Ultra Drugs Hiring Manufacturing Chemist, QA – Documentation Executive in Baddi

Ultra Drugs Hiring Manufacturing Chemist, QA – Documentation Executive in Baddi

Ultra Drugs, a reputed pharmaceutical company, is now hiring for two exciting positions: Manufacturing Chemist (Liquid Oral) and QA – Documentation Executive. Based in Baddi, these roles offer excellent opportunities for growth and professional development in the pharmaceutical industry. If you have the right qualifications and experience, this could be the perfect next step in your career.

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Job 1: Manufacturing Chemist (Liquid Oral)

Position:
Manufacturing Chemist – Liquid Oral

Location:
Baddi, Himachal Pradesh

Qualification:

• B.Pharm, M.Pharm, or M.Sc. in Chemistry, Pharmaceuticals, or a related field.

Experience:

• 5+ years of experience in the pharmaceutical industry, specifically in liquid oral manufacturing.

Designation:
Executive / Senior Executive

Interview Mode:
Face-to-face interview

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Responsibilities of Manufacturing Chemist (Liquid Oral)

As a Manufacturing Chemist for Ultra Drugs, you will be responsible for:

• Overseeing the production of liquid oral formulations and ensuring compliance with regulatory standards.
• Ensuring that manufacturing processes align with Good Manufacturing Practices (GMP).
• Managing the equipment and raw materials required for production.
• Maintaining high-quality standards and meeting production targets.
• Collaborating with other departments to ensure smooth operations.
• Preparing reports and documentation related to the manufacturing process.

This role requires an experienced individual who can manage the intricacies of pharmaceutical production while adhering to stringent quality standards.

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Job 2: QA – Documentation Executive

Position:
QA – Documentation Executive

Location:
Baddi, Himachal Pradesh

Qualification:

• B.Pharm or M.Pharm in Pharmaceuticals or a related field.

Experience:

• 6+ years of experience in Quality Assurance and documentation within the pharmaceutical industry.

Designation:
Senior Officer / Executive

Interview Mode:
Face-to-face interview

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Responsibilities of QA – Documentation Executive

The QA – Documentation Executive will play a pivotal role in ensuring the quality and compliance of Ultra Drugs’ operations by:

• Handling and managing QA documentation related to pharmaceutical production.
• Ensuring adherence to regulatory requirements and GMP standards.
• Reviewing and approving batch manufacturing records, SOPs, and other documents.
• Conducting internal audits and assisting in regulatory inspections.
• Collaborating with the QA team to improve documentation practices.
• Ensuring that the company’s documentation is up to date and in compliance with regulatory requirements.

This is an excellent opportunity for an experienced professional with a solid background in quality assurance and pharmaceutical documentation.

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Location: Baddi, Himachal Pradesh

How to Apply

Interested candidates for the roles of Manufacturing Chemist or QA – Documentation Executive at Ultra Drugs are encouraged to apply by sending their resumes to hr.recruitments@ultradrugs.co.in or contacting the recruitment team at 9369902931 or 8091506200.