Purification Development Associate Job at Revel IT (Philadelphia)

Research Associate

Prominex Inc. is a startup molecular diagnostic company with an experienced team...

Location

United States , San Diego

Salary:

Not provided

Prominex

Expiration Date

Until further notice

Requirements

Basic knowledge of laboratory procedures, established techniques, instruments and equipment
Experience with nucleic acid amplification techniques (PCR) and nucleic acid purification procedures
Able to operate under SOPs for development purposes
Experience with lateral flow technologies
Basic understanding of Universal Precautions and Basic Lab safety
Skilled with use of word processing, spreadsheets, graphical and presentation software applications
Capable of searching scientific literature to gain information about specific topics
Bachelor’s degree in Science and minimum requirement of 2-5 years of experience in a related field
Master’s degree in Science and minimum requirement of 0-2 years of experience in a related field

Job Responsibility

Executes bench experiments
makes detailed and general observations and reports data accurately and effectively
Analyzes data and interprets results
Prepares technical reports, summaries, protocols, and data analyses
Presents and discusses results of experiments within the scientific team
Works well in a team environment by being a productive team member, suggesting creative solutions to problems and providing input to project planning
Maintains high level of professional expertise through familiarity with scientific literature
Investigates, creates and develops new methods and technologies for project advancement
Helps to troubleshoots problems and institutes corrective action
Performs a wide variety of tasks, and exhibits a wide degree of creativity and latitude

Fulltime

Production Supervisor

The Production Supervisor will apply GSK Values and Expectations when managing a...

Location

United States , King of Prussia

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

BS/BA or Associates Degree with 5 or more years of directly related experience
5+ years of direct experience within the pharmaceutical or biotechnology sector OR 2+ years of supervisory experience in a manufacturing environment
Experience in production areas such as cell culture, buffer preparation, media preparation, or purification

Job Responsibility

Supervises Manufacturing Associates in operating cell culture equipment, preparing media and buffers, running chromatographic and filtration processes, and handling administrative duties
Oversees production, technology transfers (for NPI facility), and ensures training and ongoing development of staff
Leads or assists in investigations and resolutions alongside quality assurance and cross-functional teams
Acts as a departmental leader for process optimization, production scheduling, continuous improvement, and collaboration
Perform production activities alongside Manufacturing Associates and manage absences and timesheets as needed
Carry out responsibilities in compliance with Data Integrity principles, site SOPs, GSK EHS standards, and relevant legal requirements
Oversee and review documentation to confirm that the preparation of bulk biopharmaceutical intermediates meets cGMP, GSK, and other regulatory agency standards
Attend daily meetings, or assign a delegate, to discuss and adjust the production schedule as necessary
Support the implementation of new products and processes into the facility, including equipment and area changeovers
Maintain competency with current and emerging digital platforms (SAP, EBR, DeltaV, RTMS, etc.)

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes

Fulltime

Associate Scientist, Process Development (Process Validation & Business Strategy)

In this vital role you will be a part of the Process Development Drug Substance ...

Location

United States , Holly Springs

Salary:

97377.00 - 118653.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree and 3 years of Process Development or Scientific experience
Master’s degree and 1 years of Process Development or Scientific experience
2 – 4 years of experience in a Biotech/Pharma Process Development, MFG, QC, or laboratory role
Knowledge in broad aspects of biologics processing, for example cell culture, purification, analytical methods, or product quality attributes
Familiarity in operational aspects of process development lab or commercial biopharma manufacturing
Experienced with software such as Holistic Lab Execution Environment (HLEE), Tableau, MS PowerBI, spotfire, and/or databricks
Able to apply digital tool skills to solve business process issues and evaluate opportunities for process improvements
Excellent written and verbal communication
Be a self-starter with the ability to take on several projects at one time.

Job Responsibility

Lead and develop the Process Development safety, training, and compliance monitoring operation
Holistic Lab Execution Environment (HLEE) champion for the process development lab
Develop digital tools to improve business process efficiencies and identify bottlenecks within the process development operation
Develop digital tools to support process validation and process monitoring activities
Support and develop the Amgen North Carolina (ANC) PD DST knowledge management ecosystem, alignment of ANC PD business process to network practice, and optimizing the ANC PD business process
Provide process floor or lab support as required.

What we offer

Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

Fulltime

Associate Engineer, Process Development - Downstream

Be part of Amgen's newest and most advanced drug substance manufacturing plant. ...

Location

United States , Holly Springs

Salary:

82868.00 - 92671.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school diploma / GED and 6 years of Chemical, Biomedical, or related Engineering
Life Sciences
or other relevant sciences' experience
Associates and 4 years of Chemical, Biomedical, or related Engineering
Life Sciences
or other relevant sciences' experience
Bachelor’s degree

Job Responsibility

Apply a fundamental understanding of Downstream (Purification) Bioprocessing to support biologics technology transfer, process validation, and plant start-up
Support continuous process verification, process monitoring, optimization, complex investigation, and product life cycle management
Ensure safety and compliance of process development activities
Provide process on floor process support as required
Provide support for regulatory filing, inspection, and other CMC activities

What we offer

competitive and comprehensive Total Rewards Plans that are aligned with local industry standards

Fulltime

Senior/Research Associate, Drug Product Development

We are seeking a skilled and motivated Senior/Research Associate to join our Del...

Location

United States , South San Francisco

Salary:

75000.00 - 100000.00 USD / Year

NewLimit

Expiration Date

Until further notice

Requirements

MS in Biomedical Engineering, Chemical Biology, Pharmaceutical Sciences, or a related discipline with 2+ years of industry experience or equivalent experience
Experience formulating LNPs with diverse lipid components for nucleic acid delivery
Experience with purification techniques, including dialysis, Tangential Flow Filtration (TFF), ultracentrifugation, and sterile filtration
Proficiency in LNP analysis using DLS, LC-UV, LC-CAD, CGE, fragment analyzers, Osmolality, MALS, ELISA, and fluorescence-based 96-well plate assays

Job Responsibility

Formulate, downstream process, and characterize LNPs for nucleic acid delivery across diverse model systems, including pre-clinical models
Partner with the Epigenetic Editing and Product teams (Immunology, Metabolism, Vascular) to meet LNP requirements for reprogramming interventions at both small and large scales
Develop and optimize LNP compositions, downstream processing and analytical methods to establish robust production protocols
Map future formulation needs, manage material procurement, and ensure the lab is equipped for upcoming programs
Interpret complex experimental data to drive decision-making within Delivery Science and Preclinical Development workstreams
Maintain rigorous and detailed records of experimental protocols and results in an Electronic Laboratory Notebook (ELN)

What we offer

Health, dental, and vision insurance
401(k) with company match
Paid parental leave
Industry-leading paid time off (PTO) — 20 days/year for all employees + holidays
Meals and snacks on-site

Fulltime

Senior Scientist - Downstream Analytics

Senior Scientist – Downstream Analytics (Large Molecules). We’re partnering with...

Location

United Kingdom , Southampton

Salary:

45000.00 - 55000.00 GBP / Year

Cranleigh STEM

Expiration Date

Until further notice

Requirements

A PhD (or equivalent experience) in Analytical Chemistry, Biochemistry, or a related field
Strong hands-on experience in HPLC and bioprocessing within a biotechnology, pharmaceutical, or life sciences environment
Knowledge of purification and characterisation methods for peptides, antibodies, or similar large molecules
Experience with TFF or tangential flow filtration (advantageous)
Familiarity with ISO or GMP-regulated environments
Ability to lead technical projects and support team development
Strong communication and problem-solving skills
A flexible, proactive mindset with strong attention to detail

Job Responsibility

Lead downstream analytical workflows using HPLC, UPLC, PAGE, flash chromatography, and related techniques
Contribute to the purification and characterisation of large molecules, such as peptides and antibodies
Support method development and continuous improvement in analytical approaches
Collaborate with chemistry and production teams to support small molecule and oligonucleotide preparation
Maintain, calibrate, and optimise analytical instrumentation in line with ISO and internal quality systems
Mentor and support Associate Scientists and Lab Technicians
Ensure accurate documentation and maintain data integrity across workflows
Promote and uphold Health, Safety, and Environmental (HSE) standards
Manage stock levels of analytical reagents and consumables
Stay up to date on emerging trends in bioprocessing and analytical technologies

What we offer

Holidays: 25 days annual leave + 8 bank holidays
Pension: 6% employer contribution
Life Assurance: 4x salary
Flexible working hours
Long service awards and recognition scheme
Employee Assistance Programme with 24/7 remote GP access
Annual flu vaccinations
Cycle to work scheme and gym discounts
Discounts and savings platform
Professional membership reimbursement

Fulltime

Process Development Engineer

Process Development Engineer at Amgen Singapore Manufacturing. Amgen is one of t...

Location

Singapore , Tuas

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree OR Bachelor’s degree and 2 years of directly related experience OR Associate’s degree and/or 4 years of directly related experience OR High school diploma / GED and 6 years of directly related experience
3+ years of relevant work experience in the commercial manufacturing environment within the biotechnology or pharmaceutical industries
At least 2 years’ experience with regulated environments (i.e. cGMP) required
In depth cell culture and/or purification process knowledge, including single-use technologies and harvest technologies
Experience in providing floor support, troubleshooting unit operations, and resolving and documenting investigations to support cGMP production
Possess basic understanding of regulatory and cGMP requirements
Able to apply engineering principles and advanced statistical analysis in-order to solve processing issues and evaluate opportunities for process improvements
Able to escalate relevant issues to project lead and line management
Independently motivated but also work well in team environment
Strong communication skills (technical writing and verbal communication/presentation)

Job Responsibility

Applies expertise in the successful coordination of multiple, complex, non-routine activities including tech transfer process qualification, process performance monitoring, floor support, troubleshooting of unit operations
Support/lead complicated investigations, providing concise communications to teams and leadership
Compile and analyze process data using tools such as excel, JMP, SIMCA to inform future decision-making and take predictive action
Author technical protocols, technical assessments, and product impact assessments
Verify data in technical reports, spreadsheets, and regulatory filings
Utilize strong written and verbal communication skills in technical writing and presentations

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

New

Senior Associate Scientist

As a Senior Associate Scientist Biology, you will be at the forefront of our mis...

Location

United States , Pearl River

Salary:

68600.00 - 110900.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Molecular Biology, Virology, Immunology, or a related scientific discipline with 4–5 years of relevant laboratory experience, or a Master’s degree with 2–3 years of relevant hands-on laboratory experience
Minimum of two years’ experience working with NGS technologies
Proficiency with a wide range of molecular biology and analytical techniques, including nucleic acid extraction, fluorescence-based quantification, and real-time PCR
Exceptional task planning, problem-solving abilities, and ability to manage multiple priorities effectively
Effective verbal and written communication skills

Job Responsibility

Execute NGS protocols to support vaccine program initiatives
Conduct laboratory-based activities, including sample organization and preparation, DNA/RNA purification, library construction, qPCR, tissue processing, and related tasks
Operate, maintain, optimize, and manage laboratory automation systems
develop and improve automated workflows
Develop innovative sequencing protocols for pathogen and/or human genome characterization using Ion Torrent and Illumina platforms
Demonstrate advanced problem-solving abilities, including troubleshooting and resolution of technical issues with high-level of independence
Manage project timelines effectively and work efficiently on assigned tasks
Maintain current knowledge of scientific literature and emerging technologies
attend relevant scientific meetings to integrate new technologies and principles as appropriate
Perform molecular biology research, data analysis, and other tasks aligned with program needs

What we offer

401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
paid vacation, holiday and personal days
paid caregiver/parental and medical leave
health benefits to include medical, prescription drug, dental and vision coverage
Relocation support available

Fulltime

Purification Development Associate

Revel IT

Location:
United States , Philadelphia

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 11, 2026

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