QC Chemist I
The QC Chemist I at Confidential Client's San Diego site performs analytical testing and standard laboratory procedures to ensure pharmaceutical product quality under cGMP regulations. This entry-level role involves operating various analytical instruments, preparing samples, documenting results, and supporting quality investigations in a fast-paced early-phase development environment. The position emphasizes precision, collaboration, and continuous learning within a dynamic quality control team.
About Careertakes
👉 Important disclosure: Careertakes is a third-party recruiting platform supporting this hiring process. If selected, you will be employed directly by our client, pharmaceuticals and life sciences (drug development & delivery).
Applicants for this role may also receive access to additional matched opportunities through the Careertakes platform.
Location & Schedule
San Diego, CA — Monday–Friday, 8:00 AM – 4:30 PM
100% onsite
The Role
You will join a quality control team supporting early‑phase pharmaceutical development. Key responsibilities include:
- Independently perform standard laboratory techniques, including H/UPLC, dissolution per USP 711, water content analysis per USP 921, appearance assessment, and water activity per USP 922.
- Execute advanced analytical techniques with assistance, such as PXRD, DSC, FT‑IR, TGA, and SEM.
- Prepare samples and solutions; manage instrument set‑up and shutdown procedures.
- Create data packets, stability data sheets, and Certificates of Analysis that summarize analytical testing.
- Assist in Out‑of‑Specification (OOS) investigations and document deviations with Qualified Investigators and management.
- Apply cGMP, Confidential Client SOPs, and relevant ICH and FDA guidance in daily work.
- Communicate test results and escalate OOS/OOT findings to internal stakeholders and clients as appropriate.
- Perform other duties as assigned.
The Candidate
Minimum requirements:
- Bachelor’s degree in a scientific field (Chemistry or Biochemistry preferred).
- Able to be physically accessible to lab and office staff and to use standard office equipment.
- Vision sufficient for reading written documents and frequent use of a computer monitor.
Preferred skills and background:
- Applicable laboratory experience (industry or academic) preferred.
- Prior GMP exposure is a plus.
- Strong attention to detail, good documentation habits, and the ability to follow written procedures.
Pay
The anticipated salary range for this position in California is $70,500 – $72,000 annually. The final salary offered may vary based on experience, education, skills, and business needs. This range applies to roles working in California; pay may differ for positions located in other states.
Why Join Confidential Client
- Hands‑on, entry‑level opportunity to develop analytical and GMP skills.
- Supportive, fast‑paced environment focused on continuous process improvement.
- Competitive paid time off and paid holidays.
- Medical, dental, and vision benefits effective day one.
- Tuition reimbursement and career development opportunities.
- Site programs promoting employee engagement, wellness, and community involvement.
- Employee Resource Groups and diversity & inclusion initiatives.
Additional Information
This is an onsite, full‑time role in San Diego, CA with a regular daytime shift (Monday–Friday). Candidates must be authorized to work in the U.S.
Equal Opportunity & Hiring Transparency
Careertakes and our client are Equal Opportunity Employers committed to building a diverse and inclusive workforce. We prohibit discrimination or harassment of any kind. To support a fair and efficient hiring process, AI tools may be used to assist with application review or resume screening. These tools do not replace human decision-making. Final hiring decisions are made by people.
If you have questions about how your data is used, please contact us directly.
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