Analytical Scientist
Sterling Pharma Solutions
Date: 2 weeks ago
City: Cary, NC
Contract type: Full time
Location: Cary, North Carolina, US
Department: Research and Development
Reference: VN1138
Summary Of The Role
As the Analytical Scientist, you are executing development of analytical methods and improvement of existing ones to support API development programs. This requires skills and knowledge in handling, analyzing and characterizing chemicals, pharmaceuticals and related organic molecules. The role also requires hands on experience in analytical techniques such as HPLC, GC, etc. The Analytical Scientist II will independently draft analytical development reports, method qualification protocols, and execute validation protocols for analytical methods. This position will also independently perform and review chemical analysis and draft reports for analytical method development and validation. This role requires 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.
Your Responsibilities
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.
Diversity and Inclusion
Sterling values diversity and we are committed to creating an inclusive environment for all employees. All employment decisions are based on business needs, job requirements and individual qualifications, without regard to race, color, religion, sex, pregnancy, age, national origin, physical or mental disability, past or present military service, marital status, gender identification or expression, medical condition (including genetic characteristics) or any other protected characteristic as established by law.
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.
Apply now
Department: Research and Development
Reference: VN1138
Summary Of The Role
As the Analytical Scientist, you are executing development of analytical methods and improvement of existing ones to support API development programs. This requires skills and knowledge in handling, analyzing and characterizing chemicals, pharmaceuticals and related organic molecules. The role also requires hands on experience in analytical techniques such as HPLC, GC, etc. The Analytical Scientist II will independently draft analytical development reports, method qualification protocols, and execute validation protocols for analytical methods. This position will also independently perform and review chemical analysis and draft reports for analytical method development and validation. This role requires 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.
Your Responsibilities
- Demonstrates technical ability to assist in the design and execution of non-routine experiments with supervision.
- Demonstrates ability to correctly analyze data/results and interpret outcome of experiments and to propose appropriate follow-up with supervision.
- Applies basic 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.
- Performs literature searches and extracts relevant information from published protocols, and journals.
- Performs routine maintenance and troubleshooting of analytical equipment with limited supervision.
- Manages a variety of aspects of analytical projects with minimal supervision.
- Provides project related updates to internal and external customers.
- Writes project documentation (analytical test methods, developmental reports, and protocols) of medium complexity with minimal input from supervisor.
- 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.
- Bachelor’s degree in a scientific discipline such as analytical chemistry, or related field with 6+ years of experience, or
- Master’s degree in a scientific discipline such as analytical chemistry, or related field, with minimum of 3+ years of industrial experience, or
- Doctoral degree in a scientific discipline such as analytical chemistry, or related field, with minimum of 1+ years of industrial experience.
- Chemical/ API manufacturing practices/processes knowledge is preferred.
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.
Diversity and Inclusion
Sterling values diversity and we are committed to creating an inclusive environment for all employees. All employment decisions are based on business needs, job requirements and individual qualifications, without regard to race, color, religion, sex, pregnancy, age, national origin, physical or mental disability, past or present military service, marital status, gender identification or expression, medical condition (including genetic characteristics) or any other protected characteristic as established by law.
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.
Apply now
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