Job Opportunities in India
May 19, 2023
Venus Remedies
Baddi
FULL TIME
QA Officer
QA Officer
IPQA person develops and implements SOPs or the manufacturing process to ensure consistency and adherence to quality standards. Monitors and verifies the manufacturing process to ensure that it is performed in compliance with established procedures and guidelines. Conducts IPQC tests on samples taken from the manufacturing process to ensure that the product meets quality specifications. Reviews and approves batch records to ensure that all manufacturing and testing activities are correctly documented and comply with regulatory requirements. Collaborates with other departments, such as Manufacturing, Quality Control, and Regulatory Affairs, to ensure that quality standards are maintained throughout the product life cycle.
Job Posting: 05/12/2023
IPQA person develops and implements SOPs or the manufacturing process to ensure consistency and adherence to quality standards. Monitors and verifies the manufacturing process to ensure that it is performed in compliance with established procedures and guidelines. Conducts IPQC tests on samples taken from the manufacturing process to ensure that the product meets quality specifications. Reviews and approves batch records to ensure that all manufacturing and testing activities are correctly documented and comply with regulatory requirements. Collaborates with other departments, such as Manufacturing, Quality Control, and Regulatory Affairs, to ensure that quality standards are maintained throughout the product life cycle.
Job Posting: 05/12/2023
Baddi
JOB REQUIREMENTS
Mandatory Qualifications
B.Pharma.
B.Pharma.
Work Experience in Relevant Field
2-4 Years
Technical Skills Required
Should have a good understanding of c GMP regulations, FDA guidelines, and other industry standards. reviewing batch records, conducting investigations, and collaborating with other departments. Experience in In-process quality assurance in the pharmaceutical industry, particularly in injectables, is preferred.
2-4 Years
Technical Skills Required
Should have a good understanding of c GMP regulations, FDA guidelines, and other industry standards. reviewing batch records, conducting investigations, and collaborating with other departments. Experience in In-process quality assurance in the pharmaceutical industry, particularly in injectables, is preferred.
JOB DESCRIPTION
Who You'll Work With
QA department
QA department
What You'll Do
To develop and implement SOPs for the manufacturing process to ensure consistency and adherence to quality standards.
To develop and implement SOPs for the manufacturing process to ensure consistency and adherence to quality standards.
Soft Skills Required
Ability to work in a fast-paced environment and manage multiple priorities simultaneously
Ability to work in a fast-paced environment and manage multiple priorities simultaneously
Functional Area
Quality Assurance
Quality Assurance
Recruitment Status
Active
Active
Employment Type
Full Time
Full Time
Date of Joining
Immediate
Immediate
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