Scientist - NIH VRC
$53.33/hr
Purification development experience for GMP process development in biotech/pharmaceutical or related industry (experience in clinical manufacturing is highly desirable). Must be a team player who can ...
$53.33/hr
Purification development experience for GMP process development in biotech/pharmaceutical or related industry (experience in clinical manufacturing is highly desirable). Must be a team player who can ...
$53.33/hr
Purification development experience for GMP process development in biotech/pharmaceutical or related industry (experience in clinical manufacturing is highly desirable). Must be a team player who can ...
Baltimore, MD · Hybrid
Expected to provide investment insights and impact the investment process for both public and ... Basic understanding of fundamental drug development research and preclinical / clinical data ...
Baltimore, MD · Hybrid
Expected to provide investment insights and impact the investment process for both public and ... Basic understanding of fundamental drug development research and preclinical / clinical data ...
... procurement process begins, and position Emmes as a strategic partner early in sponsors ... Strong network across biotech and pharma with the ability to convert relationships into early ...
... procurement process begins, and position Emmes as a strategic partner early in sponsors ... Strong network across biotech and pharma with the ability to convert relationships into early ...
Prepare processing rooms and equipment for R&D, pilot-scale and GMP manufacturing operations ... Associate degree in Pharmaceutical Technology, Biotechnology, Chemistry, Biology, Engineering ...
Prepare processing rooms and equipment for R&D, pilot-scale and GMP manufacturing operations ... Associate degree in Pharmaceutical Technology, Biotechnology, Chemistry, Biology, Engineering ...
... Biotechnology, Biochemistry, Pharmaceutical Sciences, or a related scientific field. * Minimum 4-8 years of progressive experience in MSAT, Bio process engineering, or process development, GMP ...
... Biotechnology, Biochemistry, Pharmaceutical Sciences, or a related scientific field. * Minimum 4-8 years of progressive experience in MSAT, Bio process engineering, or process development, GMP ...
... procurement process begins, and position Emmes as a strategic partner early in sponsors ... in biotech and pharma. Responsibilities * Drive net-new business development by securing new ...
... procurement process begins, and position Emmes as a strategic partner early in sponsors ... in biotech and pharma. Responsibilities * Drive net-new business development by securing new ...
... Biotechnology, Biochemistry, Pharmaceutical Sciences, or a related scientific field. * Minimum 4-8 years of progressive experience in MSAT, Bio process engineering, or process development, GMP ...
... Biotechnology, Biochemistry, Pharmaceutical Sciences, or a related scientific field. * Minimum 4-8 years of progressive experience in MSAT, Bio process engineering, or process development, GMP ...
Oversee portfolio governance processes, including prioritization frameworks, resource allocation ... Experience in both pharma and high-growth biotech environments preferred. * Ability to understand ...
Oversee portfolio governance processes, including prioritization frameworks, resource allocation ... Experience in both pharma and high-growth biotech environments preferred. * Ability to understand ...
Gaithersburg, MD · On-site
$116K - $177K/yr
Work with consumables manufacturing and process development teams to gain information on Automation ... Experience in the Biotech or Pharmaceutical industries strongly preferred. * Experience with ISO ...
Gaithersburg, MD · On-site
$116K - $177K/yr
Work with consumables manufacturing and process development teams to gain information on Automation ... Experience in the Biotech or Pharmaceutical industries strongly preferred. * Experience with ISO ...
Knowledge of program management methodologies such as integrated timelines and stage-gate development processes in a biotech or pharma environment. * Excellent communication and interpersonal skills ...
Knowledge of program management methodologies such as integrated timelines and stage-gate development processes in a biotech or pharma environment. * Excellent communication and interpersonal skills ...
Demonstrated experience in pharmaceutical, biotechnology, manufacturing, technical operations ... process development, MS&T, quality, data, or other regulated environments. * Strong program and ...
Demonstrated experience in pharmaceutical, biotechnology, manufacturing, technical operations ... process development, MS&T, quality, data, or other regulated environments. * Strong program and ...
Demonstrated experience in pharmaceutical, biotechnology, manufacturing, technical operations ... process development, MS&T, quality, data, or other regulated environments. * Strong program and ...
Demonstrated experience in pharmaceutical, biotechnology, manufacturing, technical operations ... process development, MS&T, quality, data, or other regulated environments. * Strong program and ...
Knowledge of program management methodologies such as integrated timelines and stage-gate development processes in a biotech or pharma environment. * Excellent communication and interpersonal skills ...
Knowledge of program management methodologies such as integrated timelines and stage-gate development processes in a biotech or pharma environment. * Excellent communication and interpersonal skills ...
Demonstrated experience in pharmaceutical, biotechnology, manufacturing, technical operations ... process development, MS&T, quality, data, or other regulated environments. * Strong program and ...
Demonstrated experience in pharmaceutical, biotechnology, manufacturing, technical operations ... process development, MS&T, quality, data, or other regulated environments. * Strong program and ...
Demonstrated experience in pharmaceutical, biotechnology, manufacturing, technical operations ... process development, MS&T, quality, data, or other regulated environments. * Strong program and ...
Demonstrated experience in pharmaceutical, biotechnology, manufacturing, technical operations ... process development, MS&T, quality, data, or other regulated environments. * Strong program and ...
Gaithersburg, MD · On-site
$172.47 - $258.70/hr
Demonstrated experience in pharmaceutical, biotechnology, manufacturing, technical operations ... process development, MS&T, quality, data, or other regulated environments. * Strong program and ...
New
Gaithersburg, MD · On-site
$172.47 - $258.70/hr
Demonstrated experience in pharmaceutical, biotechnology, manufacturing, technical operations ... process development, MS&T, quality, data, or other regulated environments. * Strong program and ...
New
Rockville, MD · On-site
Provide technical engineering oversight from development, to the implementation and routine ... Individual with experience must have knowledge of unit operations typically used in biotech and ...
Quick apply
Rockville, MD · On-site
Provide technical engineering oversight from development, to the implementation and routine ... Individual with experience must have knowledge of unit operations typically used in biotech and ...
Provide technical engineering oversight from development, to the implementation and routine ... Individual with experience must have knowledge of unit operations typically used in biotech and ...
Provide technical engineering oversight from development, to the implementation and routine ... Individual with experience must have knowledge of unit operations typically used in biotech and ...
Baltimore, MD · On-site
... biotech, and self-care companies to accelerate the development, manufacturing, and delivery of life ... process development for clinical programs, with advanced development labs and cGMP cleanroom suites ...
Baltimore, MD · On-site
... biotech, and self-care companies to accelerate the development, manufacturing, and delivery of life ... process development for clinical programs, with advanced development labs and cGMP cleanroom suites ...
Baltimore, MD · On-site
... biotech, and self-care companies to accelerate the development, manufacturing, and delivery of life ... process development for clinical programs, with advanced development labs and cGMP cleanroom suites ...
Baltimore, MD · On-site
... biotech, and self-care companies to accelerate the development, manufacturing, and delivery of life ... process development for clinical programs, with advanced development labs and cGMP cleanroom suites ...
| 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.

$53.33/hr
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 24 days ago
Cape Fox Facilities Services is seeking an experienced Scientist support of the overall functions of the Vaccine Research Center (VRC) on the NIH Bethesda campus by supporting collaborative research in the intramural community of the NIH. The total hourly pay for this exempt position is $53.33 for up to 40 hours per week. This rate represents the company's good faith and reasonable estimate of possible compensation at the time of posting
In addition, for eligible positions we offer a variety of benefits including specified holidays, paid leave, health insurance, dental insurance, vision insurance, life and disability insurance, tuition reimbursement, as well as 401K with company match. This job will be posted until filled or withdrawn. Participate in projects that are complex and scientifically demanding within a specific area/field, specifically Bioanalytical separation.
Initiate, implement, plan, and execute scientific research and development. Determine scientific rigor in assessing own data and that of others, by providing detailed observations, analyzing data, and interpreting results. Ensure project goals are met within time and budget constraints.
Independently initiate, plan, design, evaluate, revise and execute projects within CGE, UPLC field, utilizing good scientific judgment. Utilize specific investigation and method development work in support of multiple projects at a time. Communicate and initiate investigations for project and process findings, draw conclusions, and act as project manager in the drafting of state-of-art work and publishing of papers.
Develop research findings and make recommendations to leadership for decision. Provide forward-looking perspectives that contribute to "go/no go" decisions by leadership. Research and recommend outside technologies for consideration.M.S degree in Chemistry, Biology, Biochemistry Life Sciences or a related discipline
Minimum of five (5) years of experience in recombinant protein purification development for GMP clinical-phase products. Demonstrated knowledge of maintaining accurate and detailed records. Demonstrated expertise in the following techniques or tools for protein purification and characterization: Column chromatography for protein purification by AEX, CEX, affinity, SEC, HIC.
Column packing and testing. AKTA chromatography system. Lab scale TFF systems.
Qualitative assays including SDS-PAGE and Western Blot. UV/vis spectrophotometer. Purification development experience for GMP process development in biotech/pharmaceutical or related industry (experience in clinical manufacturing is highly desirable).
Must be a team player who can effectively work with members from cross-functional departments. Strong oral and written communication skills. Familiarity with computer software including word processing and data evaluation.
Occupational Health/Physical Requirements and Worksite Hazards: Occupational health/physical requirements is required Cape Fox Corporation, its subsidiaries and affiliates provide equal employment opportunities to all persons and prohibit employment decisions on the basis of race, religion, color, creed, national origin, sex, age, disability, political affiliation, protected veteran status, or sexual orientation. Cape Fox Corporation, its subsidiaries and affiliates offer preference to Cape Fox Corporation shareholders, descendants and other Native Americans pursuant to Public Law 100-241.M.S degree in Chemistry, Biology, Biochemistry Life Sciences or a related discipline. Minimum of five (5) years of experience in recombinant protein purification development for GMP clinical-phase products
Demonstrated knowledge of maintaining accurate and detailed records. Demonstrated expertise in the following techniques or tools for protein purification and characterization: Column chromatography for protein purification by AEX, CEX, affinity, SEC, HIC. Column packing and testing.
AKTA chromatography system. Lab scale TFF systems. Qualitative assays including SDS-PAGE and Western Blot.
UV/vis spectrophotometer. Purification development experience for GMP process development in biotech/pharmaceutical or related industry (experience in clinical manufacturing is highly desirable). Must be a team player who can effectively work with members from cross-functional departments.
Strong oral and written communication skills. Familiarity with computer software including word processing and data evaluation. Occupational Health/Physical Requirements and Worksite Hazards: Occupational health/physical requirements is required Cape Fox Corporation, its subsidiaries and affiliates provide equal employment opportunities to all persons and prohibit employment decisions on the basis of race, religion, color, creed, national origin, sex, age, disability, political affiliation, protected veteran status, or sexual orientation.
Cape Fox Corporation, its subsidiaries and affiliates offer preference to Cape Fox Corporation shareholders, descendants and other Native Americans pursuant to Public Law 100-241.
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501 - 1,000 Employees
Ketchikan, AK, US