994 Process Development Biotech jobs in Newton,MA

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Associate Scientist I

Pace Analytical Life Sciences

Woburn, MA 01801

$28/hr

~ 30 min OnsiteUrgently HiringEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

Bachelor's degree in chemistry/biochemistry, or a closely related field; OR an equivalent combination of education, training, and experience.
Fundamental principles, practices, and techniques of chemistry/biochemistry.
Standard understanding of the administration and oversight of chemistry/biochemistry programs, policies, and procedures.
Fundamental methods to resolve chemistry/biochemistry problems, questions, and concerns.
Standard understanding of applicable chemistry/biochemistry laws, codes, and regulations.
Understanding of standard testing tools, instruments, and calibration.
Computer applications and systems related to the work.
Principles and practices to serving as an effective project team member.
Methods to communicate with staff, coworkers, and customers to ensure safe, effective, and appropriate operations.
Correct business English, including spelling, grammar, and punctuation.
Performing fundamental professional-level chemistry/biochemistry duties in a variety of assigned areas.
Overseeing and administering standard chemistry/biochemistry functions.
Training others in policies and procedures related to the work.
Serving as a team member and the development and management of projects.
Operating in a both a team and individual contributor environment.
Interpreting, applying, and explaining applicable laws, codes, and regulations.
Preparing fundamental functionals reports, correspondence, and other written materials.
Using initiative and independent judgment within established department guidelines.
Using tact, discretion, and prudence in working with those contacted in the course of the work.
Performing effective oral presentations to large and small groups across functional peers and the department.
Contributing effectively to the accomplishment of team or work unit goals, objectives and activities.
Establishing and maintaining effective working relationships with a variety of individuals contacted in the course of the work.

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Senior Director, AIRx Discovery Biology Lead

Takeda Pharmaceutical

Boston, MA 02108

Hybrid~ 11 minEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

PhD in cell biology, molecular biology, pharmacology, or closely related discipline
12-15+ years of drug discovery experience with a strong track record in target validation and disease biology
Proven contributions to IND filings; experience supporting IND-enabling biology packages
Track record designing and managing externalized CRO biology programs; ability to scope, oversee, and critically interpret study data
Ability to connect target biology to clinical hypothesis and translational strategy
AI/ML data integration experience; comfortable working with large multi-source datasets
Experience in at least one therapeutic area represented across the Takeda Research portfolio
Excellent cross-functional collaboration skills; able to operate effectively in a lean, fast-paced team
The position will be based in Cambridge, MA
This position is currently classified as “hybrid” by Takeda's Hybrid and Remote Work policy

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Research Senior Scientist, Cheminformatics

Takeda Pharmaceutical

Boston, MA 02108

~ 11 min OnsiteEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

PhD in Computational Chemistry, Cheminformatics, Computer Science or related disciplines
2+ years of experience in pharmaceutical or biotech setting
Solid programming and scripting capabilities (e.g., Python, R, C/C++) with a proven ability to design and automate scalable computational workflows
Strong expertise in cheminformatics toolkits such as RDKit
Comprehensive knowledge of the DMTA cycle with demonstrated success in deploying predictive tools across the design process
Experience leading strategic initiatives to accelerate DMTA cycle

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Biochemist

United States Army

Lowell, MA 01852

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Sr Product Development Scientist

Keurig Dr Pepper

Burlington, MA 01803

~ 27 min OnsiteEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

Bachelor's degree in Food Engineering, Chemical Engineering, Food Science, Materials Science, or related field
MS or PhD Preferred
7+ years of experience in product development or processing, preferably developing dry powders or granulated food systems (beverages strongly preferred)
Strong working knowledge of:
Powder flow and bulk solids behavior
Thermal and mass transfer
Dissolution and rehydration mechanics
Particle size distribution and morphology
Experience translating lab formulations to pilot and full-scale manufacturing

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Biochemist

United States Army

Cambridge, MA 02139

New, Posted 11 hours ago

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Sr Account Director, Business Development (Bioanalytical Labs) - US - Boston

Thermo Fisher Scientific

Newton, MA

OnsiteEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

Bachelor's Degree
5 years of experience in pharmaceutical/biotech industry, with demonstrated success in meeting/exceeding targets
Valid driver's license
Ability to travel independently
Fluent English required

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Senior Manufacturing Engineer - design, prototyping, mfg/process development - medical device

InnoTECH Staffing

Boston, MA 02115

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Sr. NPI Manufacturing Engineer

Draper

Cambridge, MA 02139

~ 12 min Onsite

Bachelor's or Master's degree in Mechanical Engineering Manufacturing or other relevant field
5-10 years of relevant industry experience
3+ years of program management experience in manufacturing operations, supply chain, or engineering
Proven success managing programs through the full product lifecycle
Applicants selected for this position will be required to obtain and maintain a U.S. Security Clearance

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Research Development Quality Inspection Management Lead (GCP/GVP)

Merck Group

Billerica, MA 01821

RemoteHealth InsurancePaid Time OffRetirement Benefit

Minimum 8 years QA experience or other relevant experience with a minimum of 5 years in Clinical QA
Bachelor's degree with a focus on scientific subjects
Sound experience with Regulatory Authorities inspections by major authorities (MHRA, FDA, EMA, PMDA)
In depth knowledge of drug development processes and respective international regulations/guidelines
Broad knowledge of relevant GxP areas (GCP, GLP, GVP)
Travel globally up to 20%

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