QRC Group, Inc

Pharma

Scientist

$75–110k ~AI est. Carolina, Carolina, Puerto Rico CONTRACT
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for executive candidates.

The Brief

“Scientist at QRC Group, Inc. Skills: Manufacturing Science, Technical Services, Process Engineering. Provide technical oversight. Support manufacturing operations”

What You'll Achieve.

Ensure manufacturing processes are reliable; Ensure manufacturing processes are compliant; Ensure manufacturing processes are capable; Consistently deliver high-quality products

Industry & Context.

Pharma
Problems you'll solve

Issue resolution; Process improvements

Eligibility Requirements

Support 24/7 operations, Issue resolutions across time zones

What They're Looking For.

Must Have

Bachelor's in Chemistry, Bachelor's in Pharmacy, Bachelor's in Engineering, 5+ years spray dry experience, 5+ years solid dosage experience, 5+ years packaging experience, Working knowledge of cGMPs, Working knowledge of global regulatory guidance

Nice to Have

Demonstrates adaptability, Collaborative mindset, Positive attitude toward change, Fluent in Spanish

What You'll Do.

Provide technical oversight

Support manufacturing operations

Ensure processes are reliable

Ensure processes are compliant

Ensure processes are capable

Deliver high-quality products

Participate in resolution of technical issues

Author change controls

Manage internal relationships

Manage external relationships

Build relationships with development organizations

Build relationships with central technical organizations

Maintain processes in validated state

Maintain processes in qualified state

Justify state of process validation

Document state of process validation

Evaluate process capability

Maintain processes in compliance

Support ongoing manufacturing

Support technical transfer

Support validation activities

Work cross-functionally

Deliver on technical objectives

How You'll Work.

Team & Collaboration

Cross-functional teams; External partners; Site management; Development organizations; Central technical organizations; Diverse technical teams; Diverse business teams; Other functions

Communication Scope

Technical writing; Effective communication; Influence across teams

Process & Methodology

Project management, Coordinating projects, Executing projects

Full Job Description

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website http://www.qrcgroup.com / to learn more about our services and solutions! We are seeking a highly skilled Scientist in Technical Services / Manufacturing Science (DRY-EM TS/MS) to provide scientific and technical support for manufacturing operations. This role is responsible for ensuring manufacturing processes are reliable, compliant, and capable of consistently delivering high-quality products, particularly within spray drying and solid dosage manufacturing environments. The position requires strong collaboration with cross-functional teams and external partners to support process performance, resolve issues, and drive continuous improvement. Key Responsibilities * Provide technical oversight for spray dry, solid dosage manufacturing and packaging processes, leveraging a strong technical foundation and previous experience supporting these processes. * Participate in resolution of technical issues, including those related to control strategy and manufacturing. * Possess excellent technical writing capabilities, including authoring of deviations and change controls. * Employ excellent communication skills to manage internal and external relationships with external partners, site management, and cross-functional teams. * Build and maintain relationships with development and central technical organizations. * Ensure that manufacturing processes are compliant, capable, in control, and maintained in a validated or qualified state. * Understand, justify, and document the state of process validation with data that evaluates the capability of the manufacturing process to meet its stated purpose. * Maintain processes in a state of compliance with US and global regulations, including cGMPs and applicable global regulatory manufacturing guidance. * Support ongoing manufacturing at External Partne

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