The Associate Engineer II will provide technical support for manufacturing activities in collaboration with CDMO partners, while also contributing to process development and process validation efforts. The position requires laboratory presence (>50%) and the ability to independently execute and document experiments, analyze data, and communicate results through technical reports and presentations. The successful candidate will collaborate cross-functionally and may interface with external CDMO partners to support manufacturing campaigns and process transfers.

This is a 12-month contract based in San Carlos, CA.

Responsibilities

• Provide remote manufacturing oversight to support batch execution, ensuring adherence to process parameters and GMP requirements.
• Participate in deviation investigations, root cause analysis, and implementation of corrective and preventive actions (CAPAs).
• Provide technical support for manufacturing and process development through data analysis, manufacturing document reviews, and supporting lab scale studies.
• Perform in-process sample testing to support monitoring of manufacturing process performance and understanding.
• Manage sample inventory, including tracking, storage, and organization of manufacturing samples.
• Maintain accurate and timely documentation in electronic lab notebook (ELN) systems.
• Analyze manufacturing and experimental data using statistical tools (e.g., JMP) and summarize findings in technical reports.
• Collaborate with cross-functional teams including Process Development, Manufacturing, Analytical Development, and Quality.
• Prepare and present technical data to internal stakeholders and support interactions with CDMO partners.

Qualifications

• BS in Chemical Engineering, Biochemistry, or a related discipline, with minimum 2 years of relevant industry experience. MS without experience; or equivalent work experience.
• Experience or exposure to GMP manufacturing environments and process development activities.
• Hands-on experience with in-process analytical techniques, including colorimetric and enzymatic assays.
• Familiarity with upstream and downstream processing technologies, such as fermentation, UF/DF, depth filtration, and chromatography.
• Experience supporting technology transfer, scale-up, or CDMO-based manufacturing is preferred.
• Understanding of deviation investigations and root cause analysis methodologies.
• Familiarity with statistical analysis tools (e.g., JMP) is preferred.
• Experience using electronic lab notebook (ELN) systems is a plus.
• Strong technical writing, data analysis, and communication skills.

Salary

• $99,840-$112,230

Why Choose R&D Partners?

As an employee, you have access to a comprehensive benefits package including:

• Medical insurance – PPO, HMO & HSA
• Dental & Vision insurance
• 401k plan
• Employee Assistance Program
• Long-term disability
• Weekly payroll
• Expense reimbursement
• Online timecard approval

R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.

• R&D Partners is an equal-opportunity employer.