usa-scientist iii (scientific).

job summary:
As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now!

 
location: Framingham, Massachusetts
job type: Contract
salary: $85.00 - 88.77 per hour
work hours: 9 to 5
education: Bachelors
 
responsibilities:
Manufacturing Science is a partner of biologics manufacturing operations and is the custodian of manufacturing processes. Manufacturing Science ensures manufacturing processes are capable, compliant, in control, cost effective, and continuously improved.

- Provide collocated technical leadership at manufacturing sites including process monitoring, CPV, root cause investigation, change assessment, debottlenecking, and continuous improvement.

- Anticipate, respond to, and permanently resolve issues that arise during production.

- Aid in design of new processes and facilities with expertise in scale up, manufacturability, PAT, capacity analysis, and cost analysis.

- Lead the creation and use of digital process data analytic systems.

Partner with internal and external functions to identify, prioritize, scale up, transfer, implement, validate, and file new product and process life cycle improvements.

Job Responsibilities

- Provide technical support and routine process monitoring for upstream mammalian manufacturing of commercial products.

- Review manufacturing processes, deviations, and/or development and production data.

- Review manufacturing batch records, protocols, and control strategies.

- Provide technical support and data analysis for investigations and deviation resolution.

- Recommend changes or additional experiments to improve quality, productivity, recovery, and overall efficiency.

- Interact with colleagues and external partners from various functions, such as Engineering, Manufacturing, and Quality departments.

- Oversee and report on overall manufacturing progress.

- Lead technical project team or cross-functional team between groups/organizations. Provide input and coordinate support from process development teams.

- Support documentation preparation for regulatory purposes and stay current on regulatory requirements that have impact on manufacturing processes and evaluate/implement changes if required.

- Provide CMC support and guidance for product life cycle management.

- Provide technical guidance and train less experienced staff.

Key Responsibilities may differ among employees with same job title and may change over time in accordance with business needs.

 
qualifications:
- Bachelor's degree in engineering or science with 5 - 7 years of experience

OR

- Master's degree in engineering or science with 3 - 5 years of experience

OR

PhD in engineering or science with 0 - 3 years of experience.

PREFERRED QUALIFICATIONS

- Demonstrated expertise applying fundamental principles to real world problem solving and providing practical solutions to difficult technical issues.

- Experience with biologics mammalian upstream unit operations: vial thaw, seed train, wave reactors, production reactors, harvest and capture column operations. Experience with perfusion cultures is highly preferred.

- Hands-on cell culture experience at laboratory or pilot scale.

- Understanding of cGMP concept and familiar with quality and regulatory framework.

- Proficiency in process data analytics.

- Knowledge of computerized systems in biopharmaceutical manufacturing environment, i.e., Distributed Control System, DeltaV Process Data Historian, LIMS, and MES.

- Experience leading projects and/or cross functional teams.

- Works independently with minimal supervision and direction. Performs work that consistently requires independent decision making and the exercise of independent judgment and discretion.

- Strong communication and technical writing skills. Experience communicating with business partners and senior management.

- Experience with root cause analysis and/or risk assessment

- Experience working with statistical analysis software

- Experience communicating with cross-functional teams and senior management

- Proficient in Microsoft Word, Excel, PowerPoint.

SPECIAL WORKING CONDITIONS

- Ability to gown and gain entry to manufacturing areas

 
skills: Chromatography, Laboratory Information Management Systems (LIMS), GMP (Good Manufacturing Practice)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

This posting is open for thirty (30) days.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.