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Research Assistant

2 months ago

San Diego, United States Planet Pharma Full time

Title: Research Associate


MUST HAVES:

  • cGMP and HPLC experience - at least 2 years, ideally 3+
  • 2-3 years working in the pharma industry minimum
  • BS degree in either Biology or Chemistry (preferred, other scientific majors are fine as well)


Summary:

The purpose of this position is to carry out assigned laboratory duties which may include sampling, testing, and evaluating analytical data on samples such as raw materials, in-process, and final products. In addition, will also develop and validate analytical methods.


Essential Duties & Responsibilities:

The following statements are intended to describe the general nature and level of work being performed by an individual assigned to this job. Other duties may be assigned.

  • Perform analytical testing in support of product development and method validation.
  • Conduct laboratory tests in compliance with established internal Standard Test Methods (STMs), compendial and vendor/partner supplied methods.
  • Maintain organized records of tests performed and results obtained by following company policies.
  • Perform basic troubleshooting and preventative maintenance of laboratory equipment.
  • Understand and comply with all company policies, safety procedures, and SOPS, including cGMPs and cGLPs.
  • Assist in the preparation analytical data for internal and external meetings and presentations.
  • Assist in performing laboratory investigations. Contribute to written investigation reports as required.
  • Maintain a level of technical knowledge and understanding in the assigned areas of responsibility that are consistent with the current scientific requirements of the company.
  • Participate in the transfer of methods to/from the Quality Control department.

Interaction:

  • The incumbent works closely with all functional areas in Research and Development, Manufacturing, Quality Assurance, Quality Control, Document Control and Regulatory Affairs.

Skills:

Knowledge, Skills, and Abilities:

  • Basic understanding of the chemical and physical principals upon which formulation, process development and analytical methodology is based.
  • Familiarity with concept of cGMPs.
  • Basic skills in using typical laboratory and processing equipment (e.g. HPLC, UV Spec, pH meter, centrifuge, etc.).
  • Ability to utilize scientific information resources within the assigned area of responsibility.
  • Good observation skill, problem solving, and troubleshooting skills (e.g. rational progression of investigation).
  • Good understanding of the scientific thinking in the design of experimental protocols.
  • Basic documentation skills (e.g. notebook, reports) with attention to detail and legible handwriting.
  • Good organizational skills (e.g. daily tasks, documentation, archived information).
  • Good interpersonal skills (e.g. working with members of other teams to achieve shared goals).
  • Good verbal and written English communication skills (e.g. able to participate in scientific discussions and written interactions).
  • Proficient in the use of computers and widely used workplace applications (e.g. Microsoft Office, Outlook, graphing software, etc.).
  • Ability to be flexible in adapting work plan to current corporate goals.
  • Basic time management skills (e.g. multi-tasking and task prioritization).

Education:

  • Bachelor’s degree in relevant field of study (e.g. chemistry, pharmacy, biology, engineering, etc.) from an accredited college or university required.
  • 1 year combined academic and pharmaceutical industry experience.