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求人Thermo Fisher

Scientist I, Process Development

Thermo Fisher

Scientist I, Process Development

Thermo Fisher

Plainville, Massachusetts, USA

·

On-site

·

Full-time

·

1w ago

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Laboratory Setting, Office

Job Description

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $35 billion. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing efficiency in their laboratories, we are here to support them.

At Viral Vector Services (VVS) a division of Thermo Fisher Scientific, we deliver from process development through commercial supply, we offer the expertise and resources to help clients deliver innovative gene therapies.

Job Title: Scientist I Process Development-Upstream or Downstream Location/Division Specific Information: US - Massachusetts – Plainville (on-site)

How will you make an impact?

As the Upstream/Downstream Process Development Scientist you will help our clients to deliver lifesaving and life changing therapies to patients in need. You will be supporting planning, executing, and documenting laboratory and tech transfer activities in support of process establishment, pilot, and transfer into cGMP manufacturing. You will also act as a subject matter expert (SME) and support transfer and operation of internally developed and client-transferred processes into the process development and pilot space. You will also be supporting tech transfer out to the cGMP manufacturing space.

Education regiments:

B.S. in Chemical Engineering, Biochemistry, Biology or related field

General qualifications:

  • Demonstrated understanding of experimental design with the ability to independently conduct laboratory experiments.
  • Collaborate with the Analytical Development team to develop comprehensive testing plans.
  • Participate in client meetings to present results and assist with drafting process development reports.
  • Prepare Process Development records, work instructions, and batch records.
  • Proficiency in technical writing, adhering to Good Documentation Practices (GDP), with preferred experience in data compilation and interpretation.
  • Strong communication skills with the ability to clearly and concisely interpret, summarize, and present scientific data.
  • Flexibility in work hours, including availability for weekends and evenings, as the need arises to meet project timelines.

Upstream Process Development Qualifications:

  • Practical experience in aseptic techniques, cell culture, single-use bioreactors (SUBs), wave reactors, and harvest/clarification processes is preferred. Familiarity with transfection and infection -based processes for gene therapy production

Downstream Process Development Qualifications:

  • Expertise in various purification techniques, including affinity and anion exchange chromatography, with proficiency in using AKTA chromatography systems and Unicorn software is helpful. Experience with filtration-based unit operations such as tangential flow filtration, sterile filtration, and depth filtration is helpful.

Knowledge, Skills, Abilities

  • Ability to analyze and summarize scientific data
  • Understanding of cGMP and regulatory requirements of biopharmaceutical manufacturing.
  • Strong interpersonal and communications skills; written and oral
  • Ability to function in a constantly evolving environment & balance multiple priorities.
  • A flexible work schedule is required including Weekend and night as needed to support lab activities.

Compensation and Benefits

The hourly pay range estimated for this position based in Massachusetts is $28.16–$36.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs

  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement

  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

  • Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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Thermo Fisherについて

Thermo Fisher

Thermo Fisher Scientific Inc. is an American life science and clinical research company. It is a global supplier of analytical instruments, clinical development solutions, specialty diagnostics, laboratory, pharmaceutical and biotechnology services.

10,001+

従業員数

Waltham

本社所在地

$200B

企業価値

レビュー

3.0

10件のレビュー

ワークライフバランス

3.5

報酬

3.8

企業文化

3.2

キャリア

3.5

経営陣

2.1

45%

友人に勧める

良い点

Good benefits and compensation

Nice people to work with

Learning opportunities and skill development

改善点

Poor management and leadership issues

Disengaged or unsupportive management

Frequent reorganizations and chaos

給与レンジ

2,092件のデータ

Junior/L3

Mid/L4

Junior/L3 · DATA ANALYST

1件のレポート

$130,000

年収総額

基本給

$100,000

ストック

-

ボーナス

-

$130,000

$130,000

面接体験

8件の面接

難易度

3.0

/ 5

期間

14-28週間

内定率

12%

体験

ポジティブ 12%

普通 63%

ネガティブ 25%

面接プロセス

1

Application Review

2

Recruiter Screen

3

Hiring Manager Interview

4

Panel Interview

5

Final Interview

6

Offer

よくある質問

Technical Knowledge

Behavioral/STAR

Past Experience

Culture Fit

Industry Specific