Upstream Process Development Scientist Experience in development of mammalian cell culture ... Basic knowledge of regulatory requirements of the pharmaceutical / biotechnology industry. Key ...
Upstream Process Development Scientist Experience in development of mammalian cell culture ... Basic knowledge of regulatory requirements of the pharmaceutical / biotechnology industry. Key ...
Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Direct the development and optimization of upstream processes including but not limited to: seed ...
Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Direct the development and optimization of upstream processes including but not limited to: seed ...
Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Direct the development and optimization of downstream processes including and not limited to ...
Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Direct the development and optimization of downstream processes including and not limited to ...
Legend Biotech is seeking a Principal Scientist, Lentivirus Upstream Process Development as part of the Technical Development team based in Somerset, NJ . Role Overview The Principal Scientist ...
Legend Biotech is seeking a Principal Scientist, Lentivirus Upstream Process Development as part of the Technical Development team based in Somerset, NJ . Role Overview The Principal Scientist ...
Scale up process developed at research stage to manufacture adequate amounts of protein to support ... Basic knowledge of regulatory requirements of the pharmaceutical / biotechnology industry.
Scale up process developed at research stage to manufacture adequate amounts of protein to support ... Basic knowledge of regulatory requirements of the pharmaceutical / biotechnology industry.
Legend Biotech is seeking a Principal Scientist, Lentivirus Downstream Process Development as part of the Technical Development team based in Somerset, NJ . Role Overview The Principal Scientist ...
Legend Biotech is seeking a Principal Scientist, Lentivirus Downstream Process Development as part of the Technical Development team based in Somerset, NJ . Role Overview The Principal Scientist ...
Regeneron's Preclinical Manufacturing & Process Development Group (PMPD) is seeking a Process ... biotech or pharmaceutical industry. A strong fundamental understanding of various protein ...
Regeneron's Preclinical Manufacturing & Process Development Group (PMPD) is seeking a Process ... biotech or pharmaceutical industry. A strong fundamental understanding of various protein ...
Experience in development of mammalian cell culture processes for the production of recombinant ... Basic knowledge of regulatory requirements of the pharmaceutical / biotechnology industry.
Experience in development of mammalian cell culture processes for the production of recombinant ... Basic knowledge of regulatory requirements of the pharmaceutical / biotechnology industry.
Regeneron's Preclinical Manufacturing & Process Development Group (PMPD) is seeking a Process ... biotech or pharmaceutical industry. A strong fundamental understanding of various protein ...
Regeneron's Preclinical Manufacturing & Process Development Group (PMPD) is seeking a Process ... biotech or pharmaceutical industry. A strong fundamental understanding of various protein ...
Bioprocesses, Biotechnology, Cell Cultures, Centrifugation, Chromatographic Techniques, Cross-Functional Teamwork, Data Analysis, Downstream Process Development, Evaluating New Technologies ...
Bioprocesses, Biotechnology, Cell Cultures, Centrifugation, Chromatographic Techniques, Cross-Functional Teamwork, Data Analysis, Downstream Process Development, Evaluating New Technologies ...
Bioprocesses, Biotechnology, Cell Cultures, Centrifugation, Chromatographic Techniques, Cross-Functional Teamwork, Data Analysis, Downstream Process Development, Evaluating New Technologies ...
Bioprocesses, Biotechnology, Cell Cultures, Centrifugation, Chromatographic Techniques, Cross-Functional Teamwork, Data Analysis, Downstream Process Development, Evaluating New Technologies ...
Global Viral Vector MSAT Lead
Raritan, NJ · On-site
This role requires collaboration and partnering closely with Process Development, Manufacturing ... Legend Biotech Privacy Notice.
Global Viral Vector MSAT Lead
Raritan, NJ · On-site
This role requires collaboration and partnering closely with Process Development, Manufacturing ... Legend Biotech Privacy Notice.
Bioprocesses, Biotechnology, Cell Cultures, Centrifugation, Chromatographic Techniques, Cross-Functional Teamwork, Data Analysis, Downstream Process Development, Evaluating New Technologies ...
Bioprocesses, Biotechnology, Cell Cultures, Centrifugation, Chromatographic Techniques, Cross-Functional Teamwork, Data Analysis, Downstream Process Development, Evaluating New Technologies ...
D. preferred in Biotechnology, Biochemical Engineering, or related field. Experience * Minimum 10+ years in biopharmaceutical manufacturing. Viral vector late processes development/manufacturing ...
D. preferred in Biotechnology, Biochemical Engineering, or related field. Experience * Minimum 10+ years in biopharmaceutical manufacturing. Viral vector late processes development/manufacturing ...
Senior Process Engineer
Bridgewater, NJ · On-site
$90K - $210K/yr
This position is responsible for supporting the activities involved in development, process ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...
Senior Process Engineer
Bridgewater, NJ · On-site
$90K - $210K/yr
This position is responsible for supporting the activities involved in development, process ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...
Senior Process Engineer
$106.30K - $137.50K/yr
This position is responsible for supporting the activities involved in development, process ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...
Quick apply
Senior Process Engineer
$106.30K - $137.50K/yr
This position is responsible for supporting the activities involved in development, process ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...
Senior Process Engineer
$90K - $210K/yr
This position is responsible for supporting the activities involved in development, process ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...
Senior Process Engineer
$90K - $210K/yr
This position is responsible for supporting the activities involved in development, process ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...
Senior Process Engineer/Process Engineer II - Manufacturing
Brooklyn, NY · On-site
$109.40K - $141.40K/yr
... process development, design, and process implementation required, preferably in medical device, pharmaceutical, or biotech manufacturing. Understanding of FDA 21 CFR Part 820, ISO 13485, and GMP ...
Senior Process Engineer/Process Engineer II - Manufacturing
Brooklyn, NY · On-site
$109.40K - $141.40K/yr
... process development, design, and process implementation required, preferably in medical device, pharmaceutical, or biotech manufacturing. Understanding of FDA 21 CFR Part 820, ISO 13485, and GMP ...
Senior Process Engineer/Process Engineer II - Manufacturing
Brooklyn, NY · On-site
$108.40K - $140.20K/yr
... development, design, and process implementation required, preferably in medical device, pharmaceutical, or biotech manufacturing. • Understanding of FDA 21 CFR Part 820, ISO 13485, and GMP ...
Senior Process Engineer/Process Engineer II - Manufacturing
Brooklyn, NY · On-site
$108.40K - $140.20K/yr
... development, design, and process implementation required, preferably in medical device, pharmaceutical, or biotech manufacturing. • Understanding of FDA 21 CFR Part 820, ISO 13485, and GMP ...
Senior Process Engineer/Process Engineer II - Manufacturing
Brooklyn, NY · On-site
$108.40K - $140.20K/yr
... development, design, and process implementation required, preferably in medical device, pharmaceutical, or biotech manufacturing. · Understanding of FDA 21 CFR Part 820, ISO 13485, and GMP ...
Quick apply
Senior Process Engineer/Process Engineer II - Manufacturing
Brooklyn, NY · On-site
$108.40K - $140.20K/yr
... development, design, and process implementation required, preferably in medical device, pharmaceutical, or biotech manufacturing. · Understanding of FDA 21 CFR Part 820, ISO 13485, and GMP ...
Biotech Process Development information
See New York salary details
$21.36 - $23.77
2% of jobs
$23.77 - $26.18
0% of jobs
$26.18 - $28.59
9% of jobs
$30.27 is the 25th percentile. Wages below this are outliers.
$28.59 - $31
20% of jobs
The median wage is $32.83 / hr.
$31 - $33.41
25% of jobs
$33.41 - $35.82
17% of jobs
$36.66 is the 75th percentile. Wages above this are outliers.
$35.82 - $38.23
5% of jobs
$38.23 - $40.64
4% of jobs
$40.64 - $43.05
4% of jobs
$43.05 - $45.45
3% of jobs
$45.45 - $47.86
10% of jobs
$21
$35
$47
How much do biotech process development jobs pay per hour?
What are the key skills and qualifications needed to thrive in Biotech Process Development, and why are they important?
What are some common challenges faced by professionals in Biotech Process Development, and how are they typically addressed?
What is biotech process development?
What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?
| Aspect | Biotech Process Development | Biotech Manufacturing Associate |
|---|---|---|
| Primary Focus | Designing, optimizing, and scaling up bioprocesses for product development | Executing manufacturing processes to produce biopharmaceuticals at scale |
| Work Environment | Laboratories and pilot plant facilities | Production floors and manufacturing plants |
| Required Skills | Process design, lab techniques, troubleshooting | Equipment operation, quality control, adherence to SOPs |
| Typical Credentials | BSc/MSc in Biotechnology, Chemical Engineering, or related fields | BSc in Biotechnology, Biology, or related fields |
While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.
Job description
A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Upstream Process Development Scientist
Experience in development of mammalian cell culture processes for the production of recombinant proteins is a plus. Knowledge of protein chemistry and purification techniques and purification process development experience is preferred. Basic knowledge of cGMP policies and procedures. Basic knowledge of regulatory requirements of the pharmaceutical / biotechnology industry.
Key Responsibilities:
Design and execute experiments for production of proteins using microbial fermentation processes. Design, analyze and interpret lab experiments, purification data, in-process trends, productivity and quality attributes to support upstream process development.
Lead efforts to evaluate different fermentation media, feeds, and feeding strategies to improve product yield and quality including proper folding of protein
Scale up process developed at research stage to manufacture adequate amounts of protein to support clinical trials
Author technical documentation including process validation protocols and reports.
Evaluate process robustness, investigate causes of process variances, and take steps to maximize process reproducibility.
Basic qualifications: Ph.D., MS or BS in Chemical/Biochemical Engineering or related Biological Sciences is required. For a candidate with a Ph.D. >3 yrs. of industrial experience; candidate with an MS >5 yrs. industrial experience and for a candidate with a BS, >7 years of industrial experience in developing upstream microbial fermentation processes for the production of bio-pharmaceuticals is required. Specific experience in development of microbial expression processes for soluble protein production is preferred.
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996