RFL Group Job Circular 2020.RFL started its journey with cast iron (CI) products in 1980. The initial main objective was to ensure pure water and affordable irrigation instruments for improving rural life. Today the company has its wide ranges of CI products like pumps, tube wells, bearings, gas stoves, etc, and has achieved prestige as the largest cast iron foundry and light engineering workshop in Bangladesh.
With a vision to serve the common people of Bangladesh with quality necessary products, RFL diversified its operation into the PVC category in 1996 and in the plastic sector in 2003. At present, it is a market leader in all these three sectors-cast iron, PVC, and Plastic in the country. A sizeable amount is also exported to different countries.
RFL Group Job Circular 2020
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Very happy to know you that recently published a job circular. The Job is the RFL Group Job Circular. You can see the job description, apply process, the start date of application and the last date of apply, the number of vacancies, apply source on Job hat Info. If you think you are the right candidate then don’t late apply as soon as possible to be a part of the RFL Group. Please read the job description carefully we show you the details below.
RFL Group Job Circular 2020
Job Summary | |
Institution Name | RFL Group |
Number of vacancies | Not Specify |
Job Nature | Full-Time |
Age | 30( general) and 32 ( special candidate) |
Published Date | October 17, 2020 |
Last Date of Application | October 31, 2020 |
Job Location: | See the image for details |
Salary: | See the image for details |
Education: | Graduate or Post Graduate |
Job Type: | Private Job |
Who can apply: | Male and female both can apply |
Employment type: | Contactual |
Application Fee: | N/A |
Source: | Online |
Website: | www.rflbd.com |
Experience | See the image for details |
RFL Group Job Circular details here
Deputy Manager/ Manager – QA/QC
RFL Group
Vacancy
Not specific
Job Responsibilities
- Receive a batch of documents. Check all required batch documents are available and updated. Review and checking of batch related documents (BMR, BPR, IPC records, QC Test reports, deviation and change control, OOS, etc.). Archive all batch release related documents, a compilation of batch document.
- Act as change control coordinator; facilitate all change control activities. Assure change control activities are performed in a timely and contentious manner. Work closely with requesting departments as required to determine the impact of change ensuring all supporting documentation/ data is present resulting in minimizing the CCF cycle time.
- Act as deviation management coordinator; facilitate all incident/deviation related activities, and assure deviation control activities are performed in a timely and continuous manner.
- Responsible for handling/supporting quality-related customer complaints, product recall activities.
- Coordinate the cross-functional investigation team in investigating customer complaints, OOS, incident & deviation investigations to find out the root cause.
- Performing/assist in managing all manufacturing operation deviation investigations and CAPA Implementations. Track /Monitor the Deviation, Complaint, Investigation, and CAPA logs. Work closely with other departments as required to determine the impact of CAPA ensuring all supporting documentation /data is present resulting in minimizing the deviation and complaints.
- Preparation, review/checking of SOPs, and other documents.
- Issuance, distribution, control, retrieval, and archiving of all documents according to requirements as & when required.
- Performing in-process control activities as and when required.
- Release of finished goods through SAP & approval of documents if the department head is not available.
- Review/Checking of APQR.
- Performing process validation and qualification activities in coordination with the Validation team.
- Document control and Document Numbering.
- Performing additional duties as when required.
Employment Status
Full-time
Educational Requirements
- B. Pharm / M. Pharm from any reputed University.
Experience Requirements
- At least 5 year(s)
Additional Requirements
- Age 25 to 40 years
- Only males are allowed to apply
- The candidate should have at least 5 years’ experience in quality assurance.
- Experience in the pharmaceutical industry / Medical device industry.
Job Location
Habiganj (Habiganj Sadar)
Salary
- Negotiable
Compensation & Other Benefits
- Lunch Facilities: Partially Subsidize
- Salary Review: Yearly
- Festival Bonus: 2

IPDC Job Circular 2020 Apply on www.ipdcbd.com
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