Save Job
Posted 3y ago

Executive/ Sr.Executive-QA validations

@ Dr. Reddy's Laboratories
Hyderabad, Telangana, India
OnsiteFull Time
Responsibilities:develop plans, perform validation, review documentation
Requirements Summary:Bachelor's degree in pharmacy, chemistry, microbiology, or related field; 3+ years in pharmaceutical validation; knowledge of cGMP; experience with equipment, facility, process, and computer system validation; strong analytical, communication, and documentation skills.
Technical Tools Mentioned:Microsoft Office, Validation software
Save
Mark Applied
Hide Job
Report & Hide
Job Description
Job Requirements

We are seeking a highly skilled and detail-oriented Executive/Sr. Executive for our Quality Assurance (QA) department in the healthcare sector. The successful candidate will be responsible for performing and managing equipment, facility, process, and computer system validation activities to ensure compliance with cGMP regulations and company standards. The ideal candidate will have experience in validation, strong analytical skills, and a thorough understanding of cGMP regulations.

Key Responsibilities:

  • Develop, execute, and manage validation plans, protocols, and reports for equipment, facility, process, and computer system validations.
  • Perform and manage validation activities, including installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) testing.
  • Review and approve validation documentation, including validation plans, protocols, reports, and change controls.
  • Investigate deviations and non-conformances related to validation activities and recommend corrective and preventive actions (CAPA).
  • Ensure that validation activities are completed on time and within budget.
  • Ensure that validation activities are compliant with cGMP regulations and company standards.
  • Participate in internal and external audits and regulatory inspections.
  • Provide training and guidance to manufacturing personnel on validation-related topics.

Qualifications:

  • Bachelor's degree in pharmacy, chemistry, microbiology, or related field.
  • 3+ years of experience in validation in a pharmaceutical manufacturing environment.
  • Strong knowledge of cGMP regulations and guidelines.
  • Experience with equipment, facility, process, and computer system validation.
  • Excellent analytical and problem-solving skills.
  • Strong attention to detail and accuracy.
  • Good communication and interpersonal skills.
  • Ability to work independently and as part of a team.
  • Proficiency in Microsoft Office applications and other validation-related software.

We offer a competitive salary and benefits package, as well as opportunities for career growth and development. If you are passionate about quality and have a desire to make a difference in the healthcare industry, we encourage you to apply for this exciting opportunity.