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High Q Pharmaceuticals Jobs (NOW HIRING)

Techengpr

CSV C&Q Technical Lead

Carolina, PR · On-site

$120 - $180/hr

... important pharmaceutical capital projects in Puerto Rico. This position is ideal for a senior ... Passionate about delivering compliant, high-quality validation documentation Why Join Technical ...

LEGACY MEDICATION MGMT SERVICE

Pharmacist

Gresham, OR · On-site

$61.75 - $74.25/hr

If you're a pharmacist who understands the importance of your role in patient outcomes and values compassionate, high-quality care, you may be an ideal fit for this opportunity within the Legacy ...

Legacy Health

Pharmacist

Gresham, OR · On-site

$82.40/hr

If you're a pharmacist who understands the importance of your role in patient outcomes and values compassionate, high-quality care, you may be an ideal fit for this opportunity within the Legacy ...

Legacy Health

Pharmacist

Gresham, OR · On-site

$82.40/hr

If you're a pharmacist who understands the importance of your role in patient outcomes and values compassionate, high-quality care, you may be an ideal fit for this opportunity within the Legacy ...

FITS LLC

C&Q Lead

Gurabo, PR · On-site

$98K - $130K/yr

If this sounds like you, and if you have a commitment to serving customers with high-quality ... providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch ...

PHARMACY RETAIL

Pharmacist - Retail

Gresham, OR · On-site

$61.75 - $74.25/hr

If you're a pharmacist who understands the importance of your role in patient outcomes and values compassionate, high-quality care, you may be an ideal fit for this opportunity within the Legacy ...

PHARMACY RETAIL

Requisition Pharmacist - Retail

Gresham, OR · On-site

$61.75 - $74.25/hr

If you're a pharmacist who understands the importance of your role in patient outcomes and values compassionate, high-quality care, you may be an ideal fit for this opportunity within the Legacy ...

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High Q Pharmaceuticals information

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How much do high q pharmaceuticals jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for high q pharmaceuticals in the United States is $23.21, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $26.44 per hour, depending on experience, location, and employer.

What is High Q Pharmaceuticals?

High Q Pharmaceuticals is a pharmaceutical company that focuses on the research, development, manufacturing, and distribution of medications and health-related products. Their aim is to improve patient outcomes by providing high-quality, effective, and safe pharmaceuticals. High Q Pharmaceuticals typically collaborates with healthcare professionals and regulatory bodies to ensure their products meet strict standards and contribute positively to public health.

What are some common challenges faced by professionals working at High Q Pharmaceuticals?

Professionals at pharmaceutical companies often navigate challenges such as strict regulatory requirements, tight project deadlines, and the need for precise documentation. Team members frequently collaborate across departments—including research, quality assurance, and regulatory affairs—to advance projects while ensuring compliance with industry standards. Adapting to evolving technologies and maintaining up-to-date knowledge of guidelines are essential for success. Despite these challenges, the work is rewarding as it directly contributes to developing medicines that improve patient lives.

What are the key skills and qualifications needed to thrive at High Q Pharmaceuticals?

To thrive at High Q Pharmaceuticals, you need a solid background in pharmaceutical sciences, regulatory compliance, and quality assurance, often supported by a relevant degree or certification. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practice (GMP) guidelines, and industry-standard analytical instruments is typically required. Strong attention to detail, problem-solving abilities, and effective teamwork skills help individuals excel in this environment. These competencies are crucial to ensuring product safety, regulatory adherence, and maintaining high-quality standards in pharmaceutical operations.

What is the difference between High Q Pharmaceuticals vs Pharmaceutical Sales Representative?

AspectHigh Q PharmaceuticalsPharmaceutical Sales Representative
Required CredentialsDegree in Pharmacy, Pharmacology, or related field; licensing may be requiredBachelor's degree in life sciences, marketing, or related field; sales experience preferred
Work EnvironmentPharmaceutical manufacturing facilities, laboratories, quality controlOffices, hospitals, healthcare facilities, client meetings
Employer & Industry UsagePharmaceutical manufacturing companies, biotech firmsPharmaceutical companies, medical device firms, healthcare providers

High Q Pharmaceuticals primarily focuses on manufacturing, quality control, and research within the pharmaceutical industry, requiring technical and scientific expertise. In contrast, Pharmaceutical Sales Representatives concentrate on promoting and selling pharmaceutical products to healthcare providers, emphasizing communication and sales skills. Both roles are integral to the pharmaceutical industry but differ significantly in responsibilities and work environment.

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What job categories do people searching High Q Pharmaceuticals jobs look for?

The top searched job categories for High Q Pharmaceuticals jobs are:

High Q Pharmaceuticals jobs near you
Infographic showing various High Q Pharmaceuticals job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 16% Part Time, 2% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $48,283 per year, or $23.2 per hour.

CSV C&Q Technical Lead

Techengpr

Carolina, PR • On-site

$120 - $180/hr

Other

Posted 22 days ago

Job description

Technical & Engineering Consulting LLC is seeking an experienced Automation / CSV C&Q Technical Lead to support one of the most important pharmaceutical capital projects in Puerto Rico.

This position is ideal for a senior Computer System Validation (CSV) professional who enjoys leading technical teams, defining validation strategies, collaborating with automation and commissioning teams, and ensuring regulatory compliance throughout the project lifecycle.

The selected consultant will serve as the primary CSV technical lead, supporting computerized systems and automation associated with manufacturing process equipment from design through commissioning, qualification, startup, and final handover.

What You'll Do

As the Automation / CSV C&Q Technical Lead, you will:

  • Lead the Computer System Validation (CSV) strategy for the project.
  • Define validation requirements and technical direction throughout the project lifecycle.
  • Partner with Process Engineering to ensure automation solutions meet business requirements.
  • Provide technical leadership during software development and testing activities.
  • Collaborate closely with Design Verification, CQV, Automation Engineering, Operations, Quality, and external vendors.
  • Develop and review:
    • Validation Plans
    • User Requirements
    • Functional Specifications
    • Design Specifications
    • Requirements Traceability Matrices (RTM)
    • Test Scripts
    • Validation Summary Reports
  • Lead execution of IQ, OQ, and PQ protocols for automation and computerized systems.
  • Support FAT and SAT activities.
  • Manage deviations, investigations, change controls, and validation documentation.
  • Develop CSV training plans and training matrices.
  • Monitor CSV milestones, schedules, and project deliverables.
  • Ensure compliance with GAMP 5, Data Integrity (ALCOA+), cGMP, and company quality procedures.
  • Support system turnover to Manufacturing and Operations.
Required Qualifications
  • Bachelor's Degree in Automation, Controls, Chemical Engineering, Electrical Engineering, Computer Science, or related discipline.
  • Significant experience in Computer System Validation (CSV) within pharmaceutical, biotechnology, or other FDA-regulated environments.
  • Experience leading CSV activities on capital projects.
  • Strong understanding of:
    • GAMP 5
    • 21 CFR Part 11
    • Data Integrity (ALCOA+)
    • cGMP requirements
  • Hands-on experience developing and executing:
    • IQ/OQ/PQ
    • Validation Plans
    • RTMs
    • Test Scripts
    • Validation Reports
  • Experience supporting automation platforms and computerized manufacturing systems.
  • Experience with technical change management and deviation management.
  • Excellent technical writing and documentation skills.
  • Strong communication and leadership abilities.
Preferred Qualifications

Experience with one or more of the following is highly desirable:

  • Large pharmaceutical capital projects
  • Automation Lead or CSV Technical Lead roles
  • Manufacturing Execution Systems (MES)
  • Batch reporting systems
  • Data Historians
  • Alarm Management
  • FAT/SAT execution
  • Lilly systems and quality procedures
  • Regulatory inspections and FDA audits
What We're Looking For

The ideal candidate is:

  • A technical leader who can influence cross-functional teams
  • Highly organized and detail-oriented
  • Comfortable working in a fast-paced capital project environment
  • Experienced coordinating with engineering firms, automation integrators, contractors, and quality organizations
  • Passionate about delivering compliant, high-quality validation documentation
Why Join Technical & Engineering Consulting?

At Technical & Engineering Consulting LLC, you'll have the opportunity to contribute to some of Puerto Rico's largest pharmaceutical manufacturing projects while working alongside industry-leading engineering and validation professionals.

We value technical excellence, integrity, collaboration, and long-term professional relationships.

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