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..
IMPORTANT: Write a Perfect Cover Letter in minutes and start getting interviews! Get expert advice as you write.) Use These Examples Proven to Work.
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.