MSAT Scientist / Senior Process Engineer - 5197

Posted 4 Days Ago
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Pearland, TX
70K-97K Annually
7+ Years Experience
Pharmaceutical
The Role
The MSAT Scientist is responsible for transferring viral vector bioprocesses into GMP production, ensuring process scalability and manufacturability. Responsibilities include process supervision, campaign reporting, managing deviations, and continuous manufacturing process improvement.
Summary Generated by Built In

Description

Verista’s 600 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values:

  • We empower and support our colleagues
  • We commit to client success at every turn
  • We have the courage to do the right thing
  • We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
  • We constantly acquire new skills and learn from our experiences to enhance our collective expertise

MSAT Scientist Responsibilities:

As a member of the MSAT Team, your are responsible for the successful transfer of viral vector bioprocesses into GMP production. As such, you are in direct contact with our clients and internal cross functional teams. This role will ensure successful process scalability and manufacturability. Scientists in this role are responsible for all the process integration-related aspects of work during campaign preparation, process supervision, reporting during and after production campaigns, leading relevant major deviations and continuing manufacturing process improvement under the supervision of a Sr. Scientist and/or Manager.

Requirements
  • 5-10 years of experience
  • GMP manufacturing support (Viral Vector or Cell and Gene Therapy preferred; microbial or mammalian processing support required if VV/ CGT background is limited or non-existent), and basic understanding of current Good Manufacturing Practices, US / EU regulations.
  • Advanced knowledge of cellular biology, cell culture, scale up, mass transfer, bioreactor operation, and / or depth filtration, tangential flow filtration, chromatography, viral filtration; buffer and media production; aseptic processing
  • Demonstrates critical thinking skills in problem solving and decision making
  • Ability to explain technical problems in terms sufficient for other technically trained people to understand the problem and proposed solutions, both verbally and in writing
  • Ability to independently lead small projects and to create, maintain, and utilize the cross-functional support of other departments within the asset for the accomplishment of objectives
  • Ability to perform basic and advanced root cause analysis techniques for resolving deviations and identifying appropriate CAPA: Five why, Kepner-Tregoe, Fishbone, Pareto, Scatter plotting, DMAIC for RCA
  • Ability to perform basic risk identification and remediation and lead basic and advanced risk assessments using standardized methodologies which could include FMA, FMEA, HAZOP, and/ or HACCP
  • Attention to detail and high level of accuracy
  • Some knowledge of statistical data analysis is a plus
  • Strong communication, technical writing, organizational and interpersonal skills; able to give accurate and complete guidance and direction to junior scientists for smaller issues and problems
Benefits

Why Choose Verista?

  • High growth potential and fast-paced organization with a people-focused culture
  • Competitive pay plus performance-based incentive programs
  • Company-paid Life, Short-Term, and Long-Term Disability Insurance.
  • Medical, Dental & Vision insurances
  • FSA, DCARE, Commuter Benefits
  • Supplemental Life, Hospital, Critical Illness and Legal Insurance
  • Health Savings Account
  • 401(k) Retirement Plan (Employer Matching benefit)
  • Paid Time Off (Rollover Option) and Holidays
  • As Needed Sick Time
  • Tuition Reimbursement
  • Team Social Activities (We have fun!)
  • Employee Recognition
  • Employee Referral Program
  • Paid Parental Leave and Bereavement

For more information about our company, please visit us at 

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.

$70,491-96,936

*Verista is an equal opportunity employer.

Top Skills

Bioreactor Operation
Cell Culture
Cellular Biology
Mass Transfer
The Company
HQ: Fishers, IN
402 Employees
On-site Workplace
Year Founded: 2020

What We Do

Verista is a leading business and technology consultancy firm that provides systems, compliance, validation and quality solutions to life science companies - enabling them to improve health and improve lives. We help clients solve their most critical and complex challenges across the GxP lifecycle, from preclinical and clinical to commercialization, manufacturing and distribution – bringing together decades of knowledge, the most advanced engagement platforms and transformative technologies. This allows clients to benefit from the ease, efficiency and trust that results from working with one partner who excels across specialties. Verista’s clients trust the company’s 650+ experts to deliver consistent, safe, and high-quality results across the product development lifecycle. Verista is based in Fishers, Indiana, Wayne, Pennsylvania, Westford, Massachusetts, and San Mateo, California. For more information, visit www.verista.com

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