NEPHRON SC logo
NEPHRON SC Verified
Pharmaceuticals, Manufacturing

Instrumentation Specialist

West Columbia, SCOnsiteFull TimePosted 1 month agoVisa sponsorship available

Is this role right for you?

Upload your resume and get a skill-by-skill breakdown — see exactly where you match, where you're close, and what to highlight. Not a mystery percentage.

Get a tailored resume highlighting what this role needs.

Required skills

  • cGMP
  • quality systems
  • FDA
  • USP
  • HPLC
  • GC
  • laboratory instrumentation
  • IT skills
  • hardware troubleshooting
  • software troubleshooting

Nice to have

  • preventative maintenance
  • SOPs
  • cost savings
  • vendor maintenance contracts
  • written communication skills
  • oral communication skills

Role summary

The Instrumentation Specialist oversees all aspects of laboratory instrumentation in the chemistry laboratory, focusing on planning, organizing, and managing preventative maintenance. This role involves creating and modifying SOPs, ensuring adequate supplies for maintenance and troubleshooting, and driving cost savings compared to vendor contracts. Key qualifications include experience with cGMP documentation, quality systems, FDA/USP requirements for instrumentation, strong IT and troubleshooting skills for laboratory equipment (HPLC, GC), and project management abilities. A minimum of a Bachelor's degree or 7 years of experience in Quality Control Chemistry and/or R&D is required.

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. 

_______________________________________________________________________________________

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. 

_______________________________________________________________________________________

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. 

_______________________________________________________________________________________

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.

Ready to apply?
You'll be redirected to NEPHRON SC's application page.

Similar roles

See how RiseMe works

Match, tailor, and prep so you send fewer applications and land more interviews.