What are the responsibilities and job description for the ENTRY LEVEL SCIENTIST position at PPD?
JOB DESCRIPTION
Assistant Scientist – Small Molecule – Middleton, WI
Company Overview
PPD is a leading global Contract Research Organization - currently operating in nearly 50 countries! At PPD we are passionate, deliberate, and driven by our purpose - to improve health. Our organization works with a diverse group of pharmaceutical companies to help bend the cost and time curve of small molecule, biologic, and vaccine product development.
This position is located at our GMP lab in Middleton, WI - the largest GMP laboratory in North America. Check out this video for a brief introduction to our lab as told by our scientists: https://vimeo.com/533240741
We hire the best, develop ourselves and each other, and recognize the power of being one team. You will receive extensive training to allow you to be successful at PPD, and it's not just talk - our award-winning training programs speak for themselves. In addition, our teams support career growth, allowing you to explore the numerous career pathways available once you become part of our PPD team.
Role Description
As a chemist, referred to as an Assistant Scientist, you will use state-of-the-art technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and analysis serve as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market.
We offer flexible scheduling to encourage a healthy work-life balance for our employees. Enjoy a Monday through Friday work week with a full time schedule you create! Lastly, we also offer health benefits, a generous PTO plan, and tuition reimbursement for all full-time employees. Let’s not forget to mention monthly Donut Day and daily lunch options catered to campus from local vendors available for purchase.
Responsibilities:
- Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing.
- Problem solves with assistance pertaining to extraction and/or instrumentation problems.
- Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines.
- Manages QC/QA responsibilities without supervisor or QA input.
- Communicates project status to project leader.
- Performs work assignments accurately, and in a timely and safe manner.
- Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP).
- Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.
#LI-LM1
Job Qualification
Qualifications
Education and Experience
Bachelor's degree (Life Sciences degree preferred) or equivalent and relevant formal academic / vocational qualification
Knowledge, Skills and Abilities
- Knowledge of applicable regulatory authority, compendia and ICH guidelines
- Ability to understand and independently apply GMPs and /or GLPs to everyday work about documentation and instrument use
- Ability to utilize Microsoft Excel and Word to perform tasks
- Ability to independently optimize analytical methods
- Good written and oral communication skills
- Time management and project management skills
- Problem solving and troubleshooting abilities
- Ability to work in a collaborative work environment with a team
Work Environment Requirements
PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
Able to work upright and stationary and/or standing for typical working hours.
Able to lift and move objects up to 25 pounds
Able to work in non-traditional work environments.
Able to use and learn standard office equipment and technology with proficiency.
May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
What To Expect Next
We look forward to receiving your application. A member of our talent acquisition team will review your qualifications and if interested, you will be contacted for an interview.
Diversity Statement
COVID-19 Vaccination Update for U.S. Colleagues
- All U.S. colleagues are required to report vaccination status. New hires will be asked to report vaccination status within the first two weeks of employment.
- All U.S. new hires who are in the following job categories must be fully vaccinated before their first day of employment or request an accommodation: executive director level and above, client-facing commercial, clinical research associates (CRAs), remote site monitors-local (RSM-L) all CRA and RSM-L line managers, clinic-based staff in early development services and accelerated enrollment solutions, and FSP within analytical services division roles. New hires will be asked to disclose vaccination status upon first day of employment and are required to report vaccination status within first two weeks of employment.