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Stark Pharma Solutions Inc

CIP C&Q Lead

Cary, NC · On-site

About the Company Stark Pharma Solutions Inc. is a global consulting and staffing partner ... CIP C&Q Lead Location: North Carolina Duration: Long Term Job Overview We are seeking an ...

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DrFirst Inc.

Director, Business Development, Pharma

Serve as the internal authority on pharma digital media budgets, competitor positioning, agency relationships, and buying cycles. * Gather and synthesize market intelligence to inform go-to-market ...

SCA Pharma

Validation Engineer

Windsor, CT · On-site

SCA Pharma is an FDA 503B outsourcing facility providing customized medications for hospitals and ... Ensure that C&Q and Validation project deliverables (i.e., Specification, SOPs; Protocols/Reports;

SCA Pharma

Validation Engineer

Windsor, CT · On-site

SCA Pharma is an FDA 503B outsourcing facility providing customized medications for hospitals and ... Ensure that C&Q and Validation project deliverables (i.e., Specification, SOPs; Protocols/Reports;

Rocket Pharma

NJ · On-site

Rocket Pharma is a fully integrated, late-stage biotechnology company advancing gene therapies with ... points, Q&A documents, and website content * Assist with quarterly earnings processes, investor ...

QRC Group, LLC

Sr Engineer

Juncos, PR · On-site

$102K - $140K/yr

Juncos, Puerto Rico We are seeking Sr Engineer with experience in Medical Devices or Pharma ... Develop C&Q plans, schedules, and resource forecasting. * Oversee and/or execute commissioning ...

QRC Group

Sr Engineer

Juncos, PR · On-site

$102K - $140K/yr

Juncos, Puerto Rico We are seeking Sr Engineer with experience in Medical Devices or Pharma ... Develop C&Q plans, schedules, and resource forecasting. * Oversee and/or execute commissioning ...

Compa Industries

Project Engineer 2

Los Alamos, NM · On-site

$60 - $65/hr

Ability to obtain DOE Q Clearance (preferred at time of hire) * Work Schedule: 4/10 preferred ... Previous experience in regulated environments (DOE, DoD, pharma, oil/gas) Education and Experience ...

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How much do q pharma jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for q pharma in the United States is $54.33, according to ZipRecruiter salary data. Most workers in this role earn between $50.48 and $63.70 per hour, depending on experience, location, and employer.

What is a Q Pharma?

A Q Pharma job typically refers to a position within the pharmaceutical industry that focuses on quality assurance, quality control, or regulatory compliance. Professionals in these roles ensure that pharmaceutical products meet industry standards, regulatory requirements, and safety guidelines. Responsibilities may include reviewing manufacturing processes, conducting audits, and maintaining documentation to comply with FDA and other regulatory bodies. These jobs are critical for maintaining product integrity and patient safety in the pharmaceutical sector.

What are the main responsibilities of someone working in a Q Pharma position?

In a Q Pharma role, your core responsibilities typically include monitoring product quality throughout the manufacturing process, conducting inspections and audits, maintaining meticulous documentation, and ensuring compliance with regulatory guidelines. You might also be involved in investigating quality issues, developing process improvements, and coordinating with production, R&D, and regulatory teams. The position often requires balancing multiple projects while supporting both routine operations and new product introductions. Success relies on close collaboration with cross-functional departments to ensure quality standards are consistently maintained.

What are the key skills and qualifications needed to thrive in the Q Pharma position, and why are they important?

To thrive in a Q Pharma role, candidates typically need a background in pharmaceutical sciences, quality assurance, or regulatory affairs, often supported by a relevant degree. Familiarity with industry-standard tools and systems such as GMP (Good Manufacturing Practices), LIMS (Laboratory Information Management Systems), and FDA or EMA regulatory standards is crucial. Strong attention to detail, analytical thinking, and excellent communication skills help professionals excel in this position. These competencies ensure pharmaceutical products meet strict quality standards and regulatory compliance, safeguarding consumer safety and organizational reputation.

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Q Pharma jobs near you
Infographic showing various Q Pharma job openings in the United States as of September 2026, with employment types broken down into 79% Full Time, and 21% Contract. Highlights an 89% In-person, and 11% Remote job distribution, with an average salary of $113,000 per year, or $54.3 per hour.

CIP C&Q Lead

Cary, NC • On-site

Stark Pharma Solutions Inc
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Job description

About the Company

Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.

Position: CIP C&Q Lead
Location: North Carolina
Duration: Long Term

Job Overview

We are seeking an experienced CIP C&Q Lead with strong experience in Clean-In-Place systems, commissioning, qualification, and cleaning cycle development within pharmaceutical or biotech environments.

Key Responsibilities

• Lead commissioning and qualification activities for CIP systems.
• Develop and optimize CIP cleaning cycles and critical parameters.
• Review P&IDs and engineering documentation.
• Develop URSs, quality risk assessments, and commissioning test plans.
• Develop and execute IOQ protocols and final summary reports.
• Coordinate automation functional testing and system verification.
• Support CIP systems from construction through completion of C&Q activities.
• Perform field activities including safety checks, LOTO, protocol execution, and issue resolution.
• Participate in FAT and SAT activities as required.
• Work closely with Engineering, Automation, Quality, and SME teams.
• Ensure systems meet project requirements, safety standards, and GMP expectations.
• Support the safe handling of caustic cleaning solutions.

Required Qualifications

• Strong experience in CIP commissioning and qualification.
• Hands-on experience with pharmaceutical or biotech CIP systems.
• Experience with cleaning cycle development and optimization.
• Experience reviewing P&IDs and engineering documentation.
• Experience developing URSs, risk assessments, test plans, and IOQ protocols.
• Experience with FAT, SAT, automation functional testing, and field execution.
• Knowledge of GMP requirements and regulated manufacturing environments.
• Experience with LOTO and field-based commissioning activities.
• Strong troubleshooting and problem-solving skills.
• Good communication and teamwork skills.

How to Apply

Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.

Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse backgrounds.