Production/Quality Supervisor/Male/HPS/2026/362

Harshplacements; Masat; On-site; TRY 79,809 - 133,016; Full time

Job summary

Harshplacements is looking for a proactive Production / Quality Supervisor located in Masat, Turkey, with 1 to 3 years of experience in the pharmaceutical industry. Responsibilities include overseeing production and quality operations, ensuring compliance with GMP standards, and facilitating smooth workflow. The position offers a salary between ₹15,000 to ₹25,000 per month and requires strong knowledge of GMP, along with good leadership and communication skills.

Qualifications

• 1 to 3 years of experience in pharmaceutical manufacturing.
• Strong knowledge of SOPs and pharmaceutical processes.

Responsibilities

• Supervise daily manufacturing activities as per SOPs.
• Monitor production processes for efficiency and quality.
• Coordinate with teams to meet production targets.
• Maintain production records and ensure GMP compliance.
• Supervise quality control activities.

Skills

Knowledge of GMP

Leadership skills

Documentation abilities

Problem-solving skills

Communication skills

Education

B.Pharma / M.Pharma

Job description

Job Summary

27.04.26 | 131944 | HPS/2026/362 | Production/Quality Supervisor | Male | 2 | 1 to 3 | B.Pharma/M.Pharma | Masat

We are seeking a proactive and responsible Production / Quality Supervisor with 1–3 years of experience in the pharmaceutical industry. The candidate will oversee daily production or quality operations, ensure compliance with GMP standards, and maintain smooth workflow within the department.

Key Responsibilities

Production:

• Supervise daily manufacturing activities as per SOPs and Batch Manufacturing Records (BMR).
• Monitor production processes to ensure efficiency and quality output.
• Coordinate with cross‑functional teams to meet production targets.
• Ensure proper utilization of manpower, machines, and materials.
• Maintain production records and ensure compliance with GMP guidelines.

Quality:

• Supervise quality control and assurance activities.
• Review sampling, testing, and documentation processes.
• Ensure adherence to quality standards and regulatory requirements.
• Handle deviations, CAPA, and documentation.
• Support audits and regulatory inspections.

Eligibility Criteria

• Education: B.Pharma / M.Pharma
• Experience: 1 to 3 years in pharmaceutical manufacturing
• Gender: Male

Skills Required

• Strong knowledge of GMP, SOPs, and pharmaceutical processes
• Good leadership and team management skills
• Strong documentation and analytical abilities
• Problem‑solving and decision‑making skills
• Effective communication and coordination

Job Details

• Number of Vacancies: 2
• Salary: ₹15,000 – ₹25,000 per month (CTC)
• Working Hours: 8 hours per day