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Associate Downstream Process Development Scientist Jobs in Connecticut

Manufacturing R&D Engineer

Durham, CT · On-site

$71K - $91K/yr

We are seeking a results-driven Manufacturing / R&D Engineer to lead process development and ... Investigate and resolve manufacturing challenges using scientific and data-driven problem-solving ...

Design, implement and/or deploy NGS data analysis workflows for data processing, visualization ... Analyzing diverse datasets (multi-omics) to find relevant drug discovery targets and downstream ...

Manufacturing R&D Engineer

Durham, CT · On-site

$71K - $91K/yr

We are seeking a results-driven Manufacturing / R&D Engineer to lead process development and ... Investigate and resolve manufacturing challenges using scientific and data-driven problem-solving ...

Manufacturing R&D Engineer

Durham, CT · On-site

$71K - $91K/yr

We are seeking a results-driven Manufacturing / R&D Engineer to lead process development and ... Investigate and resolve manufacturing challenges using scientific and data-driven problem-solving ...

Associate Scientist

Farmington, CT · On-site

$69K - $90K/yr

The Associate Scientist will serve as the platform lead for Xenium spatial transcriptomics projects ... Process Optimization & Development: Drive the continuous improvement of the platform by optimizing ...

Associate Scientist

Trumbull, CT · On-site

$49K - $52K/yr

The individual draws conclusions based on data, proposes and directs next steps in the development ... If you need a reasonable accommodation for any part of the employment process, please contact your ...

Sr Process Engineer

Milford, CT

$104K - $134K/yr

This involves using scientific tools/approaches to investigate, develop, and document the process ... Collaborates with product development team to align Process development with R&D goals. * Runs ...

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Associate Downstream Process Development Scientist information

What is an Associate Downstream Process Development Scientist?

An Associate Downstream Process Development Scientist is a professional who works in the biotechnology or pharmaceutical industry, focusing on developing and optimizing processes that purify biological products, such as proteins or antibodies, after they have been produced by cells. Their work is crucial for ensuring the final product meets quality and safety standards before it is used in research or clinical applications. They typically perform laboratory experiments, analyze data, and collaborate with other scientists and engineers to improve yield and efficiency. This role is often entry-level or early-career, providing hands-on experience in process development and technical troubleshooting.

What are the key skills and qualifications needed to thrive as an Associate Downstream Process Development Scientist, and why are they important?

To excel as an Associate Downstream Process Development Scientist, you need a solid understanding of biochemistry, chemical engineering, and downstream purification techniques, often supported by a bachelor's or master's degree in a life science or engineering discipline. Familiarity with chromatographic systems (such as AKTA), filtration equipment, and analytical tools, as well as knowledge of GMP/GLP regulations, is typically required. Strong problem-solving, attention to detail, and effective teamwork and communication skills help you navigate complex experiments and collaborate with cross-functional teams. These skills ensure efficient process optimization, compliance with regulatory standards, and successful development of biopharmaceutical products.

What is the difference between Associate Downstream Process Development Scientist vs Associate Upstream Process Development Scientist?

AspectAssociate Downstream Process Development ScientistAssociate Upstream Process Development Scientist
Primary FocusPurification and recovery of bioproductsCell culture and fermentation processes
Required SkillsProtein purification, chromatography, filtrationCell culture, bioreactor operation, media preparation
Work EnvironmentLaboratories, manufacturing facilitiesLaboratories, bioreactor labs
Common CertificationsBiotech or bioprocessing certificationsBiotech or bioprocessing certifications

Both roles are essential in biopharmaceutical development, focusing on different stages of the production process. The Associate Downstream Process Development Scientist specializes in purification techniques, while the Associate Upstream Process Development Scientist concentrates on cell growth and fermentation. Understanding these distinctions helps candidates target their skills and career paths effectively.

What are some typical challenges faced by an Associate Downstream Process Development Scientist, and how can they be addressed?

Associate Downstream Process Development Scientists often encounter challenges such as optimizing purification processes, troubleshooting equipment performance, and ensuring batch-to-batch consistency. These challenges can be addressed by maintaining meticulous documentation, collaborating closely with upstream and analytical teams, and staying current with best practices in chromatography and filtration. Proactively seeking feedback from experienced colleagues and participating in cross-functional meetings can also help in identifying solutions and improving process efficiency.
What cities in Connecticut are hiring for Associate Downstream Process Development Scientist jobs? Cities in Connecticut with the most Associate Downstream Process Development Scientist job openings:
Senior Scientist- Analytical Research and Development

Senior Scientist- Analytical Research and Development

Pfizer

Groton, CT

$93K - $156K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 26 days ago


Pfizer rating

8.3

Company rating: 8.3 out of 10

Based on 123 frontline employees who took The Breakroom Quiz

23rd of 74 rated pharmaceutical


Job description

What You Will Achieve

As a Senior Scientist, you will be at the center of our operations and you'll find that everything we do, every day, is in line with an unwavering commitment to quality. You will be recognized as a technical expert and a scientific contributor. With your deep knowledge of the discipline, you will be an active team member whose decisions impact the projects. You will perform qualitative and quantitative analyses of organic and inorganic compounds to determine chemical and physical properties during chemical syntheses, or drug product development process.

You will be using your scientific judgment to adapt standard methods and techniques by applying prior work experience. You will be forecasting and planning resource requirements for your project team. Your creativity in developing novel processes and new ideas will be used frequently. You will undertake mentoring activities to guide team members.

It is your innovative scientific temperament that will help in making Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It
  • This colleague will be responsible for developing analytical strategies in support of pharmaceutical drug substance and/or drug products during all development phases, including supporting manufacturing process development, developing, validating and transferring analytical methods, designing stability studies for shelf life assignments, and developing impurity control strategies.

  • Collaborates with colleagues and subject matter experts to assess the most appropriate analytical approach to support project activities, including use of computational predictive tools, modelling software and data visualization tools where appropriate.

  • Perform lab work and delegate responsibilities and review peer lab work as appropriate,

  • Through effective communication and collaboration with multidisciplinary team members, this colleague will have the opportunity to present data at team meetings and be actively involved in solving technical challenges that arise during development.

  • The candidate must be able to collaborate with and mentor peers as well as effectively interact with colleagues at all levels of the organization.

  • Author relevant sections of global regulatory submissions in support of new drug approvals. They will also prepare technical reports, critically review data, and may evaluate new instrumentation and analytical techniques/approaches.

  • Proficient with a wide variety of software and information systems and the curiosity to continue learning new techniques to solve complex analytical problems.

  • Proficient with a breadth of relevant methodologies such as, chromatography, dissolution, IR spectroscopy, mass spectrometry, particle size analysis and NMR, with expertise in one or more of these techniques.

QualificationsMust-Have
  • Ph.D. in Analytical Chemistry or related field, with 0 to 3 years of relevant industrial experience or MS in Analytical Chemistry or related field with 7 to 8 of years of experience.

  • Demonstrated ability to meet timelines with minimal supervision and experience leading multi-disciplinary teams.

  • Demonstrated ability to learn new techniques and solve complex analytical problems.

  • Demonstrated oral and written communication skills, including visualization of data and drafting reports.

  • Attention to detail, strong organizational skills, the ability to multitask, and effective interpersonal and communication skills.

  • Proficient with a breadth of relevant methodologies such as, chromatography, dissolution, IR/Raman spectroscopy, mass spectrometry, particle size analysis, and NMR, with expertise in one or more of these techniques.

Nice-to-Have
  • Experience in the pharmaceutical industry.

  • Prior experience with analysis of peptide therapeutics.

  • Experience with trace level impurity analysis

  • Understanding and prior experience in global regulatory submission processes.

  • Familiarity about separation technology including liquid chromatography, gas chromatography, SFC, etc.

  • Experience with a wide variety of software and information systems utilized in the pharmaceutical industry (eg LIMS, Chromatographic Software, Veeva, electronic notebooks).

  • The ability to use computational predictive tools, modelling software or data visualization tools.


PHYSICAL/MENTAL REQUIREMENTS

  • Ability to perform calculations and data analysis is required.

  • This role requires the use of laboratory equipment and working in laboratories. Some lifting may be required.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

  • Some travel may be required.

  • Relocation support available

  • Work Location Assignment:On Premise

The annual base salary for this position ranges from $93,600.00 to $156,000.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 12.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 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, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

Relocation assistance may be available based on business needs and/or eligibility.

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

Sunshine Act

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.

EEO & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.

Pfizer endeavors to makewww.pfizer.com/careersaccessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please emaildisabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available onPfizer Careers.

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About Pfizer

Sourced by ZipRecruiter

All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives. Our Health and Science System Specialists Team provides leadership across patient care settings in the complex Hospital, Health System, and Key Medical Group environment to bring value to our customers and patients in this dynamic ecosystem.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US

Year founded

1849