Associate, Manufacturing Science & Technology

  • Cambridge, MA

Compensation

: $94,360.00 - $141,170.00 /year *

Employment Type

: Full-Time

Industry

: Engineering



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Job Description

Brammer Bio is a rapidly growing, dynamic gene therapy contract development and manufacturing organization that is seeking sharp individuals to bring the highest quality processes, products and testing to our clients. Our employees are committed to making a difference in our organization, for our client partners and the patients we serve. We are looking for top talent with proven competencies and strong character to join our team and help lead our organization into the future.

The primary responsibility is to support the technology transfer teams for the late stage, PPQ and commercial manufacturing of viral vectors. This position requires close interaction with the MS&T colleagues, Manufacturing, Process Development, and other departments. This role will focus on aspects of ensuring a robust, scalable and efficient manufacturing processes to produce late-phase human clinical trial and commercial gene transfer vector products.

MST Associate will work closely with the MST teams to support client projects and with Brammer s Florida site, PD, Quality, EHS, and Manufacturing to ensure compliance and technology transfer. Additionally, based on project assignment the role executes process characterization projects for Brammer Bio.

ESSENTIAL RESPONSIBILITIES:

  • Supports cross functional technology transfer teams for cGMP DS manufacturing of viral vectors. Collaborate with another site or clients to ensure success of scale up/ process transfer. Includes authoring of upstream or downstream plan documentation and associated detail process descriptions (DPDs).
  • Partner with Brammer s Alachua/Cambridge Process Development as well as Cambridge Manufacturing and Quality organizations in tech transfer activities to facilitate project success.
  • Identify, own and resolve technical process issues arising from deviations, investigations and client programs in a timely manner
  • Generate documents (technical memos and reports, protocols, etc.,) related to tech transfer of new processes. Accurately forecast and drive schedule/project plan of assigned MST deliverables.
  • Support the MST PPQ programs to operate efficiently. This may include data management from executed runs, operational support for engineering and GMP runs, and standardization of programs to limit bespoke elements
  • Assist investigation root causes of deviations for cGMP manufacturing, and implement CAPA
  • Identifying opportunities to improve systems and practices, and drive harmonization across manufacturing platforms

Note: This job description is not all-inclusive. Additional duties may be performed, as assigned. It acts as a guideline and is subject to change over time.

Benefits:

Thermo Fisher offers an attractive benefit package to all full time employees which includes; medical, dental, and vision coverage, company paid Disability and Life Insurance benefits, and a 401(k) Plan with a generous company match. All full time employees are also provided with paid time off, paid company holidays, and an incentive bonus plan.

Thermo Fisher is an Equal Opportunity Employer and participates in eVerify.



KNOWLEDGE, SKILLS and QUALIFICATIONS:

  • Bachelor or advanced degree in Biochemical, Chemical Engineering or a related scientific discipline such as Chemistry or Biology.
  • MST Associate I: B.S. with less than 2 years relevant experience
  • MST Associate II: B.S. with 2-3 years relevant experience, or Master s degree.
  • MST Associate III: B.S. with 4+ years relevant experience, or Master s degree with 1-3 years experience
  • Strong interpersonal and communications skills; written and oral.
  • Ability to function in a fast-paced dynamic team environment and balance prioritize multiple projects
  • Laboratory experience preferred.
  • Knowledge of cell and gene therapy vector production highly desirable.
  • Ability to be hands-on

PHYSICAL DEMANDS/FACTORS:

While performing the duties of this job, the employee:

  • Ability to function in a rapidly changing environment & handle multiple priorities.
  • Work Hours: Monday through Friday, 8:00 AM to 5:00 PM. Requires overtime to work evenings, weekends or holidays, as required to meet project timelines.

Ability to lift up to 25 lbs.




Associated topics: bio, biochemistry, biological engineer, biomechanics, biosynthetic, metabolic, molecular, neuro, pain, pathogenesis

* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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