14001(2004) Certified & Reputed Pharmaceutical Company, pioneer & Leader of producing Cephalosporin products since 2003 in theGlobal/Domestic market.

Mid-Sized Firm in Pharma & Life Sciences Domain

Trainee or Jr Executive For Formulation FRD

batch process knowledge and equipment handle and document verify basically this knowledge is good

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