Instrumentation Specialist

Posted 5 Days Ago
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West Columbia, SC, USA
In-Office
Senior level
Healthtech • Pharmaceutical • Manufacturing
The Role
Oversees laboratory instrumentation programs in a chemistry laboratory, including preventive maintenance, qualification, troubleshooting, supplies, SOPs, logbooks, and compliance documentation. Maintains HPLC, GC, and other analytical instruments while supporting cGMP quality systems and FDA, USP, and industry requirements. Provides technical direction, manages projects and resources, and identifies cost-saving opportunities compared with vendor maintenance contracts.
Summary Generated by Built In

Description

  

Job Purpose:

• Oversees all aspects of the laboratory instrumentation in the chemistry laboratory 

• Assists with additional work duties or responsibilities as evident or required. 

• Performs other duties as assigned or apparent. 

• Relies on experience and judgment to plan and accomplish goals. 

• Performs a variety of complicated tasks under general supervision for which creativity is expected and latitude is given. 

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Primary Accountabilities: 

• Plans, organizes, and manages preventative maintenance of laboratory equipment 

• Creates or modifies SOP’s, forms, logbooks, etc. as necessary to facilitate the instrumentation program. 

• Ensures that supplies are on hand to perform routine instrument maintenance and that supplies for non-routine maintenance or troubleshooting are ordered promptly as needed. 

• Focuses on cost savings and value delivery, ensuring that instrument maintenance is of higher quality and lower cost than vendor maintenance contracts. 

NOTE: The Primary Accountabilities below are intended to describe the general content of and requirements of this position and are not intended to be an exhaustive statement of duties. 

Incumbents may perform all or most of the primary accountabilities listed below. Specific tasks or responsibilities will be documented in the incumbents' performance objectives as outlined by the incumbents' immediate supervisor or manager. 

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Job Specifications and Qualifications:

Skills:

• Experience with cGMP documentation systems and with implementation of quality systems. 

• Strong knowledge of FDA, USP, and industry requirements for analytical instrumentation qualification and maintenance 

• Must have strong project management skills and be able to provide technical support and direction with compliance to standards in order to meet business initiatives. 

• Must possess direct experience with maintaining HPLC, GC, and other common laboratory instrumentation. 

• Must possess strong IT skills and a strong understanding of hardware and software troubleshooting of laboratory instrumentation. 

• Must be detail oriented and have excellent organizational skills. 

• Must possess effective written and oral communication skills and b able to handle multiple projects within limited time frames. 

Abilities:

• The ability and willingness to change direction and focus to meet shifting organizational and business demands. 

• The ability to effectively manage one self, demonstrates integrity, be productive under pressure, and achieve developmental goals. 

• The ability to manage a multitude of resources and to be accurate and current with data and information 

• The ability to create new products and processes that add value to the Business, by generating new ideas and applying creative and analytical approaches. 

Education/Experience:

• Minimum Bachelor’s degree or 7 years of experience working in Quality Control Chemistry and/or Research & Development. 

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Working Conditions / Physical Requirements:

· Position requires standing (40%), sitting (25%), talking, hearing, typing and walking (35%). 

· Position encounters the following environmental factors: hazardous materials including HPLC solvents, chemical reagents, acids and other non-specified hazardous materials that are project specific.

· Position requires safety glasses, respiratory and other non-specified protective equipment to be worn as necessary. 

Additional Requirements:

· Salary range is based on experience.

Skills Required

  • Bachelor’s degree or 7 years of experience in Quality Control Chemistry and/or Research & Development
  • Experience with cGMP documentation systems and quality system implementation
  • Knowledge of FDA, USP, and industry requirements for analytical instrumentation qualification and maintenance
  • Direct experience maintaining HPLC, GC, and other common laboratory instrumentation
  • Strong IT skills and hardware/software troubleshooting experience for laboratory instrumentation
  • Strong project management, organizational, written communication, and oral communication skills
  • Ability to manage multiple projects within limited time frames
  • Ability to work with hazardous materials and use required personal protective equipment
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The Company
HQ: West Columbia, SC
Year Founded: 1937

What We Do

Nephron Pharmaceuticals Corporation is a world leader in manufacturing generic respiratory medications and provides drug compounding services for 503B outsourcing through its sterile, cGMP facility.

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