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Duration: 12 months of contract

Job Details:

Ideal candidate: The ideal candidate for this role should have a bachelor’s degree in any scientific or engineering discipline with 1 – 3 years professional working experience. Candidates with recent Master degree are also suitable if they bring strong soft skills. The candidate should possess solid working experience with standard software tools such as Microsoft Office. Experience with specialized software such as like SAP or Smartsheets is desirable but can be learned on the job. Biologic drug product knowledge is favorable. The candidate must excel in group management, deadline adherence, and meticulous documentation skills. This position leans heavily on project development (PD) and project management (PM) skills, with technical expertise expected to develop over time. Professional working experience outside of an academic setting is preferred.

Nice to have:

Tech transfer experience

Preferably from BioPharma Industry

Top 3 Must Have Skill Sets:

+ Chemical Engineering, Biotechnology, and Pharmaceutical Science Industry related experience

+ Has been working on GMP environment

+ Preferably from BioPharma Industry

Day to Day Responsibilities:

+ Apply fundamental engineering and scientific principles to resolve issues and evaluate effects of process improvements, equipment, scale, and raw materials

+ Assist in the design and execution of experiments in order to characterize and enable implementation of new capabilities and process changes such as filling, lyophilization and analytical technologies

+ Support technology transfer leads during the transfer of drug products into manufacturing sites (clinical and commercial), including make-a-batch exercises, process parameter risk assessments, process transfer documents, and change control assessments

+ Support development and maintenance of technology transfer tools (clinical and commercial)

+ Effectively communicate results of characterization studies, experimental execution and technology transfer initiatives

+ Author/review/data verify technical documents, such as technical protocols, technical assessments, technical reports and draft standard operating procedures or guideline documents

+ Conduct analysis of data generated, including statistical analysis using applicable software.

+ Development of digital tools and models by leveraging data analytics and programming skills

+ Support at scale characterization and/or process validation runs as person in plant

Basic Qualifications:

+ Master degree OR

+ Bachelor degree and 2 years of experience OR

+ Associate degree and 6 years of experience OR

+ High school diploma / GED and 8 years of experience

Preferred Qualifications:

+ B.S. in scientific or engineering discipline with 1‒3 years’ relevant professional experience or M.S. in scientific or engineering discipline with 0‒2 years’ relevant professional experience

+ Familiarity with cGxP and experience in drug product / drug substance manufacturing or process development

+ Knowledge of and hands-on experience with various drug product technologies

+ Displays critical thinking, problem solving and independent research skills

+ Ability to learn new techniques, perform multiple tasks, keep accurate records, follow instructions, and comply with company policies

+ Excellent project management skills and ability to escalate relevant issues to project lead and line-management

+ Strong cross functional team player with good communication skills (oral and written)

+ Ability to work independently and as part of a team with internal and external partners

+ Good computer and organizational skills with strong attention to detail

+ Self-motivated with a positive attitude

About US Tech Solutions:

US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com (http://www.ustechsolutionsinc.com/) .

US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.