Pharma Job Opportunity: Quality Assurance Jobs at Harman Finochem Careers
Looking for a rewarding Pharma Job in the pharmaceutical manufacturing sector? Harman Finochem Limited is hiring for the role of Production-QMS Documentation Specialist in Chhatrapati Sambhajinagar. This opportunity is ideal for candidates interested in Quality Assurance Jobs involving QMS documentation, SOP management, regulatory compliance, and pharmaceutical production operations. Candidates searching for Pharma Job openings and Quality Assurance Jobs can explore this excellent career opportunity with a globally recognized API manufacturing company.
- Job Position: Production-QMS Documentation Specialist
- Location: Chhatrapati Sambhajinagar
About the Company
Harman Finochem Limited is a globally recognized pharmaceutical company specializing in the manufacturing and export of high-quality Active Pharmaceutical Ingredients (APIs) and chemical intermediates. Established in 1983, the company operates out of two GMP-certified manufacturing sites in Aurangabad with a combined capacity of 350,000 liters. Serving clients in over 75 countries, Harman Finochem is a trusted producer of over 45 APIs, including being one of the largest global manufacturers of Metformin. With certifications from esteemed regulatory authorities like USFDA, WHO-GMP, and EDQM, the company’s commitment to quality, innovation, and sustainability underpins its success in the pharmaceutical industry.
Job Description
- This is a full-time, on-site role for a Production-QMS Documentation Specialist located in Chhatrapati Sambhajinagar.
- The role involves managing and maintaining documentation related to the Quality Management System (QMS) within the production environment.
- Responsibilities include drafting, reviewing, and updating standard operating procedures (SOPs).
- Ensuring compliance with regulatory requirements is a key part of the role.
- Collaborating with the production team to address and resolve quality-related issues.
- Facilitating internal and external audits effectively.
- Supporting continuous process improvements across production and quality systems.
- Maintaining accurate records for both regulatory and internal compliance purposes.
Qualifications
- Strong knowledge of Quality Management Systems and regulatory compliance, including cGMP standards.
- Proficiency in drafting, reviewing, and managing Standard Operating Procedures (SOPs) and other technical documentation.
- Demonstrated skills in quality control, quality assurance, and production process oversight.
- Ability to facilitate internal audits and support regulatory audits effectively.
- Proficient in attention to detail, record-keeping, and ensuring accuracy in documentation.
- A bachelor’s degree in Pharmaceuticals or a related field is preferred.
- Strong interpersonal and communication skills for collaboration across production and quality teams.
- Experience in the pharmaceutical or active ingredient manufacturing industry is a valued advantage.
