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ResourceMFG | Manufacturing Workforce Specialists

Job Information

Description

QUALIFICATIONS: • Bachelor’s degree (B.S.) in related field preferred or equivalent work experience. • Two to four years related experience or equivalent • Strong knowledge of pharmaceutical manufacturing processes, computer, and equipment validation, GMPs, and product/process validation. • Ability to develop clear, concise, and timely oral and written reports. • Experience with laboratory environment, equipment, and safety procedures. • Experience in research and development, including understanding of statistical analysis. • Commitment to excellence and high standards • Excellent written and oral communication skills • Strong organizational, problem-solving, and analytical skills • Ability to manage priorities and workflow • Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm • Acute attention to detail • Demonstrated ability to plan and organize projects • Ability to work independently and as a member of various teams and committees • Proven ability to handle multiple projects and meet deadlines • Ability to work on complex projects with general direction and minimal guidance. Working knowledge of data collection, data analysis, evaluation, and scientific method.

Job Requirements

RESPONSIBILITIES:

 

  • Analyzes products in compliance with cGMP regulations and SOPs.
  • Follow work instructions and standard operating procedures.
  • Inspect production areas, production processes, and finished goods produced.
  • Completes and maintains appropriate documentation to support testing procedures and comply with GMPs including but not limited to data capture forms, equipment logbooks, and inventory forms.
  • Monitor cleanliness of production and if unacceptable, report to direct supervisor.
  • Reads, understands, and follows SOPs; complies with current GMP as required by FDAD
  • Document all retain samples pulled in excel workflow.
  • QUALIFICATIONS: • Bachelor’s degree (B.S.) in related field preferred or equivalent work experience.

• Two to four years related experience or equivalent

• Strong knowledge of pharmaceutical manufacturing processes, computer, and equipment validation, GMPs, and product/process validation.

• Ability to develop clear, concise, and timely oral and written reports. • Experience with laboratory environment, equipment, and safety procedures.

• Experience in research and development, including understanding of statistical analysis.

• Commitment to excellence and high standards • Excellent written and oral communication skills • Strong organizational, problem-solving, and analytical skills

 

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