“QC Junior Team Member Opportunity: Apply Now with B.Pharm/MSc at Cipla”

Pharmaceuticalcarrier; Rangpo; On-site; INR 3,00,000 - 4,00,000; Full time

Job summary

A leading pharmaceutical company is seeking a Junior Team Member – QC to prepare, update, and review specifications and SOPs for material analysis. The ideal candidate holds an M.Sc. or B.Pharma degree and has 2 years of QC experience. This role emphasizes collaboration and compliance with pharmacopoeial standards and quality requirements. The position is located in Sikkim – Rangpo.

Qualifications

• 2 years in the QC department of a pharmaceutical organization.

Responsibilities

• Prepare and review specifications, SOPs, and policies for material analysis.
• Ensure compliance with current pharmacopoeia and quality standards.
• Issue documents to applicable units and maintain records.
• Execute harmonization and simplification of documents.

Skills

Collaborate to Succeed

Innovate to Excel

Perform with Accountability

Lead with Empathy

Act with Agility

Strong Domain Knowledge

People Management

Education

M.Sc. / B.Pharma

Job description

Cipla Limited is a global pharmaceutical company based in Mumbai, India. It was founded in 1935 by Dr. K.A. Hamied, and today it is one of the largest pharmaceutical companies in India and a significant player in the global pharmaceutical industry.

Cipla is known for its focus on providing affordable and accessible healthcare solutions. The company is involved in the development, manufacturing, and marketing of a wide range of pharmaceutical and healthcare products, including prescription drugs, active pharmaceutical ingredients (APIs), and over-the-counter (OTC) medications.

Cipla has a diverse portfolio that covers various therapeutic areas, such as respiratory, anti-infectives, cardiovascular, central nervous system, gastro-intestinal, oncology, and more. The company has a strong presence in both domestic and international markets, with a significant footprint in over 80 countries.

In addition to its pharmaceutical business, Cipla is actively involved in research and development, striving to bring innovative and cost-effective solutions to address global health challenges. The company has played a crucial role in providing affordable medicines for various diseases, including HIV/AIDS, tuberculosis, and malaria.

Job Description: Junior Team Member – QC

Job Purpose: Prepare, update, and review specifications, Standard Operating Procedures (SOPs), policies, and operating documents for material analysis. Ensure alignment with predefined quality parameters and compliance with relevant standards, pharmacopeia, and current Good Manufacturing Practice (cGMP) requirements.

Accountabilities:

I. Document Preparation

• Prepare documents like SOPs, specifications, and non-routine documentation.
• Ensure timely availability across the site to provide support during the analysis.

II. Pharmacopeial Compliance

• Review the latest pharmacopeial updates, supplements, and amendments.
• Evaluate updates required in the available document to ensure compliance with current pharmacopoeia through consent with regulatory bodies.

III. Quality Compliance

• Review assigned documents by referring to the relevant backup and pre-defined quality procedures.
• Ensure compliance against quality requirements.

IV. Document Issuance

• Issue documents to applicable units.
• Maintain a record in the issuance record (bound book) to ensure the current version of the common document is available at the unit.

V. Harmonization and Simplification

• Execute harmonization and simplification processes of documents.
• Reduce complexities in processes and ensure standardized procedures are followed.

Candidate Profile:

• Educational Qualification: M.Sc. / B.Pharma
• Experience: 2 years in the QC department of a pharmaceutical organization

Competencies/Skills:

• Collaborate to Succeed
• Innovate to Excel
• Perform with Accountability
• Lead with Empathy
• Act with Agility
• Strong Domain Knowledge
• People Management

This opportunity is ideal for candidates with a strong background in Quality Control, holding an M.Sc. or B.Pharma degree, and possessing 2 years of relevant experience. If you are a dynamic professional who thrives in a collaborative environment and has a passion for maintaining high-quality standards in pharmaceuticals, we invite you to apply. The position is based in Sikkim – Rangpo.