Akums Drugs & Pharmaceuticals Hiring QA – Validation & Qualifications Executives

Akums Drugs & Pharmaceuticals, a leading name in pharmaceutical manufacturing, is hiring QA – Validation & Qualifications Executives for its EU-GMP-approved Injectable Manufacturing Unit located in Haridwar.

If you have the expertise and qualifications required for this role, this is your chance to work with a company renowned for its world-class pharmaceutical solutions.

Job Details – Akums QA Validation & Qualifications Executives

Position:

• Executive

Department:

• QA – Validation & Qualifications

Qualification:

• B Pharm (Bachelor of Pharmacy)

Experience Required:

• 3 to 7 years of relevant experience in pharmaceutical QA processes, specifically in validation and qualification.

Location:

• Haridwar

About Akums Drugs & Pharmaceuticals

Akums Drugs & Pharmaceuticals is a pioneer in pharmaceutical manufacturing and has a strong global reputation for delivering high-quality formulations.

The company’s Injectable Manufacturing Unit, approved by EU-GMP, is known for its cutting-edge technologies and strict compliance with global quality standards.

Key Responsibilities of QA Validation & Qualification Executives

1. Process Validation:
   • Oversee the validation processes for injectable manufacturing.
   • Ensure compliance with EU-GMP guidelines during validation.
2. Equipment Qualification:
   • Handle qualification protocols for equipment and systems used in manufacturing.
3. Documentation:
   • Prepare, review, and maintain validation and qualification documents.
   • Ensure accurate reporting and timely submission of records.
4. Compliance Assurance:
   • Work closely with regulatory and internal teams to ensure adherence to quality standards.

How to Apply for QA – Validation & Qualifications Executives

Interested candidates can share their updated resumes at amit.sharma@akums.in.

Additional Tips for Applicants

1. Highlight your experience in validation and qualification processes in the pharmaceutical industry.
2. Emphasize any previous work in compliance with EU-GMP standards.
3. Ensure your resume is up-to-date and tailored to the role.