Bristol Myers Squibb

Bristol Myers Squibb

Parenteral Manufacturing Technician

Manati - PR - US, USA · Mid · Full-time

Sponsorship not specified$50k-$90kDetected 41 min ago
PLCVoIPGMPCommunicationCollaborationCritical ThinkingAdaptability

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odds of building a lasting career here

38Risky
Cap-exempt (no lottery)0
Sponsors this role85
Entry-level history0
PERM / green-card track0
Lottery odds (Level I)39
Fits your clock70

Thin sponsorship signal and lottery-bound (~15% per draw). A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.

Lottery odds assume a STEM candidate.

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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 44 green-card filings in this occupation, 100% were for a worker who already held the job.

Green-card follow-through: 41%

Of 27 labor certifications old enough to have been used, 16 expired without the employer filing the next step. Median time from filing to decision: 475 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.

Reported a layoff in this occupation

In a green-card filing decided 2026-01-29, this employer stated it had laid off workers in Biostatisticians (NJ) during the preceding six months. 3 such filings on record.Describes the period before that filing, not necessarily today. Unlike WARN notices this is occupation-specific and federal.

Files H-1B transfers

29 transfer filings in the last year, covering 29 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.

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About the role

  • The starting pay range(s) listed above is for full-time employees (FTE).
  • You may also be eligible for additional discretionary incentive cash and stock opportunities.

Responsibilities

  • Operates formulation, preparation, and filling equipment; performs basic troubleshooting and escalates abnormalities.
  • Performs Cleaning-in-Place (CIP) and Sterilization-in-Place (SIP) operations for tanks and systems.
  • Maintains accurate inventory of components and materials; submits timely requests to support uninterrupted operations.
  • Support Manufacturing and Cross Functional Activities
  • Supports onboarding and "on the job" training of new employees.
  • Supports validation and qualification activities within the manufacturing area.
  • Communicates status of documentation, activities, and pending actions to supervision and partner departments.
  • Maintains housekeeping and aseptic conditions within controlled environments in alignment with contamination control practices.

Requirements

  • Describe job requirements, which induce physical fatigue by means of exertion required.
  • Routine physical activity is required for equipment operation, material handling, and work inside controlled environments.
  • Must be available to work rotating shifts, irregular hours, weekends, and holidays, depending on operational needs.
  • Collects required in process samples following aseptic sampling techniques.
  • Performs batch record audits, as required.

Nice to have

  • High school diploma or equivalent required.
  • Minimum of 2 years of experience in parenteral/aseptic manufacturing, or 3 years of experience in pharmaceutical manufacturing.
  • Experience interacting with automated or computer controlled production equipment in a regulated environment preferred.
  • Prior exposure to formulation, preparation, or sterile filling operations is strongly preferred.
  • Knowledge of preparation, formulation, and aseptic filling processes, including critical process parameters and their impact on product quality.
  • Knowledge of sterilization and contamination control technologies, including steam sterilization, depyrogenation, sterile filtration, lyophilization, and isolator technology.
  • Ability to execute filter integrity testing, SIP/CIP processes, and basic troubleshooting of mechanical or process issues.
  • Knowledge of cGMP, aseptic technique, environmental control, documentation, EHS, and hygiene practices within a sterile manufacturing environment.

Compensation

  • The starting pay range(s) listed above is for full-time employees (FTE).
  • Supports annual requalification programs and area readiness activities.

Benefits

  • Handles hazardous and non hazardous waste according to Environmental, Health & Safety (EHS) procedures.
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This listing is sourced directly from Bristol Myers Squibb's careers page and normalized into a canonical job model.