Process Engineer
New Brunswick, NJ · On-site
Company Description Big Pharmaceutical Organisation Associate Process Engineer/Scientist- Drug ... Minimum of 3-5 years of experience in the Pharmaceutical or Biotechnology industry in product and ...
New Brunswick, NJ · On-site
Company Description Big Pharmaceutical Organisation Associate Process Engineer/Scientist- Drug ... Minimum of 3-5 years of experience in the Pharmaceutical or Biotechnology industry in product and ...
New Brunswick, NJ · On-site
Company Description Big Pharmaceutical Organisation Associate Process Engineer/Scientist- Drug ... Minimum of 3-5 years of experience in the Pharmaceutical or Biotechnology industry in product and ...
Brooklyn, NY · On-site
$108K - $140K/yr
Cresilon ® is a Brooklyn-based biotechnology company that develops, manufactures, and markets ... The Senior Process Engineer or Process Engineer II will support and lead manufacturing process ...
Brooklyn, NY · On-site
$108K - $140K/yr
Cresilon ® is a Brooklyn-based biotechnology company that develops, manufactures, and markets ... The Senior Process Engineer or Process Engineer II will support and lead manufacturing process ...
Cresilon is a Brooklyn-based biotechnology company that develops, manufactures, and markets ... The Senior Process Engineer or Process Engineer II will support and lead manufacturing process ...
Cresilon is a Brooklyn-based biotechnology company that develops, manufactures, and markets ... The Senior Process Engineer or Process Engineer II will support and lead manufacturing process ...
Brooklyn, NY · On-site
$108K - $140K/yr
Cresilon ® is a Brooklyn-based biotechnology company that develops, manufactures, and markets ... The Senior Process Engineer or Process Engineer II will support and lead manufacturing process ...
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Brooklyn, NY · On-site
$108K - $140K/yr
Cresilon ® is a Brooklyn-based biotechnology company that develops, manufactures, and markets ... The Senior Process Engineer or Process Engineer II will support and lead manufacturing process ...
$90K - $210K/yr
Position Summary We are seeking an innovative and highly motivated Senior Process Engineer on our ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...
$90K - $210K/yr
Position Summary We are seeking an innovative and highly motivated Senior Process Engineer on our ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...
Bridgewater, NJ · On-site
$90K - $210K/yr
Position Summary We are seeking an innovative and highly motivated Senior Process Engineer on our ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...
Bridgewater, NJ · On-site
$90K - $210K/yr
Position Summary We are seeking an innovative and highly motivated Senior Process Engineer on our ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...
$106K - $137K/yr
Position Summary We are seeking an innovative and highly motivated Senior Process Engineer on our ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...
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$106K - $137K/yr
Position Summary We are seeking an innovative and highly motivated Senior Process Engineer on our ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...
Associate Process Engineer/Scientist Location: New Brunswick, NJ Job ID: 21528-1 Duration: 6+ ... Minimum of 3-5 years of experience in the Pharmaceutical or Biotechnology industry in product and ...
Associate Process Engineer/Scientist Location: New Brunswick, NJ Job ID: 21528-1 Duration: 6+ ... Minimum of 3-5 years of experience in the Pharmaceutical or Biotechnology industry in product and ...
Parsippany, NJ · On-site
The Principal Process Engineer is the technical lead for equipment reliability and asset ... biotechnology, medical device, or other regulated manufacturing environments * 5+ years in ...
Parsippany, NJ · On-site
The Principal Process Engineer is the technical lead for equipment reliability and asset ... biotechnology, medical device, or other regulated manufacturing environments * 5+ years in ...
... biotech, academic, or pharmaceutical setting. * Core engineering background in bioprocessing of ... Experience handling the cell processing side for cell therapies, including mammalian cell culture ...
... biotech, academic, or pharmaceutical setting. * Core engineering background in bioprocessing of ... Experience handling the cell processing side for cell therapies, including mammalian cell culture ...
... CQV Engineer to support a biotechnology manufacturing expansion project in Raritan, NJ. The ... Support qualification of aseptic processing isolators and associated GMP manufacturing systems.
... CQV Engineer to support a biotechnology manufacturing expansion project in Raritan, NJ. The ... Support qualification of aseptic processing isolators and associated GMP manufacturing systems.
... biotech, academic, or pharmaceutical setting. * Core engineering background in bioprocessing of ... Experience handling the cell processing side for cell therapies, including mammalian cell culture ...
... biotech, academic, or pharmaceutical setting. * Core engineering background in bioprocessing of ... Experience handling the cell processing side for cell therapies, including mammalian cell culture ...
CQV Engineer - Biotech Manufacturing, Isolators & VHP Position Summary Validation & Engineering ... Support qualification of aseptic processing isolators and associated GMP manufacturing systems.
CQV Engineer - Biotech Manufacturing, Isolators & VHP Position Summary Validation & Engineering ... Support qualification of aseptic processing isolators and associated GMP manufacturing systems.
CQV Engineer Biotech Manufacturing, Isolators & VHP * Position Summary Validation & Engineering ... Support qualification of aseptic processing isolators and associated GMP manufacturing systems.
CQV Engineer Biotech Manufacturing, Isolators & VHP * Position Summary Validation & Engineering ... Support qualification of aseptic processing isolators and associated GMP manufacturing systems.
CQV Engineer - Biotech Manufacturing, Isolators & VHP * Position Summary Validation & Engineering ... Support qualification of aseptic processing isolators and associated GMP manufacturing systems.
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CQV Engineer - Biotech Manufacturing, Isolators & VHP * Position Summary Validation & Engineering ... Support qualification of aseptic processing isolators and associated GMP manufacturing systems.
... Engineering, Virology, Molecular Biology, or a related field. * 8+ years (PhD) or 10+ years (MS) of experience in process development or manufacturing within a biotech or pharmaceutical setting
... Engineering, Virology, Molecular Biology, or a related field. * 8+ years (PhD) or 10+ years (MS) of experience in process development or manufacturing within a biotech or pharmaceutical setting
Bridgewater, NJ · On-site
$117K - $140K/yr
Job Summary : Legend Biotech is a global biotechnology company dedicated to treating life ... on ETL/ELT processes and scalable platform engineering. Responsibilities : • The Lead Data ...
Bridgewater, NJ · On-site
$117K - $140K/yr
Job Summary : Legend Biotech is a global biotechnology company dedicated to treating life ... on ETL/ELT processes and scalable platform engineering. Responsibilities : • The Lead Data ...
... Engineering, Virology, Molecular Biology, or a related field. * 8+ years (PhD) or 10+ years (MS) of experience in process development or manufacturing within a biotech or pharmaceutical setting.
... Engineering, Virology, Molecular Biology, or a related field. * 8+ years (PhD) or 10+ years (MS) of experience in process development or manufacturing within a biotech or pharmaceutical setting.
Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Support process improvement initiatives, including enhancing programming efficiency ...
Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Support process improvement initiatives, including enhancing programming efficiency ...
... Engineering, Virology, Molecular Biology, or a related field. * 8+ years (PhD) or 10+ years (MS) of experience in process development or manufacturing within a biotech or pharmaceutical setting
... Engineering, Virology, Molecular Biology, or a related field. * 8+ years (PhD) or 10+ years (MS) of experience in process development or manufacturing within a biotech or pharmaceutical setting
$54.2K - $63.4K
2% of jobs
$63.4K - $72.7K
9% of jobs
$81.1K is the 25th percentile. Wages below this are outliers.
$72.7K - $81.9K
15% of jobs
$81.9K - $91.2K
18% of jobs
The median wage is $94.3K / yr.
$91.2K - $100.4K
17% of jobs
$100.4K - $109.7K
14% of jobs
$109.9K is the 75th percentile. Wages above this are outliers.
$109.7K - $118.9K
11% of jobs
$118.9K - $128.2K
6% of jobs
$128.2K - $137.4K
4% of jobs
$137.4K - $146.7K
3% of jobs
$146.7K - $155.9K
1% of jobs
$54.2K
$100.7K
$155.9K
| Aspect | Biotech Process Engineer | Biotech Manufacturing Technician |
|---|---|---|
| Credentials | Bachelor's degree in biotech, chemical engineering, or related field; often requires experience in process design | Associate's or bachelor's degree; focus on operational skills and equipment handling |
| Work Environment | Designing, optimizing, and overseeing production processes in labs or manufacturing facilities | Operating and maintaining equipment on the manufacturing floor |
| Job Focus | Process development, scale-up, troubleshooting, and process improvement | Executing production tasks, quality checks, and equipment setup |
Biotech Process Engineers focus on designing and improving manufacturing processes, requiring technical and analytical skills. In contrast, Biotech Manufacturing Technicians handle day-to-day production operations. Both roles are essential in biotech manufacturing but differ in responsibilities and required qualifications.

Big Pharmaceutical Organisation
Associate Process Engineer/Scientist- Drug Product, Biologics Manufacturing Science and Technology
Key responsibilities include
Execution of post-market process change activities/experiments through partnership with R&D development assets
Responsible for characterizing, optimizing and troubleshooting product and manufacturing processes of parenteral dosage forms.
Work with R&D and manufacturing sites to design and execute experiments to support product robustness, new technology implementation, and/or manufacturing investigations
Serve as technical resource to other functions, providing expertise on the product and its process.
Effectively represent biologics drug product manufacturing science and technology in various internal and external teams and committees on development, technology transfer, manufacturing, specifications, process validations and launch.
Provide assistance to sites globally to resolve significant quality events and manage complex change controls.
Bachelor's degree in relevant science or engineering discipline (chemistry, pharmaceutical sciences, pharmacy, biology, chemical engineering).
Master or advanced degree preferred.
Minimum of 3-5 years of experience in the Pharmaceutical or Biotechnology industry in product and process development and commercialization in a global environment.
Key Skills and Experience
Hands-on experience in the laboratory and in-depth understanding in sterile and liquid products, particularly biologics, formulation development, analytical methods, commercial manufacturing, and their unit operations.
In-depth understanding of Quality by Design (QbD), Design of Experiments (DOE), multivariate analysis, PAT, critical process and material attributes and CQA's.
Working competency of Statistical Process Control and related tools (JMP/MiniTab/SAS).
Able to design and execute scientifically sound, hypothesis driven experiments
Skilled in writing and reviewing complex study plans and scientific reports.
Possess high level of familiarity with sterile product processing equipment and manufacturing facilities.
Overall knowledge of parenteral technology: aseptic processing, sterilization, isolator processing, lyophilization, pre-filled syringe operations, etc.
Strong understanding of project management systems and tools
Six Sigma Green/Black Belt certification desirable
Interested candidates may contact at "Praveen.arora(@)artechinfo.com or 973-507-7593
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Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).
Recruiting and staffing services
10,000+ Employees
Morristown, NJ, US
1992