Associate Manufacturing Scientist I
The Associate Manufacturing Scientist I supports large-scale oligonucleotide synthesis and purification in compliance with GLP/GMP protocols. This role involves operating specialized manufacturing equipment, documenting processes, collaborating with cross-functional teams, and ensuring quality and safety standards in a biopharmaceutical manufacturing environment.
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, Scientific & QA.
Applicants for this role may also receive access to additional matched opportunities through the Careertakes platform.
Manufacturing Responsibilities
This role supports large-scale oligonucleotide synthesis and purification in a GMP environment. The successful candidate will follow controlled documentation and batch records, operate production equipment, and support cross-functional teams to deliver high-quality material.
- Follow batch records, SOPs, and work instructions to detail
- Document all operations in batch records and logbooks
- Comply with GLP/GMP protocols and site safety procedures
- Operate large-scale oligonucleotide manufacturing equipment (e.g., oligonucleotide synthesizer, purification skid, tangential flow filtration system, lyophilizer, ChemGlass reactors, pH/conductivity meters, peristaltic pumps)
- Prepare reagent solutions and mobile phases
- Pack chromatography columns and manage fraction collection
- Perform intermediate and product analysis (LCMS)
- Track and update raw material usage in D365 ERP
- Act as production campaign lead when assigned
- Support training for new personnel
- Maintain a clean, organized, and safety-compliant workspace
- Communicate effectively with Process Development, Analytical Development, QC, and QA teams
Minimum Qualifications
- Bachelor's degree in a scientific field OR equivalent relevant work experience
- Entry-level to 2 years experience in a similar manufacturing or laboratory role
- Basic experience with laboratory documentation and following SOPs
- Good verbal and written communication skills
- Ability to work collaboratively in a team and maintain attention to detail
- Authorization to work in the United States is required
Preferred Qualifications
- Prior experience in a GMP manufacturing setting and with controlled documentation
- Hands-on experience with oligonucleotide or nucleic-acid manufacturing operations
- Familiarity with LCMS analysis and tangential flow filtration systems
Compensation & Benefits
Wisconsin pay range: $60,000—$70,000 USD (annual). Compensation is set by our client and may vary based on experience and location. Additional benefits may include health insurance, retirement plan contributions, paid time off, and other standard employer-provided benefits — details provided by the hiring organization during the interview process.
Location & Employment Type
Madison, WI — Full-time, on-site role supporting production and manufacturing operations.
Additional Information
Careertakes acts as a recruiting partner in this process. Our client is committed to safe, compliant manufacturing practices. Reasonable accommodations are available for applicants with disabilities; please indicate accommodation needs during the application process.
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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