Flip-of Seal Supervisor

Title / Grade: Flip-Off Seal Supervisor

Department: Production/Manufacturing

Reports To: HOD

Work Experience: 05+ years of experience in a supervisory role within the packaging,

medical device, or pharmaceutical industry, with specific experience

in flip-off seal production preferred.

Salary 2.00 - 4.00 LPA

Education: Diploma or Bachelor’s degree in Mechanical Engineering,

Manufacturing, or a related field.

Preferred Industry Any Manufacturing

Job Purpose The Flip-Off Seal Supervisor is responsible for overseeing the

production and quality assurance of flip-off seals used in medical

device and pharmaceutical packaging. This role includes managing a

team of operators, ensuring compliance with quality standards, and

maintaining productivity targets. The Supervisor will monitor daily

operations, implement process improvements, and maintain strict

adherence to regulatory and safety guidelines.

Major Duties &

**Responsibilities**:

- Supervise and lead a team of operators involved in the

manufacturing and assembly of flip-off seals, ensuring

adherence to standard operating procedures (SOPs).
- Schedule daily tasks and assign duties to meet production

targets and optimize resource utilization.
- Train new team members on process specifics, equipment

use, and safety protocols.
- Conduct regular quality checks to ensure that seals meet

specified standards, including visual inspections and

functional tests.
- Maintain strict compliance with GMP, ISO standards, and

other relevant regulatory requirements.
- Work closely with the Quality Control team to identify and

address quality issues promptly.
- Monitor production processes to ensure consistent quality

and efficiency.
- Track and report on production metrics, including output

rate, defect rate, and waste reduction.
- Collaborate with the process engineering team to implement

improvements and enhance process efficiency.
- Maintain accurate records of production activities, including

batch records, quality inspections, and shift reports

Document any deviations from standard processes and assist

in investigations as required.
- Prepare and submit production reports to management on a

regular basis.
- Coordinate with inventory control teams to ensure timely

availability of materials.
- Track usage and ensure mínimal wastage of materials in line

with lean manufacturing principles

required skill set:
Familiarity with GMP, ISO 13485, ISO 15378 regulations, and

pharmaceutical/medical device packaging standards.
- Strong leadership and team management skills.
- High attention to detail with a focus on quality and compliance.
- Ability to interpret technical documents, quality standards, and

production reports.
- Effective communication skills for coordinating across

departments

**Job Types**: Full-time, Permanent

Pay: ₹16,000.00 - ₹25,000.00 per month

**Benefits**:

- Provident Fund

Schedule:

- Day shift
- Weekend availability

Supplemental Pay:

- Performance bonus

Work Location: In person