Latest Job Vacancies at Biopharma Limited

Manufacturing jobs, Pharmaceutical jobs,

Quality Assurance Officer

Requirements 

  • B. Pharmacy./ M. Pharmacy or any other related field.
  • Quality Assurance and validation Knowledge of GMP and GDP regulations
  • In-depth knowledge of quality regulations and current industry practices.
  • Minimum of 3 years experience.

Key Competencies:

  • Detail-oriented with problem-solving
  • Abilities, and conceptual thinking.
  • Ability to handle detailed tasks and work with varying types of data.
  • Ability to maintain confidentiality.

Syrup Line Operator

Requirements 

  • Conduct Qualitative and quantitative analysis of all manufactured syrups.
  • Report any anomalies is syrup making process.
  • Prepare batch as per the production plan
  • Ensure basic running maintenance is done to ensure quality performance.
  • Ensure operational safety is done before machine start up. Ensure syrup availability as per the production plan.

Qualifications:

  • At least 1-3 years hands-on experience
  • Knowledge of food Safety and Hygiene handling techniques.

Pharmacovigilance office

Key Responsibilities:

  • Completing periodic safety update reports on drugs and other treatments.
  • Flagging up early warning signs of adverse effects of drugs.
  • Minimising the risk of serious side effects on products. Completing safety audits

Qualifications:

  • B. Pharmacy./ M. Pharmacy or any other related field.
  • PPB membership.
  • Minimum of 2 years experince.

Regulatory Affairs Officer

Key Responsibilities:

  • Ensuring compliance with regulations set by the Regulatory Authorities.
  • Advise and participate in any quality management system reviews that may be necessary from regulatory guidelines.
  • Liaising, negotiating and maintaining correspondence with regulatory authorities.

Qualifications:

  • B. Pharmacy./ M. Pharmacy or any other related field.
  • 2-5 years experience in pharmaceutical manufacturing regulatory affairs.
  • Registered with pharmacy and Poisons board.

Compression Machine Operator

Key Responsibilities:

  • Responsible for Cleaning, Set Up and Operation of all equipment related to the Manufacturing processes.
  • Responsible for receipt, verification, and usage of raw materials to be used within the process.
  • Responsible to follow manufacturing order instructions, basic operating procedures process related, and procedures related to safety and Good Manufacturing Practices (cGMP).
  • Responsible for quality, productivity, and process efficiencies under execution..
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Qualifications:

  • 1 year or more in Experience in Pharmaceuticals Manufacturing
  • Strong technical knowledge in tablet compression.
  • Mechanical knowledge is an added advantage.

HOW TO APPLY

If you fit any of the below vacancies, kindly send your resume to talk2us@biopharmaltd.com indicating which position you are applying for latest by 30th january 2024.

UN Jobs Salary Scale | United Nations Salary Range

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