Analytical Development Scientist Position Available In Pinellas, Florida
Tallo's Job Summary: The Analytical Development Scientist position at Ion Nutritional Labs in Largo, FL offers a full-time role with an estimated salary range of $55.2K - $66.5K a year, along with benefits such as health insurance, dental insurance, 401(k) matching, and paid time off. The ideal candidate will have 5 years of experience in a cGMP environment, strong analytical instrumentation skills, and a Bachelor's degree in Science. Responsibilities include method development, validation, production process validation, equipment maintenance, and supporting new product development.
Job Description
Analytical Development Scientist Ion Nutritional Labs – 1.0
Largo, FL Job Details Full-time Estimated:
$55.2K – $66.5K a year 1 day ago Benefits Health insurance Dental insurance 401(k) Paid time off Vision insurance 401(k) matching Life insurance Referral program Qualifications Microsoft Powerpoint Microsoft Word CGMP Microsoft Excel Microsoft Access 5 years Bachelor of Science Writing skills Laboratory experience English Analysis skills Chromatography Bachelor’s degree Computer skills Manufacturing Senior level Communication skills
Full Job Description Job Title:
Analytical Development Scientist Reports to: R D Director
GENERAL PURPOSE
The Analytical Development (AD) Scientist validates production processes, develops and validates analytical methods to ensure that our customers receive quality products that meet all specifications and requirements.
POSITION RESPONSIBILITIES
: Implement, manage, and perform analytical method development, validation, and/or verification including preparation, review and approval of Protocols and Summary Reports. Implement, manage, and perform production process validation, including preparation, review and approval of Protocols and Summary Reports. Implement, manage and perform production cleaning validation, including preparation, review and approval of Protocols and Summary Reports. Identify, Purchase, Qualify, Install, Calibrate, and maintain analytical equipment for the laboratory as well as some production equipment. Prepare Formula Specific Product Test Details to support new product development activities as required. Maintain an active role on continuous improvement teams to identify opportunities to increase efficiency and effectiveness, and reduce costs (e.g., bringing out-sourced testing into the QC laboratory, improving and optimizing existing methods, etc.). Manage the stability program for all applicable products. Support QC laboratory Investigations with Scientific assessment of unexpected results. Identify, create, and/or source analytical and qualitative reference standards and electronic standard libraries. Writes and/or reviews Protocols and Summary Reports. All other duties as assigned. Willing to work holidays and weekends as requested by manager.
Experience:
Minimum 5 years of experience in cGMP environment Drugs or Dietary Supplements.
Knowledge, Skills and Abilities:
Sound laboratory/testing experience. Broad range of analytical techniques, including advanced knowledge and experience using a broad range of instrumentation including HPLC and FTIR. Strong analytical instrumentation experience with understanding of supporting scientific principles. Writing skills (reports, SOP’s, protocols, etc.) c
GMP / GLP
background is required. Health and safety knowledge as it relates to the laboratory. Computer skills to include full competence with MS Word, PowerPoint, Outlook, Excel, and Access. Operating and troubleshooting procedures for lab equipment. Strong communication skills. Ability to read, understand and communicate in English. Ability to lift up to 30 lbs.
Education:
BS Degree or higher in Science; Candidates with an advanced science degree and science background preferred.
Job Type:
Full-time Benefits:
401(k) 401(k) matching Dental insurance Health insurance Life insurance Paid time off Referral program Vision insurance
Schedule:
8 hour shift Day shift
Work Location:
In person
