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Dp Manufacturing Executive – Drug Product Production (Formulation / Packaging Operations)

IPCA Laboratories Limited
0-3 years
Not Disclosed
Dhar, India
1 June 4, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

DP MANUFACTURING EXECUTIVE – DRUG PRODUCT PRODUCTION (FORMULATION / PACKAGING OPERATIONS)

JOB SUMMARY
A Drug Product (DP) Manufacturing role focused on formulation, filling, packaging, and production line operations in a GMP-regulated pharmaceutical manufacturing environment. The role ensures smooth execution of drug product manufacturing activities while maintaining product quality, safety, and compliance with regulatory standards.

EXPERIENCE REQUIRED
Fresher to 3 years of experience in pharmaceutical manufacturing, production operations, or packaging departments. Freshers with technical training (ITI/Diploma) and industrial exposure are eligible.

EDUCATION QUALIFICATION
Diploma / ITI in relevant technical or pharmaceutical production disciplines.

KEY RESPONSIBILITIES

  • Perform drug product formulation and support manufacturing operations

  • Operate production machinery for filling, labeling, and packaging processes

  • Execute packing activities as per batch manufacturing instructions and SOPs

  • Perform line clearance activities before and after production batches

  • Support documentation activities including batch records and logbooks

  • Ensure compliance with GMP, safety, and hygiene standards in production areas

  • Assist in cleaning and maintenance of production equipment and work areas

  • Coordinate with QA and QC teams for smooth production workflow

  • Follow standard operating procedures (SOPs) and manufacturing instructions strictly

KEY SKILLS REQUIRED

  • Basic understanding of pharmaceutical production and manufacturing processes

  • Hands-on experience or familiarity with machine operations in production lines

  • Awareness of GMP guidelines and cleanroom practices

  • Ability to follow SOPs and maintain accurate documentation

  • Attention to detail and discipline in regulated manufacturing environments

  • Team coordination and shift-based working flexibility