Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
$72к-113к/год
$65к$80кмедиана$90к
По похожим ролям (47) ~ $80к/год
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Чётко описанная начальная лабораторная роль в крупной биофармацевтической компании даёт практический опыт поддержки производства вакцин и работы с аналитическими методами.
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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