Location: Germantown, Wisconsin, US
Department: Research and Development
Reference: VN1229
The Associate Scientist, under the direction of a senior scientist, executes chemical reactions on a gram to multi-kilogram scale and performs routine analytical procedures to monitor reaction progress. This role requires the incumbent to efficiently organize routine work with supervision and properly evaluate and interpret generated data. Exercises judgment within defined procedures and practices to determine appropriate action. The Associate Scientist II will exercise judgment within defined procedures and practices to determine appropriate action.
This position is located at our Germantown, WI site. They need to be in the Greater Milwaukee Area in commutable distance to the site and willing to be onsite full time.
Your responsibilities
This position is located at our Germantown, WI site. They need to be in the Greater Milwaukee Area in commutable distance to the site and willing to be onsite full time.
Your responsibilities
- Executes synthesis activities from gram to multi-kilogram scale under supervision.
- Performs routine analytical procedures necessary for support of development activities.
- Performs routine maintenance and troubleshooting of laboratory equipment with supervision.
- Writes project documentation (developmental reports and protocols) of medium complexity with supervision.
- Establishes and coordinates activities at contract chemical and analytical laboratories, as required.
- Assists as a technical contact for projects that transfer internally with the production groups. (i.e. research kilo laboratory to GMP kilo laboratory, or kilo laboratory to plant).
- Embody our company values, which are: be reliable, be caring, be transparent and be willing.
- Bachelor’s degree in Chemistry or related field required with 3-5 years relevant experience.
- Master’s degree in Chemistry or related field with 0-2 years relevant experience.
- Some hands on experience in analytical techniques such as HPLC, GC is helpful, not required.
We offer a competitive compensation and benefits package including medical/dental/vision/life insurance, paid time off, bonus program, 401k match, tuition reimbursement, 24/7 employee assistance program, flexible work hours, and the opportunity for career training and development. Please note that compensation is based on a variety of factors when extending offer, including but not limited to, the role, responsibilities, candidate experience, education, qualifications, and business considerations.
Candidates must be eligible to work in the United States without requiring company sponsorship to obtain or keep U.S. work authorization.
Why consider Sterling?
Sterling Pharma Solutions is a global contract development and manufacturing organization (CDMO) with more than 50 years’ experience in developing and manufacturing Active Pharmaceutical Ingredients (APIs). This is complimented by Antibody Drug Conjugate (ADC) research and development bioconjugation services.
We are a fast growing, dynamic business with facilities in the UK, Europe and the US, where we employ more than 1300 talented and passionate people who support our customers in bringing new medicines to market, improving and saving the lives of patients.
Our culture and our way of working is what really sets us apart as a business; we aim to deliver an exceptional experience to our customers and our employees. You can expect to be part of a supportive team, all working towards a shared goal: to deliver first-class science and service to our customers every day.
Sterling Pharma Solutions is an equal opportunity employer.
Be caring. Be transparent. Be willing. Be reliable.
