Shift Incharge

Job Title: Shift In-Charge – Production (Pharma)

Qualification: . Chemistry

Experience: 2–5 years in pharmaceutical production with documentation exposure

Job Summary:

Responsible for supervising production activities during shifts, ensuring adherence to cGMP, and maintaining proper documentation (BMRs, logbooks, etc.).

Key Responsibilities:

Oversee shift operations and manpower.

Maintain production records as per GMP standards.

Ensure compliance with SOPs and safety norms.

Coordinate with QA/QC and maintenance teams.

Report deviations/incidents promptly.

Skills:

Strong in pharma documentation

Good knowledge of GMP

Team handling and communication skills

• Experience

  2 - 5 Years

• No. of Openings

  1

• Education

  Graduate (B.Sc)

• Role

  Shift Incharge

• Industry Type

  Call Centre / BPO / ITES / LPO

• Gender

  Male

• Job Country

  India

• Type of Job

  Full Time

• Work Location Type

  Work from Office

• Face Interview Location

  Kanukunta plant balapur