Analytical Scientist

About Client:
The client is a prominent pharmaceutical company with a rich history and global presence. It operates worldwide, conducting research, developing, and manufacturing a wide range of innovative medications and therapies. The company focuses on several therapeutic areas, including respiratory diseases, cardiovascular diseases, metabolic disorders, oncology, immunology, and diseases of the central nervous system. It is recognized for its commitment to research and development, investing significantly in discovering novel treatments and advancing medical science.
With a workforce comprising diverse and skilled professionals, it remains committed to its mission of improving lives and driving medical advancements. Through its dedication to innovation, research, and healthcare solutions, the company continues to shape the future of medicine on a global scale.


Rate Range: $45-$50/Hr.


Job Description:

• Client is currently seeking a talented and innovative scientist to join our Materials and Analytical Sciences department located at our Ridgefield, CT facility. As a scientist, you will develop and perform scientific assays to analyze the drug formulation of New Chemical Entities (NCE), New Biological Entities (NBE), and Advanced Therapy Medicinal Products (ATMPs).
•  you will actively contribute to the discovery, development and delivery of our products to our patients and customers.
• Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success.
• We realize that our strength and competitive advantage lie with our people.
• We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance.

• Independently designs and performs analytical methods to measure drug formulations by reverse-phase and size exclusion chromatography under Good Laboratory Practices (GLP) guidelines.
• Participate in the development, qualification, and validation of new analytical methods.
• Maintains an organized and detailed notebook according to Good Documentation Practices (GDP) guidelines.
• Reports and treats data with a high level of integrity and ethics. Present results responsibly at team meetings.
• Solid knowledge and understanding of applicable GLP regulations.
• Work in a collaborative manner with members of other departments.
• Review, approve, write, and revise Standard Operating Procedures (SOPs) and Technical Reports.
• Comply with applicable regulation, perform all work in a safe manner; Maintain proper records in accordance with SOPs and polices.
• May require an ability to push, pull, lift, and carry objects up to 50 lbs.

• Masters Degree from an accredited institution with three-plus (3+) years of experience in related scientific discipline, OR Bachelors Degree from an accredited institution with seven-plus (7+) years of experience in related scientific discipline or equivalent experience in related field.
• Knowledge and experience in high performance liquid chromatography (HPLC) method development and validation for drug formulation analysis.

• Experience with HPLC related software, such as Empower, to execute experiments and analyze data.

• Ability to work independently in the lab to prepare reagents, pipette solutions accurately, and operate instruments.
• Prior experience working in a GxP environment is preferred.
• Strong laboratory skills with the ability to resolve and advise on technical issues of a moderate scope and develop new skills through on-the-job experiences.
• Experience in extracting nucleic acid (DNA and RNA) and performing qPCR is a plus.
• Experience working with viruses (lentivirus, AAV) or viral vectors is a plus.
• Clear and effective written and verbal communication skills.
• Proven problem solving ability.

Non-benefitted (other than those mandated under state or federal law).Please note that this position does not include paid time off benefits. ApTask offers subsidized insurance coverage to our employees.

About ApTask:
Join ApTask, a global leader in workforce solutions and talent acquisition services, as we shape the future of work. We offer a comprehensive suite of offerings, including staffing and recruitment services, managed services, IT consulting, and project management, providing unparalleled opportunities for professional growth and development. As a member of our dynamic team, you'll have the chance to connect businesses with top-tier professionals, optimize workforce performance, and drive success for our clients across diverse industries. If you are passionate about excellence, collaboration, and innovation, and aspire to make a meaningful impact in the world of work, come join us at ApTask and be a part of our mission to empower organizations to thrive.

Applicants may be required to attend interviews in person or by video conference. In addition, candidates may be required to present their current state or government issued ID during each interview.

​​​​​​​Candidate Data Collection Disclaimer:
At ApTask, we prioritize safeguarding your privacy. As part of our recruitment process, certain Personally Identifiable Information (PII) may be requested by our clients for verification and application purposes. Rest assured, we strictly adhere to confidentiality standards and comply with all relevant data protection laws. Please note that we only collect the necessary information as specified by each client and do not request sensitive details during the initial stages of recruitment.

If you have any concerns or queries about your personal information, please feel free to contact our recruitment team at businessexcellence@aptask.com .
 

Last updated on Aug 23, 2023