Job Description / Responsibility

• Checking, analysing & documenting all sorts of incoming sample and supplies of raw/bulk materials and packaging materials.
• Checking, analysing & documenting all sorts of vendor’s samples.
• Ensuring that routine chemical analysis of in-coming blends and finished products from production is done on time as per QAP test notes.
• Ensuring that routine in-process checks of products are done as per QAP.
• Re-evaluating or retest raw materials.
• A sampling of incoming raw & packaging materials.
• A sampling of raw & packaging materials for re-evaluation or retest.
• Performing & documenting accelerated stability test & real-time stability test of the new & existing product.
• Performing & documenting routine chemical tests for retention samples of finished products.
• Establishing expiry dates and shelf life specification on the basis of stability test related to storage condition
• Generating & maintaining QC documents.
• Performing & documenting method validation procedure (protocol & report).Assisting cleaning validation and process validation.
• Ensuring all register & log books for raw data, records & documentation are properly maintained and periodically checked, Calibrations of automated equipment, reagents and thermometers are properly maintained at regular intervals.
• Ensuring that reagents required for analysis are prepared and used in accordance with GLP.
• Ensuring that only validated/calibrated instruments are used for analytical works and immediately inform the Supervisor if any error in the instrument is detected.
• Ensuring that safety equipment/dresses are worn in accordance with GLP while in the laboratory.
• Ensuring that Product Complaint samples, Returned Goods samples, file samples, market samples of competitors are analysed as and when assigned by the Manager/Supervisor.
• Where necessary, making recommendations to improve the overall efficiency and appearance of the plant to ensure that at all time it meets the cGMP.
• Ensuring that any other work related to QCD is carried out as and when assigned by the Department Head.
• Preparing and standardizing test and volumetric solutions.
• Identifying the requirement of any significant change required in the relevant area of work and informing the head of the department about it.

 Basic Qualifications

• B. Pharm / M. Pharm/ M.Sc. in Bio-Chemistry/ Chemistry from any reputed University.
• Age 25 to 30 year(s)
• 1-2 years of experience in the pharmaceutical industry
• Communication- Speaks clearly and persuasively in positive or negative situations; listens and gets clarification; Response well to questions; Writes clearly and informatively; Presents numerical data effectively
• Leadership- Exhibits confidence in self and others; Inspires and motivates others to perform well; Accountable for behaviours and their impact on others; effectively influences actions and opinions of others; Accepts feedback from others; Gives appropriate recognition to others
• Strategic Thinking – Develops strategies to achieve organizational goals; Understands organization’s strengths & weaknesses; Adapts strategy to changing conditions. Critically evaluates quality systems to propose best practices.
• Computer skills: MS Office (Word, Excel, PowerPoint and Access).

Job Nature
Full-time

Job Location
Mymensingh

Salary Range
Negotiable

Other Benefits
As per company policy

Apply Instruction:

Or

Send your CV to jobs@genvio.com.bd

Applicant must enclose his/her Photograph with CV.

Genvio Pharma Ltd.
Villa Placidium; Suite A1; House 7; Road 2/d; Block J; Baridhara, Dhaka 1212, Bangladesh

Application Deadline: November 30, 2017