Scientist, P&P
About The Position
In this role you will support the laboratory with data review generated to comply with cGMP and Data Integrity (DI). You will be responsible to ensure raw data and electronic data are reviewed on a timely manner and comply with cGMP, DI and West requirements. You will execute daily SAP review and locking of results along with audit trail reviews. West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to [email protected]. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.
Requirements
- BS in biomedical engineering, chemical engineering, mechanical engineering, or related technical degree
- Minimum 3 years 3 -5 years of professional experience in a lab environment required
- Experience in pharmaceutical/medical device field and implementing laboratory training programs required
- cGMP
- ISO and USP/EP compendia
- Strong oral and written communication skills and attention to detail required
- Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description
Nice To Haves
- Intron/Zwick/UV/or 3D Printing & CAD experience is a plus
Responsibilities
- Perform analysis using various techniques including established and experimental test methods.
- Use instrumentation both qualitatively and quantitatively where appropriate.
- Manage projects from protocol to final report.
- Train and certify analysts as appropriate.
- Develop and validate methods.
- Keep current with new analytical technology.
- Possess ability to work independently and as part of a team with self-motivation, adaptability, and a positive attitude.
- Prepare technical reports based on data from multiple analysts utilizing multiple analytical techniques.
- Prepare work instructions, SOPs, and qualification documentation.
- Prepare lab study designs and prepare study plans and protocols.
- Interact with internal and external clients as needed.
- Willingness to learn and apply new analytical techniques.
- Perform lab investigations, OOS, and OOT as required.
- Serve as a role model for positive leadership.
- Meet individual and departmental goals as required.
- Apply required cGMP regulations and internal QA procedures
- Adhere to established laboratory safety procedures.
- Performing clean room testing.
Benefits
- Benefit programs that empower the physical, mental, emotional and financial health of our team members and their families.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
