Associate Analytical R&D Scientist

As the Analytical R&D Associate Scientist, you are accountable for driving results by supporting manufacturing activities through phase specific method development and method validation activities. The Analytical Scientist will execute the development of analytical methods and improve existing methods to support our active pharmaceutical ingredients development program. The Associate Scientist II works closely with a multifunctional team to support quality control and chemical research and development groups.

Your responsibilities

• Execute development of analytical methods and improvement of existing ones to support API development program for Sterling facilities with supervision.
• Draft and execute validation protocols for analytical methods with supervision.
• Perform and review data analysis and drafts reports for analytical method development and validation with supervision.
• Perform routine maintenance and troubleshooting of analytical equipment with supervision.
• Write project documentation (Analytical test methods, developmental reports and protocols) of medium complexity with supervision.
• Establish and coordinate activities at contract chemical and analytical laboratories, as required.
• Ensure timely completion and compliance with cGMP and all other relevant company training requirements.
• Proven ability to apply scientific principles, theories and concepts to research problems and develop solutions for analytical problems related to drug substances in compliance with appropriate Standard Operating Procedures (SOPs) and regulatory guidelines.
• Demonstrate technical ability to assist in the design and execution of non-routine experiments with supervision.
• Embody our company values, which are : be reliable, be caring, be transparent and be willing.
• An individual in this position must be able to successfully perform the essential duties and responsibilities listed above. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of this position.

Requirements for the role

What we offer

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.