Zentiva Hiring Freshers for Quality Assurance (QA) Role
Position Name
Quality Assurance (QA) – Executive I
Organization
Zentiva
Location
Ankleshwar, Gujarat
Are you eager to kickstart your career in the pharmaceutical industry? Zentiva is hiring fresh graduates for the Quality Assurance (QA) role in Ankleshwar, Gujarat. Zentiva is a leading player in the global pharmaceutical industry, known for its commitment to quality and compliance in pharmaceutical manufacturing. As a fresher or someone with up to 3 years of experience, this is an excellent opportunity to join a dynamic team in a full-time position.
Key Responsibilities
As a Quality Assurance Executive I at Zentiva, your role will involve ensuring that all pharmaceutical manufacturing processes comply with Good Manufacturing Practices (GMP) and regulatory requirements. Below is a detailed breakdown of your responsibilities:
Quality Management & Continuous Improvement
- Line Clearance: Ensuring proper clearance of production lines and maintaining shop floor compliance.
- In-Process Checks: Conducting in-process sampling and checks to ensure quality standards.
- Complaint Investigation: Assisting with the site Complaint Investigation System to address quality concerns.
- Qualification & Validation: Supporting the validation of systems, equipment, and handling changes, deviations, and corrective actions.
- APQR: Preparing and reviewing the Annual Product Quality Review (APQR) for quality compliance.
- Batch Records Review: Ensuring the accuracy and completeness of Batch Manufacturing and Packing Records.
Compliance Management
- Regulatory Compliance: Ensuring adherence to FDA, MHRA, and other regulatory bodies’ guidelines.
- Gap Analysis: Identifying and addressing any gaps in current quality systems.
- Compliance Execution: Implementing compliance action plans and tracking their completion.
Validations & Qualifications
- Equipment Validation: Reviewing and ensuring that all equipment, processes, and cleaning methods remain validated.
- Protocol Review: Reviewing validation protocols and ensuring the quality of the production process.
Documentation Control
- SOP Management: Preparing, reviewing, and controlling the distribution of Standard Operating Procedures (SOPs).
- Master Document Control: Ensuring compliance with master documents and archiving processes.
cGMP Training
- GMP Training Programs: Developing GMP training programs in coordination with other departments.
- Training Modules: Creating training modules to keep employees updated on current Good Manufacturing Practices (GMP).
Other Responsibilities
- Maintenance & Calibration: Assisting with the maintenance and calibration program to ensure the functionality of equipment.
- Safety: Reporting unsafe conditions and ensuring a safe working environment.
Qualifications & Requirements
To be considered for the role of Executive I – Quality Assurance, candidates must meet the following qualifications:
| Qualification | Description |
|---|---|
| B.Pharm | Bachelor of Pharmacy |
| M.Pharm | Master of Pharmacy |
| B.Sc | Bachelor of Science (Chemistry or related field) |
| M.Sc | Master of Science (Chemistry or related field) |
Experience
| Experience Level | Description |
|---|---|
| 0-3 Years | Freshers to 3 years of experience in the pharmaceutical industry |
Candidates with experience in Quality Management Systems, Process Validation, and Regulatory Compliance will be given preference. However, freshers with a passion for quality and attention to detail are encouraged to apply.
Skills & Competencies
Zentiva is looking for individuals with the following skills:
- Knowledge of GMP: Familiarity with Good Manufacturing Practices and regulatory guidelines.
- Communication: Strong interpersonal skills and the ability to present complex technical issues clearly.
- Teamwork: A collaborative mindset with the ability to work effectively in a team.
- Problem-Solving: Ability to resolve conflicts and propose quality improvements.
Salary
The salary range for this position is ₹25,000 – ₹35,000 per month, depending on qualifications and experience.
Why Join Zentiva?
Zentiva offers an opportunity to work with a global pharmaceutical leader committed to high-quality standards and innovative solutions. Joining Zentiva means becoming part of a team that values:
- Continuous Learning: Zentiva provides opportunities for professional development and career growth.
- Dynamic Work Environment: Work in a collaborative, fast-paced environment that encourages innovation.
- Global Compliance Standards: Exposure to international regulatory practices, including FDA and MHRA standards.
How to Apply
If you meet the qualifications and are excited to start or further your career in Quality Assurance, apply now! Submit your application with the Job Requisition ID: R2466942 to Zentiva.
Location: Ankleshwar, Gujarat
Zentiva’s Ankleshwar facility is located in the heart of India’s pharmaceutical manufacturing hub. It provides an excellent environment for growth and learning in the pharmaceutical industry.
Take the first step towards a rewarding career in Quality Assurance. Apply today and join Zentiva in delivering high-quality, compliant pharmaceuticals that meet global standards!