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QC Analyst - Bioassay Temp - 2nd Shift (1-9:30pm)

Оценка ИИ

Интересная позиция в быстрорастущей сфере генной терапии с хорошим соцпакетом (401k, страховки). Однако статус 'временной роли' и работа во вторую смену могут подойти не всем кандидатам.


Вакансия из Quick Offer Global, списка международных компаний
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Сложность вакансии

ЛегкоСложно
Оценка ИИ

Роль требует минимум 2 года опыта в QC в среде GMP и владения специфическими методами (qPCR, ELISA). Работа во вторую смену и в условиях BSL 2 добавляет физической и организационной сложности.

Анализ зарплаты

Медиана75 000 $
Рынок65 000 $ – 90 000 $
Оценка ИИ

Зарплата в вакансии не указана, но рыночные оценки для QC Analyst в Массачусетсе (один из самых дорогих биофарм-кластеров) выше средних по стране. Учитывая вторую смену, кандидат может рассчитывать на дифференцированную надбавку.

Сопроводительное письмо

I am writing to express my interest in the QC Analyst (Bioassay) position at Genezen. With over two years of experience in a cGMP laboratory environment and a strong background in cell-based assays, I am confident in my ability to contribute to your Quality Control team in Lexington. My expertise in qPCR, ddPCR, and ELISA, combined with my proficiency in aseptic techniques and cell culture, aligns perfectly with the requirements of this role.

Throughout my career, I have demonstrated a meticulous approach to routine and non-routine testing, ensuring the highest standards of data integrity and compliance with GxP regulations. I am particularly drawn to Genezen's commitment to scientific excellence and its mission to accelerate the delivery of life-changing gene therapies. I am eager to bring my technical skills and proactive problem-solving mindset to your state-of-the-art facility and support the 2nd shift operations.

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Составьте идеальное письмо к вакансии с ИИ-агентом

Составьте идеальное письмо к вакансии с ИИ-агентом

Откликнитесь в genezenlabs уже сейчас

Присоединяйтесь к команде Genezen и внесите свой вклад в создание инновационных методов генной терапии уже сегодня!

Описание вакансии

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures.

WORKING AT GENEZEN

Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.

JOB SUMMARY

The QC Analyst temporary role will be responsible for routine and non-routine QC testing within the Bioassay team within a GMP laboratory.  This is a 2nd shift, full on-site, position (1 – 9.30pm) based at Genezen’s new state-of-the-art facility in Lexington, MA.  This role supports daily operations within the Quality Control group through execution of cell-based testing, routine lab support and working within Quality Systems. This includes but is not limited to in-process testing, lot release testing, and stability testing. Support outside of standard shift hours is required occasionally and the initial training period will be on first shift. All activities are all performed in accordance with cGMP guidelines and are supported by departmental and inter-departmental policies and standard operating procedures.

ESSENTIAL JOB FUNCTIONS

  • Perform routine/non-routine cell-based testing and review of in-process, DS and DP release and stability samples in accordance with Standard Operating Procedures (q-PCR, ddPCR, cell culture, ELISA)
  • Perform peer review as SME of assay data with minimal errors.
  • Participate in equipment validation, method transfer/qualification/validation, critical reagent qualification and special protocol execution as required.
  • Review/generate protocols and reports, as required.
  • Establish, revise, review and maintain standard operating procedures.
  • Promptly and proactively communicates gaps to leadership
  • Work as an active member of internal/cross-functional teams
  • Train other analysts, as required.

SPECIAL JOB REQUIREMENTS

  • Strong understanding of GxP regulations, ability to apply to any situation, and identify deficiencies w/ some guidance.
  • Adaptability required as work schedule may change based on business needs.
  • Criminal background check required (completion by staffing agency satisfies this requirement).
  • Other duties as assigned.

KNOWLEDGE, SKILLS AND EXPERIENCE

EDUCATION / CERTIFICATIONS / LICENSESEssential/Desired
BA/BS in Biochemistry/Cell Biology or other related scienceEssential
ON-THE-JOB EXPERIENCE
Minimum 2 years’ laboratory base experience within QC testing capacity, preferably in cGMP environment.Essential
High proficiency in cell culture and cell-based assaysEssential
Understanding of industry testing requirements/standardsEssential
SKILLS/ABILITIES
Proficiency in computer applications including MS Word, Excel, and LIMS (preferred).Essential
Good/effective communication, organizational, and time management skills with the ability to work well with others and independentlyEssential
Flexibility and willingness to learn, with a proactive approach to making a positive impactEssential
Detail OrientedEssential

PHYSICAL DEMANDS

While performing the duties of this job, the employee is required to meet the following physical demands:

Work Environment

  • Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning
  • Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities
  • Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock
  • Occasionally exposed to extremely loud noise levels

Movement

  • Frequently required to stand; sit; walk; balance; stoop; kneel; crouch; use hands to finger, handle, or feel; reach with hands and arms
  • Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl

Lifting

  • Frequently lift and/or move up to 25 pounds
  • Occasionally lift and/or move up to 50 pounds

Vision

  • Frequently utilize close vision and the ability to adjust focus

Communication

  • Frequently required to communicate by talking, hearing, using telephone and e-mail

GENEZEN'S CURES VALUE-BASED COMPETENCIES

Committed to Science

We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.

Urgency in action for the patients

We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.

Resilience & Grit in operations

We are committed to overcoming challenges, learning from failures, and persistently striving for success.

Execute with Excellence & Integrity

We are dedicated to delivering quality results and upholding ethical principals.

Solutions driven for our partners

We are committed to being a proactive, collaborative, creative and open-minded partner.

GENEZEN'S BENEFITS

  • Paid vacation days, amount based on tenure
  • Paid sick time
  • 10 observed holidays + 2 floating holiday + 1 volunteer day
  • 401(k) plan with company match up to 6% of salary, vested immediately
  • Share Appreciation Rights
  • Choice of several healthcare plans
  • FSA and HSA programs
  • Dental & vision care
  • Employer-paid basic term life/personal accident insurance
  • Voluntary disability, universal life/personal accident insurance
  • Accidental Death & Dismemberment (AD&D) Insurance

ADDITIONAL DETAILS

  • Nothing in the job description for this role restricts management’s right to assign or reassign duties and responsibilities to this job at any time.
  • This position requires a criminal background check.
  • Genezen is an Equal Opportunity Employer.
  • Genezen participates in EVerify.
  • Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.

Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts.

Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world’s largest children’s museum--to name just a few reasons why this area is a great place to live.

Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

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Навыки

  • Quality Control
  • qPCR
  • LIMS
  • ELISA
  • Cell Culture
  • cGMP
  • ddPCR
  • Aseptic Technique
  • Bioassay

Возможные вопросы на собеседовании

Проверка практического опыта работы в стерильных условиях, критически важного для биоанализов.

Опишите ваш опыт работы в условиях BSL 2 и соблюдения асептических техник при работе с клеточными культурами.

Оценка технической грамотности в ключевых методах, указанных в вакансии.

С какими трудностями вы сталкивались при проведении анализов qPCR или ELISA и как вы их решали?

Проверка понимания регуляторных стандартов, обязательных для фармацевтического производства.

Как вы обеспечиваете соответствие принципам cGMP при документировании результатов испытаний и проведении перекрестной проверки данных?

Вакансия предполагает временный характер и вторую смену, важно понять готовность кандидата.

Как вы адаптируетесь к работе во вторую смену и готовы ли вы к возможным изменениям графика в зависимости от производственных нужд?

Оценка навыков работы с отклонениями, что важно для QC.

Расскажите о случае, когда вы обнаружили несоответствие или ошибку в данных. Каковы были ваши действия согласно протоколу?

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