Location: Gujarat, India

Experience:
2-5 years

Company Overview:

We are hiring for pharmaceutical company establishing a new setup in Gujarat, India.

Position Overview: We are seeking a skilled and experienced Quality Control Analyst to join our team in Gujarat. The ideal candidate will have 2-5 years of experience in quality control, preferably in the pharmaceutical industry. The role will involve conducting various quality control tests and analyses, with a focus on ensuring compliance with regulatory standards and maintaining product quality.

Responsibilities:

1. Perform routine and non-routine analysis of raw materials, intermediates, and finished products using analytical techniques such as HPLC, GC, UV-Vis spectroscopy, etc.
2. Conduct analytical testing and method validation in accordance with established protocols and procedures.
3. Ensure compliance with regulatory requirements and industry standards, including cGMP guidelines.
4. Document and report test results accurately and promptly, maintaining thorough records of all analyses performed.
5. Investigate and troubleshoot any deviations or out-of-specification results, implementing corrective actions as necessary.
6. Assist in the development and optimization of analytical methods and procedures to improve efficiency and effectiveness.
7. Participate in internal audits and inspections, supporting quality assurance activities as needed.
8. Collaborate with cross-functional teams, including production, quality assurance, and R&D, to resolve quality-related issues and drive continuous improvement initiatives.
9. Maintain cleanliness and organization of the laboratory, ensuring proper calibration and maintenance of equipment.
10. Stay updated on industry trends, regulatory changes, and best practices in quality control and analytical testing.

Qualifications:

1. Bachelor’s or Master’s degree in Pharmacy, Chemistry, or related field.
2. 2-5 years of experience in quality control, preferably in the pharmaceutical industry.
3. Hands-on experience with analytical techniques such as HPLC, GC, UV-Vis spectroscopy, etc.
4. Strong knowledge of cGMP guidelines and regulatory requirements for pharmaceutical quality control.
5. Excellent analytical and problem-solving skills, with keen attention to detail.
6. Effective communication and interpersonal skills, with the ability to work well in a team environment.
7. Proficiency in computer software applications, including Microsoft Office and laboratory information management systems (LIMS).
8. Ability to work independently, prioritize tasks, and meet deadlines in a fast-paced environment.