Every day, Kelly Scientific Resources (KSR) connects scientific professionals with opportunities to advance their careers. We are the first and largest scientific staffing company in the world, and we are currently offering an exciting opportunity to work as a Senior Analytical Chemist at a growing pharmaceutical company in Phoenixville, PA!

This is a 6 month temp-to-hire, 1st shift, weekday position.

Besides working on-site at a company doing exciting work in the field of therapeutic antibody development, by working with KSR, you would be eligible for the following:
- Competitive pay ($28-36/hour for this position, based on experience)
- Access to a comprehensive benefits package
- Access to valuable continuing education courses via the Kelly Learning Center
- Employee discounts and a recognition program
- And more!

The Senior Analytical Chemist conducts research, analysis and experimentation on substances for such purposes as product and process development and application, quantitative and qualitative analysis, and improvement of analytical methodologies. He/She also maintains the laboratory and all documentation within GLP/cGMP guidelines. The Senior Analytical Chemist performs complex activities and applies basic understanding of scientific data/ literature in areas related to Analytical Services. He/she is expected to present ideas for modifying existing procedures and suggest alternative methods for improving results and provide solutions to a variety of problems.

Essential Duties and Responsibilities:
'« Apply basic scientific principles and techniques to complete assigned complex experimental activities related to the endeavors of Analytical Services and receive limited supervision on specified tasks.
'« Develop and validate test methods.
'« Perform routine and non-routine analysis on raw materials, drug substances, reference material and drug products using a variety of instrumental and wet chemistry techniques.
'« Recognize the necessity for independent literature reading and scans literature in the area of responsibility.
'« Solve technical problems within the scope of the assignment with assistance from supervisor. Show ingenuity in resolving problems.
'« Submit progress reports as appropriate and assists in the preparation of study reports in a timely and efficient manner.
'« Monitor and assess current analytical methods and assists in improvements and amendments according to cGMP practices.
'« Responsible for following policies, procedures, cGMPs and laboratory safety pertinent to the execution of duties. Ensure compliance is maintained in all areas of responsibility.
'« Contribute to the development and/or implementation of new technology in conjunction with supervisor.
'« Assist in other parts of the department as workload and project priorities dictate.
'« Demonstrate development of technical and communication skills with a degree of professional maturity.
'« May review work from various sources, may assign work to others, and may train less experienced employees.
'« Participate as a team member, support the company mission and vision and contribute to the pursuit of the company's goals.
'« Participate actively in regular meetings.
'« Achieve expected performance measures.
'« Other duties as assigned.

Qualifications
'« At least a Bachelors¡¿ Degree or equivalent in Chemistry or related science.
'« 3 - 5 years experience in analytical drug development in a pharmaceutical laboratory.
'« 3 - 5 years experience with HPLC, dissolution and classical analytical techniques.
'« Experience in testing all aspects of solid dosage forms a necessity; controlled release and semi-solid testing experience a plus.
'« Working knowledge of experimental designs, GMPs, clinical manufacturing, validation, and report writing for regulatory submissions.
'« Proficient with interpreting and implementing cGMPs, cGLPs, ICH, USP, FDA, DEA and OSHA guidelines.
'« Demonstrated ability to work and manage effectively in a fast paced environment.
'« Must be able to manage multiple projects while maintaining efficiency and effectiveness.
'« Excellent oral and written communication skill to communicate with the team, peers, management, and external contacts.
'« Must have the ability to work effectively and independently.
'« Working knowledge of personal computers and Microsoft Office Products, including Word, Project, and Excel.


This is an exciting opportunity to learn, grow, and make an impact at a growing pharmaceutical company involved in cutting-edge research and development. So, don't wait... send your resume/CV right away to be considered for this opportunity! Or, feel free to refer a friend. All resumes are concurrently entered into our national database.

Since its founding in 1995 as Kelly's scientific business unit, Kelly Scientific Resources has emerged as the leading scientific and clinical trials staffing company in the world today. On average we employ over 400 clinical trials professionals and 4,500 scientists in temporary, contract and full-time positions - from more than 100 locations in North America, Europe and the Pacific Rim.

Kelly Scientific Resources is the scientific staffing business unit of Fortune 500 global staffing provider Kelly Services, Inc.

Kelly Services, Inc. is an Equal Opportunity Employer.

KELLY SCIENTIFIC RESOURCES leads the world in dedicated scientific and clinical research staffing, operating in 23 countries and territories throughout North America, Europe, and the Pacific Rim. Since its launch in 1995, Kelly Scientific Resources has provided staffing and placement services to a broad spectrum of industries, including biotechnology, chemical, consumer products, cosmetics, environmental, food sciences, medical/clinical, pharmaceutical, and petrochemical. For more information, visit www.kellyscientific.com

Kelly Scientific Resources is the scientific staffing business unit of Fortune 500 global staffing provider Kelly Services, Inc.