Career Opportunities in Pharmaceutical Manufacturing and Quality
A prominent Indian pharmaceutical company is conducting a walk-in interview for experienced professionals to join its teams in Production, Quality Control (QC), and Quality Assurance (QA). This presents an excellent opportunity to advance your career within a state-of-the-art manufacturing and quality-compliant environment, contributing to the development and production of a diverse range of pharmaceutical formulations.
Job Openings and Requirements:
The company is seeking qualified individuals for the following positions:
-
Production Supervisor (2 Vacancies):
- Qualification: 12th Pass with ITI
- Experience: 4-7 Years
- Responsibilities: Supervise compression and coating machine operations, ensuring strict adherence to Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and safety protocols. Monitor daily production activities, maintain meticulous records, and coordinate with teams to achieve manufacturing targets.
- Key Skills: Proficiency in compression and coating machine operation, strong understanding of manufacturing process control, and robust GMP compliance knowledge.
-
Quality Control (QC) Officer / Senior Officer (3 Vacancies):
- Qualification: B.Pharm / M.Pharm / M.Sc. Chemistry
- Experience: 2-5 Years
- Responsibilities: Perform comprehensive testing of Raw Materials (RM) and Finished Goods (FG). Conduct High-Performance Liquid Chromatography (HPLC) analysis and stability studies, operate Gas Chromatography (GC) instruments, and maintain precise laboratory documentation in line with GMP standards.
- Key Skills: Expertise in HPLC and GC analysis, stability testing, RM & FG testing, and laboratory documentation practices.
-
Quality Assurance (QA) Executive / Senior Executive (1 Vacancy):
- Qualification: B.Pharm / M.Pharm
- Experience: 7-10 Years
- Responsibilities: Manage Quality Management System (QMS) activities, ensure GMP compliance, and handle deviations, Corrective and Preventive Actions (CAPA), and change control processes. Oversee market complaints, conduct risk assessments, prepare and review SOPs, and actively support internal and regulatory audits.
- Key Skills: Strong command over QMS principles, GMP compliance, CAPA, change control, deviation management, SOP preparation & review, regulatory audit exposure, and risk assessment.
Walk-in Interview Details:
- Dates: 11th July – 18th July 2026 (Excluding Sunday)
- Venue: FDC Limited, Village Khol-Bhud, Tehsil Baddi, District Solan, Himachal Pradesh – 173205
- Job Location: Baddi, Himachal Pradesh
Eligibility Criteria:
Candidates must possess the stipulated educational qualifications and mandatory relevant experience within the pharmaceutical industry. A thorough understanding of GMP and regulatory requirements, coupled with strong documentation and communication skills, is essential for all roles.
Documents to Bring:
Interested and eligible candidates are requested to carry an updated resume, passport-size photographs, all educational certificates and mark sheets, experience certificates, latest salary slips, and a government ID proof (such as Aadhaar or PAN card) to the interview.
Why Join This Organization?
This is a unique opportunity to work with a respected leader in the pharmaceutical sector, gain exposure to modern manufacturing and quality systems, and thrive in a professional environment that fosters continuous career growth and stable employment.
For further inquiries regarding these positions, please contact the Human Resources Department.
