Quality Control Analyst

Indchemie Health Specialities Pvt. Ltd.

Website: indchemie.in
Job details:
Company Description

Indchemie Health Specialities Pvt. Ltd., established in 1986, is a leading Indian pharmaceutical company with a strong global presence in various therapeutic segments. With operations spanning South East Asia, Central America, East Europe, Africa, and Latin America, Indchemie is committed to providing quality pharmaceutical formulations and dosage forms both in India and overseas. Backed by a highly skilled regulatory team, the company has successfully filed dossiers in regulated, semi-regulated, and non-regulated markets. With a 700-member domestic field force covering over 20,000 doctors, Indchemie continues to deliver high-quality healthcare solutions. Products like CHERi, a top 10 hematinic brand in India, emphasize its focus on innovation and excellence in its field.

Role Description

The Quality Control Analyst is a full-time, on-site position based in Baddi. The role involves performing quality control tests, analyzing raw materials and finished pharmaceutical products, and ensuring compliance with company and regulatory standards. Responsibilities include operating and maintaining laboratory equipment, preparing test reports, and collaborating with the quality assurance team to ensure product consistency and safety. The role also involves assessing methodologies, implementing quality control procedures, and supporting efforts to meet compliance requirements.

Qualifications

• Strong analytical skills to interpret data and assess quality and compliance.
• Proficiency in Quality Control practices, including precision testing and compliance management.
• Hands-on experience with laboratory skills, including sample preparation and procedural adherence.
• Familiarity with operating and maintaining laboratory equipment.
• Understanding of Quality Assurance processes to support regulatory compliance.
• Bachelor’s degree in Pharmaceutical Sciences, Chemistry, or a related field.
• Excellent attention to detail, documentation, and reporting skills.
• Experience in pharmaceutical quality standards and regulatory environments is a plus.

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