United Pharma Technologies

United Pharma Technologies

Quality Control/Analytical Specialist

Edison, NJ, United States · Mid

Sponsorship not specifiedDetected 2202 days ago
GMPResearchMass Spectrometry

Stay score

odds of building a lasting career here

40Risky
Cap-exempt (no lottery)0
Sponsors this role90
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

Thin sponsorship signal and lottery-bound. A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.

Lottery odds assume a STEM candidate.

Personalize to your clock →

Employer immigration record

from this employer's Department of Labor filings

Green-card filing pattern in this occupation

Context, not a finding about this posting: of this employer's 14 green-card filings in this occupation, 100% were for a worker who already held the job.

Third-party placement is common here

92% of this employer's visa filings place the worker at a client company rather than at the employer itself, across 36 clients. Your visa, salary band and layoff exposure would follow the employer of record, not the client.Most common: REGENERON PHARMACEUTICALS · Merck & Co, Inc · MERCKFiles as an H-1B dependent employer.

Green-card follow-through: 30%

Of 10 labor certifications old enough to have been used, 7 expired without the employer filing the next step. Median time from filing to decision: 504 days.100% of their filings were for a worker who already held the job.Only certifications past the 180-day window are counted — recent ones cannot have expired yet.

Files H-1B transfers

7 transfer filings in the last year, covering 7 workers. Median labor-condition decision: 7 days. An employer that already files transfers is one that can take over an existing H-1B.

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

Community outcomes

No reports yet — be the first to help the next applicant.

About the role

  • May act as a backup to Microbiological Specialist to conduct microbiological analysis on raw materials, in-process goods, and/or finished products and make evaluation to determine conformance to specification.
  • Interface with personnel from other companies/laboratories regarding testing discrepancies and method/instrument problems.

Responsibilities

  • As needed, serve as primary lead investigator or support investigator for out of specification investigations
  • Maintain data documentation in accordance with cGMP and company standards.
  • Maintain inventory of chemicals, apparatus, and equipment for analytical laboratory and satellite laboratories.
  • Maintain the analytical lab in accordance with GMP/Plant housekeeping procedures.

Requirements

  • 3+ years' experience in a GMP-regulated laboratory required
  • Working knowledge of USP, EU compendia test methods for raw material testing.

Nice to have

  • Experience with reverse phase HPLC chromatography and Gas Chromatography a plus.
  • Experience with Agilent chromatography systems and Chemstation/OpenLab software is a plus.
  • Experience with AA and UV assays a plus
  • Experience conducting OOS investigations a plus.

Company info

  • Company Description
  • We are one of the leading technical resource provider for Pharmaceutical & life science industries.
  • We have 100+ employees working for major Pharmaceuticals Giants such as Merck, Novartis, BMS and Takeda.

Equal opportunity

  • All your information will be kept confidential according to EEO guidelines.
Apply directly at United Pharma Technologies →Create a free account for alerts like thisView United Pharma Technologies immigration profile

This listing is sourced directly from United Pharma Technologies's careers page and normalized into a canonical job model.