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Pharmaceutical Formulation Remote Jobs in Colorado

Pharmaceutical Formulation Remote information

What are the key skills and qualifications needed to thrive as a Pharmaceutical Formulation Scientist in a remote role, and why are they important?

To thrive as a Pharmaceutical Formulation Scientist working remotely, you need a solid background in pharmaceutical sciences or chemistry, often supported by a relevant degree and industry experience in drug formulation. Familiarity with formulation software (such as Design of Experiments tools), data analysis programs, and regulatory documentation systems is typically required. Outstanding problem-solving, communication, and self-motivation skills set top candidates apart in a remote setting. These skills and qualifications are crucial for ensuring effective development, documentation, and cross-functional collaboration in pharmaceutical product creation, even when working off-site.

What is a Pharmaceutical Formulation Remote job?

A Pharmaceutical Formulation Remote job involves developing and optimizing drug formulations while working outside of a traditional laboratory or office setting, typically from home. Professionals in this role use scientific expertise to design, analyze, and improve the composition, stability, and delivery of pharmaceutical products. They often collaborate with cross-functional teams, document research findings, and ensure formulations meet regulatory requirements, all through digital communication and data analysis tools. This position is ideal for individuals seeking flexibility and who have experience in pharmaceutical sciences, chemistry, or related fields.

What are some typical challenges faced when working remotely in pharmaceutical formulation, and how can they be addressed?

One common challenge in remote pharmaceutical formulation roles is effective collaboration with laboratory and cross-functional teams, as much of the work depends on real-time data and physical sample evaluations. To address this, professionals often rely on robust digital communication tools, regular virtual meetings, and clear documentation to stay aligned with on-site colleagues. Maintaining organized records and proactively scheduling check-ins helps ensure timely feedback and project continuity. Additionally, remote workers should familiarize themselves with digital platforms for data sharing and project management to stay efficient and connected.

What is the difference between Pharmaceutical Formulation Remote vs Pharmaceutical Quality Control Remote?

AspectPharmaceutical Formulation RemotePharmaceutical Quality Control Remote
Primary FocusDeveloping and optimizing drug formulationsTesting and ensuring the quality of pharmaceutical products
Required SkillsFormulation science, lab techniques, regulatory knowledgeAnalytical testing, quality assurance, compliance standards
Work EnvironmentResearch labs, development teams, remote collaborationLaboratories, testing facilities, remote data analysis
Common CertificationsDegree in pharmacy, pharmaceutical sciences, or chemistryDegree in pharmacy, chemistry, or related field; certifications in quality assurance

Pharmaceutical Formulation Remote and Pharmaceutical Quality Control Remote roles both operate within the pharmaceutical industry but focus on different aspects. Formulation specialists develop new drug products, while quality control professionals ensure products meet safety and efficacy standards. Both roles often require similar educational backgrounds and can be performed remotely, but their daily tasks and objectives differ significantly.

What are the most commonly searched types of Pharmaceutical Formulation jobs in Colorado? The most popular types of Pharmaceutical Formulation jobs in Colorado are:
What are popular job titles related to Pharmaceutical Formulation Remote jobs in Colorado? For Pharmaceutical Formulation Remote jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Pharmaceutical Formulation Remote jobs in Colorado look for? The top searched job categories for Pharmaceutical Formulation Remote jobs in Colorado are:
What cities in Colorado are hiring for Pharmaceutical Formulation Remote jobs? Cities in Colorado with the most Pharmaceutical Formulation Remote job openings:

Senior Process Engineer- Small Molecule/ Oligo/ Peptide

CRB

Denver, CO โ€ข On-site, Remote

$103K - $165K/yr

Full-time

Posted 26 days ago


Job description

Company Description
CRB is a leading provider of sustainable engineering, architecture, construction and consulting solutions to the global life sciences and food and beverage industries. Our more than 1,100 employees provide best-in-class solutions that drive success and positive change for our clients, our people and our communities. CRB is a privately held company with a rich history of serving clients throughout the world, consistently striving for the highest standard of technical knowledge, creativity and execution.
Job Description
We are seeking a skilled and experienced Process Engineer III/ IV or V with deep expertise in small molecule manufacturing to join our engineering consulting team. This role combines technical leadership with strategic client engagement, supporting process design, scale-up, optimization, and regulatory compliance across a variety of pharmaceutical and chemical industry projects.
The Process Engineer III will lead the design and execution of process scopes-such as unit operations, systems, or facility areas-on small to medium-sized projects. You will manage scope, budget, and schedule, while maintaining clear communication with clients and internal teams. This role also includes mentoring junior staff, contributing to high-quality deliverables, and supporting capital project planning and regulatory alignment.
This position can be based near any CRB location, remote option will be considered
Key Responsibilities
  • Lead and support client projects focused on small molecule API process development, scale-up, and manufacturing optimization.
  • Conduct site assessments, gap analyses, and provide recommendations for process improvements and compliance.
  • Develop process flow diagrams (PFDs), piping and instrumentation diagrams (P&IDs), and mass/energy balances.
  • Translate client requirements into actionable design scope and document decisions, open issues, and action items.
  • Identify and escalate scope changes or design deviations to project leadership.
  • Collaborate with cross-functional teams including architecture, mechanical, electrical, and construction.
  • Prepare technical reports, proposals, and presentations for internal and client stakeholders.
  • Support capital project planning including feasibility studies, equipment selection, and facility design.
  • Ensure alignment with industry standards including cGMP, FDA, EMA, and ICH guidelines.
  • Participate in advanced project activities such as:
    • Technical bid tabulations
    • Vendor package management
    • Factory acceptance testing
    • Risk assessments (e.g., HAZOP, HACCP)
    • 3D model reviews and coordination
    • Sequence of operations and functional specification reviews
  • Mentor junior engineers and design staff.
  • Lead system design programming and planning with support from senior engineers.
  • Participate in cross-discipline squad checks and drive overall project quality.

Qualifications
Minimum Qualifications
  • Bachelor's or Master's degree in Chemical Engineering or a related discipline (ABET-accredited).
  • Minimum of 5 years of experience in small molecule process engineering, preferably in a consulting or client-facing role.
  • Strong understanding of chemical synthesis, purification, and formulation processes.
  • Experience in design firm or operating company settings within a related industry.
  • Strong written and verbal communication skills.
  • Intermediate experience with applicable industry and regulatory guidance and building codes.
  • Advanced technical knowledge and experience with small molecule API manufacturing equipment and utility systems, such as chemical reactors, filters, centrifuges, dryers, vacuum pumps, scrubbers, purified water, process compressed gases, and engineered heat transfer fluid systems.
  • Experience designing and implementing engineering controls for containment of highly potent APIs.
  • Experience with cGMP practices within regulated industries (FDA, EMA, JP, etc.).

Preferred Qualifications
  • EIT or PE certification.
  • Experience coordinating and managing design within project teams and with external partners.
  • Familiarity with commissioning, startup, qualification, and troubleshooting of process systems.
  • Experience with regulatory environments and validation documentation.
  • Prior experience in engineering consulting or client services.
  • Familiarity with process safety, risk assessments, and HAZOP studies.
  • Demonstrated experience leading a small team of process engineers on complex engineering design projects.

The pay range for a candidate selected for this position who is based in Denver is typically $103,125 to $165,000 annually. The base salary range represents the low and high end of the salary range for this position. The selected candidate's actual pay will be based on various factors, including but not limited to work location, qualifications, and relevant experience. In addition, CRB offers a total rewards package that includes comprehensive insurance coverage as well as the opportunity to participate in one or more annual incentive programs based on company and individual performance.
Additional Information
All your information will be kept confidential according to EEO guidelines.
CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity Employer and it is our policy to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Employment is contingent on background screening.
CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please, no phone calls or emails.
CRB offers a complete and competitive benefit package designed to meet individual and family needs.
If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.