
Quality Assurance Associate, Clinical Supplies
Are you passionate about ensuring the quality and safety of pharmaceutical products? Do you have a keen eye for detail and a strong understanding of clinical supplies? Catalent is seeking a Quality Assurance Associate for our Clinical Supplies division. As a member of our team, you will play a crucial role in maintaining the highest standards of quality and compliance in our products. We are looking for a highly skilled and motivated individual who is dedicated to delivering top-notch results. If you are ready to take on a challenging and rewarding role in the pharmaceutical industry, then we want to hear from you! Read on to learn more about the qualifications and responsibilities for this position.
- Conduct thorough quality assurance checks on all pharmaceutical products to ensure they meet industry standards and regulations.
- Collaborate with cross-functional teams to develop and implement quality control processes and procedures.
- Monitor and review batch records, analytical data, and other documentation to ensure accuracy and compliance.
- Perform audits of manufacturing processes and facilities to identify any areas for improvement and recommend corrective actions.
- Identify and report any deviations or non-conformities in products or processes and work with the necessary teams to address and resolve them.
- Maintain a thorough understanding of current industry regulations and standards to ensure compliance.
- Participate in the investigation of customer complaints and product recalls, and assist in implementing corrective and preventive actions.
- Conduct regular training and education sessions for employees on quality assurance procedures and best practices.
- Work closely with the research and development team to ensure proper handling and testing of clinical supplies.
- Maintain detailed and accurate documentation of all quality control activities and results.
- Identify and implement continuous improvement initiatives to enhance quality and efficiency in processes.
- Communicate and collaborate with external regulatory agencies and participate in audits and inspections.
- Stay updated on new and emerging technologies and industry trends related to quality assurance and make recommendations for their implementation.
- Adhere to all company policies and procedures, including safety protocols, at all times.
Bachelor's Degree In A Relevant Scientific Field, Such As Chemistry, Biology, Or Pharmaceutical Science.
Minimum Of 2 Years Of Experience In A Quality Assurance Role Within A Clinical Supplies Or Pharmaceutical Manufacturing Environment.
Strong Understanding Of Cgmp Regulations, Fda Guidelines, And Other Relevant Industry Standards.
Experience With Quality Systems, Including Document Control, Change Control, And Deviation Management.
Excellent Attention To Detail And Strong Analytical Skills, With The Ability To Identify And Troubleshoot Issues In A Timely Manner.
Data Analysis
Supply Chain Management
Problem Solving
Quality Control
Risk assessment
Batch record review
Documentation management
GMP compliance
SOP Development
Regulatory Knowledge
Audit Preparation
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Teamwork
Active Listening
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Quality Assurance Associate, Clinical Supplies in San Diego, CA, USA is $55,000-$85,000 per year. However, this can vary depending on factors such as experience, education, and specific job responsibilities.
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Catalent, Inc. is a multinational corporation headquartered in Somerset, New Jersey. It is a global provider of delivery technologies, development, drug manufacturing, biologics, gene therapies and consumer health products. It employs more than 14,000 people, including approximately 2,400 scientists and technicians.

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