Manager/Asst. Manager Quality Assurance- Conversion (Pharma & SRC)

Job Description

Title: Manager/Asst. Manager Quality Assurance- Conversion (Pharma & SRC)

Company Name: A Well renowned Aluminum Foils Packaging Company

Vacancy: 1

Age: 30 to 45 years

Job Location: Dhaka (Dhamrai)

Salary: Negotiable

Experience:

  • At least 4 years


Published: 2026-04-22

Application Deadline: 2026-05-22

Education:
    • Bachelor of Science (BSc) in Chemistry, Materials & Metallurgical Engineering


Requirements:
  • At least 4 years


Skills Required: MS Office

Additional Requirements:
  • Age 30 to 45 years
  • The applicants should have experience in the following area(s): Chemical Industries, Group of Companies, Manufacturing, Packaging, Quality

  • The applicants should have experience in the following business area(s): Manufacturing (Light Engineering & Heavy Industry), Packaging Industry, Plastic/ Polymer Industry, Manufacturing (FMCG), Multinational Companies

  • Candidate should have work in the Factory.

  • Experience in Aluminum Foils Packaging Plant or Conversion Unit should be preferred.

  • Must have computer literacy, conversant with MS Office and ERP software

  • Must be able to work on own as well as being a team player

  • Be flexible to provide off-hour support

  • Ability to work under stressful situation

  • Strong communication and interpersonal skills with a proactive approach.

  • Working experience in ERP systems related to material release and Certificate of Analysis (COA) documentation.

  • Analytical and reporting capabilities to support audit readiness and continual improvement.



Responsibilities & Context:

Duties/Responsibilities:

  • Preparing, Sampling, Analyzing, Release, Retest & Disposal of all kind of routing samples such as Raw material, packing material, finished product, Retention sample, Sample of source approval & return goods maintaining with receive register & Machine log book.

  • Performs general maintenance & calibration of laboratory equipment as required by the departments established calibration program & GMP requirement.

  • Daily IPQC monitoring in different Section.

  • Develops, review, revises, or approves Standard Operating Procedure (SOP) as required.

  • Issue, distribution, retrieval & distribution record of all SOP, log book, BMR & BPR, all specification, all analytical method, master formula.

  • Carry-out vendor quality surveys or product quality audit

  • To handle investigation Market, complain, product recall, out of specification (OOS), deviation & assign root causes analysis, Develop CAPA, Change control & Rejection.

  • Technical efficiency report (Wastage Report, Statistical QC Report)

  • Develop professional working relationship with regulatory bodies` incl. BSTI, etc.

  • Review of action plans (CAPA) in response to audits of manufacturing facility by the external, Third-party Manufacturer and internal agencies

  • Any other Quality related responsibility assigned by the Management as per company requirement.



Job Other Benifits:
    • As Per Company Policy

    • Salary Review: Yearly

    • Lunch Facilities: Partially Subsidize



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: Production/Operation

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