Top 126 Process engineer associate Jobs

Process Validation Associate / Engineer
Krystal Biotech —Pittsburgh, PA
- Full-time
- Bachelor's degree
- 1 year
- Communication skills
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BET Associate Manufacturing & Process Engineer
Horseshoe Beverage Company LLC —Neenah, WI
- $83,000 - $90,000 a year
- Weekends as needed
- Background check
- Pass drug screening
- Ability to lift 50 pounds
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Process Engineering Professional Associate - EN234XXXJP3 - P
PEAK Technical Services Inc. —Boise, ID
- $49.04 - $57.69 an hour
- Contract
- Construction site
- Ability to walk for extended periods
- Bachelor of Science
- Relocation assistance
- Health insurance
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Sr. Associate, Process Manufacturing Engineer
L3Harris Technologies —Canoga Park, CA
- $73,000 - $136,000 a year
- Full-time
- Oracle
- Mid-level
- Microsoft Office
- Paid holidays
- Disability insurance
Composite Material Process & Physics (MP&P) Engineer (Associate, Experienced)
Boeing —North Charleston, SC
- $91,800 - $151,800 a year
- Computer science
- Computer Science
- Bachelor of Science
- Health savings account
- Disability insurance
6d
Associate Process Engineer
Brindley Engineering —Lisle, IL
- $90,000 - $130,000 a year
- Full-time
- Hybrid work
- Bachelor of Science
- Mid-level
- Ability to lift 50 pounds
- Paid parental leave
- Paid holidays
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Associate Process Engineer
FUJIFILM —Mesa, AZ
- Pass drug screening
- Mid-level
- Bachelor's degree
Associate Engineer II (Contract), Drug Product Process Development
Vaxcyte —San Carlos, CA
- $51 - $56 an hour
- Contract
- Bachelor of Science
- Mid-level
- Bachelor's degree
Associate Process Engineer
IPS Custom Automation —Arlington, TX
- $90,000 - $130,000 a year
- Full-time
- Research
- Office
- Travel
- Disability insurance
- Health insurance
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Associate Environmental Engineer
Parsons —New York, NY
- $26.59 - $46.54 an hour
- Engineering
- Office
- Entry level
- Wellness program
- Paid holidays
Associate Process Engineer, MS&T
Forge Biologics —Columbus, OH
- Full-time
- Engineering
- Master's degree
- Organizational skills
- Paid parental leave
- Disability insurance
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Associate Process Equipment and Reliability Engineer
WuXi Biologics —Cranbury, NJ
- $55,000 - $88,000 a year
- Evenings as needed
- Ability to walk for extended periods
- Ability to lift 50 pounds
- Analysis skills
Senior Associate Process Engineer (Contract)
ElevateBio —Waltham, MA
- $43 - $57 an hour
- Contract
- Mid-level
- 3 years
- Continuous improvement
Quick Apply
Process Engineering Associate I
Audubon Companies —Houston, TX
- Engineering
- Office
- Analysis skills
Quick Apply
Associate Roadway Engineer
Parsons —Minneapolis, MN
- $26.59 - $46.54 an hour
- Office
- Master's degree
- Bachelor's degree
- Wellness program
- Paid holidays
Process Engineering Associate I
ICM Ventures Inc —Colwich, KS
- Full-time
- Office
- Driver's License
- Travel
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Process Engineer - Associate
Syncreon —Carlisle, PA
- Microsoft Word
- Engineering
- Mid-level
Associate Engineer II, Automation
Arrowhead Pharmaceuticals —Madison, WI
- $75,000 - $90,000 a year
- Engineering
- Mid-level
- 3 years
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Process Engineer - Mid Level
Strategy Engineering & Consulting —Houston, TX
- Overtime
- Bachelor of Science
- Engineering
- Mid-level
- Health insurance
- Dental insurance
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Associate Process Engineer
Bosch Group —Roseville, CA
- $80,000 - $90,000 a year
- Overtime
- Microsoft Excel
- Bachelor of Science
- Mid-level
- Health savings account
- Disability insurance
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Process Validation Associate / Engineer

Krystal Biotech -
Pittsburgh, PA

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Job Details

Full-time

Qualifications

Statistics
Statistics
ICH guidelines
Bachelor's degree
GMP for research safety and compliance
Pharmaceutical manufacturing facility experience

Full Job Description

About Krystal Bio:

At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs.

Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient’s end-to-end experience.

Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology.

Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values.

Job Description Summary:

Krystal Biotech is seeking a highly motivated Process Validation Associate (1+ years’ experience) or Engineer (3+ years’ experience) to support process validation planning, design, and execution. This person will be responsible for risk assessments, process improvements, investigations, and other projects. They will also play a pivotal role in technology transfer and ensuring processes transition properly from site to site.

Primary Responsibilities:

Partner with Process Development and Manufacturing to ensure upstream and downstream processes are well controlled.
Apply QbD and traditional process validation principles to existing and new gene therapy products.
Perform and document risk assessments to capture existing process knowledge and to identify gaps.
Perform experiments (bench scale and manufacturing scale) to close gaps in process understanding and to support process development.
Troubleshoot process and equipment issues to help ensure efficiencies in processes.
Help implement a continuous improvement mindset to processes and departments.
Produce high-quality documentation that meets applicable standards and is appropriate for its intended use.
Work on development of new manufacturing facility to ensure proper transfer of technology and processes.
Work with CMC counterparts to draft materials intended for the agency review.

Minimum Qualifications & Desired Competencies:

Bachelors’ Degree in Chemical Engineering, Biomedical Engineering, or related
Relevant validation and/or engineering experience in the Biotech or Pharmaceutical industry (1+ yr for Associate, 3+ yr for Engineer level)
Background that includes knowledge/experience in GMP, GLP, and statistics
Strong knowledge of GMP and ICH requirements and QbD
Prior experience in the gene therapy field is desired
Must be a self-starter and capable of working with minimal oversight
Must be able to handle multiple roles and work in a fast paced and changing environment and know how to prioritize activities appropriately
Excellent oral and written communication skills

Krystal Biotech, Inc. is an Equal Employment Opportunity and Affirmative Action Employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this Web site or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc. will not pay fees to any third-party agency or company that does not have a signed agreement with Krystal Biotech, Inc.
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