Job summary
Job post source
This job is directly from Catalent
Job overview
The Quality Assurance Associate I, Analytical at Catalent supports quality compliance by reviewing manufacturing and analytical documents to ensure GMP standards are met, impacting product quality and patient safety.
Responsibilities and impact
The role involves reviewing and approving controlled documents, analytical release and stability data, supporting manufacturing activities, and assisting in audits to maintain quality standards.
Compensation and benefits
The salary range is $65,000 - $70,000 annually with bonus potential, medical, dental, vision benefits effective day one, 401K match, PTO, tuition reimbursement, and various employee wellness and engagement programs.
Experience and skills
Requires a Bachelor's degree preferably in Chemistry or Biochemistry, at least one year of GMP industry experience, and preferred experience with HPLC, data review, and quality systems like Trackwise and Empower.
Career development
Offers a defined career path with annual performance reviews, potential for growth within an expanding team, and opportunities for further education through tuition reimbursement.
Work environment and culture
Catalent promotes a Patient First culture with a positive, fast-paced environment, employee engagement activities, diversity and inclusion groups, and community involvement initiatives.
Company information
Catalent is a global CDMO specializing in drug development and manufacturing, delivering over 70 billion doses annually with a strong focus on innovation and patient safety.
Team overview
The candidate will join the Catalent Pharma Solutions team in San Diego, a premier pharmaceutical chemistry development and manufacturing group focused on client drug compound development.
Job location and travel
This position is on-site in San Diego, CA, with core hours Monday to Friday 8am-5pm and some schedule flexibility.
Application process
Applicants should submit their application directly to Catalent as the company does not accept unsolicited resumes from agencies; accommodations are available for disabilities upon request.
Unique job features
The job offers unique perks such as on-site fitness classes, employee resource groups, green initiatives, and a comprehensive wellness program.
Company overview
Catalent, Inc. is a leading global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, and consumer health products. The company generates revenue through its comprehensive suite of services, including drug development, delivery technologies, and supply solutions, catering to pharmaceutical, biotech, and consumer health companies. Founded in 2007, Catalent has grown through strategic acquisitions and innovations, establishing itself as a critical partner in bringing new therapies to market efficiently and reliably.
How to land this job
Position your resume to emphasize your familiarity with GMP quality standards and your experience in reviewing analytical and manufacturing documents, as these are key responsibilities for the Quality Assurance Associate I role at Catalent.
Highlight your experience with analytical techniques such as HPLC and your knowledge of quality systems like Trackwise and Empower, since these are highly preferred skills mentioned in the job description.
Apply through multiple channels including Catalent's official corporate careers site and LinkedIn to maximize your application visibility and increase your chances of being noticed for this position.
Connect with current employees in the Quality Assurance or Analytical divisions at Catalent on LinkedIn to gain insights about the role and company culture; use ice breakers such as commenting on recent Catalent innovations or asking about their experience with GMP compliance and quality systems.
Optimize your resume for ATS by incorporating keywords from the job description like 'GMP,' 'analytical release,' 'HPLC data review,' 'Trackwise,' 'Empower,' and 'quality assurance,' ensuring your resume passes automated screenings effectively.
Leverage Jennie Johnson's Power Apply feature to automate tailored applications across multiple platforms and identify relevant LinkedIn contacts for networking, allowing you to focus your energy on preparing for interviews and enhancing your skills.
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