Jobs / United States / Nivagen Pharmaceuticals INC

Nivagen Pharmaceuticals INC

GMP Cleanroom Specialist 3rd Shift Only (10:30 pm - 6:00 am)

Sacramento, CA 95834 Posted today

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Sponsorship verdict

Sponsorship possible

One solid signal, not two. Worth applying, and worth asking about sponsorship early.

  • Employer is on a government sponsor recordThe US Department of Labor certified 11 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first.
  • The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
  • No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area.
  • Confirmed live todayWhen a source last listed this job as open.
Details and sources
Employer is on a government sponsor record
The US Department of Labor certified 11 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. Source: LCA disclosure data (US Department of Labor (OFLC)).
No salary bar for this route
H-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.

US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).

A verdict summarises public evidence. It is not legal advice and never a guarantee: the employer and the immigration authority decide. Sign in to factor in where you can already work.

About the role

About the Company: Nivagen Pharmaceuticals is a global pharmaceutical company committed to enhancing lives by delivering high-quality, cost-effective generic prescription medications and over-the-counter products across the North American market. For over a decade, we have upheld our core values of excellence, integrity, and respect for people, driving innovation and quality throughout the pharmaceutical supply chain. Our team of dedicated professionals works collaboratively to advance manufacturing, distribution, and quality control processes—ensuring a comprehensive and modern approach to healthcare. Through vertical integration, cutting-edge technology, and a relentless pursuit of quality, we aim to redefine medication accessibility and affordability. We invest in our employees by offering competitive pay, comprehensive benefits, and robust training and development programs. By fostering a supportive culture and prioritizing professional growth, we empower our team to innovate and make a lasting impact in the healthcare industry. Our mission is simple yet powerful: to improve lives by providing accessible, affordable, and high-quality medications—while upholding the highest standards of excellence and ethical responsibility. Job Location: Nivagen Pharmaceuticals Inc. 3900 Duckhorn Dr, Sacramento, CA 95834 About the Job: The Cleanroom Cleaner is responsible for performing routine and specialized cleaning of Grade A through Grade D cleanroom environments. This role ensures the cleanliness and sterility of classified manufacturing areas to support aseptic processing and regulatory compliance. Duties and Responsibilities: • Execute cleaning and sanitization of cleanrooms classified as Grade A, B, C, and D environments, including surrounding areas such as airlocks, corridors, and material transfer zones. • Follow approved Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMPs) to maintain aseptic conditions. • Prepare cleaning agents and disinfectant solutions (e.g., alcohol-based disinfectants, sporicidal agents) according to specifications. • Complete and maintain cleaning logs, checklists, and records with attention to accuracy, traceability, and data integrity. • Perform daily, weekly, and monthly cleaning tasks per the Master Cleaning Schedule (MCS). • Wear proper cleanroom gowning and Personal Protective Equipment (PPE) based on area classification and activity. • Ensure cleaning materials and equipment are handled and stored appropriately to prevent contamination. • Report any facility or equipment anomalies, contamination risks, or deviation from procedures to supervisors immediately. • Support internal and external audits by maintaining a high state of cleanliness and documentation readiness. • Collaborate with Quality Assurance, Facilities, and Manufacturing teams to uphold regulatory and safety standards. Experience and Qualifications: • High school diploma or equivalent. Degree in Chemistry, Microbiology, and/or experience in Sterile Cleaning and/or Aseptic Technique preferred. • Prior experience working in a cGMP-regulated or clean room environment for a minimum of 2 years. • Familiarity with safety regulations and quality control processes in pharmaceutical manufacturing. • Priority will be given to applicants with experience in cleanroom cleaning or those who have worked in a pharmaceutical manufacturing environment. Knowledge, Skills, and Abilities: • Knowledge: Understanding of GMP, SOPs, and regulatory requirements related to clean room environments. • Skills: Strong attention to detail, excellent organizational skills, and the ability to follow precise instructions. • Physical Requirements: Ability to perform physically demanding tasks, including standing

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