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6 дней назад

Associate Specialist, Technical Operations Engineering (Biopharmaceutical Operations)

71 900 - 113 200$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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
Associate Specialist, Technical Operations Engineering (Biopharmaceutical Operations): Supporting multi-product vaccine manufacturing through laboratory-based identification, characterization, process optimization, and investigation activities with an accent on analytical testing, documentation, and cross-functional collaboration. Focus on executing critical-path laboratory work, developing and troubleshooting assays, reviewing data, and supporting continuous process improvement.

Location: West Point, Pennsylvania, United States; laboratory-based onsite role. US and Puerto Rico residents only. No relocation; no travel required.

Salary: $71,900–$113,200 annually, plus eligibility for annual bonus and long-term incentive where applicable.

Company

hirify.global's Manufacturing & Supply Division supports a global manufacturing network delivering reliable biopharmaceutical supplies, including vaccines, to customers and patients.

What you will do

  • Execute identification and characterization testing within Technical Operations Process Support Laboratories.
  • Support lab-scale process optimization, product and process investigations, continuous improvement changes, and strategic product or process initiatives.
  • Prepare, execute, analyze, document, and review laboratory experiments and data.
  • Communicate analytical data across Operations, Technology, Quality, and other support organizations.
  • Deliver assignments against accelerated, critical-path timelines with a right-first-time approach.
  • Collaborate independently and cross-functionally in a fast-paced, multidisciplinary laboratory environment.

Requirements

  • B.S. or M.S. in Chemical Engineering, Chemistry, Biology, Biochemistry, or a comparable discipline, with 0–2 years of relevant experience.
  • Working knowledge of experimental preparation, execution, analysis, and laboratory safety practices.
  • Good laboratory documentation practices, including notebook maintenance and corresponding data review.
  • Excellent written and oral communication skills.
  • Ability to work independently and cross-functionally.
  • Ability to work in a laboratory-based role and collaborate in a fast-paced, integrated, multidisciplinary team environment.

Nice to have

  • Knowledge of separation-based methods such as HPLC, UPLC, CE, or SDS-PAGE; protein quantification by absorbance or fluorescence; or plate-based characterization including ELISA and enzymatic activity.
  • cGMP experience.
  • Experience performing or developing analytical test methods for recombinant proteins, viruses, or polysaccharides.
  • Ability to manage multiple tasks simultaneously.
  • Strong problem-solving skills with a hands-on approach and willingness to investigate issues directly in the field.
  • Experience troubleshooting experimental design, assay development, and data analysis.

Culture & Benefits

  • Regular employee status with a first-shift, daytime schedule.
  • Medical, dental, vision, and other insurance benefits for employees and families.
  • Retirement benefits including 401(k), paid holidays, vacation, compassionate leave, and sick days.
  • Inclusive environment that values diverse experiences, respectful challenge, and collective problem-solving.
  • Hazardous materials may be involved; no valid driving license is required.

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