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.

---

Responsibilities

• Follow batch records, SOPs, and work instructions to detail
• Document all operations in batch records and logbooks
• Comply with GLP/GMP protocols and controlled documentation practices
• Operate large-scale oligonucleotide manufacturing equipment (e.g., oligonucleotide synthesizer, purification skid, tangential flow filtration system, lyophilizer, ChemGlass reactors, pH/conductivity meters, peristaltic pumps)
• Assist manufacturing chemists with synthesis and purification activities, including:
  • Reagent solution preparation
  • Mobile phase preparation
  • Column packing
  • Fraction collection
• Perform oligonucleotide/intermediate analysis via LCMS
• Communicate with cross‑functional teams (Process Development, Analytical Development, Quality Control, Quality Assurance)
• Maintain a clean, safe workspace and wear required personal protective equipment
• Track and update raw material usage in D365 (ERP) software
• Act as production campaign lead when assigned
• Assist with training new personnel

---

Requirements

• Bachelor’s degree in a scientific field OR equivalent relevant work experience
• Entry level to 2 years of experience in a similar manufacturing or lab role
• Good verbal and written communication skills
• Strong attention to detail and ability to follow procedures precisely
• Ability to work effectively in a team environment

---

Preferred

• Experience working in a GMP manufacturing environment and familiarity with controlled documentation

---

Compensation & Location

• Wisconsin pay range: $60,000—$70,000 USD (salary range provided by our client)
• Location: Verona, WI — on-site manufacturing role
• Candidates must have current, valid authorization to work in the United States.

---

Additional Details

• Employment type: Full-time
• This role requires compliance with GMP/GLP and strict adherence to SOPs and batch documentation.
• Careertakes and the confidential client are committed to reasonable accommodation for applicants with disabilities during the hiring process. If you need assistance, please let us know.

---

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.