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1St Shift Labware Lims Developer Jobs (NOW HIRING)

CTI

Developer Lab Applications

Milan, MI · On-site

Work with system owners to develop and maintain LabWare LIMS as a usable system within the systems ... Experience with programming languages such as LIMS Basic, Smalltalk, Postgres, Remisol, SQL ...

Biogen

NC · On-site

$98K - $127K/yr

Knowledge of manufacturing systems including DeltaV, Syncade, PI, LabWare LIMS, Oracle EBS ... Knowledge of statistical programming languages, such as R or Python * Familiarity with AI, machine ...

Unicon Pharma Inc

Quality Control Analyst I

Sunrise, FL · On-site

$23 - $30.75/hr

Quality Control Analyst 5 Months (possible extension) Sunrise, FL Shift Scheduled: Monday to Friday ... Labware LIMS and/or Empower preferred experience preferred. Microbiology testing experience ...

NCSL International

QAO Chemistry Specialist II

Irvine, CA · On-site

$96K - $118K/yr

Wednesday, Tuesday, Friday, Thursday, Monday Shift: 5X8 Relocation Available: No Requisition ID ... Utilize Empower, LabWare LIMS, SAP, and TrackWise to support data review, investigations, and ...

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How much do 1st shift labware lims developer jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for 1st shift labware lims developer in the United States is $58.55, according to ZipRecruiter salary data. Most workers in this role earn between $53.12 and $64.66 per hour, depending on experience, location, and employer.

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1St Shift Labware Lims Developer jobs near you

Quality Control Analyst II

Norton, MA • On-site

Biopharma-Consulting-Jad-Group
See more jobs at Biopharma-Consulting-Jad-Groupexternal

$24.25 - $32.75/hr

Other

Posted 15 days ago

Job description

The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation. This position enhances QC efficiency and effectiveness.

Key Responsibilities:

  • Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs.
  • Support weekend lab operations and maintain training records.
  • Assist in lab equipment and inventory maintenance, including reagent and sample prep.
  • Review data timely and qualify as a data reviewer Perform operational assignments (raw material processes, environmental monitoring, in-process testing).
  • Contribute to updating controlled documents (SOPs, work instructions, test methods).
  • Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH) Participate in continuous improvement initiatives and cross-functional collaboration.
  • Support regulatory submissions, inspection readiness, and audits.
  • B.S. in chemistry, biology, biochemistry, or related field 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent.
  • Experience in method transfer/implementation; understanding of method lifecycle management.
  • Strong technical writing, data analysis, problem-solving, and organizational skills.
  • Proficiency in LabWare LIMS, Excel, Word, and PowerPoint.
  • Contract position with possible extension
  • Location: Norton, MA, with occasional responsibilities at other locations.
  • Weekend coverage is required.
  • First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training.
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