Sansheng Pharmaceutical plc Job Vacancy

Sansheng Pharmaceutical plc (SSP) invites fresh Graduates and qualified applicants for the following Vacant positions. Anyone who is interested and qualified can apply before the application closing date.

Sansheng Pharmaceutical plc (SSP) is a GMP certified company by EFDA and is currently working for further international certifications of WHO and other country’s regulatory bodies. SSP is involved in the production of tablets / capsules (annual capacity of 5 billion units) and injection products in the form of ampules (annual capacity of 300 million ampules) and large volume infusions (annual capacity of over 10 million liters/bags) by using fully automatic and semiautomatic state of the art technology. The company also have several expansion plans in to various dosage forms that are going to be erected on its expansion project having more than 16.7 hectare total area of land.

We encourage you to read the job description carefully before you start the application process. Highlight your skills, motivation and experience and tailor your letter of interest accordingly.

Sansheng Pharmaceutical plc (SSP) are looking for energetic, enthusiastic, qualified and experienced for the following position.

Position 1: QC chemical analyst

Minimum Educational Qualification and Work Experience:

Qualifications

  • BSc Degree in chemistry, Chemical Engineering and related Fields

Requirements

  • Be hard-working and able to bear hardships; bearing good communication ability and professional dedication; proficient in conventional office software,

Experience : 0 years

Total Required : one (1)

Sex : Males and females

Age : 22-35 years.

Duties and responsibility
  • To assay raw material and finished product according to required test index and time, and report the result in time
  • To assure the correctness and precision of assaying programs, and take test results of authorized department as reference in order to develop professional skills.
  • To record test programs, archive assaying files and samples and place them in order.
  • To be responsible for security of chemical laboratory and tests.
  • To retain drugs, instruments, equipment and other assaying things. Poisonous drugs and expensive equipment should be kept in special cabinet and managed by authorized personnel
  • Responsible for the preparation, calibration and review of the standard solution (titrate), and the results are rechecked to ensure that the calibration results are accurate and true.
  • Responsible for arranging special personnel to do a good job of sample inspection, regularly do a good job of stability investigation and analysis
  • Responsible for making the purchasing plan for required instruments, standard materials (reference materials), test reagents, spare parts and other consumable products according to the inspection requirements.
  • Complete other assigned work and be responsible for it.
Position 2: QC microbiology analyst

Job Requirements

Qualifications

  • BSc Degree in Biology, Microbiology and related fields.

Requirements

  • Be hard-working and able to bear hardships; bearing good communication ability and professional dedication; proficient in conventional office software.

Work Experience: 0 years

Total required: one (1)

Sex: males or females

Age: 22-35 years

Duties and Responsibilities

  • Strictly follow the inspection SOP, Be responsible for sampling, inspection and report of microbiological analysis.
  • Be responsible for the normal use and maintenance of microbiological instruments and equipment.
  • Be responsible for culture and inoculation of bacteria required for microbial testing and preparation of bacteria solution and medium.
  • Provide accurate and reliable microbial detection results and take full responsibility for them.
  • Ensure the accuracy and completeness of the original inspection records. Abnormal situation should be reported to the immediate superior in time.
  • Has the responsibility to keep the microbiological laboratory clean.
  • Responsible for the preparation, calibration and review of the standard solution (titrate), and the results are rechecked to ensure that the calibration results are accurate and true.
  • Responsible for arranging special personnel to do a good job of sample inspection, regularly do a good job of stability investigation and analysis.
  • Responsible for making the purchasing plan for required instruments, standard materials (reference materials), test reagents, spare parts and other consumable products according to the inspection requirements.
  • Daily use and maintenance of air conditioning system for microbial testing, and make relevant records.
  • Complete other assigned work and be responsible for it.

Place of Work: Dukem, Oromia, Ethiopia manufacturing site, Oromia

Application Deadline: Sep 5, 2023

How to Apply

Closing date for receiving application is 15 days from date of Announcement. Interested candidates may send their CV by email mentioning the position title and can submit hard copy of your application, CV, credentials and other document at Dukem HR office at the address below:

Address: SANSHENG PHARMACEUTICAL PLC

Dukem Eastern Industrial Park, Oromia, Ethiopia

Email:sanshengpharmaceuticals@gmail.com

NB: Read the vacancy announcement carefully, Check the vacancy details with eligibility, Prepare your CV or Application Details, Finally, apply as instructed by the authority.

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