Catalent

Quality Assurance Associate, Clinical Supplies

Catalent

San Diego, CA, USA
Full-TimeDepends on ExperienceMid-LevelBachelors
Job Description

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.

  1. Conduct thorough quality assurance checks on all pharmaceutical products to ensure they meet industry standards and regulations.
  2. Collaborate with cross-functional teams to develop and implement quality control processes and procedures.
  3. Monitor and review batch records, analytical data, and other documentation to ensure accuracy and compliance.
  4. Perform audits of manufacturing processes and facilities to identify any areas for improvement and recommend corrective actions.
  5. Identify and report any deviations or non-conformities in products or processes and work with the necessary teams to address and resolve them.
  6. Maintain a thorough understanding of current industry regulations and standards to ensure compliance.
  7. Participate in the investigation of customer complaints and product recalls, and assist in implementing corrective and preventive actions.
  8. Conduct regular training and education sessions for employees on quality assurance procedures and best practices.
  9. Work closely with the research and development team to ensure proper handling and testing of clinical supplies.
  10. Maintain detailed and accurate documentation of all quality control activities and results.
  11. Identify and implement continuous improvement initiatives to enhance quality and efficiency in processes.
  12. Communicate and collaborate with external regulatory agencies and participate in audits and inspections.
  13. Stay updated on new and emerging technologies and industry trends related to quality assurance and make recommendations for their implementation.
  14. Adhere to all company policies and procedures, including safety protocols, at all times.
Where is this job?
This job is located at San Diego, CA, USA
Job Qualifications
  • 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.

Required Skills
  • Data Analysis

  • Supply Chain Management

  • Problem Solving

  • Quality Control

  • Risk assessment

  • Batch record review

  • Documentation management

  • GMP compliance

  • SOP Development

  • Regulatory Knowledge

  • Audit Preparation

Soft Skills
  • Communication

  • Conflict Resolution

  • Emotional Intelligence

  • Leadership

  • Time management

  • creativity

  • Teamwork

  • Active Listening

  • Adaptability

  • Problem-Solving

Compensation

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.

Additional Information
Catalent is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Required LanguagesEnglish
Job PostedDecember 19th, 2023
Apply BeforeMay 22nd, 2025
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About Catalent

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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