Executive,Quality Control
Job Description
Title: Executive,Quality Control
Company Name: DBL Pharmaceuticals Ltd. (A concern of DBL Group)
Vacancy: Not specific
Job Location: Gazipur
Employment Status: Full-time
Educational Requirements:
∎ Master of Pharmacy (M.Pharm)
∎ M. Pharm or M. Sc in Chemistry, Applied Chemistry, Bio-Chemistry from any reputed university.
∎ Skills Required: Adaptability, Time Management
Experience Requirements:
∎ 2 to 4 year(s)
∎ The applicants should have experience in the following area(s):
GMPs guideline, Pharmaceutical Quality Control, Pharmaceuticals, Regulatory Inspections
∎ The applicants should have experience in the following business area(s):
Pharmaceuticals
Job Responsibilities:
∎ Ensure sampling of concern RM as per SOP and prepare passed/rejected tags after necessary tests and arrange to the label of the same.
∎ Examine and analyze assigned material, intermediates, and products according to the written procedure (STP/BP/USP).
∎ Should have sound knowledge on analytical instruments and capabilities to handle instruments like HPLC, GC with auto-sampler and HS, PSD, AAS, Auto-titrator, UV, IR, and others, preferably knowledge of ICP-MS, etc.
∎ Should have knowledge of vendor approval, OOS/OOT, Deviation, CCR, LIR, Calibration and qualification, etc.
∎ Should be able to prepare documents such as stability protocols, finished and raw material specifications, method of analysis, transfer protocol, transfer report, SOP, etc.
∎ Should have sound knowledge on Method Validation, Cleaning validation, analytical method tech transfer, and updated Guidelines and standards.
∎ Execution and completion of IQ/OQ/PQ of new instruments and also EOP and ECP preparation.
∎ Maintain inventory control of QC instruments, spare-parts, glass-wares, and reagents/chemicals to control stock and availability in the QC lab.
∎ Perform stability study as on ICH Guideline to establish product shelf-life and to meet the regulatory requirements.
∎ Maintain appropriately qualified laboratory procedures to ensure compliance with safety, cGMP and GLP regulations.
∎ Review and updating the analytical data to maintain cGMP/GLP compliance status in the laboratory.
∎ Trouble shooting
∎ Perform other duties as assigned.
Additional Requirements:
∎ Both males and females are allowed to apply
∎ Proficient in Microsoft Office and knowledge of other QMS software is a plus.
∎ Strong knowledge of GMPs guideline /GLP/GDP/ Regulation / (WHO, UKMHRA, FDA, 21CFR part 11 etc.)
∎ Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment.
∎ Strong personal & professional ethical values are essential.
∎ Females are highly encouraged to apply.
Salary: Negotiable
Job Source: Bdjobs.com Online Job Posting.
Application Deadline: 29 May 2021
Company Information:
∎ 22 May 2021
∎ DBL Pharmaceuticals Ltd. (A concern of DBL Group)
∎ Address : Capita South Avenue Tower (6th Floor), House No # 50, Road No # 03, Gulshan Avenue, Gulshan 1, Dhaka - 1212
∎ Web : dblgroup.taleo.net/careersection/ex/jobsearch.ftl
Category: Medical/Pharma
: Interested candidate satisfying above requirements please send a complete CV with attached recent color photograph.
Source: bdjobs.com
Deadline Expired on 29th May 2021
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