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:
- 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 of 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.
Requirements:
- 3 years minimum of pharmaceutical experience required (will not consider someone right out of school, need the experience)
- Minimal lifting is required. May need to move boxes, always others around to assist. No more than 20 lbs.
- Familiarity with cGMP's, and work experience following cGMP's required.
- Basic skills in using typical laboratory and processing equipment - HPLC required
- Basic understanding of the chemical and physical principles upon which formulation, process development, and analytical methodology is based.
- Familiarity with concepts of cGMPs.
- Basic skills in using typical laboratory and processing equipment (e.g. HPLC (required), UV Spec, pH meter, centrifuge, etc.).
- Ability to utilize scientific information resources within the assigned area of responsibility.
- Good observation, 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 a relevant field of study (e.g. chemistry, pharmacy, biology, engineering, etc.) from an accredited college or university is required.
Schedule: Monday - Friday, 8:00 AM to 4:30 PM
Start Date: 07/08/2024
Estimated End Date: 12/24/2024
Hours Per Week: 40.00
Hours Per Day: 8.00
Job Types: Full-time, Contract, Temporary
Pay: $25.00 - $28.00 per hour
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Work Location: In person