Associate Scientist

Associate Scientist I-II

Kelly Science has immediate needs for multiple Associate Scientist I-IIs to join a growing client located in the Miami/Fort Lauderdale FL area.

Location: Fort Lauderdale/Miami, FL
Shift: Monday-Friday 4pm-12am
Salary Range: $30-$40/hour
12 month contract opening

Essential Duties and Responsibilities:

• Conduct laboratory activities with limited supervision, including analyzing raw materials, in-process materials, and finished pharmaceutical products for quality, safety, purity, strength, and identity, following applicable methods and relevant guidelines (cGMP, EH&S, FDA, and other governing bodies).
  
• Independently set up and operate lab equipment, prepare reagents, solvents, and solutions for analytical and formulation activities.
  
• Maintain accurate records in lab notebooks for all testing performed.
  
• Process analytical data using lab equipment such as HPLC/UPLC and enter data into spreadsheets; conduct routine calculations.
  
• Support the manufacture of inhalation drug products and prepare samples for blend uniformity.
  
• Perform equipment qualification and calibrations as directed.
  
• Execute approved method transfer protocols.
  
• Assist in training other scientists and team members.
  
• Perform additional tasks as assigned.
  
• Participate in project activities, support project timelines, and proactively contribute to meeting team objectives.
  
• Communicate effectively with team members and maintain effective relationships.
  
• Conduct lab work in accordance with SOPs and STPs and follow corporate safety rules and procedures.
  
• Comply with all corporate guidelines and policies.

Qualification Requirements:

• Associate Scientist II: BSc in Chemistry, Pharmacy, or related fields with at least 3 years of experience in Pharmaceutical R&D, or MSc in Chemistry, Pharmacy, or related fields with 0-2 years of experience in Pharmaceutical R&D.
  
• 2 years minimum industry experience with HPLC method development and Empower software
  
• Proven ability and/or experience with compendial test methods or pharmaceutical manufacturing equipment.
  
• Understanding of pharmaceutical equipment and computerized systems for operation and troubleshooting, including experience with analytical and/or process equipment such as HPLC, IR/FTIR, UV-Vis, AA, powder blenders, etc.
  
• Knowledge and understanding of FDA cGMP requirements as it applies to the pharmaceutical industry.
  
• Strong written and oral communication skills in English, with the ability to write short technical documents such as memos, laboratory investigations, protocols, and reports.

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