Sterling Pharma Solutions
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Location: Germantown, Wisconsin, US
Department: Research and Development
Reference: VN1227
As the Chemical R&D Scientist, you will lead the implementation of new methods/processes to solve problems. This role prepares and reviews summaries of observations and is capable of verbal and written presentations documented proficiently in laboratory notebooks to internal and external audiences. The incumbent will write and review SOPs, training modules, technical transfer documents, specifications, summary reports and technical reports to be sent to clients or used in regulatory filings and is responsible for ensuring complex technical information is well understood by team associates, management and clients. The position performs audits of laboratory work and reports and maintains a high level of professional expertise through familiarity with scientific literature. The Chemical R&D Scientist determines appropriate methods and procedures on new assignments.
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.
Responsibilities
Solves synthetic problems with minimal supervision. Executes synthesis activities from gram to multi-kilogram scale with minimal supervision. Isolates and purifies products and intermediates by using standard laboratory techniques. Interprets and communicates analytical data. Performs routine analytical procedures to monitor reaction progress (i.e. TLC, GC, NMR, HPLC, KF). Designs multi-step synthetic process from commercially available starting materials to target compounds. Performs routine maintenance and troubleshooting of 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. Embodies our company values, which are: be reliable, be caring, be transparent and be willing. Requirements for the role
For entry level role:
Bachelor’s degree in Chemistry or related field required with minimum of 9+ years’ experience, OR Master’s degree in Chemistry or related field with minimum of 3+ years’ experience, OR Doctoral degree with a 0-2 years of previous experience.
For advanced level role:
Doctoral degree with a 2+ years of previous experience.
Benefits
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. Candidates must be eligible to work in the United States without requiring company sponsorship to obtain or keep U.S. work authorization. About Sterling Pharma Solutions
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. Sterling Pharma Solutions is an equal opportunity employer.
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Solves synthetic problems with minimal supervision. Executes synthesis activities from gram to multi-kilogram scale with minimal supervision. Isolates and purifies products and intermediates by using standard laboratory techniques. Interprets and communicates analytical data. Performs routine analytical procedures to monitor reaction progress (i.e. TLC, GC, NMR, HPLC, KF). Designs multi-step synthetic process from commercially available starting materials to target compounds. Performs routine maintenance and troubleshooting of 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. Embodies our company values, which are: be reliable, be caring, be transparent and be willing. Requirements for the role
For entry level role:
Bachelor’s degree in Chemistry or related field required with minimum of 9+ years’ experience, OR Master’s degree in Chemistry or related field with minimum of 3+ years’ experience, OR Doctoral degree with a 0-2 years of previous experience.
For advanced level role:
Doctoral degree with a 2+ years of previous experience.
Benefits
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. Candidates must be eligible to work in the United States without requiring company sponsorship to obtain or keep U.S. work authorization. About Sterling Pharma Solutions
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. Sterling Pharma Solutions is an equal opportunity employer.
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