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2 дня назад

QC Chemistry Lead I (Monday-Friday 10pm-6:30am)

30 - 36$
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
QC Chemistry Lead I (Monday-Friday 10pm-6:30am) (Chemistry/Quality Control): Performing and supporting chemical laboratory testing, data review, validation activities, and quality documentation for pharmaceutical manufacturing with an accent on cGMP/GLP compliance, analytical accuracy, and laboratory workflow. Focus on reviewing complex laboratory data, preparing investigations and deviations, supporting validation, and training peers during the overnight onsite shift.

Location: Onsite in Irvine, California, United States; regular and predictable onsite attendance is required. Monday-Friday, 10:00 p.m.-6:30 a.m.

Salary: $30.28-$36.05 per hour

Company

B. Braun develops, manufactures, and markets medical products and services, including infusion therapy, pain management, nutrition, pharmacy compounding, wound care, ostomy care, and dialysis solutions.

What you will do

  • Perform sampling, sample login, analytical testing, data review, and validation activities for raw materials, in-process materials, environmental samples, finished products, and stability samples.
  • Complete routine and non-routine chemistry assignments in accordance with procedures, specifications, safety practices, and cGMP/GLP requirements.
  • Prepare and update investigation reports, deviations, protocols, procedures, and other chemistry documentation.
  • Review laboratory data and records for accuracy, completeness, and compliance.
  • Support peer orientation and training, work assignments, and completed-work reviews.
  • Collaborate with laboratory leads, supervisors, peers, and internal partners to resolve daily issues and maintain workflow.

Requirements

  • High school diploma or equivalent.
  • At least 4 years of related laboratory, quality control, chemistry, or testing experience.
  • Ability to follow established procedures and complete routine, repetitive assignments within defined parameters.
  • Working knowledge of laboratory documentation practices and sound judgment in resolving daily problems.
  • Effective communication and collaboration with supervisors, leads, peers, and cross-functional partners.
  • Ability to work the required overnight Monday-Friday onsite schedule; relocation is not available.

Nice to have

  • Bachelor's degree in Chemistry or another science-related field.
  • Experience in a cGMP- or GLP-regulated laboratory.
  • Experience testing raw materials, in-process materials, finished products, environmental samples, or stability samples.
  • Experience with deviations, investigations, protocols, procedures, validation activities, or peer training.

Culture & Benefits

  • Healthcare benefits and a 401(k) plan.
  • Tuition reimbursement.
  • Laboratory-based work with occasional duties in production or manufacturing areas.
  • Work involves potential exposure to toxic or caustic chemicals, with required personal protective equipment and safety procedures.

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