Vacancies at Biopharma Limited

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.

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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.
   

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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.

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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.

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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..

Qualifications:

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