Documentation Specialist III : 4529147

Artech Information System LLC

Apply to this job
Framingham, MA, us on site Until 8/21/2026 H-1B sponsor history First posted February 24, 2026 Last posted February 24, 2026
Job description

At the dawn of the new millennium, a unique information technology company was born: HCL Technologies. As narrated in the video below, HCL Technologies has demonstrated remarkable growth through the recent economic downturn, emerging as one of only eight 21st century listed technology companies in the world to cross $1bn in Net Profit, $6bn in Revenue and $15bn in Market Capitalization.

The Quality Control Chemistry Laboratory is seeking a candidate to fill a QC Documentation Specialist III position.

The individual will be responsible to review assay data for completeness in accordance with SOP s, GDP, and regulatory standards.

Must possess sound interpersonal and information gathering skills, and candidate is able to relate well with coworkers and at all levels throughout the organization.

Candidate is able to work in a team environment where collaboration and interaction is critical to work successfully.

Responsible for archiving and retrieval of QC documents, maintain systems for document storage and retrieval, and help train employees on efficient system usage.

The QC documentation Specialist may interpret and trend complex data.

Position is Monday to Friday


Skills:

Must be detail-oriented and able to work with a high volume of documents in a fast-paced environment.

Be highly organized and process-oriented.

They must have excellent oral and written communications skills to interact with all levels of the Quality organization.

They must have excellent listening skills, and be able to handle multiple requests while detailing document activity

Experience with HPLC (reversed phase and gradient) chromatography and Empower software or equivalent.

Experience with QA/QC data review in a regulated industry.

Knowledge of FDA regulations, GDP, and cGMP.


Preferred Qualifications:

Knowledge of SDS-Page, UV-Vis spectrometry (Spectramax plate analysis), and Ion Exchange chromatography (Dionex) is a plus.  

Experience working in a QC Laboratory environment complete testing and or QC or QA data review role is an advantage.


Degree in the Life sciences discipline, Bachelor degree and 5+ years of experience, or a master degree and 3+ years of experience

For more information, please contact

Akriti Gupta

(973) 967-3409

Morristown, NJ 07960 


About this role

Summary

Review assay data, organize QC documents, ensure compliance with SOPs, GDP, and FDA regulations.

Job title

Documentation Specialist III

Experience level

5+ years or 3+ years with master's degree

Industry

software

Location requirements

Framingham, MA, US, on-site, no remote work allowed

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

attention to detailorganizationcommunicationHPLCFDA regulations

Preferred skills

SDS-PageUV-Vis spectrometryIon Exchange chromatographyQC laboratory

Specializations

QC documentationdata reviewregulatory standardsHPLCEmpower software
Locations

Structured locations inferred from the posting.

Framingham, MA, USA

On-site City
Related searches