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Title

Scientist I, AD 

Category Analytical Development  
Description

Why Join Recro:

Mission and Culture:

Our leadership proactively works to create and foster a culture that exemplifies our core values and mission. We strive to provide a work environment that is diverse, inclusive, challenging, and supportive. We are committed to continuous improvement both as individuals and as an organization and encourage our employees to continue their personal and professional development in a variety of ways.

We strongly believe that every employee plays a crucial role in accomplishing our mission of improving patients’ lives through client partnerships. Whether you are working hands on developing, producing or, testing the products or if you are utilizing your expertise in any other way, through your work here you will have an opportunity to positively affect countless lives.

Benefits:

We offer a competitive total rewards package that includes health benefits, annual performance bonus, stock options, generous paid time off, holiday shutdowns, parental leave, matching 401k contributions and much more!

Your New Role:

We are looking for a Scientist I – Analytical Development to support early stage product development through commercialization efforts. In this role you will conduct analytical testing, method development and validation, method transfer and equipment qualifications. You might also write or revise standard operating procedures (SOPs), analytical procedures and other relevant documentation needed.

You will have guidance and support from more senior staff to enable you to learn and develop the skills needed to work independently.

How You Will Make An Impact:

  • You will learn how to perform method development/validation and method transfer activities, developing subject matter expertise with analytical technology transfer activities.
  • Assist in the development of analytical methods for dissolution and chromatographic analysis.
  • You will learn how to author/review laboratory investigations. Conducts investigations, determines root cause and documents results, as needed, in compliance with SOPs.
  • Proactively communicate with internal stakeholders, bringing forth any obstacles you may encounter.
  • You may interact with clients during meetings and teleconferences.
  • Perform testing and data peer review in accordance with established procedures for stability, clinical, formulation development, and method development/validation.
  • Document laboratory activities in notebooks, worksheets, electronic notebooks and the Laboratory Information Management System (LIMS).
  • Conduct daily standardization and performance verifications on laboratory equipment.
  • Evaluate and interpret test and experimental data, drawing conclusions based on results, documenting an communicating your work.
  • Assist laboratory management with acquisition, upgrade and qualification of instruments.
 
Position Requirements

Ideal Candidate Will Bring:

  • Bachelor’s Degree in chemistry or related scientific discipline is required.
  • Minimum of 6 months of prior analytical laboratory experience. Hands on experience within the pharmaceutical industry or within analytical development is preferred.
  • Technical knowledge of analytical laboratory methods and lab safety procedures is required.
  • Basic understanding of Analytical Development operations and ability to support and coordinate projects in various stages of the development process
  • Working knowledge of GLP/cGMP regulations are preferred.
  • Good technical writing and communications skills.
  • Good interpersonal skills and ability to work effectively in a team environment and client companies.
  • Ability to react quickly to changes in project priorities and timelines.
  • Basic understanding of electronic document management systems (Veeva) and chromatography data management software (Empower/Chemstation).
  • Candidates should demonstrate a general understanding of chromatographic techniques and basic trouble shooting skills for typical High Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC) related problems.
 
About the Organization Societal is a bi-coastal contract development and manufacturing organization (CDMO) with expertise to deliver on our client's needs, regardless of complexity level. These projects span pre-Investigational New Drug (IND) development to commercial manufacturing and packaging for a wide range of therapeutic dosage forms. We provide industry leading support for small molecule therapeutic development, end-to-end regulatory support, clinical and commercial manufacturing, aseptic fill/finish, lyophilization, packaging and logistics services to the global pharmaceutical market. We do all of this in our best-in-class facilities in San Diego, California and Gainesville, Georgia.

New hires will pass a background check and drug screen as a condition of employment.  
EOE Statement We are an EOE dedicated to a diverse workforce and a Drug-Free work environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other characteristic protected by law. If you require an accommodation to complete the application or interview process, please contact careers@societalcdmo.com.  
EmpID None Specified 


This position is currently not accepting applications.

To search for an open position, please go to http://Societal.appone.com



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