Deputy Manager, Engineering- Pharma Manufacturing Project

Job Description

Title: Deputy Manager, Engineering- Pharma Manufacturing Project

Company Name: Healthcare pharmaceutical limited

Vacancy: --

Age: Na

Job Location: Anywhere in Bangladesh

Salary: --

Experience:

  • At least 10 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies, Healthcare/Lifestyle product


Published: 2026-03-11

Application Deadline: 2026-03-28

Education:
    • Bachelor of Science (BSc) in Mechanical Engineering
    • Bachelor of Science (BSc) in Electrical & Electronic Engineering
    • Bachelor of Science (BSc) in Electronics
  • B.Sc. in Mechanical Engineering or Electrical/Electronic Engineering from a reputed university (local or international).



Requirements:
  • At least 10 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies, Healthcare/Lifestyle product


Skills Required:

Additional Requirements:
  • Minimum 10 years of professional experience in pharmaceutical manufacturing industries.

  • Demonstrated experience in pharmaceutical plant setup, engineering projects, or facility expansion will be highly preferred.

  • Extensive knowledge of pharmaceutical cGMP standards and adequate understanding of Quality Management Systems (QMS) to ensure effective implementation across the manufacturing facility.

  • Strong understanding of cleanroom technology, HVAC systems, utilities, and pharmaceutical process machinery.

  • Proficiency in AutoCAD, MS Project, and MS Office applications.

  • Proven leadership, communication, and project management capabilities with the ability

  • to lead multidisciplinary teams and manage complex projects.



Responsibilities & Context:

Healthcare Pharmaceuticals Limited (HPL), one of the leading pharmaceutical companies in Bangladesh, is embarking on the development of a new joint venture pharmaceutical manufacturing facility as part of its long-term strategic expansion.

This greenfield project will initially focus on the production of Oral Solid Dosage (OSD) and Oral Liquid products and will be designed and developed in compliance with internationally recognized pharmaceutical manufacturing standards. To lead this landmark initiative, we are seeking a highly experienced and dynamic professional.
The incumbent will be responsible for leading the development and execution of the
pharmaceutical manufacturing facility from conceptual design and engineering through construction, commissioning, qualification, and operational readiness. This role requires a seasoned project leader capable of managing large-scale pharmaceutical infrastructure projects, coordinating multidisciplinary teams, and ensuring compliance with global regulatory and quality standards.
Job Responsibilities:

  • Provide strategic leadership and technical oversight for the development and successful execution of the pharmaceutical manufacturing project.

  • Lead the project lifecycle from conceptualization, design, procurement, construction, installation, commissioning, and qualification to final handover for commercial manufacturing.

  • Develop and manage project budgets, capital expenditure plans, and timelines, ensuring efficient resource utilization.

  • Prepare User Requirement Specifications (URS) for process and utility equipment, conduct technical evaluation of vendor proposals, and participate in vendor selection.

  • Oversee Factory Acceptance Tests (FAT), installation, commissioning, and qualification of process and utility systems.

  • Ensure timely installation, commissioning, and qualification of process equipment and utility machinery, ensuring operational readiness in accordance with project timelines and regulatory requirements.

  • Coordinate closely with internal departments including Quality Assurance, Production, Engineering, and Commercial to ensure alignment with project objectives.

  • Work collaboratively with consultants, contractors, and international equipment suppliers to ensure timely and high-quality project delivery.

  • Ensure the facility design and operations comply with pharmaceutical cGMP standards and international regulatory guidelines such as those recommended by the World Health Organization and other relevant regulatory authorities.

  • Establish effective project monitoring systems, conduct regular review meetings, and provide progress updates to senior management.

  • Facilitate necessary regulatory, infrastructure, and environmental approvals required for project implementation.



Job Other Benifits:
    • An attractive and competitive compensation package will be offered, commensurate with the candidate’s qualifications and experience, along with other benefits as per company policy.



Employment Status: Full Time

Job Work Place: Work at office

Company Information:

Gender: Male and Female can apply

Read Before Apply: Please apply only who are fulfilling all the requirements of this job

Category: Pharmaceutical

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